How I Found Out I Have MS
My journey began July 1995, 3 MONTHS AFTER I WAS MARRIED at the age of 20! I woke up one summer morning, in our small, rural farmhouse, with SEVERELY dizzy vision and what felt like a VERY tight corset around the middle. I couldn’t see straight with both eyes open at the same time and couldn’t hardly catch my breath or move because my torso felt so restricted. (Feeling like I was wearing a corset was the way I described it to my family doctor). Luckily, I got in to see my doctor that day (20 miles away). The neurologist from the city (70 miles away) was going to be up at our rural hospital in a couple of days and I got a last minute appointment with him. I was hot and had the previous symptoms I described, but I guess 2 days was not THAT long of time to wait
A leave of absence from work was what I had to take to figure out what was going on! The couch and I spent lots of time together! I didn’t want to eat because I wasn’t sure if it was going to stay down, but I forced myself to eat a few crackers and keep drinking water. I knew I needed to put something in my stomach to help fight whatever was going on with me!
My husband took me to the neurologist at our local hospital (also 20 miles away). My farmer husband was in between summer farm work and we both wanted to hear what he had to say. Since I was so severely dizzy he got me set up to do an IV steroid drip at the hospital that day and for the next 2 days on an outpatient basis. After that he wanted me to go to his office for a series of tests including an MRI and a lumbar puncture (spinal tap)! Yes, you read that right. He thought it was MS with the vision problems, so that was the path we were going to test for.
The IV drip cleared up my vision, but not my “corset” discomfort. My local doctor did a blood test and arranged for us to go back to the city and see an endocrinologist (gland specialist). So, in that next week we were headed back to the big city to see a different doctor. This one told me it was Graves’ Disease. That meant my thyroid was an OVERACTIVE thyroid producing too much (thyroxin) secreted stuff for my body and the only treatment was removal of my
thyroid. For those of you that aren’t familiar with what your thyroid does, it is that little gland around your throat that controls most of what goes on in your body, such as weight loss/gain, your body temperature, and your monthly cycle for women.
Now back to removal of my thyroid. If you’re going to remove that gland, my thought was your going to cut my throat (look at the picture)? I think he saw the questioning look on my face. He told me he was
going to go get a radioactive pill for me to swallow and it would shrivel my thyroid so it wouldn’t work anymore and I’d have to take a pill to get that hormone every day for the rest of my life. That’s when all my super hero thoughts popped into mind:
- Is this going to work?
- How does it know what gland to “attack”?
- Am I going to appear radioactive?
- HOW is it going to work?
- What’s it going to cost if it’s that easy?
When he came back he had a glass of water, a big horse pill in a little paper cup and was wearing a pair of surgical gloves. Ok, you’re wearing gloves to bring this pill, but I just put it in my mouth and swallow it with bare hands?
Ok, my tightness did eventually go away, so I guess it killed the right organ! I later found out that pill (the size of my thumb nail) cost $800 in 1995.
My tests showed NO SIGNS of MS, none on MRI or the lumbar puncture! He said I needed to start these (expensive $1000/month in 1995) MS drug injections. I told him I wasn’t going to because we wanted to have kids and I wasn’t putting that medicine in my body when it WARNS YOU AGAINST PREGNANCY. That’s the first time I got the feeling from a doctor that if you’re not going to do what I say, then I’m not listening to you. That’s when my husband and I decided to find another neurologist as we walked out of his office.
I started having what I call MS “episodes”. It happened at random times, usually in the mornings, when I went to the bathroom, but not all the time. I would get EXTREMELY hot, start sweating, get a buzzing in my ears so I couldn’t hear anything and my vision would just black out. Once I got cool it would only last about 10-15 minutes then I could go about my day! I tried to connect it with stress, what I had done in my life, what I had eaten, the weather, but nothing was the same! I started thinking “Oh great! More lesions on the brain”. But that wasn’t the case as I got more MRIs in years to come. It still happens, but rarely!!!! The joke with the MRIs was I had proof that I HAD A BRAIN. We have great insurance so we only had to pay 20% of that MRI bill.
I went back to work about 3-4 weeks later, but soon learned that I had to cut back to 4 days a week. I couldn’t keep up working 5 days a week, helping on the farm when I got home, feeding us when my husband got done at night, plus laundry and keeping our house picked up as much as I thought a “good wife” should.