hello everyone..
33 yrs. old
RRMS - dxed in 2005
Betaseron for first 2.5 years
Curently - Copaxone
Very interested in CCSVI, but not interested in participating until all the research is done. My motto: "If it ain't broke, don't fix it."
My MS is under control and I live a normal life. mostly. I have life long numb feet and a numb left hand, cold feet - all the time, but these are things I've learned to deal with.
I'm more fortunate than others who have MS.
I also watch my diet and exercise - a lot.
Chort here...
- Karazhan
- Family Member
- Posts: 86
- Joined: Sun Mar 29, 2009 2:00 pm
- Location: Louisville, Kentucky
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Re: Chort here...
but...but...you ARE broke, we all are. Some more than others but MS is definitely "broken" and in need of fix'n.chort1313 wrote: My motto: "If it ain't broke, don't fix it."
Kara
I agree it needs fixin, but I don't want to be more "broken" until after all the kinks are worked out with CCSVI.
I don't want to fix my veins only to have them collapse again...
So until there's more of a gurantee that you don't have to keep having them 'fixed' I'll stay on the sidelines.
I can tell you I'd feel 100% different if my MS was more "active."
I don't want to fix my veins only to have them collapse again...
So until there's more of a gurantee that you don't have to keep having them 'fixed' I'll stay on the sidelines.
I can tell you I'd feel 100% different if my MS was more "active."