bdinfluence
Member
my mother has had ms for 18+ years and is in real bad shape i have told told my father ans sisters about this treatment and i`m tring to get them to make a move
thank you for posting this info
thank you for posting this info
Its not really a bad thing, it has to be published and gone through respected medical journals first and trials have to be done...Its a long process but bloody necessary...thats the worst thing bout new treatments. It prob wont be avalable to joe public on the street for years, thats if it gets accepted as a worthwhile treatment. Like i say im still waiting for the goat serum from medical grade goats.
Get busy..... My mom wouldn't be waiting.my mom has ms and she smokes weed sometimes, medicinally of course. she says she dosnt like it but it def helps her, i think she dosnt like it cuz she smokes garbage midgrades. i told her if shed let me get her some good weed then she might actually like it, but she says the prices arent worth it. i dont think shes ever smoked good weed
LOL, you should have seen my face when you said we're not supposed to eat chocolate.Basicly we need a fat free diet cuz our boody cant deal with fat cells like other ppl
My doctor gave me the choice. After reading upon the 3, it was just too obvious to go with the Copaxone. For me, it was a no-brainer. I was told Rebif and Betaseron would likely make me suicidal. Yet, my doctor did suggest the Rebif/Betaseron.Yeah real lucky lol. Are u on any treatments for ms? Im on beta interfearon once a week intermuscular injection. I hate that neeedle i dunno if i could spike myself every day too. spliff time lol
My doctor gave me the choice. After reading upon the 3, it was just too obvious to go with the Copaxone. For me, it was a no-brainer. I was told Rebif and Betaseron would likely make me suicidal. Yet, my doctor did suggest the Rebif/Betaseron.
I've got to be honest. I have little faith in the injections. Copaxone states that you "may" have an 8% less chance of progression by injecting.
I've stopped it altogether recently. Every single injection feels like being stung by a bee, but that's not the worst part. It itches and swells and then once you rotate "sites"....you irritate the shit out of it all over again.
In fact, I only used it for a few months. Using this medicine leaves pits in your skin at the injection site because it destroys the underlying fatty tissue. I'm already naturally thin, so, last thing I needed. It also leaves seemingly permanent bruises as well. It would occasionally cause aches in the joints of my hands, making me feel like I had some extreme arthritis on top of MS.
I almost feel obligated to start taking it again. I have almost 12 grand sitting in my refrigerator. Sigh.....I hate to be wasteful, but I hate those damn syringes!
For your sake, I hope you don't have the typical effect of flu-like symptoms.
As my doctor was pushing that one on me, she was telling me that most people opted to inject on the week-end (after the work week)....what a way to spend your week-end I thought...sigh.
I'm with you. Neurologists are limited in my area. I will be seeing a new neurologist soon---took 5 months just to get an appt. with a referral.crazy stuff lol. I stopped taking interfearon for about a year bout 24 months ago and have been back on them for bout a year. I know what ya mean bout the injections and the sites afterwards. I didnt see any difrance with being off it for a year but paranoia and the cost of it made me go back on it lol. I gotta nerologists appointment on the 17th, I shall ask him about Dr. Paolo Zamboni, see what he tells me lol.
has anyone taken any of this info to there neurologist, if so what did they say ? did they know about it.
has anyone taken any of this info to there neurologist, if so what did they say ? did they know about it.
im doiing this today, I shall as my nerologist and if he hasnt seen or heard of it ill give him a printed article of it.has anyone taken any of this info to there neurologist, if so what did they say ? did they know about it.