First True MS Flare-up Since Having Stem Cell Treatment

I have Secondary Progressive Multiple Sclerosis or MS and had an extremely successful stem cell treatment over a year ago. The stem cell treatment is safe and follows US medical standards of care, but is not yet FDA approved.

It gave me my life back, but it is a treatment and not a cure. I am just recovering from my first MS flare-up and have no doubt that I will recoup and be healthy once again very soon.

iLoveMyNewStemCells and all they have done and all they continue to do and all the potential they have for so many in the future.

Category:

People & Blogs

Tags:

• stem
• cell
• multiple
• sclerosis
• ms
• flare-up
• flare
• exacerbation
• solumedrol
• iLoveMyNewStemCells

[klefsky]

Have you heard of Stemehance? Its an adult stem cell booster. please email for more info.

[hollyhuber]

@klefsky I have heard of StemEnhance. It is a nutraceutical advertised like MonaVie and is sold through MLM marketing. It is a has absolutely no direct correlation or substantial scientific proof that it can benefit me more than the adult stem cell treatments I have undergone. I will stick to my supplements that I know help, like Omega-3 and Vitamin D3. Good luck with selling your StemEnhance ...

[umswagger]

I was just 100% in your shoes. I had a stem cell transplant for Crohn's disease and it worked and totally disappeared for quite some time. My Crohn's just all of the sudden flared up out of nowhere 1 year ago and I was totally unprepared. I had no Doctor, was on no meds, nothing. I was bed ridden for a bit and ending it crossed my mind a lot. It all SUCKS BAD, and I know this. I've been battling and things are slowly getting better, although the Crohn's' is back. Hang in there! You r not alone.

[DenaGoodin2010]

Sorry to see that you have had this flare up. I myself do not understand some of the neurologist around in my state of Oklahoma. I had a real bad flare up and the neuro said that I was secondary progressive now. I said well desperate times call for desperate measures and asked about having the chemo treatment to put my body into shock, and then start with the copaxone or something on that line of things. She said no and just put me on the copexone. So was just wondering if we could talk.

Thnx

[onojmai]

can i hug you? you've got a great man, and you deserve him. keep it up. as the canadians say- get 'er!

[notapplicable66]

Were you ever tested to see if you have CCSVI?

[grethomory]

Thank you so much for your honesty...talking about this helps more than anything.

[superc]

Have you tried N-Acetyl-Glucosamine?

[MSVlogSupport]

Hi Holly,

Thank you for your candor on this, it must have been very scary.

It looks like the steroids are kicking in and your improving. I look foward to hearing what your next course of action will be.

The MS hug and all that comes with it is the most painful thing I have right now and have lived with for over 2 years.

I would give anything for relief just from that, constant pain can make you go to very dark places in you head. I think many of us have felt that.

Best to you

[cliff501]

thank you for your honesty and sharing. i went to CR in 2008 and have seen no results. but i agree with your view - good science and good technology.

i hope you rebound soon. get up and see what tomorrow brings. look how much you have improved in a week.

take care and hang in there.