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- เผยแพร่เมื่อ 1 ต.ค. 2024
- Robin Roberts spoke with the actresses about their new podcast where they talk about coping with the debilitating disease, Multiple Scelrosis, and the support from family, friends and fans.
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Shortly after Christina was diagnosed with MS, i was hospitalized and then diagnosed with it myself.
The things she posted and said helped me get through that time, and honestly, i felt less alone because of her. So if you ever see this, thank you Christina 🧡
My mother lived a long life with MS (88)...get a good sleep at night and pay careful attention to your diet--and your sense of humor. You'll be ok.
Science is revealing that most autoimmune conditions are caused by leaky gut syndrome. Finding out if you have this, and remedying it, may completely halt the onset of MS
I hope you can have a good day now and then. I am glad you feel less alone. We are rooting for you and your pain is our pain--or at least I hope we could somehow distribute your pain and issues to others now and then to give you some relief.
I've had MS for 19 years, eat a healthy diet AIP protocol is a great way to eat, exercise, stretching is fantastic, use your mind.
@@deezeliz You are smart and progressively thoughtful; keep doing what you are doing. (My mum liked to swim.) My mother was told she would not live more than a decade when she was dx'd in 1953 (at 19yo)...crying on camera and talking constantly about her symptoms and "struggle" --would never have crossed her mind as a path to wellness. This sort of health propaganda troubles me.
I have MS. It's really hard. I thank these women for talking about it so freely.
Did your symptoms start with tingling in your toes too?
I've had a tingling in my toes at random times over the last few years (along with slight numbness that doesn't last long). But I'm also a hypochondriac so not sure if its in just my mind
@@Irishgui83usually it's ongoing and doesn't go away for a while. I had tingling in 2 fingers which in a month evolved to half my body. MRI said MS. It's difficult to get à diagnosis because all thèse diseases mimic each other
@@mrsremise5594 thanks for your reply and the information 👍
I also have MS and I am so grateful for this also!
Same here.
My heart is broken for her. People please don’t take your health for granted.
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
These women are infinitely more than their MS struggles. When someone goes through something like MS, it is helpful to not be alone, commiserate & support, listen & give bits of knowledge & helpful tips of what you find that helps, and I am so glad these two found each other. Not only are they helping each other, by doing the podcast, they are going to help so many more people. People going through MS, caregivers, family, friends and also those dealing with other stuff too can take what resonates with their circumstances and through these two strong, beautiful, smart, funny, talented women understand their lives more. Thank you both for sharing and thank you Robin for the interview! And So It Is! 💜💜💜
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
My dad passed away from MS in 2000, he lived 23 years with the disease and fought it till the end. Bravest, strongest and kindest man I ever knew. Thank you ladies for keeping this disease in our minds and fighting it - sending my best wishes to you both and all who struggle with MS.
How old was he?
52
My brother was diagnosed with MS in 2000 and it was foreign disease to us. He battled it for 15 yrs. The last 1.5 years, he lost his ability to speak clearly, very much like a stroke victim. So devastating to see how our family dealt (or didn't) with the progression of his symptoms, to the point of isolation and not willing step up and provide care and support. When serious illness happens, others true colors show. So grateful my husband and I stepped up and took him in. I miss him so.
My sister is battling this awful disease. I'm very sorry for your loss!
I have a difficult time with Christina Applegate crying on talk shows - particularly when I read a comment like yours. I'm so sorry for your loss; it's terrible what your brother went thru, but he was so very lucky to have you and your husband. Do not dwell on the "not dealing" ...it is normal...very normal. We spent a lifetime of struggling to deal with our mother and her MS... I think not coping is how we ultimately COPE. My mother was dx'd at 19. Proceeded to marry and have 3 kids. Lived to be 88. We squabbled over many things, but we agreed to keep her out of a nursing home ..and honestly, it's something I most proud of in my life.
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
God bless you! One of my younger sisters has MS and ultimately had a stroke and confined to a wheelchair. It is so terribly difficult at times being the caregiver.
You are a sweetheart and a good soul for taking him in. Thank you. My husband has Alzheimer's and your words struck home, hard--"so devastating to see how our family dealt (or didn't) with the progression of his symptoms, to the point of isolation and not willing to step up and provide care and support." That is my husband's narcissistic, awful daughters--all of them. I have to keep my rage at them as tamped down as possible. I've tried everything; they just refuse to give him the love and support he desperately needs--and deserves! He was a great dad! It's terribly disillusioning. Their true colors are definitely showing. Thank you again for not being like them!
My mom was dx'd with MS when I was in high school. Hers got really bad. She moved in with my aunt for a year, and when it became too much for my aunt to do alone, my mom moved into a care home that focused on rehabilitation. After a year there, her MS inexplicably went into remission, and it never came back again (she ended up dying at age 50 from a completely unrelated heart issue). I knew others with MS (friends that my mom made during her journey with the disease) and it seems to affect each person differently and to varying degrees (similar to Parkinson's, which my dad had). So take heart! So much is still unknown about MS, and there is always a chance it could go into remission and/or new therapies and meds will be developed.
Your mom had MS and your dad had Parkinson’s? Oh my goodness I can’t imagine. My father also had Parkinson’s for about 10 years. At least from the time he was diagnosed. He passed away in 2021 to 6 months after my mother did, and she died from congestive heart failure and COPD. Neither one took very good care of themselves. My dad got the Parkinson’s from agent orange during his time in Vietnam during the war. It sucks to see somebody you love slowly be taken from you. He made the comment a couple of times that he was existing not living.
I don’t suffer from MS and can only imagine 😢 but I do have a condition that is not curable and relate to the daily struggle of getting through it. Her pain, disappointment, frustration, and even anger in the eyes is so real. Peace be with you 🙏🏻 💕
My heart goes out to both of you ladies. I suffer from an invisible illness that my neurologist says mimics MS and it is hell. I mourn everything about my younger, healthier self. And just like Christina mentioned, my skinnier self. You find out very quickly who your true friends are when you have an illness like this. Hang on to Jaime Lynn, Christina, and vice versa. I hope that tomorrow is better than today for you both. 💜🌸
@tinak.3022
What is the invisible illness that you have that mimic MS?
I do the same thing. Just isolate. Once my MS progressed to where I couldn’t do normal things and go to normal everyday places, I really had to put a value on those kinds of things. I’m so thankful for things like DoorDash and Uber eats. The pandemic also aided those kinds of things for me and others with disabilities
I feel sorry for anyone suffering with a chronic illness whether it’s pain, depression, MS etc it just is brutal because it never goes away. Best of luck to both of these women they have entertained many people and given us the escape we all need from reality.
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
I also have MS and am so happy that these amazing, strong, well-known women are speaking the truth about MS. It is freaking HARD and it sucks every single day. If people based their knowledge of MS on what the drug companies advertise, they'd think we are all out there hiking and swimming with no issues. Life with MS is far from that.
Some people have MS and lead active lifestyles. I know people with MS who run marathons. Not everybody with MS is doomed to misery, especially not now with highly effective medications out there.
@@mecarr Right on. My mother was dx'd at Mass General in 1953 - she was 19. Graduated college. Married at 22; 3 kids; a career would have been difficult, but she did all kinds of volunteer work = CCD and scouts. Yes, her mobility was limited...but she was not of the yoga and smoothie generation. Lived to be 88. Never cried; never felt "ashamed." This type of interview bothers me...they are rich, ego-driven celebrities who have access to so much medical support.
I remember right there are 4 types of MS I personally know 4 people with this terrible disease. One I knew most of my life and worked for her in her home to help her because she was jazzy bound. She passed away this past year due to colon cancer from the ms. She fought a good fight she made it to her 70’s. The other lady is in her 70,s wheel chair bound the other two do pretty well on their medication but by all means it is not easy to deal with even if you don’t have as aggressive disease as someone else. I have my self two auto immune diseases. The first one is Hashimoto’s, which is very common. The other one is autoimmune and a form of vasculitis called EGPA and living each day is very hard for me as well now even with treatment because I am more advanced and the Vasculitis really affects my lungs. So it’s hard to breathe. The people in the comments be grateful for having a healthy body that’s all I can say.
@@stephmartin1148 My apologies, Steph. YOU deserve the help and attention, not these women. They will be fine. Plenty of $$$. I hope you have access to decent healthcare.
@@julieb7785
I feel the same for you sweet lady!! Just had a scan on my lungs 3 months earlier then planned from the last CT scan and my opacities from my disease are worse. On 4 steroid inhalers they are 2,000 and a biologic injection Fasenra. Starting back on Rituximab soon. It’s another biologic I think they use for MS and RA too. I did best when I was on that for two years. The EGPA disease came on in the fall of 2019 during my youngest. pregnancy. I am on the patient assistance program for the Rituximab and Fasenra biologics where my insurance doesn’t cover any biologics. VERY grateful to be alive and be here to raise my kiddos aging from 15-3. I do have a very helpful hubby. So grateful for that too. Grateful for my great specialist, so many I have to see. Autoimmune is SO rough I wish you the best, God bless you!! 💕
So many being diagnosed with this. My husband's cousin was diagnosed three years ago and she's struggling. I'll have to tell her about this podcast. I'm glad they are talking about it. Olivia Munn just announced her diagnosis and treatment of breast cancer. Another actress/comedienne recently talked about her diagnosis of Graves disease.
I'm sure people who don't like her will talk smack about Olivia just as non fans of Christina have done. You don't have to like them as actors, singers, etc., to respect the fact that high profile folks are willing to talk about their diagnoses and get the word out that if something is concerning you get it checked out. Regardless of their motives, the word is out. My dad has the same form of dementia as Bruce Willis but he didn't really know what it was until Willis's wife started talking about it.
Two wonderful women who had iconic TV dads... and such heart! They are doing what they are meant to do! Bringing light to a horrific disease.
Their friendship is priceless! They are beautiful as is ! I’m so proud of them. Keep Going 💕🙏
My life long Bestie died at 43Yrs of MS. She was The YOUNGEST person in a nursing. The visual was HEARTBREAKING
Sorry for your loss. There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
A devastating illness. My heart goes out to her and all others dealing with this. My son-in-law lost his mother to it.
Brave Woman who will help many others with their friendship and podcast, love them both and I’m glad they have support from each other..❤
What a difficult thing to go through for Ms. Sigler. You never know what someone is going through. Just no words for Ms. Applegate who I have been a fan of for decades.
I have had MS since I was 23 and boy it’s a journey great to hear them bringing awareness to the disease. Also fantastic they have a support system in place 👏👏👏💕💕💕💕
Christina has such a big place in my heart. She was my childhood and still is ♥️
Yea me too.
My brother had it for easily 25 yrs. Thank goodness it didn't an affect on his terrific sense of humor and his compassionate heart and mind. He would take these unexpected falls and everything... and he kept trying to be his best. Corona was very hard on him though he never contracted it; he died in '22. I miss him so much and I'm so proud of him.
I'm sorry about your brother...
I’m so glad you have each other. Thank you both for having the courage to share your journey. It will help so many others struggling. 🙏
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
My mother died from complications from MS in 2014 after a long battle. It's a terrible disease. I'm so glad Christina & Jamie are educating people about it because not a lot of people know about it. I wish them the best 🧡
Christina May be 40# heavier but she needs to understand that she is still amazingly beautiful! We all need to reiterate that to her! When we get the chance.
We need women like these who are not afraid to share their experiences. They are our sources and our support until women’s health becomes a priority in our health care system. Until we are no longer dismissed as stressed, anxious or hysterical and are actually taken seriously, we need to be able to advocate for ourselves and fight to get the health care that we need and deserve.
I'm so glad they are taking the torch from Annette Funicello and bringing this horrible disease that took my mom's life at the age of 53. That happened 24 years ago when I was 16 and took care of my mom at 11 when she was diagnosed. Thank you Jamie and Christina, as well as Selma.
Sorry for your loss and childhood trauma😢😢😢😢
What an absolute gem and a legend!!
She sure is.
I'm crying I am absolutely crying. Why why why why why why why why why why why why why why.
Thank you for this. I have long had symptoms that smack of MS. No official diagnosis though. I appreciate the strength of these women!
God bless these ladies.
I developed Parkinsons at age 49.
I ABSOLUTELY FEEL FOR THEM!
Two powerful women bring to light such a horrific disease. I wish them both nothing but the best and happiness as they continue down the journey, not as having the disease but as two perfect and great friends. #prayers #respect
I don’t have MS but I have other neurological issues and it’s really great how they’re speaking out and being real and transparent in Hollywood- I can relate to having to deal with a new normal
I was diagnosed in 2011 and my heart goes out to her. A sharp and self-deprecating humor really helps you cope and she truly hilarious.
MS a terrible disorder and I pray that one day soon there will be a cure 🙏 ❤. I worked with a gentleman with MS and now he's resting in eternal peace 😇🙏❤️🦋
THANKS Ladies 🙏🏻Lost my Brother to MS
My best friend died from MS…. she accepted it…..she had enough of being needled she hated needles… so she sat back and said F-this…. the toughest thing was why she had to wait to die…she’d rather have simply dropped dead of a Heart Attack!.. lol she’s never going to see another needle again…
its hard the weight when dealing with illness and medications. you are trying to deal with so much and your appearance changing as well while trying to stay confident and not worry about it because improving your illness is more important.
Is prednisone a factor as well?
Was diagnosed 9 years ago with a slow progressive MS which hasn't been totally debilitating, but screws with my walking balance. On my own, I'm lucky to know a super-skilled handyman! I did become a kinder person, always considering that I can't know what someone else's life story is - so don't rush to judgement.
Would have thought Christina mentioned her the sweetest thing co-star Selma Blair who has also struggled with ms.
She might feel it's not her story to tell .
She did. And y u would want to bring negativity into this discussion is vile. Go f urself jagweed
She did talk about her !@@evieshore3270
Kinda ironic: her initials were MS in the Sopranos
When it comes to celebrities with MS, I also think of Meredith Vieira, Teri Garr, Montel Williams, Jack Osborne, and the late Richard Pryor (1940-2005). I'm glad Ms. Applegate and Mrs. Sigler found the courage to bond together and speak out against such a dreadful unpredictable disease with no cure in place. When I saw this interview, it moved me to tears. My heart bleeds for the duo. Sisters for life! ❤
Selma Blair
@@Megannicole-ve4qj Fortunately for Ms. Blair, she went into remission though. So hers wasn't progressive.
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
Selma has permanent damage and it's Meredith Vieras husband who has MS
Montell Williams got me my ms medication for free when I had no insurance.
Obviously Jamie Lynn Sigler's MS is not too serious in terms of physical symptoms if she was able to hide it all those years without being noticeable
There are two different types. One is episodic which includes episodes and then remission and one is chronic and progressive. The progressive one is obviously harder.
Life can be rough... Bless you!
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
I love her!!!!!! Don’t tell mom babysitters dead is one of the best movies of all time!
I was diagnosed with MS in 2011. I'm very grateful that I have minimal symptoms. Slight vision problems and the right side of my right leg is cold all the time.
Often times Lyme is the root cause of MS and can be recoverable. Tons of ND’s/functional dr have seen this time n time again.
I remember reading that years ago but at the time it was getting dismissed by the medical community. But there are doctors who swear this. I've lived up and down the east coast and now in California. It never made sense to me that if you looked at a map of the US it looks like lyme disease ends in the northeast. If it's from a deer tick and there are deer ticks all over the US, then why aren't more cases diagnosed in other states?
Regardless, my heart breaks for anyone suffering with this cruel disease. And how much does Christina Applegate have to endure in this life? Breast cancer in her 30s and now this?
I was JUST gojng to say this. Lyme disease mimics other diseases such as MS, fibromyalgia, chronic fatigue syndrome and now there are connections to ALS and Alzheimer’s. With fibromyalgia lyme can also cause fibromyalgia. My sister was told she might have had MS.. nope.. it was Lyme Disease and she recovered .. to anyone reading this just keep lyme and other tick borne diseases can cause other diseases.
No relation. Lyme is bacteria; MS is a virus with an underlying genetic predisposition.
Christina Applegate so good - so damn funny. Jamie with more subtle acting. Both are GREAT!! Now they can help other women with this!! Love you both.
I hope it works for you. I’m a big fan. I’m a cusser too.
Omg.. that other lady would not keep quiet for a minute, kept talking over Ms. Applegate… someone send her in the other room, she’s obnoxious…..
I was 14 when Married at children came out. My first girl poster was Christina Applegate ❤
I was about 24 when it first came out. I too had a poster. lol
@@victorblock3421 I was always bummed she never did topless
The Wahl’s Protocol is a book about how diet, vitamins and minerals and healthy fats helped a doctor heal her MS. She was in a wheelchair. Now she rides her bike for miles.
she also had chemotherapy, which is a strong treatment for MS.
I have so much compassion for them. I don’t have Ms, but i have been living with Lyme disease since 2006.
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
Sorry if they mention it but why is Selma Blair not included in this? Applegate and Blair have starred in films together and I always found it to be a strange coincidence. Do the two not get along?
Can someone answer this: I know several people who have lived with MS for years, but not even remotely experienced the degree of negative life impact and symptoms as Applegate. There must be different levels? different varieties? or does it affect each person very differently? (i'm genuinely curious)
My mom too, although she also got a brain stroke which left her unscathed as well.
Yes. Some people with MS have little or no symptoms, while others have debilitating symptoms. Getting a diagnosis soon after initial symptoms appear and then starting treatment quickly thereafter helps considerably as the treatment can effectively stop new lesions\disability. The more time that passes without treatment means the more the MS can spread and affect other nerve functions.
I was diagnosed at 52 years old and a male. My left leg feels asleep, I have ADD, which I never had before M.S., and have short-term memory loss, I can remember a baseball game from little league, but I cannot remember where I parked my car. Other than that, I am fine. I am on Retuximab once a year IV therapy that takes like 3 hours. Sigler does Kesimpta commercials, which is another monoclonal antibody treatment. I guess everybody is different.
You can’t tell just by looking at someone. If you listen to the podcast, you’ll hear of Jaime’s horrible symptoms. I have had MS for 25 years and get frustrated when ppl say “but you look SO GOOD!” As if I was making the whole thing up.
her whole life has been so many miseries and this one is the worst. Areally strong woman for putting up with so many tragedies and still has the will ot live thru them. Oridnarily, I dont feel any sympathy for the media pepople esp the Hollywoods because these people live in another planet with no common sense and no decency and no compassion for others. Christina Applegate is an exception for being down to earth and well behaved.
I’ve always just loved Christina. She’s such a likeable person. And what an actor. She played that role as Kelly brilliantly, and at such a young age. I really wish the best for both of these awesome women. I definitely will be subscribing to their podcast!
How can i say this without sounding crude or rude. I love Christina and i feel so sorry for her suffering. Terrible to see her like this. I hope she doesn't feel the pressure to look good and please people.
At least she's very wealthy and can afford the Top Treatments and live comfortably.
Love you! ❤ I also have MS, and I've been on the Carnivore Lifestyle. My life has changed for best since Carnivore. Look into this. Wish you the best ❤
Check out Dr Anthony Chaffee, Dr. Ken Berry and Dr. Shawn Baker
Celebrities are so pathetic.. this happens to ordinary people too.. This is why Hollywood is on its way out.. 👎🖕
I applaud the honesty. As someone with MS, it makes it hard to prove to a disability court that employment is impossible for some when others are still able to work. MS is different for every person, but being stuck in hell is a good analogy. I encourage all those with sufferings like MS to offer it up to the Lord, because that’s the only thing that keeps me sated.
Well all
Of us will
Die somehow and sometime.
Two beautiful strong women coming together and supporting one another and being advocates for those suffering from MS❤️
This is hard to talk about for me I had a chiropractor break my back 10 years in bed and you're never the same after three back surgeries it's hard don't give up keep going I've been off of pain pills now for 13 years and I love you hang in there girl I've been praying for you ever since you'll be fine keep positive if you want visitors call us we'll come over. 🙏😇🌈
A chiropractor broke your back??
I’m so glad they found each other ❤
Amazing Women ❤
Christina is a great comedy actress. Her appearance in Friends is one of my favourites. I’m super sorry that both of them are going through this ❤
I grew up watching Christiana. God bless . Be strong girls
I love that they don't let go of each other the entire interview. ♥️
This touches my heart.
You ladies are so strong.
I wish you the best.
Debilitating sicknesses are real, pity no cure still are there only managing
My sister has MS, she can barely walk 😢
Lesions on brain & spine
So sad
Jamie Lynn Sigler don't seem to have it severe.
This is SO sad. I love you all. My mother was diagnosed in 1977 in California and it's so sad how it rips your world apart. Plus the drugs needed to fight this is unlawful. 😢
I don't have MS, but I have a relative of it and the daily struggle can be very real. Even with treatment...to go from a physically capable, fully functioning adult to something different is life altering. I love that these two are bringing the struggle to the forefront. More (much more) research needs to be done on these auto-immune diseases.
I have MS. I was diagnosed with it after the birth of my second child. I had a new baby and a 1 year at the time. Everything you both are saying is so true. Your entire life stops. You don’t or can’t go anywhere. You lose your independence. Thank Christina for being so real about this horrible disease.
I adore Christina!!
God I love her so much. It's so heartbroken and so amazing she finished the series I loved, even tho she had to be held up by counters and doorposts. What a woman.
When you’re dealing with MS and your daily life is “hell” … you get the right to *cuss* as much as you want. ~ Blessings to her from 🇨🇦 ♥️
Great interview. Thank you for Sharing
These women are pure example of what resilience is both of them are still beautiful and are kicking ass for girl power. I wish him both nothing but the best. I’ve always been a Christina Applegate fan ever since the Bundys married with children. And I knew something was up when I saw the second season of her Netflix series dead to me. And when she finally opened up, and everybody found out the truth, it was heartbreaking to know if she was struggling through this but yet still putting great work out their way to go ladies your true inspiration.
My heart just breaks for her with this. Shes so smart, her comic timing always so spot-on and enjoyable. Fantastic on her spots on Friends.
This truly isnt fair. Glad to see she is getting some relief through a supportive friend, and all the love she got through that standing ovation.
Love you Christina!! Sending strength to you both!
Women everywhere are starting to wake up and realize we are stronger together. We've been silenced for so long. These are strong woman who are helping us set a new standard for how we will be treated in society. I'm sorry MS is a part of your stories, ladies, but you are both an inspiration to me.
Christina is loved. Go out girl. If I saw you I’d help in a heartbeat.
Read Gabor Mates The Myth of Normal, mind/body connection. Leading expert on mind/body and how mental states are related.
I totally understand that feeling. I have had limiting vision issues that caused me a great deal of anxiety and stress from commuting to work to airport travel. I hid my issue for years because I thought I would pay a price . My life now is completely transparent about all my weaknesses so people understand and know all of me.
Christina, if you see this... I don't know what your current diet is, but give the carnivore lifestyle a try. So many people are healing all kinds of metabolic and other issues (including MS) with the carnivore diet. Give it a try. I think you'll greatly benefit and ease your symptoms if not reverse it completely. You've got nothing to loose by trying.
So crazy to see two outstanding Actresses having to fight this terrible disease. God Bless these women.❤
Selma Blair, too. Probably others we don't know about yet.
Hopefully there some breakthrough cure. Enjoy life.
What is she eating and drinking everyday? I would be interested to know what goes into and around her body that can be causing this condition?
I’ve read she’s vegan.
@@luanatringali2817 Being vegan could worsen her condition. Anybody has more information on her eating and drinking habits?
Autoimmune can be hell! MS seems to be one of the more challenging ones. Hearts out to them ❤
Has anyone in the MS community that you know of has ever heard of or tried the carnivore diet? I know I've read it reduces inflammation very well. My 26 yr old daughter is on it for endometriosis. It helped her out right off the bat, but she had to get the lesions surgically removed to really reduce her issues. She's staying on the plan, though, and we hope it keeps the lesions away.
@@kronymom I don’t know for sure but I do know that most non-animal foods are sprayed with toxic chemicals and most processed foods are stripped of nutrients and contain dangerous amounts of sugar and preservatives. I suspect that’s why keto and other carnivore diets are helping.
Christina Applegate is a great Actress ❤ Keep moving forward beautiful Lady 🙏
You ladies are being prayed for in Jesus name
These amazing women are bringing much needed awareness to an often invisible condition!
What brave exceptional women…may they keep soaring 💫✨✨✨✨
There's computer technology that helps eliminate animal and human testing and do more effective research to cure diseases. Dr. Shiva Ayadurai invented it. It's called Cytosolve. I don't know why the technology isnt being used. Look up Dr. Ayadurai's work on this.
I hope Christina sees this.......she's GORGEOUS, I had a HUGE crush on her as Kelly Bundy, and she is still HOT. I'm nearly 50 myself.
Call upon the Name of the Lord!!!!!!
She’s amazing, she truly is! I’ve loved watching her on screen for decades and I wish her all the best!! ❤
Always enjoyed her character portrayals. Wishing her the best.