FAQ/Help |
Calendar |
Search |
Today's Posts |
|
![]() |
#1 | |||
|
||||
Wisest Elder Ever
|
Quote:
How much do you take, Tricia? Is there a maximum amount you can take each day that you know of? Even the 600 mg I take three times a day isn't cutting it some days. I know I probably need to bring this up to my Neuro next time I go.
__________________
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
|||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Wise Elder
|
Jim takes 1200 mgs three times a day Kitty.
__________________
. . A woman is like a tea bag. You never know how strong she is until she's in hot water. Eleanor Roosevelt |
|||
![]() |
![]() |
![]() |
#3 | |||
|
||||
Wise Elder
|
HK - I am a light weight when it comes to meds. I take 300 mg in the a.m. and 600 mg before bed - a total of 900 mg. A couple of times they had me increase it to 1200 mg a day but I would end up being emotional and crying all the time. So 900 mg is my personal max.
The 300 mg in the a.m. lasts me all day even though Neurontin has a short half life. The 600 mg helps me during the night and seems to keep some of the spasticity from waking me up. (It could just be that 600 mg of Neurontin for me knocks me on my bu**. I take it around 7:00 p.m. and within a couple of hours I start feeling the full effects. Sometimes it's like have a few drinks and becoming more "chatty" than normal. LOL.) Some people do start to build a resistance to it and need to increase their dosage. I can't remember the maximum amount, but it is a lot higher than what I take. Definitely talk to your doc about it at your next visit. There may be something that will work better for you. |
|||
![]() |
![]() |
![]() |
#4 | ||
|
|||
New Member
|
I take Neurontin 300 mg 3x a day and it does help with the nerve pain. It does calm my lower body down more though than the upper as I still get nerve pain in my hands.
|
||
![]() |
![]() |
![]() |
#5 | |||
|
||||
Senior Member
|
I take Trileptal, for seizures believed to be a component of my MS. I think it has to do with where a leison is in my brain. Anyhoo, I haven't noticed any other benefits, except no seizures.
After reading others responses, it may be time to try Neurontin again. I don't tolerate meds well, but I'm going to ask anyway. Thanks all. ![]()
__________________
-- Beth RRMS -dx 1997 Never doubt that a small group of thoughtfully committed citizens can change the world; indeed, it's the only thing that ever has. - Margaret Mead Breathe In HOPE, Breathe Out DETERMINATION |
|||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
What meds are you all on? | Fibromyalgia and Chronic Fatigue | |||
up my meds | Parkinson's Disease | |||
Meds!!!!!!!! A Must See | New Member Introductions | |||
I know some of you have went off of your meds, | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
off meds | Parkinson's Disease |