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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#1 | ||
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Member
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Tyson,
I had you on my mind and am wondering how your first IVIG went? If I am correct you were to have it a few says ago. I have been getting IVIG for a little over 5 years now and it really helps me. I hope it will do the same for you. If you are able to post, please do so and let us know how you are and how everything went. Loving Hugs, Shari |
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#2 | ||
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Senior Member
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Yes, we are hoping it went well, and that it's the beginning of really good things for you!
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#3 | |||
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Member
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Thanks so much for asking! I was just getting on to tell you all how AWESOME it feels.
I had 4 days of it, at 40ml. Of course there were symptoms and some of my veins were appreciative, yet now, i feel honestly so good. I still have some symptoms and they may disperse yet im so much more happier because I feel somewhat normal again. Thank you guys very much for being supportive, once again! How are you all feeling? |
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"Thanks for this!" says: | redtail (10-04-2010) |
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#4 | ||
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New Member
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Hi,
I'm so glad it has helped you so tremendously! I am the ICU guy and I'm still at the hospital, I finished my 9 (yes, 9!) rounds of plasmapheresis Friday, and they just started IVIG for me (5 days, I think 70 ml?) since yesterday! When I was first admitted to the ER, they did IVIG on me a month ago, which really didn't help much at all and thats why they went on the plasmapheresis, and after the standard 5 rounds I showed *modest improvements so they added 4 more. since yesterday's IVIG, I didn't feel much different, except I actually felt noticably worse this morning ( Chest extremely tight ), does anyone feel like the symptom gets worse before getting better on IVIG? I hope this 2nd round of IVIG would actually help me and show some improvements for me soon too..! |
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#5 | ||
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Member
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Tyson,
![]() ![]() cpu90 ![]() I ,personally, have never felt worse in regards to MG after my IVIG treatments, only felt crappy from the side effects. We really don't know why a treatment works for one person with MG and not for another. As you know MG can be a very individualized disease. Don't give up though. It sometimes takes a while before they find out what medication and/or combinations of medication/treatment will work to help stabilize your MG. I'll keep you in my prayers, Shari |
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#6 | |||
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Member
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Thanks shari!
It helps with the overall weakness of legs and stuff. But my eye, and general fatigue sometimes sets in. Oh well right? Atleast I can breathe ![]() Prednisone is killllin me but whatever, ill live. Hope your well. |
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