I cried when I saw this. I remember her as Kelly on MARRIED WITH CHILDREN.. the movie THE ANCHORMAN. etc..Shes always been ...& STILL IS beautiful. My husband has Progressive MS & I know how hard it is . He went through depression & cried alot. The best thing is to join a support group. Listening to other people w/MS ,share their stories, tips, diets, etc..really helps. Sending love & prayers her way
Christina Applegate showing up at the 2024 Enmy's is one of the bravest things that she's ever done. Christina, you are still one of the most beautiful women ever. Long live Kelly Bundy. 😢
Christina Applegate's raw and real talk about her MS journey is both heart-wrenching and inspiring. Proof that even when life gives you the worst, there's still a way to make it work. 💪💖 #StrengthInVulnerability
I can't wait for the podcast. My cousin suffers from MS. She had symptoms early in life. Now she has a lot of physical restrictions. She was a nurse and didn't see the signs like Christina until she had mobility issues.
Being transparent with this and with the platform she has is perfect and brilliant and courageous, for others to see, research, and either know their own symptoms to seek help or for others to be aware and less judgemental.
Chronic illness/pain is such a rollercoaster and right when you think you've passed over that hump, something will suddenly pop up and be an issue. I've had CRPS for 9 years this year and when I connected the dots and had the realization that all dental issues will be permanent, I cried. 9 years later, I cried. That's okay, it's taken me this long to realize that sometimes you just have to cry and move on. It's crazy frustrating, a lot of MS symptoms overlap with CRPS so I can understand where she's coming from with the frustration as well. You give up so much without a choice. I was diagnosed at 15 after an untreated ankle fracture of nearly a year, it was nearly 2 yrs before I went from treating the injury to treating the pain that I'm left with.
You can see it's hard for her too bc she's so independent & now she has to depend on others. She was so fiercely independent. That is one of the worst things for her to have happened. I hope her MS doesn't get any worse.
my first thought, too! my gosh, how lovely to see people supporting each other like that. it should be an everyday thing but too often it isn't, so it's fantastic to see an instance of it broadcast
I have a Neurological condition that's very similar to MS called Autonomic Dysreflexia and Autonomic Neuropathy so I understand what you mean because I used to be a runner. I took my body for granted and was in every sport they'd let a girl be in back then and I had no fear. I grew up on 100acres of woods and was climbing and running all the time. I knew every inch of it but I also had a few accidents because I had no fear and I took chances I shouldn't have. One of those accidents was very bad on my spine but I was lucky at the time and it didn't really slow me down at all. 8 years ago I got a bad colon infection and it combined with the epidural I got when I had my twins afew years ago set off the spinal and neurological conditions. Now I'm disabled and have to use a walker for balance or I would fall over when I try to walk. My Neurologist told me that I have a wheelchair in my future and possible paralyzeation. It has also shortened my life span since it's a degenerative condition so I'm right there with you Christina! Like you said when people ask me how I'm doing all I can say is that I'm hanging in there even though I'm in excruciating pain and I'm just getting used to it! Remember were strong women and we have children and grandchildren who want us to stick around so keep fighting for them and we are in this together!!!🍒💖💖💖💖💖💖💖💖💖
how do you get used to the pain? i have peripheral neuropathy all over my body, from the vaccine booster in Nov. i am in so much pain, i truly don’t know how to live
@@emo333vampireI was diagnosed 41 years ago, it doesn't get an easier as time marches on. We just need to keep fighting and hopefully soon there's a cure. 🙏 Stay strong my MS sister. 💪
She is such a gift to all of us. She is strong and she will get past this and be back and when she is , she will flip a finger to MS and put it in its place. Look at the two women who stand with her, all of these women have survived to tell about it.
Ms doesn't define you You will always be Christina Applegate ❤❤❤❤❤❤❤❤ You're beautiful❤ Pretty face beauty stays I will keep you in my prayers not to be angry or sad 😭 we love you❤
So proud of you Christina! People like you, Jaimie, and Selma make me feel better; as I too have MS! I watched all of you throughout the years (Married With Children, Sweetest Thing, and I can go on)! I think that you are a beautiful, and strong woman! Speak out for the rest of us! I am relearning to walk again; after breaking my femur trying to walk too fast with my walker. I am living in a nursing facility; and it blows! I'm doing this for my son as well as myself! I found out I had MS in 2015; I fell and couldn't get back up! It was a total nightmare! I agree, it is my worst disease as well; I too have had bad luck with my health too! I also have Sjogren's Syndrome as well as Asthma! Lovely! Take the best care! ❤ A.W.
I'm so sorry to hear this Christina! You're so brave and have us, your fans to reach out to! You are so fabulous to talk so candidly! We love you sweetheart! ❤
It breaks my heart seeing her crying as I always see her smiling, positive and funny. I love her personality. She is also very good actress she was great at Dead To Me. It must be such hard feeling to be diagnosis with MS 😔She is a strong woman, she always looks amazing and I am sure she will cope with it but she already had battle with cancer. Also she is very energetic woman, just it must feel so unfair and disappointing for her. I wish her the best, hope gets better and have the MS effects in the minimum.💓
Hope she is able to maintain her life without getting caught up in endless rounds of tests and screenings. There’s a fine art in managing serious chronic health issues. At a relatively young age a family friend observed my autoimmune issues after I did not fully recover from infectious mono. A scenario the friend had when she had the onset of inherited type 1 diabetes. I got friendly and helpful suggestions in my early 30’s…listening with half an ear..thinking oh I will be fine. At age 67, her thoughtfulness still resonates. She managed to the age of 84. 🖼️☀️🦋🍃🌷
@@Jillybeej Best medical science can do right now is slow the progression and prevent flare ups. Even if a cure is discovered it won't reverse the damage already done.
In this dark carnival of suffering and death, where the world feels like a twisted, endless night, Christina Applegate shines like a radiant star against the pitch-black sky. Her light cuts through the gloom, giving us hope and warmth. She’s just too good to be true: stunningly beautiful, sharp-witted, funny, brave, and resilient-a beacon of inspiration in this chaotic, merciless circus. Without her, we would all sink a little bit deeper into the mire of our own despair, the sky growing colder and darker, leaving us alone in the darkness.
I’m sorry that her and these other women have this. I’m worried that I might have it. I had a focal seizure not long ago and my left side of my body keeps going numb. 😓 I’ve been sick a lot of my life with digestive problems. I was so much better for years, but now it’s like I’ve been tossed deeper into the pit. 🔥🔥🔥🔥🔥
My dad had MS , so when i found out Chrisitna Applegate and Selma Blair both have it i was so worried. I have seen what that illness can do. Hopefully they can access much better treatment than my dad could.
That's not true. Sometimes it runs in families, but not always. They don't know why people get it, or why those who get it got it. I don't have it but my daughter does -- where did it come from that she has it? Nobody in my family or her father's family has it. It came out of the blue.
Liebste Christina Applegate... Ich bete für deine Heilung und habe Gott gebeten, dass er dich unterstützt und führt auf deinem Weg ❤❤❤☀️☀️☀️ Gott segne dich... Ich Segne Dich ❤️❤️❤️ Ich wünsche dir von Herzen nur das liebste und beste... Und hoffe sehr, dass du Heilung erfährst. Vergiss nicht, nur starke Seelen bekommen solche Aufgaben, die sie auch bewältigen können. Falls du das jemals liest... Bitte beschäftige dich mit Dr. Joe Dispenza, Dr. Joseph Murphy und was Ernährung betrifft mit Anthony William. Du schaffst das... Ich würde dich zu gerne kennenlernen und wünschte, ich könnte dir mehr helfen. Du bist mehr als "nur" Schauspielerin, vergiss das nie...🙏 Und was passiert... Du berührst viele viele Menschen mit deinem Sein, mit deinem Mut und deiner Ehrlichkeit. Du gibst vielen auch Kraft und bist vielen Menschen ein Vorbild. Ich denke, deshalb hat Gott dich dafür auserwählt. Gott wirkt durch dich in dieser Welt. So denke ich. Auch wenn das manchmal schwer zu begreifen ist. Du bist eine wunderschöne Seele und ein Licht oder Leuchtturm für viele viele Menschen. Möge Gott immer an deiner Seite sein und dich beschützen. Alles liebe für Dich liebste Christina ❤ Liebe Grüsse, Annett R.❤
Hugs Christina. We’re all with you. I hate that the “authority figure” comes on and says it’s treatable. That implies that the symptoms disappear with a med - at best they slow the progression of the disease. And for those of us with primary progressive MS, there was no FDA approved medication to slow the progression until a few years ago, there’s only 1 med and it’s not appropriate for everyone. Hang in there everyone with MS. Hope for relief of symptoms.
It's absolutely not that simple. People live in their fantasy world and think that they have all the answers. I have tried your carnivore diet and it DON'T WORK. STOP TRYING TO PUSH CRAP WHEN YOU DON'T KNOW WHAT YOU ARE TALKING ABOUT. And yes I have MS and I have tried EVERYTHING
Interesting connection to that this started during a show called “dead to me.” It states that in the show, she uses anger and resentment to deal with her loss. Gotta let go of anger, bitterness and resentment. Repent and the demons causing the illness will flee. In Jesus name amen!
I cried when I saw this. I remember her as Kelly on MARRIED WITH CHILDREN.. the movie THE ANCHORMAN. etc..Shes always been ...& STILL IS beautiful. My husband has Progressive MS & I know how hard it is . He went through depression & cried alot. The best thing is to join a support group. Listening to other people w/MS ,share their stories, tips, diets, etc..really helps. Sending love & prayers her way
Best of luck to you and your husband.
She will always be beautiful to me! I pray for her strength.
Christina Applegate showing up at the 2024 Enmy's is one of the bravest things that she's ever done.
Christina, you are still one of the most beautiful women ever. Long live Kelly Bundy. 😢
So brave . 😅
@@TheresanewAuditorintownwhy isn't it brave?
Christina Applegate's raw and real talk about her MS journey is both heart-wrenching and inspiring. Proof that even when life gives you the worst, there's still a way to make it work. 💪💖 #StrengthInVulnerability
So proud of her for being so brave!! Love her even more!!
I can't wait for the podcast. My cousin suffers from MS. She had symptoms early in life. Now she has a lot of physical restrictions. She was a nurse and didn't see the signs like Christina until she had mobility issues.
I am sorry.
Having MS myself, I get everything she says. 🙏❤️🙏
I as well 6 yrs now is a horrible desease
One of the rare ones who reach fame but stayed the same person shes always been❤
Being transparent with this and with the platform she has is perfect and brilliant and courageous, for others to see, research, and either know their own symptoms to seek help or for others to be aware and less judgemental.
I just love Christina and her complete raw honesty!😊
Cristina means a lot to her public, she is so talented and wonderful, a person we care and want the best for her!
God bless Christina Applegate. She is a bright light in this world,
Christina. you are a beautiful person and countless millions have been entertained by you we are all here with you to help you through this.
Chronic illness/pain is such a rollercoaster and right when you think you've passed over that hump, something will suddenly pop up and be an issue. I've had CRPS for 9 years this year and when I connected the dots and had the realization that all dental issues will be permanent, I cried. 9 years later, I cried. That's okay, it's taken me this long to realize that sometimes you just have to cry and move on. It's crazy frustrating, a lot of MS symptoms overlap with CRPS so I can understand where she's coming from with the frustration as well. You give up so much without a choice. I was diagnosed at 15 after an untreated ankle fracture of nearly a year, it was nearly 2 yrs before I went from treating the injury to treating the pain that I'm left with.
I am so sorry love ❤
You can see it's hard for her too bc she's so independent & now she has to depend on others. She was so fiercely independent. That is one of the worst things for her to have happened. I hope her MS doesn't get any worse.
so amazing Jaime is there for her can’t imagine the pain she endures each day such a strong powerful woman she looks so beautiful a great interview
Love seeing their bond ❤
my first thought, too! my gosh, how lovely to see people supporting each other like that. it should be an everyday thing but too often it isn't, so it's fantastic to see an instance of it broadcast
Our kelly bundy ❤ still beautiful
She is being so vulnerable and brave. She is such a strong woman. This disease takes away so much.
i know you are dealing with a lot. But i see the support and affirmation around you. And i am envious for that.
I love Christina so much 😢she was one of my favorite actresses ever 🎉
I have a Neurological condition that's very similar to MS called Autonomic Dysreflexia and Autonomic Neuropathy so I understand what you mean because I used to be a runner. I took my body for granted and was in every sport they'd let a girl be in back then and I had no fear. I grew up on 100acres of woods and was climbing and running all the time. I knew every inch of it but I also had a few accidents because I had no fear and I took chances I shouldn't have. One of those accidents was very bad on my spine but I was lucky at the time and it didn't really slow me down at all. 8 years ago I got a bad colon infection and it combined with the epidural I got when I had my twins afew years ago set off the spinal and neurological conditions. Now I'm disabled and have to use a walker for balance or I would fall over when I try to walk. My Neurologist told me that I have a wheelchair in my future and possible paralyzeation. It has also shortened my life span since it's a degenerative condition so I'm right there with you Christina! Like you said when people ask me how I'm doing all I can say is that I'm hanging in there even though I'm in excruciating pain and I'm just getting used to it!
Remember were strong women and we have children and grandchildren who want us to stick around so keep fighting for them and we are in this together!!!🍒💖💖💖💖💖💖💖💖💖
how do you get used to the pain? i have peripheral neuropathy all over my body, from the vaccine booster in Nov. i am in so much pain, i truly don’t know how to live
Wondering- did the neurologist say the epidural caused it or is it just your guess?
@@emo333vampireI was diagnosed 41 years ago, it doesn't get an easier as time marches on. We just need to keep fighting and hopefully soon there's a cure. 🙏
Stay strong my MS sister. 💪
She is such a gift to all of us. She is strong and she will get past this and be back and when she is , she will flip a finger to MS and put it in its place. Look at the two women who stand with her, all of these women have survived to tell about it.
Ms doesn't define you
You will always be Christina Applegate
❤❤❤❤❤❤❤❤
You're beautiful❤
Pretty face beauty stays
I will keep you in my prayers not to be angry or sad 😭 we love you❤
Christina you are a real treasure and beautiful inside and out…..keep going ❤❤
So proud of you Christina! People like you, Jaimie, and Selma make me feel better; as I too have MS! I watched all of you throughout the years (Married With Children, Sweetest Thing, and I can go on)! I think that you are a beautiful, and strong woman! Speak out for the rest of us! I am relearning to walk again; after breaking my femur trying to walk too fast with my walker. I am living in a nursing facility; and it blows! I'm doing this for my son as well as myself! I found out I had MS in 2015; I fell and couldn't get back up! It was a total nightmare! I agree, it is my worst disease as well; I too have had bad luck with my health too! I also have Sjogren's Syndrome as well as Asthma! Lovely! Take the best care! ❤ A.W.
I'm so sorry to hear this Christina! You're so brave and have us, your fans to reach out to! You are so fabulous to talk so candidly! We love you sweetheart! ❤
Thank you for putting it out there, for helping people to understand.
I always loved Christina Applegate what a nice nice person. Why do bad thing happen to such good people? I will pray for her.
She’s still lovely. Best wishes Christina!
It breaks my heart seeing her crying as I always see her smiling, positive and funny. I love her personality. She is also very good actress she was great at Dead To Me. It must be such hard feeling to be diagnosis with MS 😔She is a strong woman, she always looks amazing and I am sure she will cope with it but she already had battle with cancer. Also she is very energetic woman, just it must feel so unfair and disappointing for her. I wish her the best, hope gets better and have the MS effects in the minimum.💓
She is so brave❤
Brave? Most of us with the disease don't sit around getting angry and just get along with our lives.
So love her! We all love her
I was diagnosed with MS over the summer. Yes it sucks!!!
Same here. August 2023.
I was diagnosed April 2023.
Sorry to hear this but we all still love her !
Hope she is able to maintain her life without getting caught up in endless rounds of tests and screenings.
There’s a fine art in managing serious chronic health issues. At a relatively young age a family friend observed my autoimmune issues after I did not fully recover from infectious mono. A scenario the friend had when she had the onset of inherited type 1 diabetes.
I got friendly and helpful suggestions in my early 30’s…listening with half an ear..thinking oh I will be fine. At age 67, her thoughtfulness still resonates. She managed to the age of 84. 🖼️☀️🦋🍃🌷
Praying for her. My grandfather had that, and my friends daughter has it. I haven't seen Christina act since Married With Children.
Poor girl. I feel so badly for her
All the health in the world to these three wonderful ones all my love and affection ❤❤❤❤❤❤❤❤❤❤
Amy you are the best and the fighter , I dont think so anyone else can fight strongly as you have done
My Dad had M.S. 16 years before he was diagnosed.
I adore her - prayers and much love❤❤❤
Glad you found someone who loves you!
Multiple sclerosis is a fully treatable disease and is by no means an incurable disease.
I believe we can overcome MS today. God bless all !!
Treatable? Yeah right! I was diagnosed 13 years ago. I know exactly how she feels.
Have you tried Ocrevus? Stopped all progression in my case.
by treatable theres things you take to help It not that it completely. goes away dont be stupid
@Lissa102 and maybe dont be rude
Treatable means there’s available treatment options. It’s not a cure. As someone who says they have had MS for a long time, should know that right?
@@Jillybeej Best medical science can do right now is slow the progression and prevent flare ups. Even if a cure is discovered it won't reverse the damage already done.
Christina is probably correct. Once it hits u finally u get it because theres no mistaking what a relapse is.
I'm having a relapse right now. I need to get my yearly MRI scheduled. I'm scared because I think the Ocuvous may have stopped working.
I love you Christina ❤️
In this dark carnival of suffering and death, where the world feels like a twisted, endless night, Christina Applegate shines like a radiant star against the pitch-black sky. Her light cuts through the gloom, giving us hope and warmth. She’s just too good to be true: stunningly beautiful, sharp-witted, funny, brave, and resilient-a beacon of inspiration in this chaotic, merciless circus. Without her, we would all sink a little bit deeper into the mire of our own despair, the sky growing colder and darker, leaving us alone in the darkness.
Prayers 🤲🙏
I’m sorry that her and these other women have this. I’m worried that I might have it. I had a focal seizure not long ago and my left side of my body keeps going numb. 😓 I’ve been sick a lot of my life with digestive problems. I was so much better for years, but now it’s like I’ve been tossed deeper into the pit. 🔥🔥🔥🔥🔥
I will make you stand and love you forever ❤️ ♥️ 💕
Bless her.
Bless you🧡🇨🇦🙏🏻
A wonderful beautiful lady ❤
My dad had MS , so when i found out Chrisitna Applegate and Selma Blair both have it i was so worried. I have seen what that illness can do. Hopefully they can access much better treatment than my dad could.
Gorgeous & brave lady...
Glad for her
I wish you can have an appearance in The Morning Show Season 4 (hoping for a Green Sisters Reunion) But that's up to you, Ms. Christina Applegate.
Take care!
Now imagine a people with medical insurance tied to their job and they have to go to work or lose their medical … America is cruel …
Oh god give her her health back so that she can enjoy and cherish upon her old days.. she deserves
I will love ❤️ you forever ♥️
That is a fucking true friend right there!
YOU MY CRASH SINCE I WAS LITLE LOVE YOU MINA
"Flippin the bird" l love her! ❤
I also have MS. I'd like to know what new treatment research she's excited about.
Support💐💐💐
Bless her heart, she went from being the most beautiful woman in a room to now not recognizing who she sees in the mirror. Prayers Christina ❤
God d bless you ❤
♥︎J♥︎A♥︎M♥︎I♥︎E♥︎-♥︎L♥︎Y♥︎N♥︎N♥︎
♥︎S♥︎E♥︎L♥︎M♥︎A♥︎
♥︎C♥︎H♥︎R♥︎I♥︎S♥︎T♥︎I♥︎N♥︎A♥︎
Damn Girl! 😢
I wish you the best God will help you
Treatable or manageable?
No cure
@@moaz9716 😞
My mother had Primary Progressive MS and got MS too, I got relapsing remitting MS.......so if you have it, so will your kids!!!!
That's not true. Sometimes it runs in families, but not always. They don't know why people get it, or why those who get it got it. I don't have it but my daughter does -- where did it come from that she has it? Nobody in my family or her father's family has it. It came out of the blue.
Liebste Christina Applegate... Ich bete für deine Heilung und habe Gott gebeten, dass er dich unterstützt und führt auf deinem Weg ❤❤❤☀️☀️☀️ Gott segne dich... Ich Segne Dich ❤️❤️❤️ Ich wünsche dir von Herzen nur das liebste und beste... Und hoffe sehr, dass du Heilung erfährst. Vergiss nicht, nur starke Seelen bekommen solche Aufgaben, die sie auch bewältigen können. Falls du das jemals liest... Bitte beschäftige dich mit Dr. Joe Dispenza, Dr. Joseph Murphy und was Ernährung betrifft mit Anthony William. Du schaffst das... Ich würde dich zu gerne kennenlernen und wünschte, ich könnte dir mehr helfen. Du bist mehr als "nur" Schauspielerin, vergiss das nie...🙏 Und was passiert... Du berührst viele viele Menschen mit deinem Sein, mit deinem Mut und deiner Ehrlichkeit. Du gibst vielen auch Kraft und bist vielen Menschen ein Vorbild. Ich denke, deshalb hat Gott dich dafür auserwählt. Gott wirkt durch dich in dieser Welt. So denke ich. Auch wenn das manchmal schwer zu begreifen ist. Du bist eine wunderschöne Seele und ein Licht oder Leuchtturm für viele viele Menschen. Möge Gott immer an deiner Seite sein und dich beschützen. Alles liebe für Dich liebste Christina ❤ Liebe Grüsse, Annett R.❤
❤❤❤
They dropped the trailer for the podcast.. Go follow people!!!!
❤
Poor thing ❤❤
Sending love. Would you consider trying one of those keto or carnivore diets that might help ? Just asking and don’t mean any disrespect.
Hugs Christina. We’re all with you. I hate that the “authority figure” comes on and says it’s treatable. That implies that the symptoms disappear with a med - at best they slow the progression of the disease. And for those of us with primary progressive MS, there was no FDA approved medication to slow the progression until a few years ago, there’s only 1 med and it’s not appropriate for everyone. Hang in there everyone with MS. Hope for relief of symptoms.
❤🙏
I loved her on married with children she was so funny
😢😢
Love those sweet ladies!
I have it and it does suck x
🤲🏾🤲🏾
She needs to be on the carnivore diet! How can I get in touch with Christina apple gate?
There is no cure for MS. Special diets are not effective in controlling symptoms or the progression of the disease.
It's absolutely not that simple. People live in their fantasy world and think that they have all the answers. I have tried your carnivore diet and it DON'T WORK. STOP TRYING TO PUSH CRAP WHEN YOU DON'T KNOW WHAT YOU ARE TALKING ABOUT. And yes I have MS and I have tried EVERYTHING
Treatable my butt. Try again Doc.
MS is absolutely treatable. I'm on an effective treatment right now. She said "treatable", not "curable".
@@EdzoH86 The key phrase to your statement is "right now". Unfortunately, down the road you'll figure out exactly what I mean by my statement.
Christina’s case seems to be much worse than Jamie’s. What caused this?💔
There are like 50 applegates on face book LOL - each one claiming to be the real McCoy
Interesting connection to that this started during a show called “dead to me.” It states that in the show, she uses anger and resentment to deal with her loss. Gotta let go of anger, bitterness and resentment. Repent and the demons causing the illness will flee. In Jesus name amen!
Don’t forget 🌱 wfpb diet like my friend Rebecca Stoner who put hers into complete remission.
U are so beautiful
At least she could get help
Coming out party
I thought she was dead