First True MS Flare-up Since Having Stem Cell Treatment

[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.

[barbaraeven]

OH NO!!! Holly thank you for being so honest and letting us know what is going on with you. John is doing good and I have seen improvement in him . This is so scary because when we saw you in Costa Rica you looked great.

It really makes me so sad .

Our friends are heading out for Costa Rica for MS treatment next month and now I don't know what to tell them??

Barbara & John

[bbcalifornia]

Holly - my heart & hope are with you. I wish there were words - but this disease is a real SOB.

Thank you for sharing the bad (putting it mildly). It is encouraging to me to see some of your feisty coming thru. I am wishing you and Raj better days ahead.

Kristi

[vbeachy]

Holly;

Like you, I didn't expect to hear that you had a flareup, especially since you had stem cell treatment.

I, and I am sure a lot of other people, are glad you shared this information, in light of the fact that it was so hard for you. Where do you go from here?