Patient oriented research on living with MS.
Many participants will ensure a good bit of data.
Patient confidentiality, Privacy
and a feeling of Power that comes with action.
Real information, collated to see patterns, what helps, what hurts,
who gets better, worse, stays the same.
If you have MS or know someone who does, please share this.
Marc, the Wheelchair Kamikaze got me thinking about joining.
Lisa sealed the deal.
Then I read these testimonials by Reputable clinicians, Experts and Patients...
I am ready to help be a part of Patient oriented Research to help slay the MonSter...