Whittled Down.

This week has been one of the absolute worst weeks ever. First being told that my condition is “just a congenital birth defect and I do not suspect will warrant any further treatment.” I have been in nonstop neck and back pain continuously. I’ve fallen and skinned my knee because of my balance issues. My memory is worsening causing me arguments with my boyfriend over stuff I’ve forgotten because I’m also very stubborn and used to having a great memory.I found out that my Papa, my mom’s dad, had a really bad infection in his elbow and had to go to the ER multiple times.

Then I was let go at work because if I were to get bitten, scratched, or catch a zoonotic disease it could delay my surgery or worse. I have been forgetting to do certain things and the pain of being on my feet all the time, cleaning, and trying to restrain pets at work was wearing at me. The animals, however, gave me much joy and happiness so I am extremely saddened. Also, I have no source of income at this point. My boyfriend is already on unemployment, so we aren’t in the best position at this point, but he assures me we will be just fine and I shouldn’t worry.

The following day my boyfriend’s car broke down with me in the backseat after we had just bought groceries. I got nauseous and threw up in the parking lot we were stuck in. We had to have it towed and get a shuttle ride because everyone who could’ve given us a ride was out of town. 

That night I had to leave class early because I was in so severe pain that I began to cry. I went straight to my moms house and laid on the ground bawling. I decided then I needed some painkillers and would get an appointment the next day instead of waiting up at the ER. I took my muscle relaxer and old pain killers from my surgery back in 2013 praying for relief.

I then found out that same night some devastating family news that crushed me. I began doubting my self. My thoughts began to stray and I fought hard to stay positive. Insomnia was horrible practically every night.

The next morning I went to school took a muscle relaxer because of the pain and had to call my boyfriend and mom to pick me up and drive my car back home because the meds did not wear off as soon as thought they would. I called my neurologist despite her earlier judgement and left a message telling her I needed pain medicine because of sever neck and back pain. I had a psychology appointment and cried my story to my psychologist who I’ve been seeing for four years and love. She assured me I was going to be ok. My neurologist called me back mid appointment to tell me she doesn’t prescribe pain medication and I have to see my primary. I thought this was a bit ridiculous because this was a side effect of the malformation of my cerebellar tonsils. My psychologist told me she was so proud of me for standing up for myself because she knows how hard it is me to fight back. 

So I called my primary’s office to find she was on vacation but I could see a nurse practitioner instead. I asked if they could prescribe pain meds and was told they can consult with a doctor and could. 

After another restless night I went to my appointment this morning. I was told that I should see a psychiatrist, which I do believe to be true, but is not my primary issue at the moment. She told me to keep taking muscle relaxer. I cried and told her I can’t sleep, I’ve been in constant pain. She said she would consult with a doctor but could give a shot of toradol which helps for 6 to 8 hours. Frustrated I left. I told my dad who took the liberty of calling the office mangers of my neurologist and the nurse practitioner and basically telling them it was unacceptable for me to be in chronic pain and have to wait because my primary is out of town. My neurologist decided not to prescribe after being told she would be reported to the board and my insurance company because she took me on as a patient and didn’t even follow up with me on my MRI findings. So she is no longer my neurologist. I officially fired her. The office manager of the nurse practitioner’s location was much more helpful and got a pain script put in for me right away. 

This whole day I had intended traveling out of town to Livingston to visit with my dad. It has been awhile and I miss him. Last time I went down was before school started. We were hoping to leave right after my appointment thinking we would leave with a pain prescription. 

So around 3 I go to HEB pharmacy: the rx is marked urgent and the technician assures me that it’ll be 30 minutes. So I ask him to call me as soon as it is ready. At this point my boyfriend and I are extremely frustrated. We head to get food and decide to wait to leave until I finish my homework and get a call from HEB. I finish my homework right before 5 and call HEB pharmacy as we drive up to pick up my prescription. At this point I’m in pain. My neck begins aching. I’m told it hasn’t been filled yet I tell the lady I had come by at 3 and told it would be filled in thirty minutes. The lady apologized and told me she would get someone to check me out so I didn’t have to wait in line again. While I’m standing at the side a red headed older lady tells me I have to get back in line which is ridiculous. She says she has been here all day and that she hasn’t had an urgent script (basically calling me a liar), I tell her that it is unbelievable that I had to wait in line when I was told it would be filled at 3:30 and ask to talk to the manager. Of course he’s not in. I’m in horrible pain at this point. I wait in line fuming. Ten minutes later when I get to the front with the cashier, she can’t find the prescription anywhere. She looks in the filing cabinet and multiple trays and consults three different individuals. The crew are all looking over at me because the red head lady is whispering to them and I’m beginning to tear up from stress and pain. The pharmacy technician finally finds it because the girl I was on the phone with put it aside to be checked out early. (So I didn’t have to wait in line) I talk to the pharmacist who was very professional and kind and tells me she is so sorry and that it was completely their faults. She states that next time I should ask to see a pharmacist and not have to wait in line when the medicine was marked urgent and I was in extreme pain. I’m just crying my eyes out and my boyfriend walked me to the car and helped me calm down. Now we are finally on our way to see my dad after a day of hell. We will be arriving almost 12 hours later than we had originally planned to. I have my pain medication that took leaps and bounds to get and I’m exhausted mentally, emotionally, and, of course, physically. I have not strength left to fight against anyone. I pray that God give me the strength to continue on. The things I am thankful for this week: 21 shirts being sold to wonderful individuals. I didn’t think that many people cared about me. I found another lady in central Texas through a mutual friend who is an expert in chiari malformation and is in the hospital fight now for a third brain surgery. She has had so many more complications than I have including hydrocephalus, syringomyelia, and a cyst blocking the flow of her CSF, but I can finally talk to someone who knows first hand what it is like. I can ask her questions about the surgery and it gives me peace and reassurance to talk. My dad’s perseverance to make sure I’m taken care of when I don’t have the strength to do it myself. My mom and my boyfriend taking care of my fragile broken state. My best friend for talking me out of a crappy mood and being there for me. Finally, the end of this week I am thankful for.

End of vent.

 

 
-Cass, chiari fighter, bullying survivor, and surviving life’s tornado.

Insomnia and Pain

Life as of Right Now

I have been having such a hard time with pain, migraines, and insomnia. Every night I either can’t get to sleep or wake up in the middle of the night and can’t get back to sleep. I’ve counted and I take roughly Twenty pills a day. Twenty!! Between my muscle relaxer for my back, my anti-anxieties to sleep, my need for tylenol, and my daily vitamins and meds. I now have an infection of my mastoid, which absolutely is painful. It’s finally stopped throbbing after three days of heat compression and antibiotics. My neck and back aches constantly from the Chiari and I really just want to lie in bed all day. I am struggling to stay positive, but I know that I am a strong individual and that I CAN do this. I miss my not having my dad and mom by my side every step of the way, but I’m growing up and this is one challenge that I’ve been given to tackle. I will continue to fight and stay motivated, it’s the only thing I can do right now.

My referral to the neurosurgeon has been approved and put in and they will be contacting me next week. I can’t wait to finally have a plan for things.

Cassandra’s Chiari

I can’t tell you all enough how much it means to me to have a support system in place. 15 shirts is incredible so far. I’m very appreciative of everyone’s love and willingness to help.

https://www.facebook.com/events/1077188662300543/
Click the Image!

Above is the link for the Facebook event to buy the shirts; Please invite your friends and family and share.

About Cassandra

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In case I have individuals who don’t know me personally reading my blog, I decided I would introduce myself and talk a bit about my passions. First of all, I’m a full time student at Texas Tech University and majoring in Biology with a minor in Chemistry. Yay science. I used to hate science in high school, but I absolutely love it now that I’m in the real world. My favorite subject is microbiology.

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I also work part-time at a wonderful little vet clinic as a vet assistant. Animals are my absolute favorite. There is nothing more satisfying knowing that I helped an animal and made a difference in their care. I am seriously thinking of becoming a veterinarian for dogs, cats, and small animals. I used to watch Animal Planet 24/7 and Steve Irwin was my idol. They have a permanent place in my heart. I love style, yet I usually dress super casual in a sort of I-don’t-care-what-anyone-thinks way, but there are occasions where I show my sense of fashion. I’m addicted to pinterest! Who isn’t these days? I actually have a board for my chiari malformation. I think it was one of my ways to cope when I found out. Pugs are my favorite animals and when I graduate, I will adopt one! I live with my boyfriend of 14 months and his brother in a cozy duplex with our Pomeranian, Eli, and our Tabby, Oliver. My mother lives right across the street so I get to see my other babies often too: Tasha and Ginger, the sweetest Chihuahuas with loads of personality. I have the most amazing parents and am so lucky to be close to both of them. My dad lives in Livingston on the lake with our Doberman, Max. He’s a nurse and served in the military for twenty+ years. My mother is my best friend and is the sweetest and most bubbly person you will ever meet.

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 I have one brother, Rhett, and sister-in-law, Jackie, the parents to my two little nieces: Emelia is almost three and a new little girl is due in January. I also have another “sister” that I’ve bonded with so closely since we were sixteen. Dianne is my other half and keeps me sane. I am so lucky to have the amazing family I do. I love my Grandparents, Aunts, and Uncles very much and my boyfriend’s family are wonderful too!

My favorite things include: science, horror films, kewpies, netflix binging (right now we’re watching Sons of Anarchy), hedgehogs, crafting (sewing, knitting, crocheting, etc.), Lily Allen music, hiking, Halloween, tattoos, decorating, vans, aliens, unicorns, stop-animation films, pugs, of course, fashion, decor, the paranormal, nature’s beautiful places, action movies, online shopping, and uncrustables.

Things I want to do: be more physically active (get in shape), visit New Zealand and Thailand, start cooking, beat this fight.

Thanks to all!

xo

Diagnosis

I got my MRI results on October 2, 2015 at 3:20 am.

My diagnosis: I have a congenital defect called Chiari Malformation Type I, my cerebral spinal fluid outflow is being blocked by my cerebellar tonsils protruding through my foramen magnum. So in other words , my skull is too small for my brain. (That’s where my smarts come from!) This is a rare disease and effects 1 in 1000. This is what is causing the pain and tingling in my arms and legs. Everything has finally matched up and I am relieved to have an answer finally. So what does this mean?

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I have to undergo decompression surgery to allow the CSF to circulate like it’s suppose to, a type of brain surgery. It luckily isn’t too invasive as they will only have to remove the bone at the back of the skull and spine. The dura overlying the tonsils will be opened and a patch will be sewn to expand the space.The goal is to relieve compression of the brainstem and spinal cord, and to restore the normal flow of cerebrospinal fluid.

The surgery will take 2-3 hours and I will be in the hospital for 2-4 days for recovery.

I do not yet have a scheduled date as I need to meet with my neurologist and my neurosurgeon.

Purple is the color to support Chiari Malformation Awareness, so I’ve changed my profile images to purple to raise awareness about this rare disease.

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If you have the ability please share or purchase one of these shirts I designed to share awareness about Chiari Malformation and to support me in my recovery, it would be much appreciated.

https://www.bonfirefunds.com/cassandras-chiari

Much Love,

Cass