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Old 05-17-2010, 11:16 AM
scrubbs scrubbs is offline
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Join Date: Nov 2009
Location: las vegas, nv
Posts: 181
10 yr Member
scrubbs scrubbs is offline
Member
 
Join Date: Nov 2009
Location: las vegas, nv
Posts: 181
10 yr Member
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Quote:
Originally Posted by rezmommy View Post
Kathie Glenn,
I guess I have some words of support, I don't know how wise they are. My original symptoms started in August 2007 and I was not diagnosed until November 2008. During those 15 months I went through a lot. The worst part was feeling depressed and that I was crazy. At the time I was 35 and the doctors couldn't understand how my different symptoms fit together. Initially they thought that I may have had a stroke. I remember being in the hospital when the symptoms first appeared and the nurse leaned close to me and said, " now is the time to tell us about any illegal drug abuse". I was so weak and stunned that I had no reply.
Until you align yourself with a good neurologist you are probably going to have more questions than answers. My first neuro was not a good fit. He sent me home to wait and see if my symptoms went away. Eventually I met a neuro who perservered with many tests, clinical observations and listened to me.
I have noticed that stress is one of the things that my MG just cannot handle. If I find myself stressed, I notice the increase in weakness immediately. I have learned to back off of being supermom and having a good support system.
I too gained 40 lbs as I was on Pred for a year. I just weaned off of it on January. I am on Imuran and Mestinon and I go for IVIG once a week. I have generalized MG so my weakness affects everything. I do know that when I feel that I am getting worse that stairs are my first indication.
Do you have confidence in your dr and the direction your plan is going in? Do you have an MG specialist in your area that you could be referred to?
I know that there are many others on this site who will respond with words of wisdom for you. If you need more support you can message me. Please take care and know that you are not alone. Melanie
Hi Melanie
I also have generalized MG that was diagnosed in Dec. 2008. Mestinon and prednisone since then. Pred down from 120 to 30mg every other day. Started on Cellcept and had my first 5 IGIVs in Feb 2009 and 2 a month since then. I have experienced everyting this disease has to offer.
I am fortunate that I have also experienced much improvement. No more double vision, swallowing or chewing problems and my stength and breathing has improved. The pain is the only thing that has been worse.
My Neuro has told me he hopes that the IGIVs can be spread out eventually.
I see you get IGIVs weekly and wondering for how long?
Have you seen improvement?
I have read a lot of post's but no one mentions how long they have been getting IGIVs.
Since I started taking Cellcept at the same time I am wondering if my improvement is a result of the Cellcept, the infusions, or a combination of both.
Maybe niether.
If you would reply I would appreciate it. Thank you.
Tony
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