The Fibromyalgia Sorority- Update

Ping Pong game by Parker Brothers, The Childre...

Ping Pong game by Parker Brothers, The Children’s Museum of Indianapolis. (Photo credit: Wikipedia)

August 5, 2012

I promised an update and I keep my promises but it’s nothing “earth shattering” as my Mom is fond of saying. It’s just the same old, same old. I did go back to the neurologist for results but everything was fine. To me, that was good. He figured out that the tingling and imbalance could have been caused by the drug Topomax, but why I fell flat on my face for no reason he couldn’t answer. To him, he looked vaguely disappointed a) because he couldn’t help me and b) I was no longer of interest to him. He made that VERY obvious. The difference between the first and second appointments were like night and day. I stopped Topomax which now leaves me to go back to the Rheumatologist but I am not in any hurry. He was the one who prescribed Topomax. (Did he not know better?) From one doctor to another, I feel like a ping-pong ball.

Today, it is beastly hot and humid and I can barely get from the house to the car, this weather is not ideal for those of us with chronic pain, imbalance, weakness. There’s only a couple of days during a few weeks when we have ideal weather but that does not guarantee feeling well.  The winter is really rough, icy winds and snow but the summer’s humidity feels like I’m suffocating.

I went with my daughter to one store for shopping for college and there was no way I was going to miss it but I sure wish there were more chairs and benches to sit on for those of us who need a break. I’ve found holding on to a carriage is helpful and sometimes, if I really feel bad while I am there I can use the electric carts. I didn’t want to do that with my daughter but that’s a blog post of a different kind…..I’m sure those of you with teenage daughters understand.

How can we look forward to any day when we don’t know how we will feel? I used to set things up in advance, make plans with friends, go into the city, or to a movie or a museum. Now, it’s like the earth has to be aligned in 940 ways before I even think about it. Not too hot, not too cold, not humid, not torrential downpours and then we have the symptom assessment. What hurts, what doesn’t (rarely an answer there) have I slept well? Everything is so complicated now. I envy my old life, pre-Fibro, but I have accepted it is gone. I wish one or two of my family members would accept that too.

People still say stupid things and most people, unless they have Fibromyalgia, JUST DON’T GET IT.  Those of us who have it are unlucky members of a very big club. We understand EACH OTHER.  Fibro sufferers, if nothing else, be glad we have each other. Perhaps we could all become sisters (and some brothers) in a Fibromyalgia Sorority. Fi Kappa Fibro anyone?

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5 thoughts on “The Fibromyalgia Sorority- Update

  1. I’m glad you found out what was causing the imbalance and the tingling. With Topamax you need to take mega doses of Vitamin C to stop the tingling and it may help with the imbalance. Topamax depletes your Vitamin C drastically. (oh yes, I’ve been on it…was on it for a long time)
    I don’t know why it would be prescribed for Fibro….but I don’t know all the uses for it. I was on it for Migraines…that’s the most common use for it. And I was on it for Manic Depression…an off label use for it. But it did well for a while. then it stopped helping the headaches…so it wasn’t much use in taking it.

    Good luck in finding something that works. I was diagnosed with fibromyalgia years ago, but when I stopped eating gluten most of the symptoms when away. I still have some pain all the time, but it’s not like it used to be. I used to feel like I had the flu all the time. I’m so sorry you have to go through all of this…pain is a horrible thing to live with.

    again…I do so hope you can find something that works for you.

    Like

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