Selma Blair opens up about journey to recovery from MS treatment l GMA
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- 게시일 2021. 10. 10.
- The actress, who is releasing a new documentary this week titled “Introducing, Selma Blair,” received an experimental treatment for multiple sclerosis.
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#GMA #SelmaBlair #IntroducingSelmaBlair #MS - 엔터테인먼트
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She's almost 50 and she is stunning! Doesn't look a day over 35.
Soo stylish too:)
Omg is she?!?!? She looks better than my self of 35
Wow I didn’t know she was that ‘old’ , looks incredible…
And…shes been through hell in back. She does look gorgeous. 🙏🏼
For real!!! I need to do better…
It's' not about her being famous as much as it is about showing her humanity in the face of adversity. May she be blessed with a long healthy life.
For a better life we need better love and affection enjoy the better
cute beagle
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@@crubbythebeagle57 This isn’t about you. Stop trying to get people to watch your channel. This is about Selma only!!
@@auntielisalisabopeepsa Thank you for saying that👋
God bless you!
She's so sweet. I pray there's a cure in her lifetime. 🙏🏻💖🕊🙏🏻
I have SO MUCH respect for her for being not only willing, but adamant about showing a genuine picture of what MS looks like. Like she said, visibility is so important. So beautiful!
Ms can Look Like anyone
I agree. This is too painful to watch and full of courage.
@@ippg9099129061 But why doesn't she seem to have difficulty walking in After 1 & 2?
@@giosy0072 people have flareups. sometimes it is much harder to walk,/speak than others ... people have good days and bad days. it can be a very very bad flareup and sometimes it is not as severe.
It’s a nerve disorder, so the muscles are healthy. Sort of like; the hardware is ok but the software is malfunctioning. So the signals being sent to the legs can get there just fine sometimes, and sometimes not. I hope this helps the question.
She looks badass with that stick and that haircut. More power to you, girl!
I was thinking the same thing. She looks absolutely gorgeous. I know it’s not the focus of any of this but I think it should be noted.
💯
agree, she still shines her beautiful essence which illness cannot blur
exactly
Her struggle brought me to tears. It definitely is a reminder never to complain about life when we’re healthy.
Me too.
Babe' 13 years and got other auto immune. She has support & money. PS, ms doesn't kill you, it's the symptoms.
@Maria EXACTLY when I see ppl complaining about petty things I SMH🤦♂️
Amen
I agree
She looks way better than in last year's interview. I hope her story triggers more research into MS
Yep
Hopefully one day there will be a cure
Same here; she has made so much progress and so brave as all her effort to take on these treatments will push the needle
I agree so much better!
Definitely, please
My Dad was diagnosed with MS at 21 years old. He did experimental drugs including chemo to try and find a cure for this disease. Unfortunately,the chemo made him go from using a cane to a wheelchair really fast. He fought so much and helped so many with the MS society. He was the President of the MS society and even won Father of the year twice from the MS society. The disease eventually took over his whole body,he ended up in a nursing home at the age 43 years old. He passed away at 46,I miss him so much but have joy and peace that he's free from this disease and is in Heaven. He suffered so much but always had a smile on his face. He's my inspiration❤
As a woman who’s been battling chronic pain for 26 years, Selma is an inspiration! She has such a better attitude than I do, and her illness is so much more serious. Selma is one brave lady and she gives me hope! I wish her as much healing as possible! She’s absolutely gorgeous! Inside and out!
YES 💝 solidarity sister 💕 I am living a similar situation and feel the same pride and inspiration when someone in the community is thriving and using their strength for good - when they could be saving their energy for themselves, still fight the good fight for the rest of us still battling. Big love. Thank you for your words 🫶🏼
@@DancingTehani
Thank you! I’m so happy to see Selma is in remission!! Sending much love and light to you sis!! 💕✨🙏
I have MS too, watching the way she struggles makes me cry. It's harder than people think. I'm so glad she's doing better than she was.
🧡🧡🧡🧡
Prayers for you🖤🖤
Same here...she is an inspiration and so are you.
I wish you the very best.
You're not alone 🧡🧡
She IS FREAKING ROCK STAR FOR BEING SO TRANSPARENT. GOD BLESS HER.
DEFINITELY ADMIRE HER HONESTY, GOD BE WITH HER🙏
god? Stop.. why would god torture her..>>??? Good plan it had....
The strength of this woman is incredible God bless her.
I agreed she is so inspiration Wow
Bullshit artist.
@@sandrabarnett1499 and it stf wasn't fake gods doing!
god f'ed her....
@@mikehd3904 u ok?
Disabled people deserve to share these stories. I’m disabled and this was incredibly validating. You go Selma! Thank you for helping our community!
She looks well and she’s talking so much better.
I know. She is doing amazing and her voice is practically back. Love seeing this. Saw the first video when she first came out.
Indeed!
Talking better? Wow...must've missed earlier videos
That's the good & the bad with MS. It wasn't until I started falling and eventually got a walking cane...ppl thought I was drunk due to my walk & the falls left me looking like a domestic violence victim. Prayers up for Selma.
@brookekelly
@Julie4evert please don't look it up. Auto immune diseases like MS are day by day. I can almost guarantee she may be feeling like crap. The lesions take over when they see fit. So there might be a picture taken of her next week when she's at a level 1 & perhaps her gait is off. I would implore ppl to celebrate her for today and pray her unconventional treatment works. 🙏
She is so brave to show the reality of this disease.
Hello how are you, I hope you have a great day.
She's amazing & courageous..
Most importantly I think she's trying to help spread the awareness of this disease & to show it as raw as possible is much needed here.
I was diagnosed with MS in 2021, I almost lost my complete eyesight, still can’t see very well. Walking without a stick has become impossible for me, too. This disease is so scary and different for each single person. It gives me strength to see people like her! Never give up, even if there is no cure .
I have MS and had HSCT in Puebla, Mexico at Clinica Ruiz. I highly recommend anyone with MS, especially early in the disease and with a low EDSS, to look into HSCT
Try to take enough vitamin D at least 2000 IU per day ...
This is so sad and heartbreaking, yet it’s inspiring and strong. I care more about her story than her acting.
@@chris1960 Well with that attitude I hope your condition begins to accelerate uncontrollably in a more pronounced way. That way the rest of us can focus on a more positive and empathetic world without your input of negativity and judgment. 😊🌞⛅️
Her last sentence when she said "I never felt that before" broke my heart 😭😭😭She is so right!!
Hi how are you doing today, I hope you have a wonderful day.
My coworker got MS. She was fine one day and then she wasn’t fine the next. It really is that fast once it starts to manifest. She looks up to Selma Blair for inspiration.
Had a coworker experience the same. One day she was fine and the next week she was going blind, walking with a cane. 30 years old with twin toddlers 😞 I felt for her. ❤️ wishing anyone going through this all the best.
The important thing to remember is that MS is a very variable disease. Each person will experience it differently. Not everyone will be affected quickly or at an even rate. A diagnosis of MS is life changing but not a guarantee of immediate disability.
@@GFSTaylor You are so right much more enlightened.
@@GFSTaylor {A diagnosis of MS is life changing but not a guarantee of immediate disability}or guarantee of any lasting disability, it can be reversed &/or potentially cured. I turned around my life, haven't re-experienced the 1/2 body numbness/pins n needles, & feel healthier than before it all happened. I rewrote all of my recipes cutting out the things research said might cause or aggravate it & would rather take a little potential inconvenience over the alternative.
Not everyone is blessed with Stemcell treatment bc of cost and insurance denials. I'm happy for her improvements however, I would like to see and hear them advocate for insurance approval nationwide
Exactly and bringing up the subject doesn't detract from her pain or her struggle but it is an important point to make that many people with MS don't have the privilege to get experimental treatments like this person of privilege was
Absolutely. IT SHOULD BE AVAILABLE FOR EVERYONE, NOT. JUST. THE. WEALTHY.
@@stormyweather9570 how come?
@@stormyweather9570 in cali?
@@stormyweather9570 oh ok. I guess I just assumed she had it done in CA.
My wife was diagnosed with MS in July 2020. It’s been a struggle for her but she isn’t anywhere near as bad as this. Oddly enough 3 other women locally have MS but kept it quiet and my wife found out for support. It was shocking. Don’t let one person’s story scare you and make you think this is what MS is. Because it isn’t. Each person is completely different. Don’t let her story scare you
Thank you!
I'm sorry to hear about your wife but please keep in mind the best and brightest scientists are working extremely hard to find better treatments and a cure for m.s. patients. I wish your wife & you well.
Hate to hear that about your wife 😞yet glad she found support from others with our crazy invisible illness . Tell her keep the faith it’s been 6yrs for me and first couple of years was my worst and was definitely a struggle and I lost everything and felt like why me? until I learned my body and MS and what it likes and doesn’t what works and what doesn’t . Tell her too do research ALL the research she can and too be her OWN advocate …because drs just want too write scripts and get paid and our meds are NOT cheap but like all meds have irreversible side effects so take heed in that. I wish her well and she’ll be well 😊 as long as she keeps a positive attitude even when it’s hard don’t stress and kick MS ass because we have it it doesn’t have US unless we let it. Much love to her and you and make sure you give her as much love and attention as possible so you too will know when she’s not having such a good day because everyday isn’t always good but have faith. 🤗🧡
It's nick named the snowflake disease for a reason because no 2 people battle it the same way.
I was diagnosed last year as well. I've had it for at least 11 years before I knew it (that's the 1st recorded dr. Visit I had complaining of numbness)
Selma's MS is more progressive compared to some and others are far more severe, like my husband's friend, who passed away 2 years ago with it. Just as many other diseases, its ugly and isn't any fun. But I tell myself each day that it could be far worse
John Nolan Don't think she put her story out there to scare people. She is making people AWARE of what MS CAN look like.
She really shows priorities in life, and the priorities she's choosing. I really appreciate her comments about people with chronic illnesses and chronic injuries. Thanks Selma!
Always love to see Selma she’s such a beautiful soul and so strong to show her real self, I certainly hope she does more movies in the future.
agree. now I want to watch Hellboy again.
With her speech, I’m not sure if she’d be able to. I don’t say that to be mean, but Hollywood seems pretty ableist. Disabled people are usually played by able bodied people.
Brave lady to show herself being less then perfect as most in Hollywood only show! Bless you I wish you all the best in life ❤
@@joanpaterson7605 I agree, i say she's strong n AMAZING woman I hope n PRAY for her wellness.
@brookekelly Michael J. Fox has Parkinson's disease, not MS.
I really hope she gets better because she was a fine actress I watched her all through the years we growed up together I really hope she gets well
I am amazed by Selma's bravery. I cannot imagine how she has raised a beautiful son and kept her positivity. MS is a terrifying disease.
She's so beautiful and inspiring. God bless her.
Hello
🌹🌹🌹🌹🌹🌹🌹🌹🌹
For a better life we need better love and affection enjoy the better
cute beagle
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She is hermosita ! she is the spitting image of her Mama . seeing her crippled reminded me of my gran with parkinson .
She is beautiful, my goodness look at her… gorgeous!
having any chronic condition can take a toll on one physically, mentally, and emotionally. it can also take a toll on those around them also. keep on fighting.
Yes @PJF so very well said and stated...👏🏽
Correct. Whether severe mental or physical illness , seen or unseen.
truly. as a very chronically ill person i’m not sure who it’s harder on, me or my father. the guilt is as unbearable as the pain.
Chronic pain and illness is so so draining!!
@@meowzy2439 i think it could be equally draining to both of you just in different ways. just like you might feel guilt, it is quite possible your father feels guilt or other negative feelings but for different things. it doesn’t minimize your feelings or his feelings. personally, i think it matters more how you deal or cope with those feelings. some people project them. some people deal with it and then move on. some people use it to victimize themselves while others turn it into something that they are surviving, overcoming, and learning to cope and adapt too. for some people it turns into or stays as depression, anxiety, etc. it isn’t easy on anybody, and it can make it easier or better when those feelings are acknowledged by all parties involved. take one day at a time and baby steps. do what you can when you can.
I watched Selma's documentary and I cried. Her strength is phenomenal. Her openness about her relationship with her mother. The brilliant and loving relationship that she has with her son. The loving support that Selma is given by friends, family, ex-lovers, and business associates is awe inspiring!! For all the hell that Selma is going thru I am happy to see how truly blessed she is during this fight for her life!
Yes! You said it all perfectly!
want to cry, I had no idea she was struggling this hard. She is freaking amazing, total hero.
She’s so beautiful, she looks healthy, thankful for you sharing your story.
Hi Jenny how are you doing today, I hope everything is going absolutely perfect with you...
Selma Blair’s courage and strength are astounding. She deserves ALLLLL of the best.
She is a true inspiration. She looks totally AMAZING, wish her the very best and continues to kick butt.
What a powerful woman. She looks amazing too. Wish you the best, Selma.
Her story is inspirational to both health and unhealthy people. If you’re healthy enjoy life to the fullest. If you’re not healthy, take care of yourself and continue to live your life to the fullest.
For a better life we need better love and affection enjoy the better
cute beagle
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THIS!!!!
Yes But if you're healthy help people who are unhealthy because a lot of disabled people do not at all have to help that's actually needed in an inaccessible ableist World practicing eugenics
Her son will be so proud of his mom. Selma has such a great sense of humour and ability to make others smile
she looks incredible, god bless this brave woman, she is an inspiration
WOW. I dont even know where to begin, so i guess I'll start here.... ♡ My mother has been suffering with MS for as long as I can remember. She was diagnosed when I was 7.
She has been through HELL & BACK, then back to hell, then BACK AGAIN.
You are an incredibly strong woman for deciding to share your story. 💜 💖 You will never know how many lives you've touched & saved. God Bless You, angel! 😇
What an inspiration she is! As someone who also struggles with MS , I am so very appreciative of her courage to use her platform to share her important story. I also am very grateful to Robin for her role in bringing Selma's story to us. Thanks, Selma and GMA.
Same here and know first hand what a struggle it is. Selma sure is an inspiration.
I constantly tell myself, It can always be worse. 😁
i don't have MS but i can understand living with conditions that impact your day to day and will never go away. When you said courage, i believe it. On top of the ways on which people can suffer there can be a stigma in voicing it. i feel like when people who were on the spotlight step up and share their experiences, it really can help make a difference, both for those who can identify and for raising awareness. There's definitely more i could learn about MS, so it's a learning opportunity for me. i found it really interesting listening to her talking about "natural only" then relating the instant change chemo has made in reducing the inflammation. In particular i found it courageous for her to speak when her speech is affected and to not shrink away. That's easier said than done but like she said, shrinking away.. it's tough on the soul. I fully embrace this interview. We all need to learn more about this condition IMO which affects more people than i think the average person might imagine.
Hi. She said she's never felt well her whole life. Is it something you always feel even though it hasn't reached such a state yet? Good luck to you.
Indeed me too! MSer here… she just gives me so much hope.
Was looking for this post and here it is! I am 28 and on Ocrevus for my MS, was diagnosed officially right before I turned 26 but my doc even agrees that I had likely been struggling w/ it for at least 3 yrs prior based on symptoms. I already have another autoimmune disease which was diagnosed when I was 20 along w/ an accident I got in that year and then a car accident at 25 and so a lot of that caused my MS diagnosis to be delayed. This video brought tears to my eyes as she is SUCH an inspiration, and then also my dad just passed away right before Christmas this past year and the last trip he and I went on together was 2 weeks before he ended up in the hospital. He went w/ me to Mayo Clinic in Rochester to try and get some more opinions and better treatment for my MS. Well the doctors were truly awful except the urologist who was a legend forsure and I was so angry bcz I also have arthritis so the change in pressure from flying tends to cause my arthritis to flair up which then tends to cause my MS to be more severe than normal (I don't get MS flairs really since I live w/ the symptoms every day) and so by the time we went to fly back home, I was so sick that I was downing double shots of Henny at the airport bar even though I don't drink much anymore bcz I thought "ill feel like shit later but at least theres my medical mj at home and in the meantime this will help me make it on this last flight without wanting to kill myself." Well now after my dad has passed and everything, I look back on that trip in a totally different light, as it was the last time I got to spend any real 1 on 1 time with my father and our relationship was garbage when I was growing up. By the time both of us had changed & thus fixed our relationship about 7 yrs ago, I was already sick to a fairly decent degree, and so our relationship was also a lot about me being his daughter who didn't feel well, his daughter w/ the one problem that he couldn't fix even as a doctor and so I felt that in my soul when Selma spoke about her mom. I like to think that my dad is watching over me and that he is part of why the Ocrevus that i'm on may not be helping a ton SO FAR, but it's improved my overall symptoms by 25% so far and it hasn't even been the full 12 weeks yet so fingers crossed it'll help even more. My mom is still alive and has always been my bestfriend and I would give ANYTHING for us to be able to go back to how we were---mother & daughter duo who joked and had a good time all the time and were both grown women living their own lives vs now where i've reverted to being a dependent essentially. Sorry for talking about myself so much it just kind of came out
I feel her pain, in 2006 I was diagnosed with myositis, I was in a wheelchair with my head having to be strapped to it because I only had movement from my knees down and elbow down. I would drink water and it would come out of my nose. I needed a caregiver 24/7.In 2008 I did a clinical study for a drug infusion of Rutixan..Not only did it help my disease, I was able to return to work , driving, walking etc in a preschool. I need the infusion every 2 years and pray that a drug comes along to battle MS
Selma is a gem to humanity. Listen people!!!
We all have struggles, but when you see that there is always someone who has such a heavy struggle like hers, it is very humbling. God bless her, and all who carry such hard struggles.
Dr Adrain on KRplus have permanent cure for any kind of Viruses or Diseases
She’s a stunningly beautiful person inside and out.
💯👍
Autoimmune diseases can be so tough. So inspirational and brave sharing her story like this!
I was so inspired and encouraged by this beautiful woman. I’ve stuttered since I was 6 years old & went through kidney failure at the age of 27. I started bawling when they said her son’s name is Arthur 😭💗 That’s my son’s name too & he’s 8 right now 🥰 God bless, comfort and strengthen Selma Blair 😘
Love you rock😎
Selma is such a beautiful person and she has a loving heart. You'll always be beautiful Selma Blair ❤
I know someone who had ms for almost over 15 years, she was bed-ridden for a long time and one day she woke up and started to walk again. Doctors didn't understand how it could happen but she is fine and lives her life now. Anything can happen. Miracles do happen in life. It's really inspiring how Blair keeps fighting.
I so wish that kind of miracle could happen for my Mother. As her daughter I wish to see her heathy during both are lifetimes. She’s been sick my whole life. She can talk pretty good and we can laugh together still which is a positive.
Did you ever ask your friend what she believes happened to cause her to walk again?
Did something change within her?
Im curious as i had a neurological issue 22 years ago resulting in loss of feeling in some places.
The feeling suddenly started returning mid 2020 including muscle recovery.
Thing is i know what caused my healing and i want to see if its the same for your friend.
There’s periods of remission with MS.
There is something called the Wahls Protocol that promises to reverse the symptoms of ms. It is based on a diet of raw foods. Please if you know of someone with ms, have them check this out.
@@skellington2000 Thank you that's good to know.
She is so beautiful!!!!!! I am so glad she is accepting this new reality. Acceptance can be very healing, even for your physical self. I am so proud of her. More beautiful than EVER! STRENGTH IS TRUE BEAUTY!
Selma, I suffer from a chronic, painful condition called EDS [Ehlers Danlos Syndrome] and I want to say, KEEP ROCKING GIRL. You look stunning, you are strong, take it day by day sweet love. I am in your corner, fighting and hoping you recover to the point you can lead a pretty normal life.
I am in the healthcare field and have seen EDS in textbooks countless times but I never read that it is actually a chronic painful condition. Thank you for sharing.
Selma Blair is lovely. She has the strength of character to openly discuss her MS. It seems challenging. I will pray for her on her road to recovery. God bless.
Her strength is so admirable and moving, i can’t help but cry. I’ve allowed her as she’s such an incredible woman.
Hello pretty
For a better life we need better love and affection enjoy the better
cute beagle
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She looks great from the last time she got interviewed. She is a warrior
So people who die or get worse with their conditions are not ''warriors''? You're only applauded when you recover by this logic, right? I love and applaud Selma btw.
@@yevgeniyaleshchenko849 you.are graping at straws.
For a better life we need better love and affection enjoy the better
cute beagle
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I met Ms Selma Blair today, she asked my name and hugged me. Didn't even hesitate. She doesn't know it but she made my year. Just a beautiful person inside and out.
She looks amazing...Cannot believe someone here said she is almost 50! What a strong woman to have so much hope and optimism! I wish her well!
I’m admired by her strength and determination. Living with an autoimmune disorder and/or a terminal illness is traumatic. She gives me courage and hope 🌷
😘😘😘 love and blessings, sweetheart ... thinking of you.
I love her! And the fact that she has shown this part of her life is going to help soooo many! Gorgeous 🙏🏼❤️
For a better life we need better love and affection enjoy the better
cute beagle
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krplus.net/bidio/odGGiKh2mW7HqJQ .....,,
I have primary progressive MS and this is so hard to watch but also so amazing at the same time. I thank her for her vulnerability.
My husband has primary progressive ms and it took me 3 days to watch her documentary and probably 6 boxes of tissues I hope your doing well we have our good weeks and bad but thankfully people are trying to slow it to a stop let's hope science figures out more advance methods soon
I'm sorry to hear of your struggle. I don't remember if the is the type Dr Terry Wahls has or not, but if you have the time to watch her tedtalk it is definitely worth it. I have never been as bad as Selma, she is inspirational. I have mitigated my symptoms through dietary change, vitamin D, positive attitude & the stubbornness to declare the deterioration my art teacher had experienced is not going to happen to me. I wish you the best with the greatest possible outcome!
"I wish she could see I am ok" is where she got me. Salma, you are brave and you are an inspiration. Wish you all the best. To you and to your lovely son. :)
Can we just talk about how gorgeous she is, and how beautiful her hair is as well. She looks in credible and your outlook on life is impeccable
She looks better than ever
She’s so so brave. I had a teacher back in grade school with MS and she was one of my favourite teachers.
Me too! MS is a scourge.
Selma is an open and transparent person. Beautiful through and through.
HER BRAVERY IS HER STRENGTH....
BLESS THIS WOMAN.
Selma, your mother knows just how well you’re doing. She is closer than you know.
You are so right !! Blessed be ❤
She is a real warrior and I am really pulling for her.
She's a real rock star. Absolute inspiration. I'm so rooting for her and others with this condition🙏🏼
Selma looks great.. i love her hair cut, it makes her look like a strong fighter. I wish her well because she is truly inspiring. I suffer with chronic pain from injury and i wish her well because it’s not easy to deal with pain and recovery.
Two amazing women, Selma Blair and Robin Roberts. Thank you, for your wonderful influence on society
I've never seen MS effects like hers. Bless her heart. She's a brave and vibrant soul.
Because it’s exaggerated to high hell. That’s why.
As we have unique nervous systems, no two people with MS will have the same symptoms. They may have “similar” but each journey is different.
MS is incredibly complicated. I think that’s why we haven’t made a ton of progress. Some people can go on living normal lives and retain bodily function, but some people can lose functionality fast. I know she “came out” as having MS recently, I wonder how long she has known. The earlier you find out and get treatment the more likely you are to prevent attacks and to get to a stage like where she’s at
@@allie9015 go back into your hovel, troll.
@@allie9015 You don’t get it … until you get it 🤷🏽♀️
Sending Trillions of angels Selma's way what a beautiful soul she is!
Amen! 🕊🕊🕊 Such a beautiful soul ✨✨✨
Prayers 🙏🏼 for those going through disability or illness.
As someone who has MS, I am so happy to see Selma doing so well and sharing her journey. Thank you for being open and genuine about your life. I needed to know that even through the hardest times, joy is what keeps us surviving
🧡🧡🧡🧡
Wishing everyone with MS healing...new effective treatments... happy and long lives🙏🙏🙏💗💞
I was diagnosed with Ms in 2012 I really didn't believe I have it I woke up one morning and just fell down on the floor couldn't Walk or talk didn't understand what was going on with my body. I saw three different doctors I also had a spinal tap which caused me some side effects that never got reverse living with Ms everyday is hard "BECAUSE most people do not understand what's going on inside your head you look normal but you don't feel normal. there's a lot of things that's going on in your body sometimes you're embarrassed to talk about or also you don't even understand. Explain to people MS symptoms will go away for months for me and then all of sudden just comes back with a bang. it's a very hard disease sometimes I have very bad left side weakness sometimes I don't remember things or people if they don't talk to me for a while sometimes you feel like being alone sometimes you don't want anyone to talk to you. certain sounds and smell that bothers you environmental problems things around you people voices lots of people have different symptoms sometimes very hard for people to relate to you even if they have MS because everyone has different symptoms sometimes you struggle to talk sometimes it comes out clearly sometimes you think you're talkin clearly but it's not clear to others people so it's kind of frustrating and for me everyday I wake up to something new sometimes the house look different to me sometime sometimes if I don't talk to a person two days I forget they exist until they call me a lot of people don't understand that Ms is not just a physical it's emotional and mental disease are drained you it makes you feel depressed sometimes most doctors told me I was fortunate because I can still walk and talk in a lot of people don't get to walk and talk which I know because I took care of a lot of patients with MS didn't walk and talk but when it becomes you you struggle to understand a lot of things but I'm grateful that the days I can talk clearly and some days that I struggle I repeat things and sometimes people say why you repeating things and they don't understand that it's not something you're trying to do it just happens sometimes to get you even said something less than 5 minutes so you repeat it again. For Every with MS YOUR not ALONE stay strong take each Day as a BLESSING.🌹🌹🌹🌹🌹🙏🦋
Thank you for sharing your journey! Made me cry while reading. Have such empathy for people with chronic illnnesses ❤ May the power and light of the LORD be with you always!! ❤❤❤
@@bravesoul5743 Ameen ! thank also with you .i appreciate your kind words🙏🌹🦋
Yes, Ma'am. I will strive not to forget your words. God Bless you and your family, Nicola. Keep talking to us. The more that you speak, more will listen. I am listening out here and talking less; and I am praying. Huuuuuuuuuuug.
@@bravesoul5743 Amen.
I pray that they find a cure soon so you no longer suffer.
I really love what she said about finding joy in life even through the pain and struggle. Even when things are hard, there is strength in finding opportunities to experience joy and make a positive impact on the people around us
Bless her, I’m glad to see she’s doing well. I got sick 5 yrs ago and chronic illness is no joke. We need more awareness and understanding
Much love to Selma Blair. I've always been a fan and much more now.
She’s such a strong person. I’ve always loved her work
Huge bravo to Selma, she's an inspiration with her drive to fight on. And she looks amazing!!
She instantly brought me to tears. So strong, so beautiful, so much wisdom and beautiful strength. Keep up the fight Selma! #multiplesclerosis
Selma is such a sweet person
Living her best life
Continued good luck and health
Pretty hair
Hello pretty
How are you doing
Hi....
She looks absolutely gorgeous here. I can’t wait to see her in a new movie❤️❤️
Hello pretty
Hi how are you doing today, I hope everything is going absolutely perfect with you.
@@travistaylor2823 Boy Travis you’re a busy man.
know I'm not, Where are you from my friend.....
@@travistaylor2823 look at the title of my name. That will give you a big clue
So happy to see she is improving and very confident. Tears came rolling down.
This woman along with my mother, is my hero. May God bless you Selma!!!!
Pray everyone with MS can access good treatment too. Such a tough condition. Lets keep researching to prevent this dreadful disease.
Such a strong spirit. God protect her and keep her strong ❣️
I will never recover from my crush on Selma Blair. She is so beautiful and sweet and kind and wise. She is much admired and appreciated. Many Blessings to her.
MS pissed me off, 20 years ago I was diagnosed, Fired from my job, went to many doctors appointments. MS is growing
She’s always been such a beautiful woman, she’s so strong and inspiring
She looks amazing, I happy she's doing so much better, I really hope she gets back into acting soon I miss seeing her on screen.
Selma Blair is such an amazing person.....her honesty gives open mindedness to those who are unaware and hope to others with MS. T
Selma Blair... You are an amazing woman. I suffer from a lot of medical problems and went through a lot of ridicule because I was undiagnosed for so many years and it left me defeated. Finally one doctor took me seriously and hooked me up with a specialist who finally gave me a concrete diagnosis. Finally... Validation. I also suffered from childhood on. You keep up the good fight. You are in my prayers. You go girl!!!!
I can't imagine what kind of journey this has been for her...
I lost my mom March 2021, and every single struggle without your mother after losing her...is hell. I am so thankful for my health, my husband, my amazing daughter, and my little unborn baby boy whose kicks remind me every day the preciousness of life.
MS is freaking horrible..I've seen people really struggle with that disease and it's horrible. I'm going to give that documentary a watch.
She is amazing. I had no idea she had MS until I saw this. She’s an inspiration to others by sharing her story even to me. I don’t have MS I have fibromyalgia, back issues etc and she inspires me not to give up and give in. I wish her all the best 🌹❤️
I know what you mean about your mom, Selma. My mom has struggled right alongside me, through my illness. If I get well, I hope she’s still here so I can pay her back a fraction of the care. ❤
I have MS too. Wishing you strength & courage! ❤🙏
I never knew she was going through this and I grew up watching her! So strong, so intelligent, and sooo empowering to listen to. I’m going to keep up and watch her documentary. May she keep telling her story and is getting the chances to live her life gleefully. SHES SO BRIGHT YOU CAN SEE HER GLOW 🥰❤️🩹
I thank her for her years of talent she shared. And the ultimate strength in showing her journey through MS! I love you, only wishes for the best forever on !
This is what happens when a beautiful person outside is just as beautiful on the inside, she has no flaws, no one is perfect but she is perfectly imperfect.....Beautiful.
I have to say I bawled like a baby watching her struggle in the documentary but I also busted out laughing at her jokes & smiled really big at the end. I have always loved her. I pray that she can stay in remission & raise her son with all the love she has to give. ❤🙏
Hello
Could you please tell me what the documentary is called ❤
@@aineeva34 Hi, yes its called, Introducing Selma Blair & I think at this time its streaming on Discovery Plus & Hulu. Its a very personal in depth look into her life with MS & its heartbreaking & inspiring at the same time. Excellent Documentary. Enjoy ❤
@@southernbelledebbie7705 thank you so much Debbie God bless ❤️❤️🌹
Selma is so awesome! She's honest, humble and beautiful... I cannot express how thankful I am for her sharing her courageous journey with all of us. She's helping people suffering with MS and other autoimmune diseases ...when you feel like your life is over because you are suffering but then you see her fighting so gracefully, you realize you too can fight for a better life and health as well!
I love her brave soul
Hello
Very brave and inspiring person. Thank you for sharing your story
What a brave soul. Nothing but respect and love to her and her little boy
I have had MS for almost 5 years and my heart aches for her. She is looking fantastic and I glad she's doing well with her treatment. 💕 I love learning new things about MS and discovering other celebrities with MS. She'll always be amazing. 😊
I have MS and had HSCT in Puebla, Mexico at Clinica Ruiz. I highly recommend anyone with MS, especially early in the disease and with a low EDSS, to look into HSCT