Myasthenia Gravis Support Group
Myasthenia gravis (MG) is a neuromuscular disease leading to fluctuating muscle weakness and fatiguability. The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and...
I tend to feel worse after ivig for a couple of days. I only get one day of infusion every three weeks. I rarely get a huge bump from ivig but can definitely see an improvement and can tell when it is time for ivig again.
Cathi
TERRY....
BLESSINGS TO YA........
so glad to hear you are feeling better this am.. When I was taking IVIG I was getting it every 2 weeks gosh, I think that was it... my memory fails me.
After the first initial doses how often will you have ivig?
Hope you have a resful day.
Annette
Once I felt it the night of treatment, but it usually kicks in around 5-7 days! Stay hydrated!
I am trying to decide if the bigger the side effects the night of treatment (headache, fever) give me the best relief , so far it seems true... but I don't now for certain.
Love, Becca
Is hydration a big part of not feeling so bad after treament with this I was more than likely told that but like my wife tells me I never listen and like I keep telling her I have a married ear and a single ear usally she is talking to my single ear and it don't hear a word she is saying.?
you so made me giggle about the married ear and single ear... I could so hear my husband telling me that. I always say he has selective hearing... only when it benefits him... lol
You will find with IVIG at least for me sometimes it did not bother me sometimes it did. I only had a few times of the bad headach etc. Just be sure drink lots of water starting a few days before and drink the day of..
Don't you just love the mg roller coaster ride... NOT but all we can do it make the best of it.. keep on keepin on
hugs
Annette
Hope this treatment gets you feeling stronger sooner that later.
Don't know if you are on facebook. If you are, there is a IVIG page called--
IVIG Patient & Provider Support Room
(don't know if you need to join it or not. Probably so since it would be a private page) There are many on that have been receiving IVIG for years for different conditions---very helpful when needed.
Be sure to keep drinking lots of water for a week after treatment ends.
hugs
sherry
I hope things work out for you Bear!!!!
Darci from Chicago