Ive just started watching the Miranda sitcom and there's so much physical comedy in it to think she was dealing with chronic pain and fatigue at the time is mindblowing! I absolutely love love love the show I'm binging through it actually. Sad that I only have a couple of seasons to go now but I'll check out her other work after. Hilarious Lady, I wish her the best
Knowing now how symptomatic she was during her “Miranda” show, I’m amazed at how she was able to make her physical scenes look so effortless. I watched the series years ago & loved it. I really admire this woman for sharing her illness; I’m sure she’s helped many as well as making us laugh! ❤
I’ve had M.E 17 years now. It’s great to see Miranda talking on this morning. Any talk about M.E is great as most people I speak to done even know what it is or they have never heard of it. It changed my life completely. Lost friends, job and partner because of it. It is like living in a nightmare. Terrible pain and can’t even look after my grandkids as too tired.
sorry to hear that. losing friends sounds terrible what w4nkers. you're better off without them and your partner as well. was it a bloke? they usually abandon women when women are at their lowest because men cannot cope with not being the centre of attention.
So sorry you have ME. I do, too. What a horrible illness to deal with. I, too, lost friends and had to leave my job. Luckily, my husband stuck with me. For that, I'll be eternally grateful. I have improved. I hope you have, as well.
My son got bit by a tick on his 1st birthday. Within 2 years he couldn't walk and every time we touched his arms or legs he would cry. Thankfully one doctor asked the right questions and he was cured. Miranda I wish you well and thank you for sharing.
I’m sorry to hear you feel isolated, but I completely get the complex emotions we go through. Not wanting to burden people, not being able to do things for our friends and families, not being able to join in, just feeling like there must be something better, just to name a few. It’s very lonely sometimes. Look for a support group online, it might help just to hear from others and to be able to share your feelings. Take care, you matter. X
@@x-Xx7xX-xexcept it's not. I was in the best shape of my life when I started experiencing debilitating fatigue, leaving me without the energy to even get out of bed in the morning. I was diagnosed with PCOS when they found giant cysts on my ovaries, which is an endocrine disorder and can cause extreme fatigue. My partner is a registered nutritionist who was able to write me a diet plan and yes a good diet is very helpful but it's not a cure and that kind of attitude is very ignorant
It's breath of fresh air to see M.E being spoken about on a largely televised platform. I've had CFS symptoms since I were 11 years old and diagnosed when I was 15. I'm now 30. Back then, no one really knew what it was and it was scary. I'm so thankful to Miranda bringing awareness to this hidden illness. Let's hope it gets less and less where people's responses are "what's M.E?" Or "oh so you just get tired alot?" 🤦♀️
I just love her! I'm so glad she's doing well, and speaking up about this. So many illnesses and disabilities aren't visible, and so many people are suffering.
Thank You Miranda. A couple of weeks ago I heard about your journey. Myself 30 yrs plus dealing with Lyme that was late diagnosed, triggering so many other issues and constantly struggling with flu symptoms, and the extra pain in forcing yourself to get up and work everyday even though sometimes that causes more damage, it wasn't the path I had planned for myself. Now two weeks later, I realized that you made a difference in my life by sharing your story. Whilst I haven't read your book yet, I thank you.
I have ulcerative colitis and someone wrote, "if you want to know what the fatigue is like, stay awake for 3 days straight and then try and function" I am glad you finally got some answers.
Loved her show! We watch reruns all the time. Her lines have become imprinted forever in our brains and at appropriate moments they come out and we have a laugh. She’s made quite an impact on me, my daughter, and hubby. So sorry to hear of her health struggles! Glad she found love. ❤️
Wading through treacle, exactly. Not being able to lift your arm/fork etc... so familiar! I had CFS/ME after contracting glandular fever EBV virus as a teenager and very slowly improved but never back to the person I was before. Experienced so much misunderstanding. So thankful to Miranda for raising awareness of this condition! Looking forward to reading the book!
I’ve had CFS/ME for 30 years and in some of those years life has been very full, (I’m laying a patio at the moment, just to give you a level of improvement), but it’s taken years of learning to listen for the signs that I’m over stretching myself. I was one of those people who couldn’t lift my head at one point. Visitors were lovely to see but also exhausting. If every year you improve a little, then cling to that hope, as I did. Eventually, I worked full time but only if I slept in the car through lunch, I could shop for hours, but only if I stopped for a cupper as I grew tired. Managing your energy is so important by only doing what feels manageable, whether it’s lifting an arm or walking 3m. It’s all keeping muscles working. Never give up and always hope that tomorrow will be an improvement, no matter how tiny.
As a fellow chronic illness/chronic pain fighter, I listened to Miranda reading this on Audible and ... I FELT HEARD! ❤ It's hugely informative! Miranda did some serious research. I will be buying a physical copy too because I want to bookmark, highlight & refer to it, as I too make my way through the darkness back into the light. Which feels much more possible since reading this book. Thank you, Miranda! Love from your "MDLC" ❤
@karenbourke3751 My MRI's, diagnosis, rheumatologist, and injecting myself fortnightly with biologics to prevent my bones fusing together (even more so), say otherwise. I exercise daily, it's very important to keep my mobility and obv it's good for mental health too. One of the hardest obstacles initially, other than a life changing disease, was learning how cold and judgemental people can be. Even complete strangers.
It's so hard to explain about fatigue so well done Miranda. I have MS and the fatigue is dreadful, very hard at work to say i can't do that and people looking at me. Hidden health conditions are not easy to live with, i only work three days a week and my managers just don't get it and compare me to how other people work.
Oh my life!! That fatigue is so real. I have hEDS (hypermobility Ehlers Danlos Syndrome) and chronic, unending fatigue is part of the condition. I'm still learning how to pace myself, so I can get through a day. Many days I can't function. I'm glad you've shared your story. ❤️
Such a brilliant lady, I remember the many PJ parties we had watching Miranda re-runs over and over, doing gallops up our hallway ❤ I wish her well and so happy she found that special someone
Loved her in Call the Midwife. I've had ME/CFS since 1999, so can fully empathize with debilitating chronic fatigue. Thanks for bringing attention to this horrible type of illness.
Miranda, you are so talented yet so down to earth. Thank you for your books, your shows and the hope and encouragement you pass on to all of us just by being YOU!! I bought your book via audible because my eyesight is not what it used to be and I'm finding it informative as well as uplifting and motivating. Congratulations on finding the love you so deserve💞
I love Miranda with my whole heart & the fact that she's talking about living with a chronic illness. I've been living with fibromyalgia since I was in my early teens. It's very isolating & there's not a lot of awareness so I'm grateful she's highlighting this.
Lovely 🌹 to see miranda back and feeling better i hope I havemirandas book its brilliant Congratulations Miranda on your marriage to your wonderful husband Please keep comments Respectful All The trolls judt STOP If you cant be KIND just dont message anything At the end off the day shes been so poorly for years Ask Yourselves hiw would you like it ?? If people were writing horrible cruel words Miranda we love you What an inspiration you are A beautiful lady inside and out Well done on your new book i am reading it excellent work on this vook sending you loads off love and hugs Miranda ❤️❤️❤️❤️🤗🤗🤗
Having a chronic undiagnosed illness is one of the worst things that’s happened to me and I feel so happy that Miranda has found answers and doing well. Drs need to take their patients more seriously.
So lovely to hear the bit about not even being able to pick a glass of water up because you're so tired. Feel so heard with her sharing this story. Thank you, Miranda. I've had situations where I'm sitting in my chair in the lounge thinking I need to rest before I crash, then getting up to go to the bathroom and I can't get up or even crawl. Big hugs to everyone.
When Miranda said about the glass of water, I felt like I cold finally explain fatigue to my loved ones. I have Lupus, Rheumatoid Arthritis and Crohn’s disease. I feel lucky everyday for the humour afforded me and the funny people around me. Stay awesome Miranda
I understand what your going through, I also have lupus, fibromyalgia, severe raynouds syndrome, asthma and a condition that makes my immune system destroy platelets (I.T.P) . Every day is a struggle, the pain never really goes away even with strong pain meds, the fatigue is constant, every day I tell myself I'm going to do x y and z, I'll be lucky if x gets done. I am fortunate to have a very supportive husband who never mentions that the hoovering didn't get done or we've run out of his favourite food, he just gets on with helping out,, even though he still works full time in a very physical job n is nearly 61, I'm sure the last thing he wants to do when he gets home is start again but he never complains. Hope this new year see you as well as you can be. X
She started talking about her symptoms and I knew it was Lyme. We had dogs with Lyme & being in the woods ourselves we learned alot about it. I wish her well!
I’ve had it for about 3 years now and it was a huge shock because then I developed Lupus on top of the CF/ME and I’ve been stunned by the harshness of some of my symptoms! I’ve just realized that I’ve actually forgotten friends of 30 years 😱👋🇨🇦
It’s terrible when you know someone else has ME, but it is validating when someone with a larger platform can speak about it. I’m looking forward to reading her book. 😊
You are wonderful. CONGRATULATIONS on your marriage and your new book which I will purchase. I have suffered from debilitating pain for 20 years now so you are not alone. I loved Miranda it was such fun and everything you've done. Much love to you from Arizona, USA I didn't vote for Trump ever so not my fault.
As a New Yorker, lime disease is so prevalent here in the states. Being aware of deer is very important for the animals & and we, the people who share their environment.
I discovered her show " Miranda " and loved it! Happy she discovered finally after all these years what she has and now she knows what to do and that she found love and got married!🎉🎉🎉🎉❤ from Israel 🇮🇱
I've had the same condition for the last 40 yrs and possibly much longer. Thank You, Miranda. You've given me many laughs at times I thought it impossible. I'm so appreciative. Congrats on marriage. ❤
Loveyy Miranda! I have Lyme dicease also, non help with doctors, non. And don't tell my friends how it is every day.. I must thank You for saying and doing something with us all suffering❣️ I watch your show almost every day because need such fun, thank You!!! 💕
Thank you for sharing this. I identify with everything you have mentioned. I'm 59 and was diagnosed with ME at the age of 30. I'm looking forward to reading your book. You're an incredible inspiration for those of us who are tired of being tired❤
My son was like that. His body was shutting down. We went to the NHS. They didn’t know what was wrong. Then we found someone who could help we found out he had Lyme disease, he drank 3 litres of water and took natural drops , now he is well Thankfully We thank God every day for this
I had a college best friend. We were both music majors. She had cronic fatigue. Luckily she had many good friends who helped her out with studying. I never judged her for being lazy. I could tell it was the real deal.
Back in the yuppy flu days, before I was diagnosed with ME, the doctor told me that I was depressed, which I knew wasn't true. I had to do my own research before I was eventually severely disabled and in constant pain for almost 20 years. Faith...healthy food and complete surrender to this life threatening dis-ease and CBT, or pacing myself, enabled an almost complete recovery. I just have to listen to my body and rest if I get a virus or whatever. Travelled the world since recovered, on my own, published a book, Not a Complete Shambles etc etc, decluttered my life ...diseases involving severe fatigue don't need to be a life sentence.
I knew someone who had chronic fatigue syndrome (she'd earlier had leukemia). Her husband was a doctor. She had the kind of job where she could work from home and build her schedule around her abilities to get out and about.
I've been sick with Lyme for years - my symptoms resembled ME and cause autonomic dysfunction and a wide range of neurological and gastrointestinal symptoms. The NHS doesn't help with long term treatment so we are forced to pay out of pocket despite 700 peer-reviewed studies showing Lyme and co-infections can persist despite antibiotics and therefore be chronic. So far treatment has helped 25% but more intensive treatment would likely help more if the NHS could give us appropriate care.
I wish Miranda all the happiness she deserves, imagine having a ME-like illness and working so hard with millions of people watching you every day. She is so brave and an inspiration.
WOW what an amazing lady, to share this and highlight this, as I for one had no idea just how awful this is for so many people, bless all of you and sending love for everyone's health into the universe ❤❤
So sorry to hear this … Miranda you have been an amazing inspiration to me, especially when I’m been having flare ups amongst chronic conditions. I wish you well ✨❤🙏🏄♀🌊🤗❤✨
It's not well, just improved. There's currently no full cure for ME sadly. Miranda still has days where she's wiped out - seen on Instagram. She's doing a fab job educating people on an area that causes misery for so many. That misery is compounded by other people "not getting it" and making you feel like you're exaggerating or lying - you're constantly being gaslit, which in itself is exhausting. This amazing woman is helping millions with her interviews! The book is great, I've just finished it.
@@katealison6087 oh it's back to ME now? Wasn't it called fibromyalgia when they realised ME wasnt getting any credibility, has the terminology fallen out of favour
There is a physical basis for most ME/CFS although many os us who have it are very sensirive emotionally i think too.....some is triggered by Lyme or viruses...or toxins....I've had it a few times in my life and now know it was a combination of all the above....my most recent phase was.after carbon monoxide poisoning and B6 toxicity. It's took me two to three years to recover this time. I'm a lot better but still get flares. My chiropractor has helped me reset my neck and spine issues after I read about Dr Raymond Perrin and his Perrin technique in the UK. He teaches how to help the lymph system which can be affected by neck or spine issues affecting the bodies ability to detox and heal.
I have Rheumatoid arthritis and yes the fatigue was like you sleep and "wake up" and you physically can not keep eyes open. You feel like you have not slep anything because of adrenal glands shutting down
I can’t thank Miranda enough for highlighting chronic fatigue conditions. It’s so good hearing my everyday experiences being spoken about!
Like Miranda, I send you my best wishes, Toni x
She’s one of my favorite actors ! She’s also incredibly funny and brilliant - so happy for her ❤
Ive just started watching the Miranda sitcom and there's so much physical comedy in it to think she was dealing with chronic pain and fatigue at the time is mindblowing! I absolutely love love love the show I'm binging through it actually. Sad that I only have a couple of seasons to go now but I'll check out her other work after. Hilarious Lady, I wish her the best
oh that series will be with you forever. I have a comfort binge basically yearly, even though I know all bits by heart.
She is fantastically funny, isn’t she??!!👏🏻👏🏻👏🏻
I've binge watched the show (all seasons) three times and laughed knowing what was coming. Miranda is amazing. Loved her in "Not Going Out."
I've watched for years. I love her humor so much. I re-re-rewatched all of her shows. ❤😂
Knowing now how symptomatic she was during her “Miranda” show, I’m amazed at how she was able to make her physical scenes look so effortless.
I watched the series years ago & loved it. I really admire this woman for sharing her illness; I’m sure she’s helped many as well as making us laugh! ❤
I’ve had M.E 17 years now. It’s great to see Miranda talking on this morning. Any talk about M.E is great as most people I speak to done even know what it is or they have never heard of it. It changed my life completely. Lost friends, job and partner because of it. It is like living in a nightmare. Terrible pain and can’t even look after my grandkids as too tired.
sorry to hear that. losing friends sounds terrible what w4nkers. you're better off without them and your partner as well. was it a bloke? they usually abandon women when women are at their lowest because men cannot cope with not being the centre of attention.
Yes a bloke but better off on my own. Thank you 🤩
So sorry you have ME. I do, too. What a horrible illness to deal with. I, too, lost friends and had to leave my job. Luckily, my husband stuck with me. For that, I'll be eternally grateful. I have improved. I hope you have, as well.
Even so, people don’t understand the level of fatigue.
Nice to see Miranda as herself rather than through a persona.
My son got bit by a tick on his 1st birthday. Within 2 years he couldn't walk and every time we touched his arms or legs he would cry. Thankfully one doctor asked the right questions and he was cured. Miranda I wish you well and thank you for sharing.
What did he ask?
I have chronic illness and it really is invisible. Feels very isolating at times. Good on her for bringing this issue to light.
I’m sorry to hear you feel isolated, but I completely get the complex emotions we go through. Not wanting to burden people, not being able to do things for our friends and families, not being able to join in, just feeling like there must be something better, just to name a few. It’s very lonely sometimes. Look for a support group online, it might help just to hear from others and to be able to share your feelings. Take care, you matter. X
I like Miranda.I loved her in Call the Midwife.she was so good.i hope she goes on to have better health.❤
Great to hear someone in the public eye talk about fatigue - based conditions. They are completely debilitating. Thanks Miranda for opening up! 🫶🏼
Cured by a good diet and exercise
@@x-Xx7xX-x if only good diet and exercise was a miracle cure for everything. Unfortunately that's not the case.
@@Carla0297 Excuses
@@x-Xx7xX-xexcept it's not. I was in the best shape of my life when I started experiencing debilitating fatigue, leaving me without the energy to even get out of bed in the morning. I was diagnosed with PCOS when they found giant cysts on my ovaries, which is an endocrine disorder and can cause extreme fatigue. My partner is a registered nutritionist who was able to write me a diet plan and yes a good diet is very helpful but it's not a cure and that kind of attitude is very ignorant
I'm a bit selfish I think fatigue based illness is better than chronic pain which I suffer from
It's breath of fresh air to see M.E being spoken about on a largely televised platform. I've had CFS symptoms since I were 11 years old and diagnosed when I was 15. I'm now 30. Back then, no one really knew what it was and it was scary. I'm so thankful to Miranda bringing awareness to this hidden illness. Let's hope it gets less and less where people's responses are "what's M.E?" Or "oh so you just get tired alot?" 🤦♀️
I just love her! I'm so glad she's doing well, and speaking up about this. So many illnesses and disabilities aren't visible, and so many people are suffering.
Thank You Miranda. A couple of weeks ago I heard about your journey. Myself 30 yrs plus dealing with Lyme that was late diagnosed, triggering so many other issues and constantly struggling with flu symptoms, and the extra pain in forcing yourself to get up and work everyday even though sometimes that causes more damage, it wasn't the path I had planned for myself. Now two weeks later, I realized that you made a difference in my life by sharing your story. Whilst I haven't read your book yet, I thank you.
I have ulcerative colitis and someone wrote, "if you want to know what the fatigue is like, stay awake for 3 days straight and then try and function" I am glad you finally got some answers.
Same
Me3❤it's a very lonely battle having an invisible disease 😢
I am such a Miranda fan! She comes across as such a genuinely nice person…
Loved her show! We watch reruns all the time. Her lines have become imprinted forever in our brains and at appropriate moments they come out and we have a laugh. She’s made quite an impact on me, my daughter, and hubby. So sorry to hear of her health struggles! Glad she found love. ❤️
She is a great artist
Wading through treacle, exactly. Not being able to lift your arm/fork etc... so familiar! I had CFS/ME after contracting glandular fever EBV virus as a teenager and very slowly improved but never back to the person I was before. Experienced so much misunderstanding. So thankful to Miranda for raising awareness of this condition! Looking forward to reading the book!
I’ve had CFS/ME for 30 years and in some of those years life has been very full, (I’m laying a patio at the moment, just to give you a level of improvement), but it’s taken years of learning to listen for the signs that I’m over stretching myself. I was one of those people who couldn’t lift my head at one point. Visitors were lovely to see but also exhausting. If every year you improve a little, then cling to that hope, as I did. Eventually, I worked full time but only if I slept in the car through lunch, I could shop for hours, but only if I stopped for a cupper as I grew tired.
Managing your energy is so important by only doing what feels manageable, whether it’s lifting an arm or walking 3m. It’s all keeping muscles working. Never give up and always hope that tomorrow will be an improvement, no matter how tiny.
I'm one of the millions who have a similar illness.I'm so glad that Miranda is speaking up-Her book is helping me so much.
As a fellow chronic illness/chronic pain fighter, I listened to Miranda reading this on Audible and ... I FELT HEARD! ❤
It's hugely informative! Miranda did some serious research. I will be buying a physical copy too because I want to bookmark, highlight & refer to it, as I too make my way through the darkness back into the light. Which feels much more possible since reading this book.
Thank you, Miranda! Love from your "MDLC" ❤
Cry me a river.
@@NihonKaikan rude
Sounds more like depression. Do you exercise - didn'g think so.
@karenbourke3751 My MRI's, diagnosis, rheumatologist, and injecting myself fortnightly with biologics to prevent my bones fusing together (even more so), say otherwise. I exercise daily, it's very important to keep my mobility and obv it's good for mental health too. One of the hardest obstacles initially, other than a life changing disease, was learning how cold and judgemental people can be. Even complete strangers.
It's so hard to explain about fatigue so well done Miranda. I have MS and the fatigue is dreadful, very hard at work to say i can't do that and people looking at me. Hidden health conditions are not easy to live with, i only work three days a week and my managers just don't get it and compare me to how other people work.
Loved her as Chummy ❤
Same
Oh my life!! That fatigue is so real.
I have hEDS (hypermobility Ehlers Danlos Syndrome) and chronic, unending fatigue is part of the condition.
I'm still learning how to pace myself, so I can get through a day. Many days I can't function.
I'm glad you've shared your story. ❤️
Such a brilliant lady, I remember the many PJ parties we had watching Miranda re-runs over and over, doing gallops up our hallway ❤ I wish her well and so happy she found that special someone
Loved her in Call the Midwife. I've had ME/CFS since 1999, so can fully empathize with debilitating chronic fatigue. Thanks for bringing attention to this horrible type of illness.
Miranda, you are so talented yet so down to earth. Thank you for your books, your shows and the hope and encouragement you pass on to all of us just by being YOU!! I bought your book via audible because my eyesight is not what it used to be and I'm finding it informative as well as uplifting and motivating. Congratulations on finding the love you so deserve💞
I love Miranda with my whole heart & the fact that she's talking about living with a chronic illness. I've been living with fibromyalgia since I was in my early teens. It's very isolating & there's not a lot of awareness so I'm grateful she's highlighting this.
So glad Miranda is back. Oh i do hope wish for another Miranda series. Such fun!! ❤❤
Miranda, I hope you feel better. You always make me laugh and smile.💕
I’ve had ME since i was 11, I’m now 21
Thanks for spreading awareness Miranda and This Morning!
Well done Miranda!
Have had this condition for 12 years. .CFS/ME.
Thankyou for talking about it.
This invisable illness is exhausting . x❤
Yeah, I've had ME/CFS since 1999. It's been a long, awful road, and I am doing much better now. Hope you are, too.
Lovely 🌹 to see miranda back and feeling better i hope I havemirandas book its brilliant Congratulations Miranda on your marriage to your wonderful husband Please keep comments Respectful All The trolls judt STOP If you cant be KIND just dont message anything At the end off the day shes been so poorly for years Ask Yourselves hiw would you like it ?? If people were writing horrible cruel words Miranda we love you What an inspiration you are A beautiful lady inside and out Well done on your new book i am reading it excellent work on this vook sending you loads off love and hugs Miranda ❤️❤️❤️❤️🤗🤗🤗
Good actress love this interview ❤I hope she well now and carries on with her amazing career 🙏 ❤
Having a chronic undiagnosed illness is one of the worst things that’s happened to me and I feel so happy that Miranda has found answers and doing well. Drs need to take their patients more seriously.
The book cover reminds me of the time she was on “Would I lie to you?” where she wore an orange jumper and Lee Mack climbed into it with her.
Loved that episode
I love Miranda Hart!!!!! I miss her show!!!!
So lovely to hear the bit about not even being able to pick a glass of water up because you're so tired. Feel so heard with her sharing this story. Thank you, Miranda. I've had situations where I'm sitting in my chair in the lounge thinking I need to rest before I crash, then getting up to go to the bathroom and I can't get up or even crawl. Big hugs to everyone.
When Miranda said about the glass of water, I felt like I cold finally explain fatigue to my loved ones. I have Lupus, Rheumatoid Arthritis and Crohn’s disease. I feel lucky everyday for the humour afforded me and the funny people around me. Stay awesome Miranda
I understand what your going through, I also have lupus, fibromyalgia, severe raynouds syndrome, asthma and a condition that makes my immune system destroy platelets (I.T.P) . Every day is a struggle, the pain never really goes away even with strong pain meds, the fatigue is constant, every day I tell myself I'm going to do x y and z, I'll be lucky if x gets done. I am fortunate to have a very supportive husband who never mentions that the hoovering didn't get done or we've run out of his favourite food, he just gets on with helping out,, even though he still works full time in a very physical job n is nearly 61, I'm sure the last thing he wants to do when he gets home is start again but he never complains. Hope this new year see you as well as you can be. X
@debbiepierce3045 your situation appears very similar to mine, we are survivors you and I. Stay strong❤️
I have suffered years with fibromyalgia. Another chronic pain and fatigue issue. I feel your frustration.
She started talking about her symptoms and I knew it was Lyme. We had dogs with Lyme & being in the woods ourselves we learned alot about it. I wish her well!
I’ve had it for about 3 years now and it was a huge shock because then I developed Lupus on top of the CF/ME and I’ve been stunned by the harshness of some of my symptoms! I’ve just realized that I’ve actually forgotten friends of 30 years 😱👋🇨🇦
one of my favourite actors on call the midwife sad when she left nice she is bringing awareness to something that is often brushed aside or ignored
Love to you ❤ and thank you for telling your story. May you and all those suffering with CFS be blessed with better health. ☀️
Really good read and very insightful. Listened to it also on audio.
Loved her in Call the Midwife!!
It’s terrible when you know someone else has ME, but it is validating when someone with a larger platform can speak about it. I’m looking forward to reading her book. 😊
I've missed you Miranda!!! Love you ❤
I was chewing on a candy.
Then she said "in me book, what's out now"
and smiled that...Miranda smile,
and the candy fell out of my mouth.
You are wonderful. CONGRATULATIONS on your marriage and your new book which I will purchase. I have suffered from debilitating pain for 20 years now so you are not alone. I loved Miranda it was such fun and everything you've done. Much love to you from Arizona, USA
I didn't vote for Trump ever so not my fault.
Voting for Trump gives you lime disease? I’m confused.
Miranda is inspirational….I absolutely loved being a DLC, such a brilliant book! Thank you Miranda 🧡
As a New Yorker, lime disease is so prevalent here in the states. Being aware of deer is very important for the animals & and we, the people who share their environment.
Congrats Miranda. You’re a genuine star.
Loved the book ❤
I discovered her show " Miranda " and loved it!
Happy she discovered finally after all these years what she has and now she knows what to do and that she found love and got married!🎉🎉🎉🎉❤ from Israel 🇮🇱
I've had the same condition for the last 40 yrs and possibly much longer. Thank You, Miranda. You've given me many laughs at times I thought it impossible. I'm so appreciative. Congrats on marriage. ❤
I could watch Miranda all day.
Loveyy Miranda! I have Lyme dicease also, non help with doctors, non. And don't tell my friends how it is every day.. I must thank You for saying and doing something with us all suffering❣️ I watch your show almost every day because need such fun, thank You!!! 💕
Thank you for sharing this. I identify with everything you have mentioned. I'm 59 and was diagnosed with ME at the age of 30. I'm looking forward to reading your book. You're an incredible inspiration for those of us who are tired of being tired❤
My son was like that. His body was shutting down. We went to the NHS. They didn’t know what was wrong. Then we found someone who could help we found out he had Lyme disease, he drank 3 litres of water and took natural drops , now he is well Thankfully We thank God every day for this
Natural drops?
@@jonnawyatt
Well done to Miranda sharing her story
I had a college best friend. We were both music majors. She had cronic fatigue. Luckily she had many good friends who helped her out with studying. I never judged her for being lazy. I could tell it was the real deal.
I have seen numerous women go through this. It can feel quite hopeless. Thank you Miranda for sharing your experience. Good for you for finding love
Yes you just get used to being ill...so true...TY
Love her sm❤️
Back in the yuppy flu days, before I was diagnosed with ME, the doctor told me that I was depressed, which I knew wasn't true.
I had to do my own research before I was eventually severely disabled and in constant pain for almost 20 years. Faith...healthy food and complete surrender to this life threatening dis-ease and CBT, or pacing myself, enabled an almost complete recovery. I just have to listen to my body and rest if I get a virus or whatever.
Travelled the world since recovered, on my own, published a book, Not a Complete Shambles etc etc, decluttered my life ...diseases involving severe fatigue don't need to be a life sentence.
I knew someone who had chronic fatigue syndrome (she'd earlier had leukemia). Her husband was a doctor. She had the kind of job where she could work from home and build her schedule around her abilities to get out and about.
I've been sick with Lyme for years - my symptoms resembled ME and cause autonomic dysfunction and a wide range of neurological and gastrointestinal symptoms. The NHS doesn't help with long term treatment so we are forced to pay out of pocket despite 700 peer-reviewed studies showing Lyme and co-infections can persist despite antibiotics and therefore be chronic. So far treatment has helped 25% but more intensive treatment would likely help more if the NHS could give us appropriate care.
Same for me in US
I wish you luck 🍀🍀
@@papabear2515I hope that it changes, good luck.🍀🍀
@@margaretlovelock7031 thanks so much. All the best to you!
Loved you in Emma. Congrats on your marriage. Hope you get better soon.
I wish Miranda all the happiness she deserves, imagine having a ME-like illness and working so hard with millions of people watching you every day. She is so brave and an inspiration.
Lyme disease… it is very hard to deal with. Miranda, thank you so much for bringing this up!!! Best wishes to you from Texas!!!
WOW what an amazing lady, to share this and highlight this, as I for one had no idea just how awful this is for so many people, bless all of you and sending love for everyone's health into the universe ❤❤
I just love this woman!!! I am so happy that she is now happy and healthy!!💕💕💕🫶🏻🙌🏻🧚🏻♀️✨✨
Absolutely love Miranda! Much healthier and health to her!!!❤
I experienced the similar things and was finally after 2009 diagnosed with fibromyalgia
It's heartbreaking, the stuff she's been through. All the best, sweetheart!!!!!🎉🎉🎉🎉🎉❤❤❤❤❤😊😊😊😊😊
LOVE, love, love Miranda!!!!
What a wonderful lady
What a honey and what an inspiration :)
I just love her,she is great.❤❤❤❤❤❤❤❤❤
Miranda is a national treasure ❤
Awe so happy she has found a man to share her life. Congrats Miranda❤❤❤❤
This is a great book. ❤❤❤
I have always loved her. She was brilliant in Call The Midwife ❤
Love her and as someone who has CFS along with several other autoimmune disorders, I thank her for sharing her story❤️👏🏻❤️
So sorry to hear this … Miranda you have been an amazing inspiration to me, especially when I’m been having flare ups amongst chronic conditions. I wish you well ✨❤🙏🏄♀🌊🤗❤✨
Love her ❤ But she'll always be "Chummy" to me 😊 Glad to hear things are finally turning around for her. 🙏🏻👍🏻
Glad to hear all is now well ! 💪
It's not well, just improved. There's currently no full cure for ME sadly. Miranda still has days where she's wiped out - seen on Instagram. She's doing a fab job educating people on an area that causes misery for so many. That misery is compounded by other people "not getting it" and making you feel like you're exaggerating or lying - you're constantly being gaslit, which in itself is exhausting. This amazing woman is helping millions with her interviews! The book is great, I've just finished it.
@@katealison6087 oh it's back to ME now? Wasn't it called fibromyalgia when they realised ME wasnt getting any credibility, has the terminology fallen out of favour
@@John-k5y3ifibromyalgia is a different condition
I remember thinking, if the house was on fire I couldn't get out of bed
I love Miranda ❤️
Wwonderful.human beauitful soul❤❤❤❤❤
Love her humor. 😂😂😂😂
I have just listened to her podcast of her new book. Sooooooo awesome
Oh my goodness that sounds so much like my experience. Thanks for your bravery. You are a goddess.
You are a super star💗
Oh! Miranda! I’m so glad to see you…I’m an admiring American..and thank you for your courage.
There is a physical basis for most ME/CFS although many os us who have it are very sensirive emotionally i think too.....some is triggered by Lyme or viruses...or toxins....I've had it a few times in my life and now know it was a combination of all the above....my most recent phase was.after carbon monoxide poisoning and B6 toxicity. It's took me two to three years to recover this time. I'm a lot better but still get flares. My chiropractor has helped me reset my neck and spine issues after I read about Dr Raymond Perrin and his Perrin technique in the UK. He teaches how to help the lymph system which can be affected by neck or spine issues affecting the bodies ability to detox and heal.
I love Miranda. Honest and real 🤩🥰🤩
I am so happy for her !!!!.........That's hope for all of us....😊
I have Rheumatoid arthritis and yes the fatigue was like you sleep and "wake up" and you physically can not keep eyes open. You feel like you have not slep anything because of adrenal glands shutting down
She’s lucky she had the resources to diagnose this and get treatment. Many of us not so blessed.
I love Miranda!
The ever-amazing Miranda ❤