Miranda Hart Opens Up On Secret Health Battle & Love At Last | This Morning

[@WelshToni]

I can’t thank Miranda enough for highlighting chronic fatigue conditions. It’s so good hearing my everyday experiences being spoken about!

[@rachelwebber2120]

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

[@nvrmnde]

oh that series will be with you forever. I have a comfort binge basically yearly, even though I know all bits by heart.

[@RosePetal17]

She is fantastically funny, isn’t she??!!👏🏻👏🏻👏🏻

[@cherrlyn381]

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."

[@SylviaDavis-e5u]

I've watched for years. I love her humor so much. I re-re-rewatched all of her shows. ❤😂

[@reenb4124]

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.

[@Oxford322]

She’s one of my favorite actors ! She’s also incredibly funny and brilliant - so happy for her ❤

[@Battlady57]

I like Miranda.I loved her in Call the Midwife.she was so good.i hope she goes on to have better health.❤

[@SueWatson-f5g]

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.

[@babypicassoeisenstein]

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.

[@SueWatson-f5g]

Yes a bloke but better off on my own. Thank you 🤩

[@jackienaiditch7965]

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.

[@susanarojo3906]

Even so, people don’t understand the level of fatigue.

[@KathrynTanner-t8f]

Nice to see Miranda as herself rather than through a persona.

[@cherylp.3347]

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. ❤️

[@stellagrau8871]

She is a great artist

[@LovinPeaceVibe]

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.

[@egl3369]

I have chronic illness and it really is invisible. Feels very isolating at times. Good on her for bringing this issue to light.

[@CAZZIEK321]

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

[@teresaearl5688]

Loved her as Chummy ❤

[@rapunzelrose68]

Same

[@alyzu4755]

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.

[@Carla0297]

Great to hear someone in the public eye talk about fatigue - based conditions. They are completely debilitating. Thanks Miranda for opening up! 🫶🏼

[@C_Xx7xX]

Cured by a good diet and exercise

[@Carla0297]

​@@C_Xx7xX if only good diet and exercise was a miracle cure for everything. Unfortunately that's not the case.

[@C_Xx7xX]

@@Carla0297 Excuses

[@Carla0297]

​@@C_Xx7xXexcept 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

[@charlottebruce979]

I'm a bit selfish I think fatigue based illness is better than chronic pain which I suffer from

[@CAZZIEK321]

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.

[@Rachel-qo4ry]

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!

[@carolmarshall4341]

I am such a Miranda fan! She comes across as such a genuinely nice person…

[@nicolepowell5470]

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.

[@naomibray5341]

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?" 🤦‍♀️

[@peachesmcgee4795]

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.

[@Bexamina]

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. ❤️

[@marilynbook4211]

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.

[@coreygilles847]

Same

[@allisonanderson5224]

Me3❤it's a very lonely battle having an invisible disease 😢

[@FeckaDoodleD00]

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" ❤

[@NihonKaikan]

Cry me a river.

[@tammydonnelly7902]

@@NihonKaikan rude

[@sunshine9016]

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💞

[@karinamurison1537]

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.

[@jackienaiditch7965]

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.

[@sonyah6699]

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

[@mary-ellendurkin163]

Miranda, I hope you feel better. You always make me laugh and smile.💕

[@hlhappy2793]

So glad Miranda is back. Oh i do hope wish for another Miranda series. Such fun!! ❤❤

[@ashly1911]

I’ve had ME since i was 11, I’m now 21 Thanks for spreading awareness Miranda and This Morning!

[@nadineburke6027]

Well done Miranda! Have had this condition for 12 years. .CFS/ME. Thankyou for talking about it. This invisable illness is exhausting . x❤

[@jackienaiditch7965]

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.

[@jacquiwmch]

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

[@PatBackPatBack-x4n]

I have suffered years with fibromyalgia. Another chronic pain and fatigue issue. I feel your frustration.

[@nataliestownsend4211]

Good actress love this interview ❤I hope she well now and carries on with her amazing career 🙏 ❤

[@annegreenwood3624]

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

[@Wannaloom]

Loved her in Call the Midwife!!

[@danae7054]

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❤

[@StarGirl-l5l]

Really good read and very insightful. Listened to it also on audio.

[@mauricepowers3804]

I love Miranda Hart!!!!! I miss her show!!!!

[@nadine4062]

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 ❤️❤️❤️❤️🤗🤗🤗

[@Mrstigger747]

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 😱👋🇨🇦

[@gloriamoline678]

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!

[@Marcia_Toms]

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.

[@travelwell6049]

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.

[@laurahall3094]

Loved that episode

[@rebeccajoy3539]

Love to you ❤ and thank you for telling your story. May you and all those suffering with CFS be blessed with better health. ☀️

[@PaulaDixon-e6i]

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. 😊

[@londonengland1231]

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.

[@IsaidwhatIsaidUK]

although i dont have lime disease i know the feeling with depression the struggle it is to be motivated to do even the smallest of tasks. its so nice and inspiring to see that you can still be successful in life whilst also having an illness like that.

[@christinemoore7704]

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

[@jonnawyatt]

Natural drops?

[@marystrenke3050]

I've missed you Miranda!!! Love you ❤

[@mademoiselledusfonctionell1609]

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.

[@cookielicious82]

Loved the book ❤

[@226Plots]

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!!! 💕

[@SylviaDavis-e5u]

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. ❤

[@AH-em3zl]

Yes you just get used to being ill...so true...TY

[@apgx6032]

Congrats Miranda. You’re a genuine star.

[@tracybailey1034]

Miranda is inspirational….I absolutely loved being a DLC, such a brilliant book! Thank you Miranda 🧡

[@FromG2eminor]

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.

[@ChronicAdvocate]

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.

[@papabear2515]

Same for me in US

[@margaretlovelock7031]

I wish you luck 🍀🍀

[@margaretlovelock7031]

@@papabear2515I hope that it changes, good luck.🍀🍀

[@papabear2515]

@@margaretlovelock7031 thanks so much. All the best to you!

[@floridastitcher1]

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

[@hazelmccloy1136]

I could watch Miranda all day.

[@shawnfuzy3191]

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.

[@cherylp.3347]

Voting for Trump gives you lime disease? I’m confused.

[@eliranpinhasov5940]

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 🇮🇱

[@CassandraSeer]

Loved you in Emma. Congrats on your marriage. Hope you get better soon.

[@nicolarollinson4381]

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.

[@charlottecariaga1548]

Love her sm❤️

[@jmcg6189]

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.

[@katherinesgrannysquares]

Well done to Miranda sharing her story

[@shelleykent5392]

Absolutely love Miranda! Much healthier and health to her!!!❤

[@curlywurly661]

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 ❤❤

[@rapunzelrose68]

I experienced the similar things and was finally after 2009 diagnosed with fibromyalgia

[@RosePetal17]

I just love this woman!!! I am so happy that she is now happy and healthy!!💕💕💕🫶🏻🙌🏻🧚🏻‍♀️✨✨

[@cdmc965]

I remember thinking, if the house was on fire I couldn't get out of bed

[@katewebber1131]

Awe so happy she has found a man to share her life. Congrats Miranda❤❤❤❤

[@Batirtze-b6x]

It's heartbreaking, the stuff she's been through. All the best, sweetheart!!!!!🎉🎉🎉🎉🎉❤❤❤❤❤😊😊😊😊😊

[@AdrianneSteeley]

LOVE, love, love Miranda!!!!

[@vivienneoneill5400]

I just love her,she is great.❤❤❤❤❤❤❤❤❤

[@Oofoofoofoof3]

Miranda is a national treasure ❤

[@MIB80]

What a wonderful lady

[@petergasper6593]

I love Miranda ❤️

[@JimTimber]

Glad to hear all is now well ! 💪

[@katealison6087]

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.

[@John-k5y3i]

@@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

[@saradh3385]

@@John-k5y3ifibromyalgia is a different condition

[@anncarroll2204]

Oh my goodness that sounds so much like my experience. Thanks for your bravery. You are a goddess.

[@wendygore2709]

Love her ❤ But she'll always be "Chummy" to me 😊 Glad to hear things are finally turning around for her. 🙏🏻👍🏻

[@Suze69]

What a honey and what an inspiration :)

[@susansalter566]

Wwonderful.human beauitful soul❤❤❤❤❤

[@jmpht854]

The ever-amazing Miranda ❤

[@jenniehalbroeder3652]

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.

[@gloriamontgomery6900]

I love Miranda!

[@jayterra2060]

She’s lucky she had the resources to diagnose this and get treatment. Many of us not so blessed.

[@kathyminassian1375]

Sounds like Chronic Fatigue Syndrome. My Daughter was and is a perfectionist, she suffered from CFS when she was about 24 this led to Scarlet Fever and every virus that came her way.

[@ruthgaffney8786]

Thanks a million Miranda for opening up the discussion about fatigue based illnesses. I can’t help feel that Alison Hammond is just NOT a good interviewer about heart felt topics. She is so uncomfortable discussing deep topics. I love her for a laugh but not for anything deep and meaningful.

[@floridastitcher1]

This Morning is a refreshing break from political shows

[@MrBrownnn696]

Very personal thing to talk about… she’s very brave.

[@jeanlaubenthal698]

Lyme disease stories seem to involve years of struggles before diagnosis. It’s tragic.

[@cherrlyn381]

Love Miranda.

[@analissalowe8469]

How does one get it diagnosed?

[@HettiedeKorteDiplomaat]

I love her.

[@taviakane2807]

❤ Miranda try Carnivore, get hold of Dr Shawn Baker! Love your work, wish you the wealth of health 🙏

[@edwi3719]

I get very nervous when people say they did their own research. I had cancer but I wasn’t my own oncologist

[@MissCBwasadancer3]

I have Severe ME, POTS & MCAS - mine was triggered by vaccine injury. I was a dancer. I’m now 26 & I’ve been Bedbound since 2015, tube fed & IV fluid dependant since 2016 & now TPN for past 3 years. At one point I was oxygen dependent, non-verbal, having seizures & mast cell reactions daily. I was completely neglected by NHS so had to fundraise for private consultant & treatments. I’m glad this is being talked about by a public figure but Miranda’s experience doesn’t represent everyone’s. In her book it states she only addressed her symptoms by reducing stress/trauma & realising her true authentic self with behavioural techniques etc (which sounds like CBT and/or the lightning process). These have been completely disproven to aid any physical improvement and have infact caused patients harm. These were removed from NICE guidelines as a treatment and would only be appropriate to recommend CBT for ME patients with depression or struggling to cope as a result of the chronic illness & pain. I’m of course pleased she’s doing better but concerned she’s been a victim of one of these expensive mind-body programs that convince you that you can will yourself better (but when it doesn’t work it’s your fault, not trying hard enough!) or she’s been in spontaneous remission and going to relapse… Like many people who have had ME for decades tend to do. I’m not hating on her, I’m worried for her. She already got brainwashed into thinking she had agoraphobia and anxiety for years by incompetent doctors! 💔

[@melindahall5062]

Why did you need tube feeding? The fact that you are posting this long and complicated Message on KZbin makes me think you are somewhat able. I wonder why the NHS “ignored you”? How did you get TPN for 3 years. That requires a PICC line or another Central line. Who put that in? Things just don’t add up hon…….Physician here.

[@Bella-fz9fy]

I agree,feeling you are not able to able to pick up a glass due to fatigue is a bit different from being able to do it and then getting paralysed and having extreme malaise from your activity,I think that’s the difference between having chronic fatigue that could maybe respond to CBT etc and ME where you’re not just ill and fatigued,you’re body can’t do physical or mental activity without a severe deterioration.,and of course some people’s physical baseline can be extremely low like yours was.

[@SP-fw1xe]

I knew it was gonna be Lyme Disease before she even said it. Surprised it took her so long to get that diagnosis.

[@hippychick2879]

i love miranda