the best thing anyone can do when they lose a pet, is to get another one. it oh so helps the healing!!...
anyone check for lyme?...
i'm sorry, i don't really have any answers--nobody does--but it does seem to me that the more resigned and depressed one is, the faster they go downhill, or maybe the faster they go downhill, the...
hi amanda, i've been given a dual diagnosis lyme and ms. feel your pain. pray and trust the answer i've done the abx's now i'm onto copaxone, i'm lucky to have a PA that helps me sort through the...
i don't remember too much, mine was done under fleuroscopy(?)while i layed on my stomach. it only took about 15 min to get 4 vials-i don't know the pressure no tilt, no cough i did have one hell of a...
it sounds strange, but i was very happy to see your post. i too have "fake heart attacks", not every day, maybe once a month. i don't have shortness of breath with them-just pain- usually midsternum,...
i was first dx w/ lyme, back in the early eighties,still tested pos. couple years ago. now they're saying ms. did repeat abx tx, now i'm going to start copaxone. my neuro and second opinion said pos....
:cry: my neuro gave me a month(merry christmas to me) to decide what tx i'm starting. she said i've put it off long enough because the mri shows worsening, but i don't feel any different. after...
i've been told i have both, i was treated for several months with various abt's with very little results. i began feeling better a few months after stopping abt's but still have lingering neuro sx....
i'm in central ny and ended up traveling to nj for an llmd. none in syracuse. sorry...
my main neuro has said since i'm not showing any worsening, to continue with the vit d and i'll see her in a few months. possible follow-up mri's before starting any new tx. other than not being able...
i find swimming makes me feel a whole lot better...
i still am not sure what i'm going to do. 4 out of 5 doctors say i should start ms tx because of where my lesions are located, pos csf,and flunked the evoked potentials. the llmd(i don't like) is the...
hi louise, sounds like i could almost have written your post. i got tired of not being able to use my hands and a surgeon sent me to a neuro for nerve conduction. a couple years, lots of tests, a...
before my ms diagnosis, the gastro told me what i now know to be ms hug, was from GERD irritating various nerves running through the area....
once i had pain in my leg that was like combination sciatica and a charlie horse. thank God it hasn't come back....
sorry things are so crappy for you. i sometimes wish my husband would leave so i could blame him and i wouldn't feel like such a burden....
i miss a life not dominated by health concerns...
i don't have any answers for you carly. just wanted to say that i understand your frustration. i've been dealing with specialists always finding their specialty. now with ms and lymes, even the...
has anyone here been diagnosed with both? i've read that minocycline treats both. i did doxy and amox for lyme. my neuro wants to start tx(after a second opinion)for ms because my lesions are growing...
I have asked lots of questions and got short dismissive answers, he acted like i had a lot of nerve to question him. i'm glad he worked for you, but i'm now beginning to wonder if this whole lyme...
i'm not sure where i belong. i was told i have ms and lyme disease, but i was telling my sister i feel like i'm having a very slow stroke, because everything seems to be happening on my left side....
he was in howell. i'm really furious now. when i first called him i asked if he could tell if i had an active infection or not. i know i had lyme before and had positive antibodies. he assures me he...
met my llmd. don't like him. not very informative. he just put me back on doxy and said see you next month....
i've been told i have both. don't really know if i believe it. one thing i haven't found is anything definitive. good luck....
central jersey...
thanks scorpio, i have a vision test scheduled next month with my neuro....
thank you everybody, just got back from initial visit with llmd. just waiting for test results now...
hi springsjean, i ended up traveling to nj to find a llmd. i haven't got my test results yet, so i can't really comment if he's any good or not. but my search came up with alot of llmds in nj. good...
i was hoping to find out if there was a way to tell them apart. i was bitten and treated for lyme 25 yrs ago, recently(maybe 5 yrs) i've had neuro and muscular symptoms. my drs. say the treatment...
i was hoping to fine out if there was a way to tell them apart. i was bitten and treated for lyme 25 yrs ago, recently(maybe 5 yrs) i've had neuro and muscular symptoms. my drs. say the treatment...