i take 20 mg of baclofen at @ 5am,12pm, and 8 pm. at one point i was taking 100 mg per day.
mfg. states that 80 should be the max dosage per day ________________________________ From: Janice Nichols <jan...@centurytel.net> To: Susan Kleinz <skle...@cox.net> Cc: celr...@aol.com; tmic <tmic-list@eskimo.com> Sent: Tuesday, November 29, 2011 1:02 PM Subject: Re: [TMIC] quiet ot Susan, I am taking your advice and not just taking it at nite too. It is helping. Thanks Janice From: Susan Kleinz Sent: Monday, November 28, 2011 6:32 PM To: Janice Nichols Cc: celr...@aol.com ; tmic Subject: Re: [TMIC] quiet ot Savella is a new drug designed to help people with fibro myalgia. It's purpose is to help neuropathic pain. It definitely works for me. For 20 years I took Baclofen at night only. I ended up taking way more than I do now, which is 10mg 3 - 4 times a day. My doctor, at BNI is a specialist in MS and TM. I am grateful for his care! Susan, Phx, AZ On Nov 28, 2011, at 4:20 PM, Janice Nichols wrote: Susan, >I am on Baclofen, Neurontin, and Zoloft too. What do you take Savella >for? Maybe I am missing out on something! >You are right about the website. It has done wonders for me. Great for >information and for handling the “isolated” feeling of TM. >When I first joined, I had lots of questions that I asked everyone to respond >to, and of course, they did. It kept things pretty active >for a while, but things have slowed down again. It is a wonderful >group - take a bow everyone of you!!! >Janice > >From: Susan Kleinz >Sent: Monday, November 28, 2011 10:33 AM >To: celr...@aol.com >Cc: tmic >Subject: Re: [TMIC] quiet ot > I was busy with Thanksgiving... > >My two lesions are at T-7, so I do not have the brain thing going on. >My first episode, I did have slurred speech...as there is a 3rd lesion in my >brain that doesn't seem to be activated now. >I would take any drug that would help me. Ritalin included. >I'm on Baclofen, Neurontin, Zoloft and Savella. I should be smiling all day >long! > >I am grateful to this website. I joined the TM Association and received a >bunch of good literature. Also ordered The Official Patient's Source Book on >TM. >I am amazed that my neurologist didn't recommend these resources. Nor did I >know how rare this illness is... > >My husband says I'm one in a million. > >Susan K., Phoenix, AZ > >On Nov 28, 2011, at 7:10 AM, celr...@aol.com wrote: > >I hope everyone is ok. It has been very quiet on this site since before >Thanksgiving or maybe I am kicked off again. Missing you. >> >>Jane/Splendora Tx >> >
