Christina Applegate and Jamie-Lynn Sigler speak out about battle with MS
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- Опубликовано: 20 сен 2024
- Christina Applegate and longtime friend Jamie-Lynn Sigler tell Robin Roberts about their lives since being diagnosed with multiple sclerosis and their new podcast, “MeSsy.”
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I so appreciate Christina's brutal honesty. Years ago, I was diagnosed with cancer and it enraged me whenever I saw some chirpy TV commercial portraying the process of surgery, radiation, chemo, pills, ect., as a positively glowing walk down some yellow brick road. I was pissed and I hated the fact that I felt I couldn't say so because I was expected to be an inspiring Hallmark greeting card. I wish nothing but the best for her.
I won’t give you the “everything has a purpose” speech because frankly it feels like it implies you *have* to look on the bright side (or you’re ungrateful, negative, or fill in the blank) - it sucks, and bright bubbly feels *fake* and disingenuous - I know people are trying to be nice when they ask how you’re doing, but it’s draining to have to explain anything in detail, and I’m pretty sure they want to keep it superficial anyway - it sucks because you can’t say you’re not doing well for fear of sounding negative so it’s a no win situation to even answer the question. It might sound harsh but I started being more honest about what *I* was comfortable talking about and now I will say “can we change the subject?” or “thanks for asking but I’m too draining (or not in the mood) to talk about it right now”. If people aren’t ok with hearing that then they don’t care much in the first place and it will be apparent - if they do care then they will appreciate you setting boundaries (so to speak) and being upfront and honest. But whatever you do, don’t pretend like everything is fine - by being honest, you are giving someone else permission to say what they really feel also. Not trying to be all “lecturey” but I hope more people say what they’re really thinking.
Thank you so much for taking the time to post regarding your cancer diagnosis. At 16 I was diagnosed with metastatic cancer. I vividly remember an older gentleman telling me “to roll with the punches” after my 2nd neck surg. I was inpatient for two weeks that first year year. After that I was isolated for inpatient high dose radiation therapy and was given enough radiation to drop an elephant. Had 3 annual inpatient high dose radiation treatments. There was a big black and yellow radiation sign on my door to warn people not to enter. Nurses and drs were only allowed a total of 30 minutes in my room every 24 hours. What went in my room stayed in my room. When I was discharged my pj’s even had to stay. I was cancer free until my recurrence at 35. It wasn’t until my recurrence I understood exactly how much radiation they had given me. The oncologist told me I was a hair away from my lifetime limit before I become high risk for bladder cancer and luekemia. I can’t complain too much because I’m still here at 60. But I definitely can relate to your comments!
@@altamoab ❤❤❤ 🫂 🙇🏾♀️🙇🏾♀️🙇🏾♀️🙌🏾
I felt the same in 2021 when I had breast cancer. It was horrific, and I'm not going to pretend I was stoic and brave. I was exhausted, in pain, terrified, and trying desperately not to lose myself in the process. I felt like a big, self-pitying baby, being told that little kids were grinning their way through their chemo, while I felt like lukewarm death!
My biggest fear is that I may be faced with all that (or worse) again, because I just don't know how the heck I'd get through that again!
@@obnoxiousbluebird6634 The kids that grin their way through it are just trying to comfort their parents. Some of them have spoken about that as adults, and said they felt so much pressure to be as strong as possible because they saw their parents breaking. Some even faked seeing heaven just to give their parents comfort.
I love Christina ❤️
Not enough is talked about around this, early symptoms and the type of support that is needed.
It looks like air Pollution, like in Los Angeles, and Environmental factors highly increase the risks of getting MS. Also Vitamin D deficiency
@@ChristinaTaft I have family in the boonies of Oklahoma with clean air and clear skies. It's not environmental, it's from inflammation- starting in the gut.
@@coolcatzclub…😮 that’s scary. Thank you for sharing.
My mom had MS. It's awful to see the struggles and loss of independence over time.
Prayers for Christina and Jamie.💕
Thank you. I had a tumor surgically removed from my cerebellum. I went from being an able bodied person to a disabled one over the course of one single surgery and nobody talks about how angry you are. It’s taken me seven years to not be so angry. You really don’t get it unless it happens to you or a friend/family member. Good luck.
I’m so sorry! It seems unfair! I hope there is a cure soon!
💪🙏🫂
@@RnW9384 Everyone heals at different rates and a stroke leaves brain damage often times and the stroke might have injured your brains ability to heal emotionally too. I’m very sorry that this happened to you! I wish you love, peace and healing!
i get that -
me too with the anger, and other people don't understand
I am so sorry that you're going through this. I've had severe balance problems that no one can diagnose. I used to go to the gym and do whatever I wanted. Now I rely on a walker or disability scooter in some instances. I do understand the anger and grief. I have managed to deal with the anger (even after over 20 years I'm not sure) but the grief is still there. Take care❤
So many things stand out in this video, but i have to say , Christina saying " I had to ask for help" is what stayed with me. 😮 I feel like we all have this part in us where we dont ask for help , we think it makes us look weak and think we need to do alone...I think her asking for help is the most courageous thing to do!!!!
I’ve been diagnosed since January 2003. There are high and lows. However I wouldn’t want my worse enemy to be diagnosed . Any other with it stay encouraged!
You are an inspiration ❤
Keep staying strong💪 easier said than done, especially hearing that from someone who does not have it..But my Aunt has it so I have seen the high and lows but she keeps on going ...
I wish you good thoughts and prayers ! And continue with that fabulous attitude and out look on life..I bet you inspire a lot of people❤
I was diagnosed in 2009. I wouldn't wish this on anyone either.
2021 for me. And still can't believe this is really happening.
@@vendomanic saying a prayer for you & all of us struggling w/ this!🌷
I have a coworker who one day said she started feeling "really really really weak" and had to go sit down in the break room. She felt better after that and figured it was probably just exhaustion. Years later she developed odd symptoms and was diagnosed with MS. So you definitely can have it for a long time without knowing it.
True !
To answer your question Robin, she may not act on a big tv show or movie because MS can affect cognitive abilities. I think ppl see us (I have MS) on the outside & think they look great & are doing better. That's all relative. Ppl with auto immune diseases like MS move in silence. Stay strong ladies.
Amen sister. You too ❤
They so ignorant media sucks. Don't bother Robin should know better it's only been years😂
That is exactly how it is.
So true. You can’t look at me and tell that I have it.
@@koreyb MS makes it difficult to exercise. For instance I have MS and heat is a trigger for me. When I get my heart rate up and my body gets too warm, I start to feel sick. So I can’t do traditional types of exercise. She mentioned that she is in a lot of pain. Heat causes me pain and the last thing I want to do is exercise, so losing weight is difficult. She probably has trouble with exercising.
Thank you Robin, I have lived with MS for 20 years. I bet you don't know how many of my Black sisters have MS. Astonishing & just down right terrible. Thank you for bringing it to light thru actresses.
Exactly. Many African Americans struggle with this disease. I was diagnosed at 19 years old, I am 41 now thank God.
I have lupus transverse myelitis so at first I was diagnosed with MS because the symptoms are similar. It’s hard because when I couldn’t walk properly people thought I was exaggerating. I only missed work when I was hospitalized, other than that I just have enough energy to work, come home and sleep. It’s not because of a depression but I literally don’t have the energy. Other than the immunosuppressants, I think an an inflammatory diet like a Mediterranean diet has helped. Best wishes to all.
#correction anti-inflammatory diet has helped. Dr. Terry Wahls (learned about her through Ted Talks) also helped.
I hope you are doing well
Love to you MS Warrior 🧡
I've been dealing with MS for 16 years and I really feel her pain. It's really hard to explain to people about this.
Christina is incredible. Being chronically ill and all that comes with it is brutal. The grieving you experience is not something people understand if they aren’t ill like this. You truly lose your whole self. My feelings are almost exactly the same as hers.
I have a number of friends like this. So thankful for them.
I was recently diagnosed with MS (at age 57) and I have to agree with what Christina said--"I will never wake up and think 'this is great.'" AMEN sister!! MS truly SUCKS. Christina and Jamie-Lynn are lucky to have each other. Not everyone is lucky enough to have someone to stick by them no matter what
I’m 51 and was diagnosed at 27. Most days are fine, but there’s some things that will never go away. One thing that has kept me well is knowing that Gd is holding my hand the whole time. I’m grateful for each day I’m well enough to work because it feels like I’m doing work that helps others. Every day I’m given ability to help others is a gift. It’s the only thing that makes life worth living. ((((Hugs full of hope to you!))))
I have been struggling for two years to be taken seriously, mostly because it’s a 6-10 month wait to see a neurologist. I finally found someone I like and they are starting testing while telling me I can’t have MS because “no one get’s diagnosed in their 50’s” ….obviously they do!
I’m so sorry you have been struggling. I hope you get a diagnosis soon so you can get started on the meds that help. I was told for 2 years that my issues were ‘in my head’, that I was making everything up, or it was written off as menopause. Doctors need to start listening to us!!!
Chronic diseases are such an important topic. It’s surprising how little people understand about the word chronic. They expect you to either get well or die. I have been dealing with one of the “invisible” diseases for almost 20 years. It’s a huge grieving process because you lose so many important parts of your life. Physical and emotional pain are with you 24/7 and you can’t get a break from it. I’m so sorry for Christina and Jamie Lynn and all of us who have one of these chronic, incurable health problems. These ladies will help so many with their honesty on the podcast.
Thank you for this because I've been diagnosed with some rare autoimmune disease called NMOSD and no one talks about this it has no traction whatsoever it's so debilitating. She is correct because I had this disease since I was little but didn't relapse until 2020 the little symptoms were showing up but you just think it's normal sickness.
I have MS. dont isolate yourself too much. I did it for 7 years.... isolated myself from everyone. what helped me cope was telling others about disease. when the time came, i saw that i was giving those who knew about my ms a little piece of me. It helped with my ongoing stress. Stress and depression makes MS worse. we will live with it for the rest of our lives, but it doesn't define who we are. ❤️ You got this.
Honestly, you can use your success and platform for MS awareness. I am sure there are many of us out there that may have MS and do not know. Also, it helps the vast majority of the world to understand this disease..
Wonderful Friends can help
Move mountains. Praying for everyone with MS. Stay strong. Your Fans Love you no matter what. Praying for you & your Family. Thank you for sharing your amazing story. Your Beautiful shines through. ❤❤
I can relate to you so much. I have rheumatoid arthritis, another invisible disease, and I'm in constant pain and isolated as well. I feel for you.
I used to have arthritis pain for 20 years until I totally stopped eating grains, gluten and dairy. And I follow Maria Emmerich’s clean Ketogenic Lifestyle. I also limit nightshades like tomatoes, potatoes, peppers and eggplant. Cayenne is the only chile pepper I use with no problem. I know that everyone is different. ☮️💟
I have neurosarcoid as well as RA-I feel you. Good days and bad days and people think you’re faking on good days-it’s maddening and SO painful-sending you good vibes 🤍🙏🏻
My sister has rheumatoid arthritis and MS and she’s going through a lot. Try to stay strong I know it’s difficult
Sorry to hear you are in pain. Hope you have a doctor who can help provide you with some help, even though I know it won’t alleviate all of your pain. 🌺
I’m sorry to hear that……..I have weird things happening to me lately…..my feet curl like a dead bird’s feet…….my muscles cramp up sometimes….and I get light headed 4 times a week…,should I trip out! What do u think it is? Thanks !peace!
what a beautiful friendship
Having any kind of chronic illness SUCKS!!!! It’s hard and we have to take it day by day!!! So sorry you both are having to go through this!!! Will be keeping you both in my thoughts and prayers.
As usual Christina has a refreshing humor and realness- even in such a difficult time. I have disability and it’s a relief when those in the spotlight can be real and honest about things.
I was diagnosed with MS about 10 years ago, and it cost me my career, my ability to walk, my ability to clean my house. Cost me the ability to do almost everything. But, life in awheelchair is not the end of the world and I’m lucky to live in a place in California where they have access transport to get me around with my wheelchair. Seeing her positivity really helps all of us!
My first symptoms of MS came when I was in my late 20's, but I wasn't diagnosed with MS until I was 46 and the emergency room doctor thought I was having a stroke.
This was a very touching and open interview and I really appreciated everything that Christina and Jamie-Lynn said and what Robin said too. My life turned upside down last September 20th 2023 when I went to the office of the company I work for and my bosses insisted I go to an urgent care facility because I could barely breathe and looked green so I went and after some tests the doctor told me I had three days left to live at the most. I had very definite plans to go out of town the next weekend for a special ceremony for the equinox but I went to my local ER at 5 in the morning and was told I had maybe 36 hours. Turns out I had been bleeding internally for a while and had cancer. I spent 5 days in the ICU and am feeling better but I take each days as it comes and yeah it can be very difficult but I keep telling everyone I am doing as good as can be expected and everyone says well you look very good for having cancer! And I went back to my full time job a week after getting out of the hospital because that is what gives me energy and yes I have to take several meds and more vitamins every morning. But I am also a master healer too. I don't listen to podcasts but I think I will listen to the MeSsy one.
❤Love, lightness & healing, brother❤
@@marygoff3332Thank you very much sister. Let's keep our focus on Christina and Jamie-Lynn though. I only wish I could help them too as I have helped many clients. I am still trying to live up to my Indian Chiefs knowing of me.
I appreciate the honesty of this video of the sad truth that it sucks to have a debilitating medical problem. My daughter has been sick and bedridden most of her 18 year old life. She has been diagnosed with several different medical problems. Recently, she passed out while getting out of bed and broke her ankle. When EMT's came, my daughter's blood pressure was so low, the took her to the ER. That situation led to test, specialist and a diagnosis of Dysautonomia/POTS. It's a life long fight as it is a chronic illness. People who don't suffer with invisible illness don't really understand. Thank you for shedding light on such issues with the bravery you both are showing. Being angry, it totally normal. Mourning the life that is gone is also normal. Thank you again for sharing. ❤
I remember Montel Williams being transparent about the struggles he was going through and how that helped so many people and also himself. Prayers for Christina and everyone going through this challenge.Support means the world.🙏🏼
Although I don't have the same illness, I have severe mobility issues due to osteoarthritis in both of my knees and hands, I can relate so much , people don't understand it because they look at you and think you are ok but in fact you are living in pain , I also was a latin dancer, I cannot go and do none of the activities my friends do, so I just stay home.
My family members say , "i'm lazy, which it really hurts. My last job was working with children, something that did not pay enough, but I loved to do it. I totally understand her. I relate with her in everything she said. ❤
I see you sis. I have arthritis and degenerative disc disease of the spine -went from being a runner and event organizer in the fitness industry to a useless feeling shut-in. I was treated exactly the same, as though I was a lazy crybaby. Regardless how many times I’d remind those close to me how much I’d always loved working out so it made no logical sense that I just one day got lazy or wimpy to pain they just didn’t get it …not until they saw me have to get a complicated spinal fusion, only then did it sink in that I wasn’t blowing my pain out of proportion. ❤ Hang in there
I love the bond of female friendships like this, just watching Jamie’s face immediately turn to an encouraging smile when Christina was starting to break down was very heartwarming
“I wake up and j am reminded of it everyday”! “It’s hard to explain”! Christina, I UNDERSTAND and FEEL the SAME way about EVERYTHING you said!!!!!!!!!!
What a good friend ❤ love the way she looks at her just holding her with her gaze
Why do women always say corny things like this?
@@helicoptergunshipwhy do you hate women and repress all your emotions, loser 🙄
@@helicoptergunshipProbably because we aren’t taught to stifle our emotions from a young age like men are. You should try it, you’d prob be a happier person
@@Angela98923 FWIW, I didn't think it was corny in this case. It was a really good summation of what seems to be an extraordinary person.
🎉❤Amen sister @@Angela98923
My husband was diagnosed in his late 30's. He had been having symptoms in his legs for years but it was always brushed off because "he was a healthy young man". Must be a pinched nerve or he slept wrong 😑. It took a doctor with some previous MS experience to get him the tests and specialist referrals he needed to diagnose him finally. Glad they are talking about this.
I have MS, I try to stay positive but some days are harder than others. I am glad she is speaking out yse most have 0 understanding of this disease. My own family is clueless
Yeah, 2018 mine was dismissed. Didn't get diagnosed until 2022. Had a shutdown like her, which is why they finally looked further.
I love the friendship & support they share! 💗My friend's been living with MS for about 20 yrs, but I forget because it's not outwardly apparent. She's been taking Tecfidera (before bed) for many years and it's kept her symptoms at bay.
It doesn’t keep the symptoms at bay, it slows the progression of the disease.
@@0329Christine Sorry if I didn't say it correctly. Semantics. I guess we're kind of saying the same thing. I'm just her friend and relaying what I see and what she's told me. 🙏🏼🌷
@@0329ChristineI'm also on Techfidera
She and I are the same age almost to the day. I can't imagine what she's going through, and I find it scary. I hope the best for her.
This made me cry. It sucks when your life changes and you can’t do all the things you loved any longer. You have a right to be mad. Life changed for me when I got RA. But you are also so very blessed with wonderful friendship and support. I look forward to their podcast
I have ms and I had it for awhile before I was diagnosed…women are so strong we just push through. I finally lost my eye sight and the ophthalmologist (I think)knew right away. I’m doing great now. I know I’m luckier than most. Christina and Selma got it very aggressively.
I wonder if it’s NMO (neuromyelytis optica). I hope you are well.
@@Jacqueline-xb5nk I really am and I can see…I guess I didn’t say that lol thank you!
I have RR ms. I do really good most days. We believe the ms has effected my right optic nerve (it had a good lunch, I guess). My vision is stable 20/50 with glasses. but if it gets any worse I will be legally blind in that eye. Fatigue is another issue. People just don’t understand that part of MS. You just can’t do anything. My physician said I probably won’t get any worse but I feel for those that do.
I was diagnosed with MS last year at the age of 13, sending prayers!
What a beautiful thing to see friendship like this. The support, the looks, the love. Beautiful!
This is true for many people. I don’t have MS, but I was injured almost 10 yrs ago….. fell one step, shattered ankle and knee. I am basically homebound. I have mobility issues, balance issues, fragile bones, and could go on.
I looked forward to grandkids, traveling, volunteering when I retired, instead I am disabled. I try to keep a positive attitude….but there are days my husband hears me stating I hate my life. I was a nurse….i helped others, now I require assistance.
Wishing Christina and Jaimie the best as they fight their disease.
I've suffered from chronic pain since 2008 and it has steadily got worse. I really feel for these ladies. I know what it does to you physically and mentally. Sometimes the mental part is worse. I'd love for there to be more choices for treatment. I love Christina and her boldness and fierceness.
Yes!! 🙌🏼 I went from being an avid runner who organizes worldwide online fitness tracker events for walkers/joggers to an isolated broken depressed pile of goo due to a degenerative disease. Thank you Christina for voicing the anger and desperation so many of us feel -especially when others cannot outwardly see the disease or chronic pain.
Christina is my new inspiration. I was diagnosed with MS in 2012. I’m currently experiencing the worst relapse I’ve ever had. This lady speaks the truth ❤
It took 20 years to get diagnosed for me! Love you Christina!
I was born with it and it came and went. I also had leukemia too. I’m making thru it barely. Yeah my MS is kicking my eye sight down. 😢 peace and love everyone Christina always a great actress ❤❤❤
Yep my doc said it was a brain virus active brain legions all over. Did steroids to stop the activity I have had nerve pain sense all over plenty of nerve ablations so maybe one day I will be diagnosed
There is not a day that I don’t need to lay down it sucks
The love I have for these two is undeniable! I will be Messy right with them! 💛🤍💜🖤
She is such a beautiful woman. I was in tears when i saw her starting to tear up. God Bless you. You are loved by so many fans.❤❤❤❤
This has helped a lot in those of us with MS who aren’t just 70/80 but younger people who are just working through it! I’ve got the rarest form of MS at 23 so to see Christina and Selma, it’s meant the world!
I am being referred to a neurologist to be screened for MS very soon. I have fibromyalgia and osteoarthritis. Since 20, I have had a ton of MS symptoms. After the birth of my daughter. The pain is excruciating. My rheumatologist said it looks like that’s what it may be. I am not looking forward to this at all. I am a traumatic brain injury survivor. I was finally getting better. Now I have sharp pains in every joint and bone in my body, including my toes and fingers. it’s not arthritis she said. That’s mostly in my knees. If I stubbed my toe, it hurts my entire foot almost up to my shin. Pushing the microwave buttons make me feel like my finger and wrist will break. Pill bottles are very hard to open now every day migraines. I have put together a symptom chart from since I was five years old. I also researched a brain abnormality I have for my neurologist so they have it all. God bless everyone who is struggling with MS.
Thank you Christina, Jamie. Selma for being so honest! Showing how we have no choice but to get used to living with the uncomfortable and awkwardness of chronic illness and disability but that it is still possible to still be us! The hardest part is knowing and becoming ‘comfortable’ with knowing we are not going to get better but still making sure to embrace any positives to help lift us to get thru our days 🤗
My Aunt had MS, I was just a little kid this was back in 1960. She was young 22 years old when diagnosed. I remember reading Annette Funicello’s book she was on the original Mickey Mouse Club. She didn’t want to tell anyone because she didn’t want to let her fans down. Finally her best friend Shelly Fabares asked her what’s wrong? She told Annette that people think she’s drinking. So she was on a magazine cover and shared her story. She said she did it to help others going through this. After that she really became proactive, raising awareness. She started a teddy bear company and perfume called Cello, which was to raise funds for research for MS. She was one strong beautiful lady, with the sweetest, kindest loving heart and soul. 🥰
Thank you for speaking up. I have MS for the past 20years. It SUCKS!
🙏❤️
I love that they are doing a podcast!! Good for them!!!❤❤❤
Love you Christina , way back from married with children. Hang in there, be encouraged. You’re not alone ❤❤. Thank you Jamie Lynn for sticking with her. You be encouraged as well ❤️❤️
So nice to meet you Christina! I too spent my life pretending to be a happy bubbly person but I am not. I got hurt in 2010 and after too many surgeries and countless doctors I now only have 25% use of my core, spine, hips and legs. And that is on my best day. I live with so much pain so I get how you feel. Anger, self pity, giving up on living. Keep going girl, for you and you alone. I hope you start having more moments without pain.
Christina Applegate is such an honest and beautiful soul. Her sense of humor and transparency is an inspiration. Much love to her 💙💯
These ladies are awesome. ❤
Absolutely!
And hot 🔥
My sister has been diagnosed a decade ago, thank God she is still great. Humour, acceptance, respect and freedom to have bad days is important.
I have lupus and pbc . I live in pain daily. Chronic pain is hell.
🙏🏾
I've been learning to live a new life with a brain injury, neuropathy and learn how to adjust, I understand all those feelings. Its a completely new existence and every day is different. I appreciate videos like this to see celebrities share their humanity in such a real way 🤗 thanks for sharing your truth ladies!! #BadassBabes
Wow, I'm so glad I found this because I just got diagnosed with MS and seeing this pretty lady being so strong really helps me! MS is rough and so hard on the body. The day to day struggles with pain, walking and fatigue are so hard, but she really helped me ❤
My Mom went over 20 years without a diagnosis ( MS) ! Never gave up had 4 children after me worked & Lived her life to the Fullest ! She was amazing my Hero Prayers for all you have to suffer with this disease! Two very Strong Women right here ❤ them Both
I was diagnosed with epilepsy at 29, but I knew something was wrong before that. I didn’t go to my doctor for 4 years prior. Mostly because I was caring about others more than I did about my health. Focusing on helping family members and perfect attendance while being a teacher who did not like the concept of taking off work is now a huge regret. Working with young students, and having colleagues , children, restaurants, stores and family see me have seizures is the most embarrassing thing to me. So I appreciate Christina Applegate’s honesty about her MS, and I understand how she’s angry. I sleep a lot to pastime. NOW, I have taken off work without pay. My aunt has MS. Overall, I appreciate Christina having a podcast with a good friend and I believe it will help a lot of people.
My very first foster mama, the lady that loved me more than anyone has ever loved me suddenly died from MS one month after my ninth birthday. She never let on that she was sick, she never mentioned to anyone that she was unwell. I remember she was tripping and falling a lot; she also was eating very little (I understand now that she was having trouble swallowing). She also became incontinent. She was so sickly a few weeks before she died, but it was our secret because we were afraid that we would be separated😔. But one morning, I found her on the floor and I couldn’t help her up, my goodness I tried😢… she begged me not to tell but I had to get a neighbor. She was hospitalized for two weeks then she died. I was with her when she died. The lady I was living with at the time was kind enough to take me everyday to be with my foster mama. I think of her everyday still, it’ll be 20 years this April 4th that I last kissed her beautiful face💔🕊️
❤❤❤❤
I love her honesty. Just because she’s been an actress for all these years she’s still human n lives her life like everyone else. I am sorry she is dealing with MS but it’s wonderful to know she’s honest about n how it’s affected her life.
ALL diseases and chronic pain are invisible- it’s why we should be kind to everyone we encounter
Amen. No one knows what hardships & suffering goes on behind closed doors.
Jamie Lynn looks amazing and she's such a good friend to Christina is just wonderful to have somebody on your side and you have your back.
My heart goes out to them. My father had MS and I understand the hardship and pain you go through. My thoughts and prayers for them to overcome this. But so so happy they have each other to get through the rough days ahead. And admitting it’s hard is the first step.
Still can’t believe she did DTM Season 3 while dealing with all of this.
I am looking forward to watching their new podcast! I started having symptoms of MS 20 years ago and was diagnosed in 2006. I am so, so happy these two beautiful and intelligent women will educate the public about MS. The medicine and therapies available in the past 15 years do dramatically slow the progression of MS in the majority of people. I am still walking and taking care of myself and most people do not believe I have MS. There can be chronic pain and pain is invisible. A big lesson I learned to not be hard on myself or others for not understanding or remembering that sometimes we get tired easily from heat, stress, walking, riding in a car...and that it is o.k. to rest. In fact it is normal. Pacing oneself is important to achieve daily tasks...take breaks or take a few days get a project done but do not let it stop you.
She’s so strong and honest and it’s so beautiful and so needed in this time. Thank you Christina and Jamie-Lynn. ❤ Best wishes to you both.
I love her sense of humor. My Mother was diagnosed with MS a few months ago; she is about the same age as Christina. A hard pill to swallow for her, but she is also remarkably strong. There are days when I feel the impotence to not be able to help her the way I wish I could, but I always try to be there to the best of my abilities. While I cannot change the fact that she now has MS we can change the way we view the world. It jolts you into a new perspective whether by choice or not. But there is no failure here sweetheart, just when you quit. ❤
I’m glad you are there for your Mom. Sometimes because of the energy depletion you want to be around people and socialize but don’t have energy, try to coordinate social events that take less energy like movie nights, ordering dinner etc. I wish you the best .
I did know about her cancer and now ms, but I am so glad she explains it.
We should all be able to speak out loud what it is and especially how we feel.
I hope that every person has his little moments of joy. Don't let this take you away.
Much love and respect❣️
I was diagnosed in 2007. Part of the grieving, fear, loss comes from having your body failing you. It sounds obvious, but unless you’ve experienced it, you just don’t know.
Please KEEP TALKING ABOUT It many many many of us need you to KEEP talking x
Through the years, I've witnessed the remarkable strength and grace of two extraordinary women as they have enchanted audiences worldwide. As life has stripped away much from me, I find solace in the one precious gift I still possess: my health. With heartfelt sincerity, I would willingly shoulder the burdens of pain and suffering endured by Christine and Jamie-Lynn, if only to safeguard the health that enables these incredible talents to continue illuminating the world. Christina, with her timeless beauty and the joy she brought us as part of the Bundy Family, is a national treasure. My thoughts are with both of you, offered with deep empathy and genuine serenity. xo
I am an old man. And I have had to deal with many illnesses and heart breaks in my life. I have been in so much pain I actually judged God, and said, "This is Not Fair.!""This is too hard for anyone to bear.!" But I was wrong.
I have found that, "This too shall pass." (in most of our difficulties)
And that, Acceptance, is the first stage of overcoming any situation.
It breaks my heart to see these women go through this, but I believe, that they will be better people for it. I am praying for you Christina. God will make it right, somehow. ❤
I have MS 10 years.. and i dont tell anyone unless i have to! I just say to myself everyone has problems and no point in me telling people about it... as i know there are people out there with all types of illnesses suffering in silence and i appreciate people in the public eye explaining what its really like.
I will be watching the podcast.
I keep telling my mates... enjoy yourselves... retire early if u can as u don't know whats around the corner.
My thoughts to the family and friends of Rob Burrows... Fantastic Rugby league rugby player (uk), and fellow Pontefract...YORKSHIRE lad...and a thanks to everyone that helped him and his family, being a private person himself his strength shone through. (Passed away this week with MND)
I am going to look for your podcast now thanks.
Christina, its nice just to see & hear you. I loved you in the series Dead to Me and felt that I saw you as a deeper more complicated actress. Now I see you as a deeper, more complicated person. Thank you for the things you and Jamie shared in this interview!
This definitely made me tear up. I love Christina. Can’t imagine what it took for her to fight through all these emotions and voice her struggles. Testifying about such a brutal disease, I hope she realizes how many people she’s helping even though it’s not a platform she asked to be on. But you’ve got to love seeing women be there for each other. We’re expected to support everyone else. It’s such an awesome thing seeing us support one another. I look forward to listening to their podcast. I think it’s going to be awesome!!
I’m 65 alone and was diagnosed in 16 I wish I had them for supporti hate being alone I isolate and in pain everyday love you two❤
It’s amazing how such good friends can be affected by the same or similar health issues. My friends from hs and I all reconnected after going through similar health issues and it’s bonded us for sure in such a genuine way. It sucks that we all have it but it’s so nice to have support from ppl who truly understand what it’s like to suffer.
Glad Jamie and Christina have each other...
I was diagnosed 2 year ago and man, it's truly so refreshing to hear total honesty about how truly awful MS can be
Chronic grief ... I can relate ! From Quebec, Canada ! I have MS
God bless these two ladies.❤❤❤❤❤❤❤❤❤❤🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉😊😊😊😊😊😊😊😊😊😊
This brought me to tears..I can well relate. Prayers for both of them to get through it all.
Christina is blessed to have a friend like Jamie.
I love Christina and have always been a fan. Prayers to her 🙏🏼
I feel bad for her..but she had many years before this disease free. Feel gratitude..my disease is similar to hers but it expressed itself early. Now I’m 63. Everything is hard. I get so mad about everything it has taken from me. I understand. But I’m still grateful because I’ve had a beautiful life.
I suffer from several painful invisible chronic illnesses and also i lost my hair. I have felt anger and loss as well. I suspect if you examine many people's lives, you will find people struggling with all sorts of invisible debilitating conditions and loss. It angers me when i look at the world and see this perfect celebrity culture reflected back at us. I am glad these women are sharing their own issues. I will say many of us have been here allbalong, waiting for a voice.
Her description also happens to perfectly fit myalgic encephalomyelitis, a disease I have; invisible disability, incurable, chronic fatigue and pain, fluctuating symptoms, grieving the loss of who you used to be, everything…I’m so glad she’s bringing light to chronic illness!!! It is so underrepresented and misunderstood 😢
So beautiful and moving. I can't wait to hear the podcast. I connect to what she is going through, with my own illness. I send her blessings and healing and thank you for being vulnerable to show the messy with us so we can all learn and be a part of your journey.
I've been dealing with MS for 10 years now and it never gets easier. A lot of things were robbed from me like running, wearing heels, and normal conversations. I have balance problems, heat and cold intolerance, speech problems, extreme fatigue, and tingling feelings in my hands and different sections of my body.
I totally understand her struggle because I too was diagnosed with multiple sclerosis back in 2013. Very difficult disease but if you let it get to you then it'll take you out more quickly that's with anything I believe
Prayers for Christina & Jamie 🙏 I understand your anger. I have Cancer & I'm pissed & Cancer sucks
This was a beautiful conversation. I'm so excited for the podcast!
As a disabled person who personally wouldn't change a thing, I very much appreciate this. It's ups, downs, but also opportunities.
Prayers for both of them.
You have your "Judy " in real life!! God Bless You Christina, your not alone. ❤
MS does suck and I've been battling it for 20+ years (since early 20s and while attending college). I hear you ladies as it's so difficult for people to understand. I see you and I love you 🧡🧡🧡
Don' t isolate yourself. I will pray for both of you ladies, my neigh or fights ot every day is in pain and rides a .bike, forces herself to move , and she said to stay alone is. No good. Keep exercising no matter the pain. And no😢 sugar, no gluten. Helps tremendously with the pain.❤❤❤❤
57 years this month living with an undiagnosed disorder. My cancer surgeon attempted to find me primary care help 21 years ago. I have been grateful every day and have not the heart to contact her and thank her for her wonderful care. I have since moved to another state. I have seen many primary care physicians. To a fault they insist my extreme sensitivity to sunlight is a psychiatric disorder.
At age 67 I manage my condition that now includes long Covid. I am a much happier person keeping my distance from the healthcare system. A thoughtful psych counselor I speak with Telemed 5 minutes monthly is my sole connection with medicine.
My grandfather was a teaching physician so I grew up among many capable physicians and learned by listening how one can think through healthcare problems. I never dreamed it would become my best resource to surviving the neurological and various other symptoms that began occurring seasonally from the spring of 1967.unable due to a recurrent malaise to travel with my family to see the cherry blossoms in Washington DC. ☀️💥🌺