Christina Applegate
Region: US
Friday 04 September 2026 13:54:03 GMT
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user724507660028 :
One of the greatest things about social media is making people living with disabilities normalized. Thank you for your voice.
2026-09-04 15:23:53
592
Spencer Jordan :
love Christina she's still hot.
2026-09-04 21:04:29
37
Heather Gwenn Baxter :
The worst part about not having a MS friend to talk to is when I tell non MS people about my symptoms and they reply “yeah I have that too”. NO YOU DONT !!
2026-09-04 18:52:07
192
mike Putnam❌ :
Veronica corningstone forever 🥰
2026-09-09 10:50:33
1
Johnny V :
She is sooo great. So down too earth. What a PERFECT advocate for this terrible disease.
2026-09-09 10:04:32
0
Who dat? :
If you know one person with MS, you know ONE PERSON with MS. It’s a spectrum of symptoms for sure. Thanks for taking point on this!
2026-09-04 15:59:37
51
Jenesa77 :
I wanna know Ms if I have it I think I have it but idk what to ask my doctor
2026-09-09 10:43:28
0
Lisabella :
Thank you
2026-09-09 09:18:57
1
Eva :
Hope you’re able to make the best of it.
2026-09-07 21:33:15
0
Stephanie Bertrand :
MS is the fucking worst
2026-09-05 02:28:29
14
RooCorral :
I have been diagnosed with MS, lupus, sjogrens, RA, MCAS, POTS, and Ehlers Danlos Syndrome all since Nov. It has been a wild ride that I would like to get off of. All the doctors keep saying I won’t feel this way forever, but how long is that?! Every damn day is a struggle!
2026-09-04 19:13:39
7
Dee :
Please take care of yourself 💜💜
2026-09-05 15:53:21
7
Wait what? :
MS is a lot like what’s going on in the world. You wake up and there’s always some new thing to worry about.
2026-09-04 15:57:44
32
Wtzhpnn :
First attack in July of 1999. 💔
2026-09-04 17:53:16
6
Mary Williams :
We miss you!! 😘 😘
2026-09-09 05:10:01
1
Annie :
I have MS too and I fucking HATE it. I’m forever angry that this happened to me. It’s been nearly a decade since my diagnosis and I think it gets worse the older I get 😳
2026-09-05 13:23:43
6
freezing 91☮️ :
Yes I have a great MS doctor in Winnipeg.
2026-09-05 22:33:33
5
AnaBanana :
MS and Fibromyalgia. can we get a bl@dy cure now. I'm tired of cancelling "life"
2026-09-05 20:13:09
7
N :
My mum had progressive MS for 25 years. At the start the worst bit was people not believing her - she got fired from teaching by a principal who thought she was faking. Her resilience throughout the years and her adaptation was astonishing to me. She had incredible friends too. I love your advocacy Christina and my heart goes out to every single one of you.
2026-09-05 18:59:37
7
Nettie :
Wishing you a lifelong remission💗
2026-09-04 21:05:45
7
Karen Qualls :
My son was diagnosed with PPMS at 22. He is now 27 and been on infusions this entire time.
2026-09-05 19:59:40
7
leelee :
I’ve enjoyed watching you since you were on married with children.
2026-09-04 14:14:43
8
Mandy ❤️🔥 :
We love you 🥰
2026-09-05 01:51:32
6
Shelly1966🇨🇦 :
I wish the US had the same dedication to MS that Canada does.
2026-09-05 19:32:47
18
sharonfink :
My son and I both have MS . I use a walker and he’s in a wheelchair. Hate my symptoms.
2026-09-04 16:11:07
18
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