Christina Applegate and Jamie-Lynn Sigler open up about MS challenges
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- Опубликовано: 16 июл 2024
- The actresses talk with ABC’s Robin Roberts about their struggles and common bond battling multiple sclerosis and the launch of their new podcast, “Messy.”
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I have MS. It's very hard to deal with, but I just always try to find the blessings in things that may not seem like a blessing to others. I'm in pain almost every day, but my motto is that I'm thankful that I still have feeling. I can actually feel the pain. That may seem silly, but in order to live with this horrible disease, you cannot wallow in self pity. Days are tough and hard, but you have to keep your mind strong in any way you can.
Everything she said-is how it was for many of us in the beginning. You mourn your old self- and mourn the idea of other things.
But you don’t give up. In three weeks, I’m wearing a ball gown like Cinderella, and if I can stand only an hour, then it’s an hour. If it’s two then it’s two.
It takes a special person to understand the ups and downs of MS-I am grateful more people get it than nineteen years ago when I was diagnosed.
Thank you Robin for your reporting. This is National MS awareness month- many of us are participating in walks across the country.
Omg!!! I need this. I feel like Christina but isolating sucks 😢 wish I could hear them everyday ☺️
"We are all hopelessly human." Life is challenging no matter who you are.
Yes! Best comment !🎉
I love you Christina ❤❤❤
Love and prayers for Christina.❤️🙏 I’ve always loved her. Jamie Lynn I’m so proud of how brave and strong you are and what a fantastic support and friend you are to Christina. Heros can be found in many ways.❤️🙏
I have neuromyelitis optica which is a super rare form of MS. So glad they made a podcast. Watched every episode. Brilliant 💜
I have a rare muscle disease and it honestly helps so much to not be alone! Physical disability sucks!!! I want so bad for my muscles to stop wasting away but the hardest thing of all is having to be so vulnerable in public!!! Thanks for giving a regular face to physical struggle!!
I totally relate to them!! I became very sick overnight with Chiari Malformation, syringomyelia and Lyme disease back in 2018 and was deathly ill and I’m still very sick but after many brain surgeries and medicine and most importantly….ACCEPTANCE, I’m doing better but it’s HELLLLL!! Keep on keepin on ladies ❤️❤️
I’ll keep all of you in my prayers 🙏🏼😘
I got a primary progressive diagnosis in 2012 when I was 19 yo. There is no getting better with progressive MS. Only getting worse, and there are no medications for us…
💙😢💙
♥️
There was a doctor who used ultrasound to stop a shake in a Parkinson's patient that he had for several years and it only took this doctor 2 hours to permanently stop the shake. The video is on RUclips and the same doctor also used ultrasound to permanently stop Alzheimer's in two patients.
First
How many have gotten ms since being the covid vax?????
Don’t do that garbage here!!
@@sallypea3202 I know two people that got ma after vax, facts. Don't do what, save lives, wake up the excepting of tyranny or violations of the neurenburg trials. Research stop hating thinkers n researchers. Be a Patriot, not a door mat.
I would love to see a list of what they were eating and I could tell them why this happened. This country is poisoning us.
No dum dum. Your diet doesn't cause MS. What an ignorant and uneducated thing to say.
Just shut the fuck up this is about supporting people!! What even is your point!! My father did everything right his whole life but his brain is rotting from Alz!! So just go away!!!