Thanks for sharing your video, i'm 32 and my gp thinks i have MS, so do
half of my family but i didn't go to the doctor for a year (i know stupid
me, i just though my fibromyglaia was getting worse) but this is just how i
walk between the burning,pins and needles ,numbness and the shear weight
plus trying to keep balance my walking has gotten pretty bad at the moment,
but thanks so much for sharing :)
Olga, I have lost 15 lbs since filming this video clip. My MS has gotten
worse not better. I am still working on losing more weight. I was slender
before MS robbed me of the ability to exercise. MS is why I gained weight.
Hi nancy, thank you for posting this video, it was very helpful to me. I
too walk the same way so i understand your struggle and I am afraid that I
might have MS. I go for my MRI later this month. all the best
Here we see, my cousin Jessica walking with the help of Lauren. Multiple Sclerosis aka MS has no known cure at this moment but we will continue to pray and ...
Tanya amazing video! My name is Sergio Rodriguez and I like Jessica also
have MS.
I appreciate you putting it out there the way you have. I have been
struggling with finding a way of putting my story "out there” too, in the
hopes of connecting with others in similar situations, and also, because I
want to help those who are still learning about life post diagnosis. I’ve
started using my counterpane.com; it's a modern-day journaling tool that
allows individuals to blog using video, text, and pictures in a way where
others can easily find your story. Because you’re doing video, you know
that video posts have the ability to change the course of one's individual
journey and can also inspire others. I’ve found that counterpane.com allows
you to blog in a new way that's more user-friendly and emotionally
compelling than YouTube. You can also organize your old posts in a visual
way to see how far Jessica has come. I’m curious what you think. Let me
know if you have a second to check it out.
thank you all for the comments, yes she does have a fb but she is a private
person. i am due to visit her soon with my uncle and sister soon. steve,
thank you and hope your journey to recovery as well.
I have SPMS, And walking was getting harder so i started to strech and
exercise more, so far this is helping I walk about 30 to fifty feet a day
when i can and when i have the help...Good luck to all.
March 2013 Walking update ~ Stem Cell Treatment #1 for Multiple Sclerosis
//msrelief.com I am feeling very strong after the Stem cell treatment about three weeks ago. I am able to do exercises that I haven't been able to do for ...
Family means strength Strength means just that Strength to keep fighting
regardless of the obstacles in our way. MS cannot weaken you because I see
strength in you, you have the heart of a Warrior. My blessings go out to
both you and your wonderful family...keep fighting. No Warrior is ever
forgotten, always remember this. -Kurt
Jeremey, I have Multiple Sclerosis but I understand that the stem cell
treatment is helping people with all kinds of conditions! I can't wait to
do my 2nd treatment in August! ~Linda
I'm glad people are seeing these videos ~ it really is accountability... I
want others to know that there is life after the diagnosis, and it can be a
good one!