... Hi! My name is Jeny. I have been taking Rebif since April and I am starting to find it hard to take my shots. I DREAD each Mon, Wed & Fri...if it wasn't...
Nice to meet you Jeny. Ty for the reply(didnt know if I would get one) I have been on Rebif for about 5 yrs now. I will not do my legs, hurts to much. I know...
Hi Tara. I so know what you mean...about it hurting in the legs...that was actually my spot of choice untill very recently. Even though I dread the days I...
HEY JENNY, MY NAME IS AMY. I HAVE BEEN ON REBIF SINCE 2005 AND LETSN JUST SAY IT HASN'T GOTTEN ANY EASIER...WE CAN CHAT IF YOU'D LIKE ... wall ... it, ... you...
... legs...that was actually my spot of choice untill very recently. Even though I dread the days I have to inject, I will not stop using Rebif (for now...
Hi Cindy. I am happy that have have someone to talk to about doing the shots. I dont know anyone else that does Rebif or betaseron. i was on betaseron after I...
Hello, My name is Matt. Forums is all new to me so a friend is helping me to get started, I must also confess that my hand is not able to stay still enough to...
Hello Matt, I have primary progressive MS and on 7.5 mg of methotrexate per week. I tried LDN first but it was no help to me. MS is an awfull disease. I...
I have chronic progressive ms since 2001 was dxed with rr in 1993. I tried all the shots body couldn't tolerate any of them. Right now the only treatment I'm...
I'm doing much better with my shots right now, I just need to tell myself how important they are and how much they have helped me. I have been attack free for...
Hi all, My name is Sharon Aschaiek, and I am a Toronto-based freelance writer. I write for a magazine called Rendezvous, which is published by pharmaceutical...
I have been reading what people have to say about how they have moved fron RRMS to SPMS and I must say it scares me. I am RR without a attack for maybe 4-5 yrs...
Well, I don't know what you mean by an attack. My MD thinks I have "mini Exacerbations". I have had stomach problems all my life and they are much worse now...
Hi.... I'm 53 and have been blessed with a diagnosis of RRMS for about 4 years. I have terrible foot drop and leg drag. One hand is more of a pain than any...
Has the drug helped? If it has, it is the real. thing. I know tis drug (used to be in pharmaceutical industry and have been keeping tabs on pipeline drugs),...
Actually ... I have had 2 appointments and my "latest" high tech MRI ... (50 minutes long, I was afraid they found a void!) yesterday. I have another ...
Oh Paul, I hear you. The medical profession has gone down hill faster than an Olympic skier. I certainly hope you are on the drug and it is working for you....
I have 3 years on you for diagnosis. My symptoms are constant numbness and stomach problems (but I have had those most of my life as I am type A++++)....
Thank you. I have a cerebal (spelling) flare up. numb on the face forehead and right side of head. take rebig as well. 62 of age. work full time. I think...
judy I live in alabama. Are you sure you and I dont have the same neuro. I get there at 7:30 and back at work before 8:45 and I have to drive 14 miles back...
Carole: Good for you. You are my inspiration. I left my job of 16 years in July and have been looking for a new job since September. Unfortunately, I worked...
HI Carole, as you see, I read backwards. Xanax acts as a smooth muscle relaxant for me. When I get the bladder spasms (and believe me you know - you MUST go...
Hey Carole, at least you get an MRI. I have not had once since diagnosis! He judges me based on my ADL's. Which are status quo I guess. I tell him if I am...
