Full Selma Blair: Walking from the ‘White House to the South Lawn’ in October was ‘healing’
Actor and advocate Selma Blair sat down with Meet the Press Moderator Kristen Welker after her visit to the White House to mark the 50th anniversary of the Rehabilitation Act.
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#SelmaBlair #MeetThePress #RehabilitationAct
Keep speaking for us Selma & thank you! I feel all of this. I was diagnosed with MS in 2004. The struggle is painstakingly real.✌️💙
She is not lying at all... I lived with hyperthyroidism for many years and it wasn't diagnosed until 2022 when I was rushed to the ER and after all the testing the doctor told me I was going through a thyroid storm! I wish more Doctors took the time to hear us. Thank you Selma❣️
Thanks to MTP and Ms Welker for this really important interview - and many thanks to Ms Blair for her advocacy and for so bravely sharing her story.
Thank you for your advocacy! My best friend and I have different chronic illnesses and are so appreciative of you speaking out
Dear Selma Blair, So good to see you finding your way to feeling better. You seem better than the last interview and you are able to speak better. Your determination, your fight is remarkable. 💙💚💜
she is an inspiration!
Thank you Selma!!!
I have been a fan on Selma even since I first saw her as an actor. And I always will be. Great lady.
Selma is inspiring and a great example of using bad things that happen to you for good. I am so glad to hear her MS is in remission! I had no idea that MS could manifest in young kids. The fact she had signs something was going on when she was only seven is eye opening. On a girly note, I love her blonde bob. ❤
Thank you.
shame we dont have her in uk to speak out not just for disabled but carers too! great interview!
To say she felt better on chemo broke my heart. I can’t imagine the pain she has to go through. She’s incredibly strong.
Love u Selma!! I am from India and I was 26 when i was diagnosed with MS in 2016. Living with MS for years, i cannot express my pain and problems to anyone. Each day i struggle and battle with my pain. Worst part is there is no cure for this disease. We can delay relapses by taking injections and medicines but no ultimate cure. Waiting for that day in my life when i will hear FINALLY I AM MS FREE!!
I have MS and now I'm in a wheelchair 😢
Some doctors do a disservice to their professional vocation. They do harm.
Just love her . I am going to be tested for MS she is so inspirational…🙏❤️✌️
Dr Burton!!!! I begged him to take me!!! It’s 120,0000! Well back in 2017
Love Selma. Kristen is over the top and annoying.
I think males might be taken more seriously than females (if that's true) because they are far less likely to actually go to a doctor, so when they do, it is considered to be something legit.
This is so true.. its a man’s world
Why did the president touch her like that?
get a hyp0allergenic dog GROSS thats a GIANT DOG eye would NOT LET that into my CAR either
Please find Donna M. Pritchett from Revere Ma and help her. Lesions in spine, Lesions on her brain yet no real assistance for her. Just sharing