FAQ/Help |
Calendar |
Search |
Today's Posts |
|
Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
Reply |
|
Thread Tools | Display Modes |
|
11-02-2009, 11:20 AM | #1 | |||
|
||||
Member
|
Hi everyone,
I was wondering if anyone has experienced worsening weakness from Mestinon? I know if you take too much it will make symptoms worse but I only take 60mg 3 x a day. It seems to be worst after my first dose in the morning. It is a really odd feeling of weakness and feeling shaky but when I look at my hands you can't see it. I am also on 40 mg Pred every other day but I don't believe it is connected to that because like I said it seems to be at it's worst in the mornings. This morning I woke up feeling really good but after the Mestinon I am now feeling the shaky weakness. I am truly stumped but feel there has to be a connection. Kendra |
|||
Reply With Quote |
11-02-2009, 11:23 AM | #2 | ||
|
|||
Member
|
Ask your Dr, you may need to lower your dosage. Or it maybe evn have your pred lowered. Keep us updated
|
||
Reply With Quote |
11-02-2009, 11:34 AM | #3 | |||
|
||||
Member
|
Kendra, I "think" that the Prednisone "might" be doing its job -- and you might not need as much Mestinon -- or maybe, not ANY Mestinon. But, this IS, definitely, as Joanmarie said, something that you should discuss with your doctor.
The whole point of taking Mestinon is to feel STRONGER -- not weaker. The "shaky weakness" does sound like "overdose". BTW, if it were me, I'd prefer to lower that Pred. Using the lowest possible dose of Pred WITH Mestinon seems to be the course with the fewest long term "nasty" side effects. But, tapering off of Pred is a S-L-O-W process -- may take MONTHS or even YEARS -- and MUST be done under a doctor's supervision. |
|||
Reply With Quote |
11-02-2009, 11:57 AM | #4 | |||
|
||||
Member
|
Joan Marie and Jana,
I think I will try only taking 30 mg of Mestinon this afternoon and see if that makes a difference. If it doesn't make a difference I will call my Dr. in the morning. The Pred is a double edged sword. It makes me feel so much better but I am terrified of the long term side effects. I don't think lowering my dose of that is an option right now. It was precribed by my Pulmo to see if it will help with Interstitial Lung Disease and she wants me on it 3-4 months. Jana I think you may be right that I may be overdosing on the Mestinon since I am now on the Pred too. This disease is so confusing and the Mestinon is so tricky because too little or too much makes MG worse. Thanks, Kendra |
|||
Reply With Quote |
11-02-2009, 12:04 PM | #5 | |||
|
||||
Member
|
[SIZE="3"]Kendra, I was just going to start a thread about Mestinon. It does sound like you may not need it in the morning. I'd calll the doc and let them know.
here is a link that might be helpful. [http://mestinon.com/ I've never had it cause me to get weaker, but I've started to have little eye muscles twitch, and have little spasm when I'm over due for it. And then I take the mestinon, and it all calms down. mestinon, does not help with my double vision, but it helps when I'm tired, and of course it makes a world of difference with my breathing. Best of wishes Love Lizzie /SIZE] |
|||
Reply With Quote |
11-02-2009, 12:16 PM | #6 | |||
|
||||
Member
|
Lizzie,
I will be looking for your thread on Mestinon! I will check out the link too. Thanks so much!!! I also have the eye twitches. Kind of a wierd feeling but nothing that bothers me much. I'm so glad it helps with your breathing. There is nothing scarier to me than not being able to breath. Luckily I have never had that happen but it is definitely my biggest fear. Kendra |
|||
Reply With Quote |
Reply |
|
|
Similar Threads | ||||
Thread | Forum | |||
I swear the Avonex is making it worse. | Multiple Sclerosis | |||
Therapy, might be making it worse | Thoracic Outlet Syndrome | |||
B12 defiency making RLS worse? | Vitamins, Nutrients, Herbs and Supplements | |||
PT Making Things Worse? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Hot weather making me feel worse | Trigeminal Neuralgia |