With MS, it's always a "wait and see" scenario. My neurologist typically wants for me to wait at least a week after a symptom appears. The body can often re-myelinate damage. Typically, I won't go to a doctor unless forced to because I need to get labs or a prescription renewed. I have no health insurance and am uninsurable.
Interestingly - the only things that seems to help my symptoms are vaping ... or illegal.
Thanks everyone. You folks are family to me.![]()
Rave... without your going into explanations here about insurance coverage, there is a website that really helps my husband and I (as his caregiver) with all similar issues. I give him a daily injection of a medication called Copaxone. On it's own it's prohibitively expensive... in the range of $4,000 a month. We only pay $16 a month. There is also help given for the uninsured and underinsured as well. Maybe there is help here for you too.
Insurance and benefits investigation I Shared Solutions® | COPAXONE® (glatiramer acetate injection)
This is the main website "Shared Solutions"
COPAXONE® (glatiramer acetate injection) | Shared Solutions®
This has really helped him. Hope it may help you too.



