 |
|
| Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
| Reply |
|
|
Thread Tools | Display Modes |
06-21-2009, 07:55 PM
|
#1 | |||
|
||||
|
Member
|
Hi. I have been having trouble with my computer...just got a new touch tablet PC....so much easier on my fingers....
I was doing great after my last dose of IVIG...(back in May).....but my symptoms have relapsed again within about 5 weeks of the IVIG. Doc put me back in for 3 more days of IVIG. I am so scared that I will get aseptic meningitis again. They have slowed my rate to 35cc/hr...each infusion is lasting around 12-13 hours. 
__________________
Cricket . |
|||
|
 Reply With Quote
|
|
06-21-2009, 09:42 PM
|
#2 | |||
|
||||
|
Member
|
Hi Stephanie,
great to hear from you  Sorry to hear you've relapsed  Will be thinking of you as you get your ivig, and sending positive vibes that all goes well Kate
__________________
Outside of a dog, a book is a man's best friend. Inside of a dog, it's too dark to read. Groucho Marx |
|||
|
|
Reply With Quote
|
|
06-22-2009, 09:53 AM
|
#3 | ||
|
|||
|
Member
|
Cricket, So sorry you are having trouble. Listening to all the problems some people have with IVIG makes me glad I don't take it. I really hope all goes well and that your strength returns soon.
|
||
|
|
Reply With Quote
|
|
06-22-2009, 11:12 AM
|
#4 | ||
|
|||
|
Member
|
Hi Stephanie,
Nice to hear from you. Sorry you haven't been feeling so well. Hope you start feeling better soon. Glad you got a new laptop! Take care. Hugs, Pat |
||
|
|
Reply With Quote
|
|
06-22-2009, 03:28 PM
|
#5 | |||
|
||||
|
Senior Member
|
Hey honey! I'm so sorry to hear that you aren't feeling well and that IV IG gives you such a hard time! was whining about mine being set @ 150 mL an hour- now I feel like such a big fool!
 Why doesn't your dr give you the plasma exchange? It just seems logical to me that if you get so sick, your body is telling you something.........My neuro was worried about my first IV IG and told me that if I had really nasty side effects, it would be my last - the plasma exchange would be my only option - fortunately I haven't had any yet........  When do you go back in to the hospital? Do they make you stay IN the hosp for the full time or are you able to go home after your treatments? Some very lucky people are able to get it at home - an option I would LOVE! I'll add you to our prayer list - if that's alright with you! Big, big hugs! Erin Quote:
__________________
Erin . |
|||
|
|
Reply With Quote
|
|
06-22-2009, 10:06 PM
|
#6 | |||
|
||||
|
Member
|
Stephanie, I am so sorry, you have to go through that fear. I am allergic to some of the antibody's of the IVIG, & get so sick from it. We are going to try high dose IV pred. Instead. I should be bouncing of the walls with energy !
My Neuro has given me pred before the IVIG, to hold back the rejection of the antibody's. I hope you get feeling better soon ! Mary
__________________
Mary . |
|||
|
|
Reply With Quote
|
| Reply |
|
|
Similar Threads
|
||||
| Thread | Forum | |||
| Hey Guys ...... | Social Chat | |||
| See ya later guys! | Survivors of Suicide | |||
| Hey guys | Epilepsy | |||
| Hey guys | Epilepsy | |||
| hey you guys | New Member Introductions | |||
Hello Guys!
Hi Stephanie!
Linear Mode
