A.S. Face 1261: Tiffany Bordelon
In December things got really bad for me, I was having problems walking; I started to use a cane as something to support myself so that I could walk to and from my classes. Silly me thinking that I could take 18 credit hours my second quarter of college were my classrooms would also be spread all over the campus giving me 10 minutes to walk from one side of the campus to the other as to not be late for class, in the middle of winter. I had long ago forgone the traditional backpack, as I couldn’t carry anything, for one on wheels. After a spontaneous trip home to see my regular doctor I was once again left frustrated and with yet more anti-inflammatory’s. I went back to school and toughed out the rest of the quarter and when I went home for spring break I saw my regular doctor again; she decided this time to do some blood work and told me to see a rheumatologist. Turns out that I was HLA-B27 positive. But that was only the beginning of my struggle.
I started my final quarter of my freshman year of college without any more answers. I tried to get in to see a rheumatologist around my school but no one would take my case, and in late April my parents and I made the decision to pull me out of school. During the time I was processing all of the paperwork I had contacted several places back home hoping that someone would take my case on. And finally I found Dr. Sidhu. He was booked out until June but I didn’t mind waiting, what was more time when you had spent nearly a year in constant pain. When I finally got in to see him he ordered a long list of blood work and x-rays and MRI’s to be done. I didn’t see him again until July; exactly one year after everything had started. I won’t lie that was a very long month for me, during that time I had lost feeling in my leg completely and could not pick up my foot at all, I used crutches to walk refusing to use a wheel chair. And when I did see him, he had no answers for me, so he ordered more tests and gave me another anti-inflammatory that he said should have stopped the pain. Well the rest of July passed, I had taken all of the medicine and it had made things worse. I started to lose feeling in my left leg too but I could still move it most of the time. When August came, my next appointment t came with it. That was when my entire life changed. He told me I have this really weird disease called Ankylosing Spondylitis, I had heard of it before but I knew next to nothing about it. I’m really glad I had my dad there that day because I didn’t follow anything after that, I cried right there in front of the doctor, I was so thankful to have a diagnosis after over a year of struggling with this debilitating disease. Finally when I had recovered enough, I asked the dreaded questions, was there a cure and what were my treatment options? He said that no there is no cure at this time, and that because I had a stubborn case and the anti-inflammatory’s hadn’t worked we were going to use a TNF blocker called Simponi. It is a once monthly shot self-administered and it will suppress my immune system. Each shot costs 3,000 dollars. They gave me one trial shot that day and two more trials to take home and use.
Three weeks later I could walk again, I didn’t hurt as bad anymore. It has now been 10 months sense I got my diagnosis and I’m noticing more and more pain. I still can’t sit or stand for long periods of time and I have a lot of trouble sleeping. I see a chiropractor every week at least once if not twice. I won’t ever have a normal life though, as the shots cause me to be so tired that I cannot do anything for a week after receiving them, they also make me sick every time. I have been getting worse lately but I am trying to stay strong. This has been a long road for me and it seems like it will only get longer, but I know that with the help of my friends and family I know that nothing can stop me, and AS isn’t going to change that.
Washington, United States of America
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