Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
i just moved to houston,tx. went to see Dr Loftus yesterday, seems to good to be true. does anybody know this doctor. i'm from ill and kinda scared to start with a new doctor when i have no one to refer me that i know. need some input on this doctor. he wants to start me on tsybari immediately. i've tried all the abc drugs and i just cant tolerate them, well copaxone i could but could not get used to shots everyday and the endents in my thighs. so i stopped. he also is testing me for devics disease instead of m.s. because of his evaluation. any input on this disease? i have had m.s. for 6 yrs why now think its something else.
CASMIRA
I would stay on Copaxone and not Tysbari...that is such a hard drug...just my opinion though.
kellygrn
I was going to the MS Clinic at UT downtown. Been going there for 5 years. Since I now have SPMS, I decided to go to a local (The Woodlands) doc. I am starting Tysabri next month.
deleted_user
so kellygrn what are your thoughts?
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I have been here before, a long long time ago and now I am back.Forgive me for not just saying what I want to say,even under a triple dose of antidepressants it is still raw and seeping and I am hesitant at revealing it as at least under the bandages around my heart I don,t have to look at how raw and wounded.My child was cleaved from my heart by his own actions. my child of ten,turning eleven...
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theatre and I are there already. I'm having a very berry tea with crackers, cheese and cherry tomatoes and she's having a joint with some beer and we're both on really comfy recliners on thick pile carpet. we need some help with the decor if anyone is around??
