Oct 12, 2016

Writing again

I am writing again.
In the past writing has brought me peace, helped me process my thoughts and feelings, but since my last surgery I've found it difficult and exhausting. I haven't written a single journal entry, blog post, or even a simple poem for four years. Then, I started reading my old blog posts. I felt the strength of my thoughts, the pain in my words and the anxieties that come with chronic health problems, which made me sad. I also found many happy memories, joyous moments captured in time, and positive support from readers. With all that in mind, I decided even though sometimes it hurts to face life head on, sometimes feeling the hurt is the only way to move into the light and feel the joy. So, after not writing for a very long time, I picked up my journal and wrote. It felt good. I felt calmer after putting my joys and sorrows on the page, it felt like talking to an old friend. Now, I have decided to start writing my blog again. After reading comments left by a few readers saying my words helped or inspired them, I realized that's what I want right? To tell my story, process my feelings, and maybe end up making someone else feel better with my words.

I'm not going to try to update the past four years, but my oh my how things change. Don't get excited, my health is still poor and life is still hard most days...but L (my son) has grown into an amazing young man, we moved into a great house in the same town as my family and I haven't had a surgery since 2012! We have added an extremely sweet, extremely affectionate little rescue dog, named Piper, to our family. Overall, the past few years have been pretty good. I've added a few diagnoses, I've had to accept the fact that I won't be having the second baby we've always wanted and some major dramas have occurred, but as usual we found a way through it as a family.

Today, I will leave you with a happy story...
When L turned 10 years old the only thing he wanted for his birthday was to adopt a dog. We already had a pooch, Gordon, but he was very attached to me and L wanted a dog to bond with him in the same way. So, we started looking. L found a little, reddish brown, twenty-five pound, eight month old girl that was in an animal foster home. We made a deal that L would care for her, clean up after her and take her through the 4H dog obedience program. (I know what you're thinking, but let me finish.) The day this little, fury baby came home we discovered she had been returned to the foster group twice, she didn't really know her name or the word "no", and she wasn't properly housebroken. All of that aside, she was moody, hungry, and had a habit of hiding toys instead of playing with them. The first night L scooped her up to take her to bed with him, she lay down on top the blanket with her back to him and growled when he tried to snuggle. L was patient, kind and consistent with this little red dog he named after a Phish song. He cleaned up her messes, fed her, played with her, lover her, and with a little help, quickly housebroke her. Over time Piper became the most affectionate, sweet, gentle dog I have ever had in my life. She began sleeping under the covers, as close to Logan as she could get, then she discovered room on his pillows for her sweet face. The next spring L and Piper joined 4H. He learned how to be a good dog owner, how to train her in basic obedience and she learned to be good, polite, sociable pooch, she learned to focus on L's words and body language. The two of them completed three years of the 4H program, three obedience competitions, and two years of another competition called Rally.
There are many days Piper's love and affection bring light to my world. This little dog with a huge personality, with so much love to give. Most would say we rescued her, but really, she was just always meant to be with us. She lays next to me as I type, comfortable and secure between my legs and the back of the couch, her breathing slow and steady, this amazing dog that was returned twice so we could bring her home forever.

Aug 6, 2012

My little scholar


Logan is getting ready to start fourth grade. He will be ten years old in November, he is thin but tall for his age, he is extraordinarily smart and can interact with any adult, but he is still an extremely silly nine year old boy.

This past school year he was placed the 'high ability' program. This meant being in a mixed third/fourth grade REACH classroom following a fourth grade curriculum, with fourth grade field trips, standards, and specials. We were asked to teach him multiplication/division prior to the first day of third grade and there was some differentiation in reading, math, and spelling. Logan made straight A's, tested very well, and rarely had any homework, all while he was sick three months of the last school year. Late in the school year they announced that the high ability program was being revised. They are switching from a 'classroom model' to a 'cluster model'. The incoming fifth/sixth graders will still be in a 'classroom model' mixed class for one more year, but the incoming third/fourth graders will move to the 'cluster model' and be grouped in classrooms with their age group peers. The problem with this is the fourth graders are basicly repeat the same fourth grade curriculum, with a few changes in materials and a few additional enrichment projects. For many of the students this will be fine, probably a good idea to review concepts they had difficulty with last year, but for Logan this far from appropriate. I am not one of those parents that just thinks my child is the best - Logan really, truly is amazingly smart. The Asst. Principle of Logan's school put it this way, "Logan is like having a special education student on the other end of the spectrum." We are currently in the process of having him assessed for giftedness in hopes it will help us to know how to meet his needs emotionally and academically.

I have spoken with the school a few times now, but there is no clear plan for a kid like Logan. No way to guarantee he will be challenged and stimulated in a classroom that is following the same standards/curriculum as last year. Our options are limited now that school starts in a week and we don't have the personal funds for private schools. At this time we are planning on enrolling him in one of the state's two public virtual schools for fourth grade, with hopes of returning to 'brick & mortar" school next year. I worry about whether or not we are making the right decision for Logan's future. I wish I could look into the future and see that our choices are going to give him all he needs to grow and learn. We cannot be afraid of trying new things - who knows, this may turn out to be the perfect learning situation for Logan and if its not, we can always go back to the local, traditional public school.

If you have any ideas, tips, or recommendations please leave me a comment or send me an email. I hope you're having a great day! Go outside, enjoy the sunshine, and all the beauty around in your life. I'll post again soon.


Jul 30, 2012

Life lessons


I've been thinking a lot about Logan's upcoming birthday . . . ten years old. First of all, I cannot believe my little man is almost ten years old already! Then, I started asking myself if I have taught him all the things he needs to know by this point in his life? He knows all the basics that any ten year old should know: brush your teeth at least twice a day, tie your shoes when they come untied, eat well, do your homework, respect others, and try to make good choices. I know he is a very intelligent boy and he will be an amazing adult, but as his momma there is more I want to teach him. . .

Treat others as you would like to be treated - this includes living beings,
Always save some of your income - you never know when a storm is coming,
Read daily,
Laugh big,
Pet and play with your dog every single day,
Live well,
Take time to appreciate your life - moments big and small,
See the beauty in your surroundings,
This family will always have your back and love you no matter what,
Work hard, then play hard,
Don't ever be afraid of a challenge,
Don't ever be afraid to fail,
Treat yourself,
Treat your family with love, respect, and kindness,
Be positive,
Love with all you have,
Respect yourself and take care of your body - you're the only you we have,
And never, ever forget your momma loves you more than words can say

I would also like for him to learn Spanish and a musical instrument, but that is a slightly different kind of lesson than the list above. I'm sure there is more, but that is off the top of my head.

I know Logan can do amazing things in life, especially with the right guidance - I just hope we are giving him the best start he could have. This is something I think about daily, but in the end all I can do is hope we're making the best choices for his future.
I know I write a lot about my motherhood anxieties, but this is my "full time job". That's all for today. As always, I hope you're having a wonderful day and take the time to see the good in your life.

Jul 27, 2012

2012



If I had to sum up this year so far in one word it would be: challenging. . .
Logan was sick off and on from October to January, then consistently from January to April. He missed almost three months of school before it was over, was very sick, and had me sick with worry. After a trip to Riley Hospital and many painful days, Logan's colon started functioning again, he regained his strength and went back to school! He was able to maintain straight A's on his report cards and score 100% on Indiana's I-READ3 mandated test. In March the principal called and asked that I bring him in for testing, then he could come home as soon as he was done. . . Logan still scored in the 'pass plus' range for both math and language on the third grade I-STEP testing. Thankfully, he is doing well now. He returned to school full time the first week of April and is now off all meds. The silver lining to this big, black cloud is that he was scanned to look for Chiari Malformation and it was NEGATIVE!!

Around the same time my neck started having pain, clicking, and cracking.  My local doctors feel surgery is needed do to problems with my cranial cervical fusion.  My next post will have more details, but surgery number five is being scheduled soon.

There have been several other bumps in the road this year, but these are the two biggies.   A few good things have happened too. . . My sister-in-law married a great man, Logan/Caleb/mother-in-law/father-in-law and I  went to Chicago for spring break, and Caleb/I celebrated our tenth anniversary.

I will try to be a good blogger and post more frequently;)  Between trying to keep up with Logan, enjoy summer, organize my messy house, and spend some time with family it has been a busy summer.  Oh, and there is the matter of the little surgery I'm trying to schedule. 

As usual, I hope you are doing well and taking the time to enjoy the little things in life! 


Jul 10, 2012

Really real


In the past two months my neck/base of my skull have been awful.  I woke up one morning, rolled over in bed, and my neck started clicking, popping, shifting, cracking, and feeling like someone kicked it.  I called my primary care physician for an xray order to see if any hardware was broken.  Then, we contacted my local orthopedic surgeon and after a CAT scan my fears were confirmed - I need a revision on my cranial cervical fusion.  We tried injections with nerve blocks and steroids with no positive effects.  I restarted physical therapy/cranial-sacral therapy, but this is beyond the help of all these modalities.  Evidently my NY surgeons left the two titanium fusion rods two levels longer than the vertebrae they secured the rods to with screws.  Now, six years later, the bottom of the rods are to close to my C-6/C-7 restricting motion, rubbing the vertebrae, and bone is trying to form between vertebrae and the rods - in other words, the clicking and popping noises in my neck are metal and bone hitting each other.  To top that off, my left C-1 screw is protruding out the back of my vertebrae into "vessels".  This seems to be causing odd shifting sensations, "creeky" hinge noises, cracking, pain, and squirty/bubbly sounds along the occipital ridge/base of my skull.

In the past few days I've realized my life is about to get really real - again.  People walk through life everyday without real problems, true stresses, or issues that will truly effect their life long term.  So many of us create the majority of our stress and anxieties by making poor choices, over reacting, being negative, or treating others badly.  Sometimes its hard for me to have sympathy for people when they could easily alter there behavior and fix the problem... some of us aren't so lucky.  It is hard to describe what it feels like before major surgery when you've already had several and know you'll have more in the future.  The anticipation of the upcoming procedure mixed with the memories of painful past experiences leaves me anxious, stressed, and thinking about how long I can ignore the whole thing!  I'm in the process of deciding who will do the surgery and where they will do it… Do I need to go back to NY?  Did my NY doctors make a mistake when they installed my cranial cervical fusion hardware in 2006?  Is any of my "residual pain" actually do to poor screw placement or rod length?  Can my amazing, local orthopedic surgeon do the surgery here in IN safely?  Should I get another opinion from another Chiari specialist?  If so, who - an Indy doc, the renowned specialist in CO, or a doc in Chicago well known for his Chiari work?
Its just gotten so complicated.  Three doctors agree, so far, that this is necessary surgery. They also agree it will not be an easy procedure for me.  My surgeon will have to remove the left C-1 screw and right C-5 screw, plus shorten my two titanium rods by two vertebral levels.  All of which is lies snuggly under layers of muscle, scar tissue, arthritis and a solid fusion. . . Did I mention I also have a large area of cerebral spinal built up at the base of my skull?  And that my connective tissue disorder makes healing more difficult?  Like I said, its gotten very complicated.
The more I talk about it or think about it the more real it seems.  I'm scared. I'm sad because this may rule out any chance of a baby.  I guess all I can do today is focus on the current task and worry about tomorrow, tomorrow.  This surgery is inevitable, but I'm not in a hurry.  My family and doctors seem to disagree, so we'll see how long they let me get away with ignoring the situation and concentrating on Logan/I having a great summer!
I'll update once I have more information- I'm waiting to hear back from my NY surgeons after they view my latest CAT scans.  Any prayers or good thoughts you can send my way would be appreciated.  Thank you and I hope you're having a good day! 


Feb 7, 2012

Has it really been this long?



Well, it seems my blogging runs in cycles with my pain and stress level. It occurred to me this morning that I haven't posted in a while. . . more like four months!!! I'm going to play a little game of catch up, so that you can understand why I have been so neglectful.

1. My last post was about my dear, sweet Ava and her first birthday. I am VERY excited to announce Ava's mommy/daddy are pregnant and due in July! Please, send the Bryan family lots of good thoughts, love, and prayers.

2. In early October I started having some rather annoying pain in my low back/abdomen. I went to my doctor, who ordered some tests and they found hemoragic cysts on my left ovary - note the cysts were on my left side, but the pain is on the right. The right sided pain was chalked up to free floating fluid from the cysts, and I was treated for ovarian cysts. A few weeks later the exact same pain, on my right side, in the exact same place was back and it was worse than ever. I went back in for a abdominal CT scan and this time there was a kidney stone on the right, and my right lung was infiltrated with pneumonia. Well, this explains the right sided back/abdominal pain. In December I was re-scanned and the kidney stone hadn't moved, but my lung was clear. Since then I have been having a lot of pain and spasming with this kidney stone. I have seen a urologist, but she isn't convinced the primary cause of the pain is my kidney stone. She believes there is a problem in my colon/intestines and it is causing inflammation which is then effecting my kidney and the small stone inside. I am scheduled to see a gastroenterologist later this month - I've been to many over the years, so I'm not sure what they're going to do, but it probably will involve some sort of scope and won't be any fun. I know I have gastroparesis due to vagus nerve damage, which is why I am not always able to digest food, but we will see what this new doc has to say.

3. Logan played his first season of basketball. We live in Indiana and around here kid's basketball programs start as young as 4 yrs. old. My husband/I have tried to expose Logan to several sports and at some point he will choose the what he likes to play. Out of all the sports we've tried - football, soccer, t-ball, swimming - basketball seems to come easiest to him. Now if I could just figure out how to make him more aggressive/competitive on the court he'd be good little baller. Logan really enjoyed the season, he learned a little about the sport, made some new friends, and had a great time. . . even though his team was 2-12.

4. The holidays were rather uneventful. No big fights at family get togethers, no major drama - just good family time, a few laughs, and Logan was spoiled rotten. As usual I sent out photocards and made some goodies to give away. A few of my crafts took longer that expected, but most of it worked out in the end.

5. My gorgeous little man, Logan, has been sick for weeks now. It all started in November when he was put on anti-biotics to treat bronchitis and it constipated him almost immediately. By Christmas we thought he was back on track. Three weeks ago I got a call from the school to come pick up Logan because he wasn't feeling well. He was home one day and then we sent him back. Later that day I brought him home early again, we end up finding out he has strep throat and he goes back on anti-biotics. After ten days, he is no better and had the strep rash upgrading him from strep to scarlet fever, so we start him on a stronger anti-biotic. Now this whole time Logan does not have a fever, is complaining of headache/abdominal pain, and his tonsils/lymph nodes are swollen, but he doesn't complain about his throat. Five days into the stronger anti-biotic he doesn't seem to be getting better, so I take him in for a mono test and abdominal x-ray. The mono test is negative, but the x-ray shows severe constipation and his entire large intestine is impacted. He is automatically put on a laxative and stool softener. Three days later, this past Wednesday,he spiked a fever, so he had an abdominal CT scan to make sure the appendix isn't inflamed and look for infection - luckily, it came back clean. So, Thursday he was put on a "super-laxative" and we were told he would be cleaned out within 48 hours. It is now Tuesday of the following week, Logan is still miserable with belly pain and he has had maybe four good sized bowel movements, but he's no where near cleaned out. Each morning he is waking up in pain, I find him moaning in fetal position begging me not to make him move. Its so much easier being the patient. He missed twelve days of school, and this is his second day back. I feel horrible forcing him to go to school when he is so uncomfortable, but we are doing all we can to get him feeling good again. Logan is going to a pediatric gastro next week - I just pray we can get some answers and help.

6. My sister-in-law, Emily, got married! Logan was the ring barer, Caleb walked their momma down the isle and I got to take LOTS if pictures. We all had lots of fun, Emily was beautiful, and I'm no longer the only "in-law" in the family!

I think that covers the basics. I will post more details later, and try to keep you all updated on Logan's belly. The past few weeks and months have been hard for me, but I'll try to keep posting regularly. I'm trying to stay positive, look at the bright side, and just keeping moving.


Oct 20, 2011

Purple is her color.


If you have read many of my posts you probably remember my some written about my angel, Baby Ava. She came into this world to teach us all a little something about life, but she was not meant to stay with us for long. Ava Jean Bryan would have turned one this coming Tuesday. We all miss her, love her, and would do anything for her to be with us - but that just wasn't His plan. As this milestone comes closer I have seen Ava's momma, Angie, find the strength to settle into her new life. Don't be mistaken, she will never move on, get over it, or be without that pain, but she is starting to settle into what life will be without Ava. I'm sure some of you have lost someone close to you and there are always moments when you stop to think, "I wish they were here," to feel this joy, see this beauty, or be part of a life changing moment. . . I can only imagine that she feels that everyday. Even in moments of pure joy, somewhere in her heart Angie will be thinking, "I wish Ava was here."
I was with Angie last night while she was working on a baby book for Ava. It was a beautiful, handmade scrapbook one of her crafty friends made as babyshower gift, so all she had to do was put in the pictures and captions. Angie made the comment that this was perfect for her because most traditional baby books have pages for writing things like babies first tooth, baby's first word, favorite food, and so on. I had never even thought of that. There are so many little things that people take for granted . . . how many of you have a baby book that you never even took the time to write in? I was reminded in that moment we all have something in life that is really hard, we all have something that consumes us at some point, but it is up to us to find a way to make it through. Angie is so strong and amazing, she is finding a way to live her life in the shadows of a deep loss and profound sadness. She is finding a way to move forward through all the pain, sadness, anger, and tears.
Ava helped me to remember that even on my darkest days, in my most painful moments, when I think I just can't do this anymore - there is always someone in more pain, more misery, and worse health. I wish my life were different and some days it is hard to accept that I will be in pain every second of the rest of my life, but I'm here with an amazing family and good friends. I may not be living in my dream house, drive a fancy car, or go on lavish vacations, but I don't need those things to have a full life and be happy.
Ava fought over two months to stay strong, beating the odds time after time. Angie's hope, love, and devotion never fading for a second. The two of them have a bond stronger than most mothers/babies. They made a deal in one of their many late night talks - Angie understood she had to go, she understood she was meant to change lives and she did, so now Angie would have to carry on her message. As hard as it has been, I know Ava is proud of her mommy - Angie has started an annual Baby Ava Legwarmer, toys, and clothes drive to benefit the children at Riley Hospital for Children, and has plans to start a Baby Ava Charity. I continue to feel connected to Ava, just before Mother's Day after thinking of her all day I felt a very strong need to dye Angie a purple scarf. Purple was Ava's color, and I know she wanted me her mommy to have a beautiful, purple scarf for Mother's Day.
It is so easy to get caught up in our own lives - we may not talk to the people that mean the most to us as often as we should, we may not make time for the simple moments like just spending time with a good friend or taking advantage of the little time we have with you children. Life is hard enough, take the time to celebrate the good in your life, take the time to enjoy your life! Whether you realize it or not, every life is a gift not a given. . . Ava taught me that.

Oct 6, 2011

The sun will come out tomorow.


I know I promised more detailed posts on our August adventures, but first I there are a few things that have been on my mind . . .

1. I'm thirty-three years old and I will be in pain everyday for the rest of my life. I will wake up in pain, move through the pain (when possible), and then go to sleep with my pain. Each morning the first thought that registers in my mind is, "ouch". I am SO tired of being in pain and having to find a way to live as normal a life as possible - I want to have fun with my family/friends, I want to work to contribute more to my family, I want to ride roller coasters and horses, I want a break from this pain, I want to be better. I don't sleep well, due to pain and nerve/brain damage I never reach REM sleep which is the deepest, most restful stage of sleep. I'm just getting tired. I know it seems like I am so positive and appreciative about my life, but even I have my moments when it all seems hopeless and impossible.

2. Monday morning Logan woke up to the sound of me puking up my undigested dinner from the night before. It was early, and I didn't think he was awake so I used his bathroom since my husband was in our shower. He was awake, he did hear me, and it makes me so sad. . . Logan is aware that most mommas do not have brain surgery, come home multiple times with several staples holding surgical wounds closed, or puke undigested food from dinner the night before. He knows when I'm hurting more than usual, he knows when I can't eat because I'm nauseated, he has seen me in the hospital connected to all the tubes and wires - all of these things make my heart hurt. This is not the life I wanted for my son. . . I think most all I want him to not have to see his momma sick anymore.

3. There is a stigma with being a chronically ill, legally disabled, pain patient. (Now, you need to know I am no longer on any of the really "good" pain meds and I no longer see doctors that are at pain clinics or specialize in pain treatment - some would not classify as a pain patient anymore. I do not like pain medications, or any medication for that matter.) Sometimes when I'm at family gatherings politics may come up and in the past comments have been made about whether or not US citizens should have to "pay for other people's lives". There have been many instances of similar conversations, but I think you get the idea. My point is that I worked as long as I physically could - when I got sick I had been to school, built a business, gotten married, built a home, and started a family. I did EVERYTHING I was supposed to and my life literally fell apart when I got really sick. I didn't do anything to cause my disorders, but I have been treated like a lower class citizen by several people because I don't have a job, or I am on medicare. When our lives fell apart and a lot of our remaining income went to medical care/treatment it was my doctors that encouraged us to apply for Social Security Disability. (By the way, we were twenty-four and twenty-five years old with a one year old baby.) I don't think we had a choice, and I don't feel bad about taking it, even though some out there probably think I should. I guess what you should get out of this is that you don't know what you would do when your life disappears and your future is forever changed. You don't know what its like until you are staring in the face - I've always felt like heart surgery, cancer, brain surgery, and anything lifelong or terminal are kind of like exclusive clubs . . . you just can't know what is really going on inside until you join one. Try to remember, this is not an equal opportunity world, and some of us got the shit end of the deal.

4. When you see me, please do not assume I am healthy or feeling good because I am pretty and wear a smile on my face. One of my doctors, the horrible one that left me without my pain patch cold turkey, once said, "you just LOOK so healthy, its hard for my staff to understand." I will never forget that statement. If nurses in a neurological office thought I was too healthy for the level of treatment I was receiving, then what were people that didn't have my chart and a medical background thinking? I look this way because my body stopped digesting food properly and I have to maintain some level of physical therapy to strengthen my muscles so my degenerating joints/discs have more support. Not to mention that gaining weight is not an option, according to my many doctors it would triggeran array pain, back, and joint issues. So, I am truly sorry if I "look healthy and happy", but I choose not to let the whole world see me vulnerable and in pain. . . even though that is who I truly am.

Well, sorry for being such a Debbie downer, but sometimes this is how I feel, sometimes it is just too hard, and I'm trying to be honest about my life. Don't worry about me, I'll get up, do my physical therapy, and put on a happy face. The alternative is to lay here, feel the pain and nausea, feel sorry for myself and stay miserable while life passes me byand I just can't let that happen! Have a good day, and thank you for reading my venting - I'll try to be a little more upbeat next post!

Oct 3, 2011

Where do I begin . . .



Well, where do I start? I know its been a few months since I've posted, sorry for that, but my pain level went up and my days got busy. I guess I'll start with early August and catch you up . . .

August 4 - I had an appointment with my orthopedic surgeon to look my T-8 area of my spine and the pain radiating from it. I had a full body work up last December, so we knew something was wrong with my T-8 vertebrae and at some point it would need to be addressed. Over a few months I had been having pain around my thoracic spine and that's when I knew it was time. Dr. Joseph Riina is an amazing surgeon with OrthoIndy, an amazing group of docs/therapists/facilities, and he did my 2009 lumbar fusion/discectomy to treat my spinal fracture/herniated disc. When I went to see him in August I could tell there was something wrong just by looking at the films. (You would think after all my MRIs, x-rays, and CT scans I would be good at recognizing a problem - this is only the case when there is something blatantly wrong.) Thanks to the combination of my cranio-cervical fusion and my lumbar fusion I have acquired a seventeen degree curve in my thoracic spine. But the good news didn't stop there . . . my T-8/T-9 vertebra are degenerated significantly causing pain, instability, and early onset arthritis. The bright side: I don't need surgery at this time, my nerves are not being compressed yet, and I can still treat with physical therapy, ice, TENS unit, meditation, yoga and massage. I have found most doctors like and encourage my treatment program, and since I don't like taking meds this works well for me at this time. I must admit since Logan has gone back to school my eating has not been as frequent or healthy as it should be, but that is one of many things that I need to change.

August 5 - Caleb, Logan, and I went to meet Dr. Torres-Martinez at the Riley Hospital for Children Genetics Clinic. After a very thorough physical exam, long family history review, and a brief exam of my EDS it was decided Logan was at very low risk of having my genetic disorders . . . he didn't even order an MRI! Logan is having a heart ECHO tomorrow to check on a "muffle" heard from his heart, and he is to see an opthamologist one more time - but, the big news is NO EDS, NO tethered cord, and most importantly he is NOT considered at risk for Chiari! I could have kissed this wonderful man telling me my son is healthy, and I should not be concerned. Dr. Torres-Martinez also told us that any child I have will have a 50% chance of inheriting the Elhers-Danlos Syndrome gene, which has not been identified so there is no genetic test for it at this time. This wouldn't be good, but I'm not sure it would be a serious enough reason to not have another child? Luckily, Chiari malformation is MUCH lower at around 12% chance of passing on my disorder according to my neuro-specialists in New York and the doctors at Riley Hospital for Children. My surgeons have told me before they do not feel families should refrain from having children due to Chiari, unless it would put the mother's health at risk.

I am SO thankful Logan will not have to deal with my medical disorders!!! I have thanked God everyday of Logan's life for his health, happiness, kindness, and intelligence - I'm not a religious person, but I do believe there is some sort of energy out there, bigger than all of us and I call it God, or the "the big E" as a dear friend once said. I believe things do happen for a reason and I believe something good can come out of most situations no matter how horrible it feels in the moment. Maybe, I am sick to help others learn how to see the light even on the darkest days, or so my son can be healthy and amazing. Maybe, I am here to learn patience, focus, or how to endure hardship and not forget my blessings. I'll never really know, but I do believe we all have a purpose and we are all have something to offer this crazy world.

August 6 - Caleb, Logan, and I head to Clifty Falls State Park in Madison, Indiana. We had a great time on the trails and just spending time together. I'll have to give this its own post later.

August 10 - I turned 33!! I LOVE my birthday, this year I spent my actual birthday on the lake with my dad, uncle, and Logan. That weekend we had a small party at our buddy's house, and then a boat afternoon/BBQ with all the Beems.

August 16 - Logan started 3rd grade! For the first time I made it through day one without crying, but day two there were a few tears. Between school and football I have barely seen Logan since early August! Logan is in the GT classroom, gifted and talented, which is made up of half third graders and half fourth graders. We really like his teacher, we'll call her Mrs. W for blogging purposes, and he likes his classmates - seems to be much less frustrating for him than being in a classroom where everyone is asking him questions constantly or just do things that Logan finds to be ridiculous. I found out recently that Mrs. W has had some of her own experiences with medical world that give her a unique understanding of our family and Logan's life outside the classroom. I hate to hear about anyone having medical problems, but it is very comforting to meet someone that has a true understanding of what my life is really like.

Logan also started tackle football! His team is the Jaguars, they've only won two games, but those boys have SO much fun. I'll post about our junior football adventures later, but had to mention it for my August update.

The end of August brought a family trip to Florida for my cousin Bob's beach wedding.
I'll have to write a whole other post for this because it was a BIG, fun week!

Well, this has been a very long winded post, so I'm going to say goodbye for now and I promise to post regularly again. Unfortunately, the past few months my pain level has been very high and I just haven't felt like doing or thinking anything beyond what is necessary. Now that life is settling down, and hopefully my pain level will go back to a 3 on the daily pain scale so I can continue writing. I'm not sure if any of you really enjoy reading about my life, but this helps me to get out some of my thoughts/stress so thank you for taking the time to read my blog.

As usual, I hope you are having a wonderful day. Oh, I discovered Pinterest.com recently thanks to one of my best friends . . . if you haven't seen it or want to check out my boards go to: http://pinterest.com/beem78/ .

Jul 22, 2011

Gordon the fish.


My dog, Gordon, is three years old and has always loved the water. He loves to boat, swim, play on the beach - he's a water dog at heart. Gordon is basenji/chihuahua mix, only ways eighteen pounds, is very agile, very fast and very smart. When we adopted him we thought he was a white german shepherd/basenji mix, which would have made him at least fifty pounds, but he's turned out to be perfect. We found him at a local Humane Society, fell in love with him right away, plus it felt good to teach Logan to adopt a puppy versus buy a puppy!
This week Gordon has been quite entertaining during our lake adventures. . . He has been obsessed with swimming with Logan, so whatever Logan is doing, Gordon is doing. He is running down the dock jumping in, he's eating the spray off the waterguns, he's having snack breaks with Logan, he's fetching the ball - I should say at this point that this warms my heart, watching my boy and his dog having a great summer together. I usually float on a raft, talk to my dad/uncle, throw the ball with Logan/Gordon, and judge Logan's many jumps off the dock. Gordon uses my raft as a 'home base' - he jumps off the dock, swims to me, climbs up onto the raft, and hangs out until he's ready to jump in and swim again. He is a very busy dog at the lake, he LOVES it and its impossible to keep him out of the water. One day last week he had been swimming for a few hours when he climbed onto my raft, rested for a minute, then I hear, "Hey mom, Gordon's peeing on your raft!" Yes, I said peeing on my raft! I was off the raft by the time Logan finished his sentence, and so was a very startled pooch. We swam over to the dock, got him out, and let him finish relieving himself up on the seawall. I was shocked! I've been boating all me life and I've never seen a dog pee off dry land. A few days ago, we were swimming off the dock again and Gordon was stoked as usual - first, he was jumping from the dock to the toon floating the boat lift and fell between the toon and a metal bar, didn't even stop his little legs from running, I don't think he even noticed. Then, an hour later I was relaxing on my raft when I look up and see Gordon peeing off my raft into the lake! This time it wasn't landing on my raft so I didn't dump him, but seriously have you ever heard of that? I guess he just didn't have time to head to dry land.
This dog is becoming a fish. Gordon is the first one in to swim, he wants to ride the tube with the kids, and he loves a good boat ride! I love my little pooch and his love for Logan and the water. Gordon got very sick a few days after we brought him home, with treatment and time he made a full recovery. The vet told us the rescue group that was scheduled to take him would not have had the funds to treat him, so I've always felt that this little pooch was meant to be with our family.
Gordon does lots of funny, entertaining things, but he has become quite a showoff at the lake! You've never seen a happier dog than our little Gordon.

Jul 21, 2011

Pretty pink fingers and pretty pink toes:)



For the past few weeks I haven't posted much, I just haven't had much to say. I've never been an anxious person - if you know me, you know I can be stubborn and opinionated, but not anxious. Recently however anxiety has crept in, and I don't like it.

Here I am, just trying to have a great summer, but when its time to go to sleep after a long fun day my mind starts to go a little crazy with anxious thoughts. . . What should I have gotten done that day? Am I doing my best to be a good mom to Logan? Am I doing my best to be a good daughter/wife/friend? Will I ever feel better? Will I feel good enough to get up in the morning? How many days do I have with Logan before he goes back to school? I'm sure most moms have run away thoughts, especially at night, but I'm thirty-two and have really only felt anxiety about three things: my health/surgeries, Logan growing up way too fast, and having another baby. So, when this started recently I was surprised. My dad has been a worrier ever since I can remember, I know he lies awake at night turning things over in his head, but are nightly anxieties hereditary? All I know is I don't like it! I've always had a hard time sleeping, but thats due to neurological damage not a wandering mind.

I'll let you know how the anxiety goes - I don't expect it to lighten up until after we get through a few doctor appointments, and Logan is back in school. August 4 I am scheduled to see my orthopedic surgeon to talk about a pain I'm having at my T-8 (my eighth thoracic vertebrae). Last December an MRI showed a slight bulge at that level, and now I'm having pain. So, I'm hoping he's just going to tell me to go to physical therapy and use ice/heat, but this may cause a problem with us trying to get pregnant again. Of course, right when I feel like I can get off my meds and start trying soon, something will go wrong with my health. Let's hope/pray its nothing major and won't effect our plans.

Then, August 5 Logan is scheduled to go to the Riley Children's Hospital Genetics Clinic. I received a letter/paperwork from them, and apparently they do some testing the day of the appointment. I am dreading the testing - Logan has been lucky enough to have never needed bloodwork or anything requiring a needle outside of childhood vaccinations. I'm sure there will be blood drawn, a skin biopsy, and who knows what else. There will be another appointment to discuss the results, any diagnosis, and what to do with that information - including further family planning.

For now I'm trying to do things that make me happy - spending as much time as possible with Logan, hanging out on the lake with my family, loving on my hubby, eating yummy food, reading a good book, watching a little reality TV, and enjoying sweet treats! Oh, I can't forget - my pink fingers and toes! I wasn't a "girly-girl" until after Logan was born, but ever since he came along I've loved pink. My mom would tell you I hated wearing anything pink as a little girl, or as a big girl for that matter, but as a momma I love pink. So, as simple as it sounds, having pretty pink fingers and pretty pink toes just makes me smile. Recently I went to a bridal shower for my cousin's fiance - each party goer was given a little hemp purse filled with things to keep your nails looking good at the beach! The wedding is in Florida this September and now all of us girls will have pretty, bright fingers and toes. Each of us were given super bright, fun nail polish and I LOVE my color! I've never worn neon colors on my nails, but I discovered its a nice way to brighten my day.

What are the little things that bring you happiness? Is it eating a piece of chocolate, hugging your kids, kissing your husband? All those little moments strung together can make a very happy life filled with simple pleasures, laughter, and true joy.

Jul 13, 2011

The luckiest girl in the world.



The past few weeks I have focused on Logan, my husband, my family and having a good summer. I would say so far I have had a great summer, there have been a few moments of stress, but overall life has been very good. (This is where I knock on wood, cross my fingers, and say a little prayer for this to continue.)

I don't ever forget how lucky I am to be surrounded by my family, floating in a lake, drinking a hard lemonade, any day I feel like getting myself out of the house. The best part is my family feels lucky to have me around too!

Fourth of July weekend we celebrated my cousin's thirtieth birthday, my mom's fifty-ninth birthday, my nephew's first birthday and our ninth anniversary - I know, its a BIG weekend in our family. Technically our anniversary and two of the birthdays are on June 29, but we usually celebrate the Saturday before the Fourth. We were also thrilled to be able to talk about my cousin's upcoming wedding, to a woman we love, this September in Florida. This was a busy, but great weekend! At one point my son counted twenty-four people floating off the dock, hanging out on boats, and enjoying the day together. How lucky are we to have so many people coming together to celebrate each other and our lives together!?

Most days this summer Logan and I have gone to the lake and spent the afternoon with my dad and uncle. There have been varied guests - my soon-to-be brother-in-law, a childhood friend and her family, Logan's buddies, Logan's teacher, and many of my parent's friends, but the main cast rarely changes. I love my family, I love the way I was raised, I love the relationship Logan has with my family, I love that my parents tell me they love me everyday of my life - I feel so blessed.

There will be many more days on the lake this summer, and this fall we will all come together in Florida and celebrate the love my cousin shares with his fiance. Its been a long time since we had a big family adventure in Florida, and this one may be the best one yet! A beach side, barefoot wedding, Logan is a ring barer, and I can't wait to part of their day. My husband and I were married under a white archway, lakeside on the lake I've grown up on, leaving by boat with my cousin at the wheel and honestly, the beach is the only other place we would've had our ceremony. So, I am thrilled my cousin chose the beach, and not surprised at all. . . we were raised together and have similar ideas on how to enjoy life. I love him like a brother, Logan calls him Uncle, and we've always been able to count on each other. He was the only one I ever asked how he felt about my husband shortly before we got engaged, what he thought mattered to me, and we had a very honest conversation - I was happy to hear he good things to say.

I hope you all have family in your life, people that have known and loved you longer than anyone else. I am blessed with a son, husband, parents, cousins, aunt and uncle that has been with me every step of the way - we've had our problems, we've had our disagreements, but in the end we always come back together, usually stronger than before. I am lucky - my family loves my unconditionally and they have proved it time and time again.

When I think of the best memories, the best moments in my life, my family is part of almost all of them. Birthdays, vacations, holidays, or just simple moments in time that stay with you always. . . spending time together almost everyday growing up, training our dogs together in 4H, years of tubing/boating/riding waverunners, two weeks in Yellowstone, Christmas vacations in the sun, many beach trips - watching my uncle walk Logan into the Gulf of Mexico for the very first time, and countless hours just floating, talking and being together in the lake. I really do feel like one of the luckiest girls in the world!

Well, I'm going to go call my dad and tell him I love him, maybe you should do the same!

Jun 24, 2011

The day of my first surgery . . .


I have been hesitant to tell you the story of the day I had brain surgery. . . it is a day I will never forget, but would if I could. This isn't the average surgery, its BRAIN surgery! Mine became complicated by a one in a million arterial anomaly, and quickly turned into a nine hour surgery instead of a six hour surgery. If you're a fellow zipperhead you probably have similar memories that haunt you occasionally, if you are a chiari patient pre-surgery you may not want to read this post, and if you have a "normal" brain you may find this story useless - I guess I don't really know what people will think.

Nov 17, 2004

5:00 am: It is cold and dark outside our run down, Long Island motel. I stood in the shower staring at the cobalt blue tiles covering the walls, the hot water filling the room with steam. I ran my hand down the back of my neck - it is still whole and unchanged by a surgeon's scalpel. After a long time, I left my steamy cocoon and came out into a shabby motel room where my husband and mother are waiting. I sit down on the bed and when I see myself in the mirror, for a moment, it is like looking at someone else. The mirror covered walls make it easy to see what they are doing behind me as I sit wishing time would just stop - I do not want to do this.

5:45am: We leave the security of our little motel room, and walk out into the crisp, winter air to climb in the cab. I am even more nauseous than normal, but I just keep moving.

6:00am: Caleb and I arrive in the pre-surgery registration/waiting room - this is a tiny room considering the number of surgeries performed in this huge hospital each day. We sit together, waiting for the nurse to call my name so I can change into my hospital gown and socks. Once I'm changed, and all my information is double checked, the nurse lets Caleb sit with me until my ride comes. It isn't long before Dr. Remy, one of my surgeons assistants, walks in to tell me he's ready. As we walk to the gurney I get a huge wave of fear and begin telling them, "I've changed my mind, I just want to go home . . . please don't make me do this!" Poor Caleb, he has no choice but to kiss me, tell me he loves me, and help me on the gurney. As Dr. Remy wheels me away I'm overwhelmed and begin to cry, he said, "If you weren't scared I'd be concerned - this is normal and I promise we will take very good care of you."

7:00am: I am in the operating room, doctors are attaching electrodes, someone is placing IVs in three locations, and thankfully, a nurse gives me a shot that finally makes me feel at ease. A few minutes later my anesthesiologist asks, "What music would you like to hear as you take a nap?" First, I ask for anything with Jerry Garcia, which he does not have, and my second choice is Frank Sinatra and this he has. I hear a little bit of Come Fly With Me and then I drift off to a warm, deep sleep.

At this point, I am obviously unaware of anything so, this part of the story is based on what I have been told since this day. . . After kissing me, telling me he loves me and that everything would be okay, my husband walks down the hall to the tiny, overheated room marked Surgery Waiting Room. My mother is there waiting, along with a room full of other patient's concerned family members. The surgery is supposed to take six hours, so might as well get comfortable. From what I've been told, it is overcrowded, hot, and there is one very loud family sobbing over their relative having an appendectomy. At some point they would go to eat, stretch their legs, but ultimately they would wait for nine hours to see one of my surgeons. Evidently I have a "one in a million" arterial anomaly running right through the path tmy surgeons were going to cut into my brain. Thankfully, with the use of doplar technology (which no other surgeons in the world use) they saw this anomaly, found another way to my brain malformation and literally saved my life. This is one of the rare fatal complications that are seen in this particular brain surgery.

4:00pm: At this point one of my surgeons, Dr. Paolo Bolognese, comes out to speak to my husband and mother about my surgery and complication. He tells them I am doing well, and my primary surgeon, Dr. Thomas Milhorat, will be out to speak with them as soon as he finishes closing me up. Dr. Milhorat will show them a sketch of my anomaly, tell them the surgery went as well as could be expected with a complication of that sort, and they could see me soon.

Some time that afternoon/evening: Everything is very foggy, it is hard to focus, I can hear voices, and feel severe pain. "Jennifer, you're in the recovery room. You're okay, just relax." I slip back into a hazy sleep, and pain retreats momentarily. Slowly, I become more aware of my surroundings, pain, and body. . . I can hear two, unfamiliar voices directly next to my bed, they are talking about my vitals and one of them says they are going watch me for a while. I can feel someone watching me, but when I open my eyes I cannot see her. I can see the white tile ceiling of the recovery unit, I see the tops of the curtains on each side of me, and then, my nurse's face. "Hello, how are you? How is your pain?"
Oh shit, I am in more pain than I have ever felt in my life! Damn, why did I do this? I can't focus from the pain, the sleepiness, and there is no way I can speak. "ahhh. ouhhh." My nurse responded by saying, "Do you need something for the pain? You can have something for muscle spams soon too." All I can get out was, "yes." She then shoots something into my IV, my insides get a flash of warm, and I relax a little.
Next time I wake up, I realize I'm laying on my back, and I really want to move. My head is being propped up by a metal, v-shaped wedge lined with foam, but it feels like my brain is trying to rip through the back of my skull. So, I tried to roll on my left side - this did not go well at all. The nurse standing at the foot of my bed watching me quickly stopped me and insisted on rolling me herself. As she rolls me the my left, I puke up the fluid in my stomach, feel extreme pain run through my head, and my neck spasms all at once. She gets me situated on my left side, with my knees slightly bent, and uncomfortable pump cuffs on my lower legs to prevent blood clots. Now, I can see the three or four beds between me and the unit door, I see the nurse updating my chart then observing me from the end of my bed, and I continue to drift in and out of consciousness.
Finally, I hear two familiar voices - my husband and my mom, the two people I wanted to see more than anyone in the world. As I open my eyes, I see Caleb's face . . . he looks tired, but relieved. All I can manage to say is, "it hurts, it hurts, it really hurts." He takes my hand in his, holds it tightly and says, "Dr. Milhorat said it went better than could be expected, and they could see your spinal fluid flowing again with the naked eye. You did it! It went well. I love you. We only have ten minutes now, but we'll be back at visiting hours." A minute later, he lets my mom up close to hold my hand. She kisses me gently, strokes my hand with hers, and tells me, "You're going to be okay. The surgery went well, and you're doing well. I love you, punkin." My mom very gently, strokes the little strip of hair the doctors left along my forehead, and kisses the back of my hand. Then, it is time for them to go until visiting hours in a little later. With help from the nurse, and a break to puke, I turn to my right side, push the button she gives me for my pain pump and fall back into a haze of pain and meds.
The rest of the night goes this way - in and out of consciousness, trying to communicate, and pushing my pain pump button as much as possible. At some point I noticed the recovery room- it was one big rectangular shaped room, patients lining the walls, and a long nurse's station running down the middle. There are so many patients in this room, I can't see everyone so I can't tell you how many. Some patients are sitting up talking, obviously here for an outpatient procedure, and some are moaning and unable to move, like me. About midnight I am moved to a room on the neurological floor, my vitals are checked again, and I am left alone in my dark, quiet room.

Well, that is the story of how I spent my son's second birthday. For some reason I thought that day would be hazy, or at least fade over time, but the memories from that day are quite vivid. Honestly, I've always been happy I wasn't the one in the waiting room.

Jun 23, 2011

Baby love


Logan and I are babysitting my nephew today. He is almost one year old, and very cute. We are really enjoying our time with him, and he adores his big cousin Logan.

There is something I have to get off my chest . . . as much as I love my sweet, little nephew, it is sometimes hard for me to be around him. I have always wanted at least two babies, and would have loved more, but so far that has not happened. I have wanted a second baby since Logan was three, but instead I've had surgeries. Seems like every time we think we're going to be medically cleared to try for a baby, something happens with my health and it is delayed. The last delay was my spinal fraction/disc herniation found in Sept. 2009, the same month my sister-n-law got pregnant.

I am very happy for people that are blessed with happy, healthy babies - it is just hard for me at times knowing that may never happen for me again. Logan has been a wonderful, amazing blessing in our lives, and I am beyond thankful for him - I just don't feel like our family is complete, I feel a strong need to me a mommy to another soul.

I still have hope, I still pray everyday. Hoping our family will be blessed once more, and feel complete. I've always wanted to be a mom, I babysat, taught swim lessons for years, life guarded at the local pool, and have always loved kids in general. So, I'll keep hoping, but for today I'll give lots of love to my handsome, little nephew.

Jun 22, 2011

Ten Things Tuesday: Authors Logan and I like to read

It may sound strange to include my eight year old son's favorite authors in the same group as mine, but it in Logan's case it isn't. The end of the year testing for second grade showed his reading level as MUCH higher than his grade level, and frankly, he reads as well as me. Also, I wasn't what you would call a 'reader' before Logan. . . I read to him nightly from birth, but by the time he was four we were reading books like The Chronicles of Narnia. So, for these two reasons, my ten things Tuesday list of authors will include authors I enjoy, authors Logan loves, and authors we have read together.
These are in no particular order:

1. J.K. Rowling - Harry Potter series. Logan and I read this series together over a year when he was seven. We fell in love with the world she created and these books are what finally gave me a love for reading! Child, teen, or adult, this series of books is amazing! PS. Don't judge the boooks by the movies, they're much better.

2. Rick Riordan - Percy Jackson series, Kane Chronicles series, and Lost Hero. This is one of Logan's favorite authors! He read all the Percy Jackson series last summer over two weeks, and it was hard to get him to put them down.

3. Chris Cleave - Little Bee and Incendiary. These are intense stories, but well written and beautiful. When I bought Little Bee I had no idea what to expect, and although it wasn't a light, easy read, it is a really good one. I am looking forward to reading the next book from this author.

4. Emily Giffin - Something Borrowed, Something Blue, Baby Proof, Love the One Your With, Heart of the Matter. This is one of my favorite 'chick lit' authors. When I'm looking for an easy, entertaining read this is the perfect author.

5. C.S. Lewis - The Chronicles of Narnia, series and several other titles. I have not read any of his work beyond Narnia, but these books are amazing! Logan and I read them for one of our bedtime stories when he was four and it sparked a love for reading in him. This is also a series my husband read as a child.

6. Stephanie Meyer - Twilight Series and The Host. This is a stay-at-home mother that had a dream about vampires and wolves, wrote it down, and ended up having four best-selling books published. All of her books are wonderful! The way she writes makes it hard to put down, but the books are eight-hundred pages so I had to put it down more than I liked. Again, please don't judge these books by their movies - the books are MUCH better.

7. Dalai Lama - he has authored many books, but the one I would like to mention is How to Practice: The Way to a Meaningful Life. This is an awesome book, touching on Buddhism, and focusing on just being a good person, appreciating life, living in the moment, etc. I think everyone should read this book.

8. Cornelia Funke - Dragon Rider, Inkheart, Inkspell, Inkdeath, Reckless, and several others. This author is thought of as an author for young adults, but the magical worlds she creates are entertaining to any age. Her stories carry you away on adventures to a place where books come to life, and children have the power to save the day. Right now Logan is reading Dragon Rider and loves her style of writing. This is another good author for fun, entertaining bedtime stories.

9. Carl Hiaasen - Skinny Dip, Strip Tease, Lucky You, Tourist Season, and several more titles written for adults in the satirical mystery genre. He also writes youth mysteries - Hoot, Scat, and Flush. All his books take place in Florida or off the coast, and really make you feel like you're right there with the characters.

10. Christopher Paolini - The Inheritance series. This is the series of books Logan and I are currently reading together. We are reading Eragon now, and it is a very good read. . . this author weaves a detailed world that draws you in and makes you want to root for the lead character. So far we have really enjoyed the story!

Well, that's my list! There are other authors we enjoy, but these are our favorites. If you haven't read some of these authors you should find them next time you head to the library. If you have any great author recommendations for Logan or myself please leave a comment or email. . . I am looking for a good summer read now and Logan is looking for a good book every other week!

Jun 20, 2011

Bee Free

Well, so much for my goal of posting everyday. The past few days have been busy, but that's not why I haven't posted. . . it has been raining here for the last four days, so my head pressure has been higher than usual and my head pain has been worse. I've used every extra minute to relax my neck, lay down on my left side and give my head a chance to feel better - unfortunately its hard to type a blog laying in fetal position on the couch.

Its getting late, but I want to tell you about a great little bakery with gluten free goodies. Logan Street Bakery, in Noblesville, IN sells goodies made by Bee Free Bakery - gluten free baked treats that actually taste like treats! The owner/founder is a friend of mine and the mother of a boy with Asperger Syndrome which is on the Autism spectrum. Several years ago she found eating gluten free profoundly changed his ability to focus, and seemed to make processing stimulation easier. The big problem was finding food that tasted good, and was gluten free. . . after trying many brands and products she decided to start making her own treats. With family tested/approved recipes she started her own bakery making gluten free cookies, cakes, pizza dough, other yummy items, and her own Bee Free flour mix so you can bake at home. Her products are sold at Logan Street Bakery, Green B.E.A.N. delivery and several other locations in the Indianapolis area, which can be found on the website: www.beefreegf.com.

Over the past year I have been dealing with painful, swollen joints - one of the things that can be helpful is eating an "anti-inflammatory diet". This means lots of veggies, lots of fruit, limited fats, limited processed foods, and limited gluten. I was surprised to find a low gluten diet would benefit me too. So, before you think you would have no need for this special little bakery, maybe you should try the yummy the treats or see how eating less gluten could benefit you!

Jun 16, 2011

A day in the sun


Today was one of those almost perfect days - one that I hope to have many more of this summer. Logan and I were lazy most of the morning, playing cards and watching cartoons. After lunch we met one of my closest friends, Angie, and headed to my dad's for an afternoon on the lake. The weather was not too hot, but warm enough to swim and play in the water. We loaded the cooler, put on our sunscreen and stopped by my uncle's dock to pick him up. Then, we took a nice cruise to show Angie part of the lake, and beached the boat on a small island for Logan and Gordon to play.

I think I've mentioned my dad and uncle were stay-at-home dads, so we have spent a lot of time together my entire life. Now they are both mostly retired and I love being able to spend time with them on a regular basis - its no secret I'm a daddy's girl and my uncle has always been like a second dad. We have a lot of fun together, Logan loves spending time with both of them, and we have made so many amazing memories over the years. I cannot imagine what life will be without the three of them to laugh with, swim with, or just hanging out in the summer sun and be silly. We're kindred spirits, my dad, my son, my uncle, my cousin, and me - we love our summers, we love our lake, we love our time together.

My life is hard. . . it is filled with pain, nausea, vomiting, joint pain year round, but in the heat of the sun I feel a little better. In the summer I feel a little less miserable, and I feel blessed to be able to take advantage of that time with some of the people that mean the most to me in life. I've always said that I have plenty of reasons to be thankful - these people, these memories, these almost perfect days top that list.

Jun 15, 2011

Have you seen my shoe?

Okay, confession time - I have been making beautiful scarves, and several people have wanted to wear or buy them. I want to start an ETSY page, sell them in a boutique somewhere, or start dyeing dresses, but with my health I worry that it will all fall apart again.

I feel like I'm constantly waiting for the other shoe to drop. Throughout my youth I had many medical problems, and several symptoms including pain, but I still worked, played, and was very active. It was after I had started building a massage business, gotten married, and had a one year old that my symptoms became so severe I needed brain surgery. I had a wonderful husband, beautiful son, a home of our own, a blossoming business, and our friends/families around us all the time. . . literally everything I had ever wanted. Obviously having lots of money, or a house on the lake would have been nice, but I had everything I REALLY wanted. I was a massage therapist working with chronic pain patients, I know it's ironic, I scheduled sessions around my family and was able to stay home with Logan when my husband worked. We had just built a house in a town close to our families and Logan had just turned one...then, it all stopped. My pain level skyrocketed, my stomach stopped digesting food, and all my other symptoms went crazy.

Most mother's spend their child's second birthday celebrating, I spent Logan's having brain surgery in NY. (I'll tell you the story of that day in tomorrow's post.) My recovery was long, and hard. I wasn't allowed to be alone with Logan for three months, no diaper changes, no holding him - just snuggles, no bathing him, and it definitely took its toll on my heart. No riding in a car for three months, unless it was for an doctor's appointment, and then everything was extremely limited for three more months after that. I felt pretty good for several months, then my symptoms flared again. Eighteen months after my first surgery I was back in NY for number two, a cranio-cervical fusion. A similar story between surgery number two and three - sixteen months between my fusion and spinal cord detether/discectomy. I made it a whole two years and one month between my third and fourth major surgeries. So far it has been nineteen months since my lumbar fusion/discectomy in December 2009, and there are no surgeries on the horizon. . . At this point I'm knocking on wood, and keeping my fingers crossed.

Unfortunately, it seems like every time I get into a good routine, or start to move forward with my life my symptoms flare, and it all stops again. I'm afraid when I start to really put my heart into this idea, the other shoe will drop and I'll be stuck feeling miserable with scarf orders to fill and a family that needs me. I want this - I have dreamed of turning my creativity into a way to help support my family. Massage therapy is never going to be an option for me again, and working in a conventional setting is difficult when you don't know what days you'll be puking, or in severe pain. There is a reason I've been legally disabled since May 2004, and none of my doctors expect my situation to change - ever. So, this plan makes sense to me. . . I can sit on the couch to tie the scarves, and the dyeing can be done when I am physically able. It sounds like a good plan, but so did my massage therapy business. I'm scared, frustrated, and unsure what to do next.

As usual, I am trying to stay optimistic. I have been able to stay off twenty-four narcotic coverage for three months, and have had reasonable pain control so far.. . my pain level on a scale of one to ten is never a zero, but on a good day is between a one and three. There haven't been any hospital visits due to pain yet, so I'd say it is going well. I use physical therapy, ice, TENS unit, Theracane, meditation, yoga, and meds to keep my symptoms from being out of control, but nothing makes me feel free of pain. What do you do when all you want is a "normal" life, but your body won't allow it? How do you plan the next day, let alone a new business? I don't know what to do, think, or feel. I just want to be able to move forward and not worry that tomorrow I'll be in so much pain I can't even think straight. This is my life, I'm accepting that, but I don't want to feel trapped by my disorders - unable to do anything outside of caring for myself and waiting for the next flare up. (Big sigh.)

So, now that you know my little secret and I've allowed a little time to wallow in self-pity, it is time to stop whining and focus. Its time to decide how to move forward from here and what is the best path - do I proceed with Threads To Dye For, or just make scarves as gifts and for fun? What will benefit my family most, what will make me happy long term? These are the questions I have to ask myself, these are the questions I have been asking myself. . . I think I know the answers, but a little extra thought won't hurt. Hopefully you'll keep reading my blog to see what happens next!

Please, feel free to email me anytime with questions, concerns, or opinions at Zipperhead1978@gmail.com. Obviously I'm not shy about my medical situation, so don't hesitate to ask anything related to any of my disorders or surgeries. Knowledge is key, and over the years I've gained a lot of it when it comes to my medical issues.

Jun 14, 2011

Ten Things Tuesday

Recently I have been reading several other blogs on a regular basis. One of the regular posts I always enjoy is 'Ten Things Tuesday', so I decided to give it a try myself. I hope you enjoy. . .

This is my very first Ten Things Tuesday list so, instead of picking one topic to write about, I'm going to tell you ten things you may or may not know about me.
1. Some of my favorite things are: chocolate, snuggling with my son to watch a movie, my pooch, potatoes, diet coke, green tea, my lake, my family, swimming in the summer sun, my friends, being crafty, tie dyeing, live music, yummy food, reading a good book, camping, hiking trails, and laughing as much as possible.
2. Our pooch, Gordon, is a BIG part of our family life. After our German Shepherd died, I found Gordon at a local Humane Society. He was just a puppy, the last of his litter, and was scheduled to go to a rescue group the very afternoon I adopted him. A little, white pup with tan spots on his right shoulder, and ear - he was adorable. I was just six weeks post-op from spinal cord detether/discectomy, so my uncle drove Logan and I to get Gordon. Of course we all fell in love with him at first sight, and he has been spoiled rotten from that moment on. You will see him in my posts, he travels with us a lot, boats with us always, and is generally in the middle of whatever we're doing. He has been an amazing addition to our family, and I encourage everyone to adopt or rescue a dog instead of buying one from a pet store or breeder.
3. I love to watch cartoons with Logan! I love all the Marvel movies - Ironman, Hulk, X-men, all of them. We spend more time than we should watching cartoons and movies, but it is something for us to enjoy together even on my worst days. I don't think it has be harmful to him, but it isn't something that I think is good for him either. Right now we are watching the Avatar series, its a great if you haven't seen it, and we both really like this time we spend together being lazy on the couch.
4. About a year ago a friend talked me into reading the Twilight series. . . I had said I would never read this series of books, but once I started the first one I was hooked! Some of my other favorite books are: Harry Potter series, books by Emily Giffin, Meditation as Medicine, The Host. If you have any recommendations please let me know - I'm always looking for a good read, especially in the summer.
5. All the artwork in our house is either framed Logan art, or framed concert posters. When my husband and I travel it is often to see live music, generally Phish. We have started a collection of signed, numbered concert artwork and love displaying it in our home. I also love showing off Logan's artistic ability by framing his artwork - I'm getting ready to frame his second grade artwork and using it to decorate our bedroom. I also am working on a wall of black and white photos of our grandparents and great-grandparents. I am trying to surround myself with things that have meaning in my life and let go of the rest.
6. Good music is something that brings a smile to my face. I enjoy most types of music, and honestly feel that music makes the soundtrack to our lives . . . how many memories of yours are connected to a song, or album. My childhood was accompanied by the Beach Boys, Neil Diamond, Buddy Holly, and many of the 'golden oldies'. During my early teen years I listened to Elvis, Bon Jovi, Snoop Dog, Counting Crows, Led Zeppelin, Bob Marley . . . until I found the Grateful Dead. At that point I found a whole new world of music: Jerry Garcia, Miles Davie, Davis Grisman, The Band, CCR, Buddy Guy, Clapton, and so many other artists the list could go on forever. Now that I'm all grown up I still enjoy a lot of the same music, but have added Jack Johnson, Talking Heads, Phish, Adele, Nora Jones, Jonny Cash. After my first Phish show I was hooked! The music, the light show, the energy of the crowd, and the people watching. Now we try to see them a couple times a year and we listen to great music everyday - Logan loves music, and he has grown up listening to all types: blues, jazz, jam, classical, oldies, rock. Music makes up the soundtrack to our lives - what does yours sound like?
7. I'm a pretty crafty girl. I like to scrapbook, photography, make mosaics, sew, tie dye, or anything else that sounds fun to create. I've made blankets for many of my friends babies, each one designed special for each baby, and for a dinosaur blanket for Logan. I love to design something and then create it! My most recent creations have been hand dyeing scarves - they are tie dyed technically, but not with lots of colors, just different shades of one color. It has been so much fun to draw a design for a scarf and then actually have it in my hands hours later! We will see what happens with my scarves - I'm in the process of starting an ETSY page, but need have a wholesale source, and a business name first. I'm thinking, Threads To Dye For. What do you think?
8. I don't know about you, but I've turned into a bit of a reality TV junky. The Real Housewives shows and the Kardashian's array of shows are my favorites. I'm the first to admit it is mindless, pointless TV, but sometimes that's exactly what I need.
9. I would probably be classified as 'all natural'. . . I don't wear makeup, trendy clothes, or high heel shoes. Don't get me wrong - I think other woman look good in all of those things, its just not for me. I like to be comfortable, and wear things that make me feel good, whats "in" doesn't really concern me. I'm not saying I'm a 'natural beauty' or anything, but I am comfortable in my own skin.
10. This blog has gone from a little way for me to write down a few of my thoughts and feelings, to something that I look forward to writing. I'm trying to write everyday, and I hope you enjoy what I have to say. Those of you that know me know that I am extremely extroverted and would talk to just about anyone about anything. So, I am going to set the goal of writing a post everyday, and hopefully you all won't get bored by what I have to say!

Well, that's it. My very first Ten on Tuesday blog! Hope you enjoyed finding our a little more about me. . . Next week I'll try to be a little less self-absorbed and find a topic that isn't based solely on myself;)
Have a great day, and, as usual, I hope you can find a reason to smile!

Jun 13, 2011

Why the big secret?


Before Logan was born I was a nanny for four beautiful boys. I took care of them for about two and half years. . . my first day the boys were 6wks, 18mos, 3yrs, and 4yrs old. Caleb and I were married on this family's property - four acres sitting on the lake where I have boated my entire life, it was an outside wedding under a big white tent, overlooking my lake. We had a dance floor, a good DJ, yummy food, and most of the people we love. It was the perfect ending when we left by boat, my uncle's Baja, with tail pipes set to rumble and "just married" sign on the back. Much of that day was a gift from this wonderful family. My last day I was having contractions all day, twenty minutes apart and Logan was born two days later. I thought my experiences with my boys and their parents had prepared me completely for being a mother of a new baby, and had given me a preview into day to day married life. . . it makes me laugh to think I truly believed that once upon a time.
Our nine year anniversary is the end of this month. Wow, we were so young when we got married - twenty-two and twenty-three at the time. Its funny how the view changes, I vividly remember during that time thinking the exact opposite - "We're not too young to get married. We're adults, supporting ourselves in this world and we're ready." In the spirit of totally honesty - we had been together for three years and we were given the miraculous surprise of Logan. I had been told I would not be able to have children, so he has been and always will be the biggest blessing of our lives. We had decided we were going to be married, Logan just upped the time frame.
People tell you marriage is hard, "it takes work". And they're right it does, but most things worth having take work. . . No one is perfect, and no one can be calm, cool, and collected all the time so, there are disagreements, and yes there are moments you may not like each other, but at the end of the day this is your partner in life. I love my husband - I love him for being my friend, lover, biggest fan, and for always wanting only the best for me and our son. He was twenty four when I had my brain surgery, and he was supportive, kind, and strong. Not all twenty four year olds could handle something like that, with a two year old and work also depending on him. He would never admit that he did anything special, but to me he has always been my strength and my protector. I believe that all this has made us stronger, I hope I'm right;)
About a month after Logan was born I started to wonder why no mother ever talks about this time. . . the time period when being a mother is much harder than you ever dreamed. No sleep, feedings every two hours (yes, I breastfed Logan until he was 1yr), the baby cries - but you don't know why, and the world just keeps on moving without you for the first time in your life. You only know what I'm talking about if you've had a baby, there is no other way to understand that first three months.
So, what's the big secret? Why not just be honest? Why not tell every mother out there that the first three months is REALLY hard? I remember feeling like I must not be doing something right, because sometimes he would just cry and I couldn't figure out how to help him. No one told me that sometimes- especially in the beginning when the baby is recovering from birth - babies cry just because! It doesn't make you a bad mother if your baby doesn't come out of the womb eating, sleeping, and cooing "like a baby." Even with my time as a nanny for an infant, and three young boys I didn't know what was coming my way. I loved those first months- the new sounds, smells, and feelings of being a new family, watching the person you created seeing the world for the first time, or just holding him for hours dreaming of our lives together. However, those first weeks were sleep deprived, emotional, isolated, and difficult. . . I felt lonely, frustrated, and tired.
I was dumbfounded as to why no one had ever talked about this part of early parenthood, why all the secrecy? I actually asked the mom of the boys I cared for and she said she didn't really know why mothers don't share these experiences openly, but everything I was going through was "normal". There was one baby book she gave me explaining why babies cry, how to identify different cries, and what to do about them. Then, it tells you sometimes they cry because they were in a warm, soft, quiet place before we plunged them into this bright, loud, cold world and they're not very happy to be here. This book was enlightening!
I think most mommies want to appear to be perfect, beautiful, and under control at all times . . . if you have a child you know that is an unattainable goal! So, we should all be honest with each other - stop trying to appear perfect for the world and start sharing all your little secrets: Logan cried a lot as a newborn, ate every other hour, and was NOT a good sleeper; Caleb and I fight sometimes, we get on each others nerves, and at times he drives me crazy; my house is so unorganized it irritates myself and my husband but still I can't seem to get it under control; Logan is probably the smartest kid I know, but he doesn't remember basic day to day things and sometimes he talks in gibberish. These aren't huge revelations or anything, but its a start. It is normal for mommies to have imperfections, it is normal for us to have needs, and it is okay to let the world see that.
Accept help, ask for advice, and share your worries - I promise it feels good, and there is a reason for the saying, "two heads are better than one." Think of your friends and family as guides to help you on your journey through life, we all have our own experiences and have something to offer each other.
So, no more secrets, no more false perfection, time to be honest with yourself, your family, and your best friends. If you want to share any of your mommy worries feel free to leave a comment:)