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Met her in real life months before this diagnosis. Fucking racist ass little bitch. Karma got you boo.
😇 So Brave, Beautiful Soul, Bless her 💗👏👏👏
It’s amazing. You see all these spoiled losers making up fake oppression and acting like spoiled brats... Selma’s like “pfff hold my cane.” Amazingly strong and funny!
Wow still cant believe she has ms. Good for her not letting it keep her down.
Go Selma! You are an inspiration! Just wonderful! 💫💫💫💫💫💫💫💫
this is all cry for help self interest...spreading awareness bullshit...
Hurry on with the stem cell things already..!
She's an inspiration. Always been a fan of hers. Her character in the sweetest things is one of my favorite characters.
When she picked her son up, I cried 😭
Selma is so inspirational.
Rise!! you got this Selma. Fuck MS!
Rise!!. you got this Selma!! fuck MS!
She’s old Hollywood beauty and grace. Very elegant.
thank you Selma!
I feel less embarrassed to use my cane. Thank you for that, Selma:)
love love love love my darling Selma
She's just an amazing everything! Person , inspiration, sunshine, just everything I seriously can't love this woman anymore
this make me so sad :( she doesn’t deserve that. God bless her and beautiful Sarah Michelle who show what real friends are
I have M.S and I'm still amazed how many people dont know what it is. I explain it as this your nerves are like a extension cord. The wires covered. With M.S it s like when you vaccum over the cord and expose the wires. Our nerves have cuts in them exposing the nerve. It causes bad reception from your brain signals. Causes pain, motor skills such as talking to be labored, walking, a little bit of every problem that your nerves are responsible for. This is a serious disease and now when actresses or actors have it is the only time we pay attention. Richard Pryor, Annette foti cello,montel williams,jake osborne....we all are suffers. Treatment is self injections but there is no cure. Thank Selma Blair for giving us a voice. Its I believe the most ignores disease. Shouldn't be!!! Help someone today with M.S.
Hang in there sister, we love you!❤❤❤❤
And the award of woman of the year was given to a man dressed as a woman called Caitlyn Jenner...how absurd...
I hope drugs gives relief.Experiment.
Brawe Women very sad story
Such a inspiration. She's just amazing. Want to hear more from her.
Breaks my heart 💔 You rock this girl 👊🏻
She is a-m-a-z-i-n-g. Bless her sweet little heart.
She jinxed herself.
I can relate to her experience a lot! When I was diagnosed, it hit me really hard and I lost a lot of functioning. Thank G-D I've had a really nice remission. It still scares the hell out of me though
so its like the end of Buffy when Buffy shares her strength to other women!
You're Amazing Selma!!
Selma Blair is so beautiful
She got so much better! God bless her! She’s a warrior! And she’s going to win this
wow I love her
I was terrified when she picked up that little boy.
She's a fighter. Not even a single tear in her eyes meanwhile I'm here crying like a baby. Damn!
First time posting and sharing.I was told Friday to get checked for MS by ER Dr cause of symptoms like burning thighs, numbness, tingling achy thighs legs, tremors inside and outside. Muscle twitching. Hard to move my legs, knees walk, I can barely stand on my legs they ache especially upper thigh area. I get tingling feelings in my face right side sometimes. I had it in my head for a few days then went away. I get these hot little spot I call like rain water drops feelings that burn ever now and then. A tight pull in my stomach. When I lay on my back or stomach the tingling and constricting of the thighs legs increase. When I sit it's the worst it increases it and I tremble . I don't see really anyone talking about the thigh upper leg issues. I had xray and CAT scan of back no problems they said. I don't have a lot of the other symptoms as others like virtigo, headaches, drop foot. Just tired of pain and not knowing what it's from. Sorry for the long rant and post. Thanks for listening.
Don't give up.Find a neurologist that specializes in MS
Need MRI not CT and x-ray .
Strong will power god bless you Selma love you!
The wall hits them all.
It is incredible how bringing up how MS affects you makes you start almost having like a mini relapse! As a person who has been living with MS for almost 10 years, I feel this struggle all too well. Keep on fighting, Ms. Blair!
What a brave young lady. I wish her health, success, and happiness.
Not taking anything away from Selma or this wonderful cause, but can we talk about how young Sarah Michelle Geller looks for a minute? I was like what the fuck! She looks not one day older than she did in 1997!
My sister in law has MS and I admire Salma for raising awareness and fighting this battle with courage and hope. I have seen my sister in law have good days and bad days. Thankfully for her it’s been mostly stable, but I know that it won’t always be the case. #hopeforthecure
She should see a Nucca Doctor. That may help with her symptoms
Blessing and prayers xoxo
😭😭😭😭 love her! What a great mama and person. ♥️♥️♥️♥️
Her son is so cute!
Just look at it as the biggest role you will ever play. Life. Make it worth watching. I know you will. Love everything you're in.
She makes me cry so much. Go Selma!!!
Autoimmune diseases are very weird I have Sjogren's
What an actress.......😳
❤️😢❤️ god bless you Selma
I've had MS for 11 years but I believe that I have had it my entire life. I went blind in the beginning, paralyzed, and terrified. I regained my sight and was able to walk again, but my fear of losing those things again are always on my mind. Now, my body has fallen apart and because of all my other problems, it;s hard to know if it's my MS that is messing with me or something else. I hope one day that MS can be stopped. It would be nice to walk without my cane and maybe even run again, Congrats to Selma. I've always loved her.