Lemtrada????
I've been on Copaxone which was a joke for me, then Tysabru which was great but I am JCV positive and now I'm on Aubagio and it feels like my symptoms are getting worse. Any thoughts about Lemtrada? I realize everyone is different. I have an appointment with my neuro nurse and am thinking about asking her.
So for 5 days and then you are off for a year? Wow that is the way to go!
I was given Lemtrada last year early on in my MS journey! It has all been good so far no reactions so far! Just the Lemtrada rash which after taking Piriton and a cool bath it went by morning! I feel very blessed by giving me the opportunity early on in my diagnosis! My husband tells my disability is better than before! I guess I don't notice because I am dealing with it daily! I certainly feel better! I will be having an MRI again in August! If you want to ask me any questions feel free! I know there are some adverse interactions with other DMT's check with your consultant and nurse! I am really pleased I made this decision, things could change tomorrow but that could be true for everybody! All DMD's carry risks, but not as dangerous as travelling on the motorway or freeway these days!
Yes Lemtrada is an IV infusion for 5 days in a row first year, then 3 days the next year.
Is There Anyone That Has Had The Lemtrada Infusion? Thoughts? Side Effects?
What Is The Steroid Infusion 3 Series They Have ?
Does Anyone Know Anything About Lemtrada Infusion Medication
Sign up for free!