Selma Blair shares the latest on her battle with MS l GMA

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In a candid Instagram post, the actress opened up about her struggles and revealed she has undergone a stem cell transplantation.

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#SelmaBlair #MS
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God bless you Selma. I’m praying for you and others with a chronic illness. 🙏💕

janedoe
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We are SO proud of you. You are SO BRAVE! Go Selma.

mariannemccarthy
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I hope with all my heart that this treatment works 💛💛

roxans
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I’ve always loved her acting. I hope Selma keeps up being optimistic!

Star-hkgc
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Selma Blair.
You are Very brave for sharing your story and bringing awareness about
About MS and her diagnosis of your condition.
Praying for your
Continued Strength...
Continued Hope...
Continued Confidence...
Continued Endurance
Continued Health and Wellness...
Continued Positive Health progression....
Continued Peace during any difficult moments.
Selma Blair, May you continue to Persevere, Overcoming...
Please Don't ever give up.
God Bless Selma Blair and her family.

jasonsandifer
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I had HSCT 18 months ago in Mexico. I have had improvement, but not to the extent that was shown in this story. There are still daily struggles, but I only regret not doing it sooner. My life would certainly be worse if I had not done HSCT. #MSWarrior

jessicam.
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I propose, we all pray for her, and, send good vibe towards her, to swift recovery, and, victory.
AMEN!!!

jorgea.amador-hernandez
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Thanks for sharing
Hang in, there are better days ahead.

lulun
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It's wonderful to think that this treatment will work well for Selma and others. What a miracle that would be !! I hope the grueling effect of taking the treatment is alleviated. All the best to Ms Blair and others needing help with MS. Put money into research for cures of diseases like this - not money for wars.

KindCountsDeb
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#HSCTheals I had this done at Northwestern as well, 5/9/18 is my bday. Recovery is hard but its worth the fight. We are warriors! #GoSelma PS- a lot of misinformation in this clip. But I suppose they had to get approval from their drug company advertisers.

mamawolf
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Hats off to science, scientists and Salma Blair !

warhammerfantasy
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I had optic neuritis twice, 1 percent away from MS
Best wishes to you

Not sure what to say if this is ever read. People are behind you. One day at a time
See the beauty...anyway you will help people with this disease just by speaking out


.

dianewillson
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The worst so far for me was 5 to 10 months post HSCT August 2018 for RRMS.

kristyhugg
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It would be very amazing when they find a cure to make a huge difference i. A persons life or safe their life, they would give the treatment but if your not famous or rich that chances of getting treatment is hard to get. Don’t get me wrong I am super happy for Selma. My best to her always and many people fighting this illness.

maggiepena
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I think they're saying this treatment is not covered by Medicare, by Medicaid or by regular insurance and not available to regular middle class or poor Americans.

Time will tell if it ever (hopefully) becomes available. Meantime millions will continue to suffer, untreated.

smh.

andreawallenberger
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Greece were the first country to use this treatment :) !

angc
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Why doesn't her doctor want to talk to the press, since she is giving daily updates?

oeyiwzj
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Without a good amount of money some of us won’t be having this

brichi
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How much is it. Well patients be able to afford it

emstmerant
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This is where Ben Carson is needed! Not in housing! Surgical Talent wasted #Disappointed

bphoxay