- In a new Instagram post, Selma Blair shared a video of herself one year ago, before she was diagnosed with multiple sclerosis.
- The video shows how much has changed in a year for Selma and her son Arthur.
- Notably, the video shows how Selma’s voice sounded before MS made it difficult for her to speak.
It’s no secret that Selma Blair has had an intense year—but her positivity and attitude in the aftermath of her MS diagnosis has been downright inspiring.
Selma shared a cute video on Instagram from a year ago of herself and her son Arthur talking about their plans for the day. “One year ago today! From #Minecraft to #fortnight in one year,” she captioned the video of her son gearing up to play video game Minecraft. “And I have shorter hair now. That’s the only difference for me. Not. What a difference a year makes.”
One year ago today! 🖤From #Minecraft to #fortnight in one year. And I have shorter hair now. That’s the only difference for me. 😂. Not. What a difference a year makes. 🤯
A post shared by Selma Blair (@selmablair) on
Selma revealed in October that she had been diagnosed over the summer with multiple sclerosis, a chronic and often debilitating disease. “I am disabled. I fall sometimes. I drop things. My memory is foggy,” she wrote on Instagram at the time. “And my left side is asking for directions from a broken GPS. But we are doing it. And I laugh and I don’t know exactly what I will do precisely but I will do my best.”
I was in this wardrobe fitting two days ago. And I am in the deepest gratitude. So profound, it is, I have decided to share. The brilliant costumer #Allisaswanson not only designs the pieces #harperglass will wear on this new #Netflix show , but she carefully gets my legs in my pants, pulls my tops over my head, buttons my coats and offers her shoulder to steady myself. I have #multiplesclerosis . I am in an exacerbation. By the grace of the lord, and will power and the understanding producers at Netflix , I have a job. A wonderful job. I am disabled. I fall sometimes. I drop things. My memory is foggy. And my left side is asking for directions from a broken gps. But we are doing it . And I laugh and I don’t know exactly what I will do precisely but I will do my best. Since my diagnosis at ten thirty pm on The night of August 16, I have had love and support from my friends , especially @jaime_king @sarahmgellar @realfreddieprinze @tarasubkoff . My producers #noreenhalpern who assured me that everyone has something. #chrisregina #aaronmartin and every crew member… thank you. I am in the thick of it but I hope to give some hope to others. And even to myself. You can’t get help unless you ask. It can be overwhelming in the beginning. You want to sleep. You always want to sleep. So I don’t have answers. You see, I want to sleep. But I am a forthcoming person and I want my life to be full somehow. I want to play with my son again. I want to walk down the street and ride my horse. I have MS and I am ok. But if you see me , dropping crap all over the street, feel free to help me pick it up. It takes a whole day for me alone. Thank you and may we all know good days amongst the challenges. And the biggest thanks to @elizberkley who forced me to see her brother #drjasonberkley who gave me this diagnosis after finding lesions on that mri. I have had symptoms for years but was never taken seriously until I fell down in front of him trying to sort out what I thought was a pinched nerve. I have probably had this incurable disease for 15 years at least. And I am relieved to at least know. And share. 🖤 my instagram family… you know who you are.
A post shared by Selma Blair (@selmablair) on
Since then, she has described details of her MS flares, revealed that she relies on a cane to walk, and shared that she has spasmodic dysphonia, a disorder associated with MS that makes her voice shake and break (if you listen to Selma’s throwback video, you can hear her voice, shake-free—quite a change from how she sounded during her latest interview with Good Morning America.
Selma also recently revealed that her eyelashes are falling out—not necessarily a direct symptom of MS, but something that may be linked to a medication that she’s taking.
Still, Selma has repeatedly stressed that she’s happy and thankful for the things she has, including friends like Sarah Michelle Gellar and Jaime King, who sends her fresh flowers every week. With an attitude like that, it’s easy to see why so many people have found her inspiring.
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