Living Proof - Stories of Hope
Living Proof - Stories of Hope
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GP Education Series: Medicine & the Mind-Brain-Body Connection - Intro
In summer 2024, Living Proof launched our first accredited course for healthcare professionals: 'Medicine & the Mind-Brain-Body Connection - a GP Education Series'.
This course provides a comprehensive introduction to the neuroscience behind chronic neurophysiological (or 'mind-body') symptoms - and the neuroplastic approach to recovery.
The course is accredited by the British Society of Lifestyle Medicine - and is written and presented by Dr Sarah Hadfield (GP and Mind-body Practitioner).
To find out more about the course, visit our website: www.livingproof.org.uk/practitioners
To preview the course - and meet the course author and presenter, Dr Hadfield, take a look at this short preview video.
มุมมอง: 153

วีดีโอ

Living Proof - Stories of Hope - Recovery from ME Chronic Fatigue Syndrome
มุมมอง 20K2 ปีที่แล้ว
Fiona lived with ME for 14 years, until finally discovering a route to recovery through science which taught her that her symptoms were caused by her brain and nervous system. By employing a range of mindbody tools and techniques she was able to fully reverse all her symptoms and regain a healthy and active life. Many thousands of people are now recovering from 'misunderstood' health conditions...
Living Proof - Stories of Hope - Recovery from Chronic Pain
มุมมอง 9K3 ปีที่แล้ว
Meet Charli, a 24-year-old biochemistry student from London, who shares her moving story of recovery from over two years of chronic pain. She describes the science behind the ‘mindbody’ approach to calming her nervous system, and her hopes that medical practitioners will start to bring the vital link between emotions and physical symptoms more into their practice. This is our first in an antici...
Sarah Hadfield (GP)
มุมมอง 2983 ปีที่แล้ว
Sarah discusses the Mindbody approach from the perspective of a GP
Liz Hardy Phsyiotherapist
มุมมอง 1313 ปีที่แล้ว
Hear Liz (Phsyiotherapist) talk about how incorporating Mindbody work into her practice has made an impact on patients and their recovery.
Irralee (Phsyiotherapist) talking about the Mindbody connection
มุมมอง 1493 ปีที่แล้ว
Hear Irralee (Phsyiotherapist) talk about how incorporating Mindbody work into her practice has made an impact on patients and their recovery.
Practitioner Testimonial From Pippa (Osteopath)
มุมมอง 1403 ปีที่แล้ว
Hear Pippa explain how they adopt the mindbody approach in her Osteopathy practice.

ความคิดเห็น

  • @portia_zar
    @portia_zar หลายเดือนก่อน

    There is no evidence for many of the claims you make. Also "Chronic fatigue" is not Myalgic Encephalomyelitis.

  • @stephenhocking9467
    @stephenhocking9467 หลายเดือนก่อน

    I’m lost for words. What has happened to medicine. I’m embarrassed for you.

  • @1966jbc
    @1966jbc 2 หลายเดือนก่อน

    Fiona, your story on Curable convinced my son to try it and he recovered from "Long Covid" or post covid sequale after many months of being bed bound. We will forever be grateful for you sharing your story. I know your mother's pain and am grateful for not having to have as suffered as she had to. He's back at college, he's traveled, he is back to weight training and running and he's back to being the wonderful loving boy that he once was.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 2 หลายเดือนก่อน

      Wow this is very much the kind of story that we love to hear! We are so happy that your son has recovered his life, this will help inspire many others on similar paths. I'm not sure how old your son is, but if he might be willing to share his story further, to help others also towards recovery, we are currently inviting UK-based 'recoverees' to feature on our forthcoming 'Recovery Wall' on our website: www.livingproof.org.uk. He can contact us on hello@livingproof.org.uk if he might be interested - he can offer as much or as little detail as he'd be happy with. Very best of luck to him going forward!

    • @fionasstory6126
      @fionasstory6126 2 หลายเดือนก่อน

      Thank you for writing this here, it means a lot (and I hope will give some a nudge to try the same techniques). I'm so pleased for your son.

  • @krugerfuchs
    @krugerfuchs 2 หลายเดือนก่อน

    Total rubbish

  • @angelm6497
    @angelm6497 3 หลายเดือนก่อน

    Ever consider that you did not have chronic pain, you were just suffering from stress? It took in excess of 10 years to have a diagnosis of chronic pain and that was only given by a pain specialist and only after attending stress and lifestyle management courses and 6 months full time group therapy. I have lived with this condition for over 30 years, following a spinal injury, and well this podcast is an insult to those living with this condor, but a rather sad reflection of a failing NHS. It's only popular because the NHS is currently sponsoring a rather poor attempt at pain, sorry stress management course and brain washing of already traumatized patients who actually have underlying conditions., and in an attempt to reduce their prescription bill. Let's not talk about the GP pushing this or her true motivation for this destructive work. The NHS is a disgrace at the moment, as it's assets are syphoned off for corporate interests. This podcast is featured alongside a sketch from the American Office joking at Pavlov's experiments on dogs, and presented as researched human behaviour.

  • @hollywalker775
    @hollywalker775 4 หลายเดือนก่อน

    Is there a place where the mind body program you practiced is referenced?

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 4 หลายเดือนก่อน

      Hi there, yes Fiona used the Curable app. You can find out more about it on our website: www.livingproof.org.uk/list-of-resources

  • @loriewert5267
    @loriewert5267 4 หลายเดือนก่อน

    I have been doing this mind/body approach for about six months. After eight brutal years of chronic pain I am finally getting relief. This s stuff really works and although I am still a work in progress I am about 40% better and it’s wonderful!

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 4 หลายเดือนก่อน

      Hi - really pleased to hear you are making progress. It really does work! :)

    • @angelm6497
      @angelm6497 3 หลายเดือนก่อน

      Over 30 years with this condition and the first treatment given was therapy and stress lifestyle management. I'm glad to hear that your appear to have addressed the psychological overlay, but true chronic pain is constant, as in every day, the only thing that changes is the level of pain, which does however need the use of various pain management techniques.

  • @hilpei3675
    @hilpei3675 4 หลายเดือนก่อน

    I'm in it. And there's a way out. Working on the mind/body approach and pain reprocessing therapy. Hope.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 4 หลายเดือนก่อน

      Hi - you are on the right track now that you have found this approach. There is indeed hope. Good luck and keep going.

  • @josieramirez9483
    @josieramirez9483 5 หลายเดือนก่อน

    ❤❤❤❤❤❤ I am happy for her. I look forward to recovering my health too. I want to feel good in my body again and go on adventures like she is doing too.

  • @thedancingdivaofdaviestree2320
    @thedancingdivaofdaviestree2320 5 หลายเดือนก่อน

    Thank you, this is an inspiring story of recovery! You describe the science behind your recovery so simply and well, and the suffering you and your family went through was heartbreaking. But isn't it wonderful so many of us are recovering - even those of us disabled by MEFM for decades! I DO understand - I was disabled by ME/CFS and Fibromyalgia myself for 20 years, mostly housebound and bedridden. Then thankfully I got OFF benzos and elavil, both prescribed for the pain and insomnia of MEFM. To my astonishment, 6 months after I tapered off those and quit 3 other equally useless prescriptions, I began to recovery my health. By facing the griefs and trauma that let to my becoming dependent, I released emotions trapped in the body and healed even further. Eventually, by listening to mind and body and learning new ways to cope like creativity, community, counseling, Chi Gong, and communication skills - I healed by 80%, mostly on my own. Through stories such as these, I learned about neuroplasticity and began doing brain rewiring and somatic tracking work with videos found on TH-cam, and by reading books like Alan Gordon's The Way Out. I discovered I could recover completely - even after over half a century! It's a slow process when you've believed you were disabled by an illness for this long, but I've seen huge results. Long Covid symptoms like being unable to sing without coughing are gone and I'm singing like a canary. I dance, perform, exercise and socialize. Not bad for a senior once bedridden for 2 decades! I still have symptoms to deal with and am learning to create safety so my crocodile brain doesn't see danger in normal stresses, and turn on the Fight or Flight state. It's taking a while, as I've been hypervigilant since birth, when I was born early as a result of a major car accident and was later bullied. Thankfully I learned to fight back, which kept me from depression - but the trauma resides in the body. Now I'm learning ways to release old trauma with Peter Levine techniques from books and videos, and somatic work. What a revelation all this is! I'm thrilled to hear you are completely well now, and look forward to joining you in that wondrous place in the future. Thank you for the video, Fiona and Living Proof - you ARE living proof we can ALL recover if we empower ourselves and take action.

  • @aglemonlover7709
    @aglemonlover7709 8 หลายเดือนก่อน

    This was very empowering, thank you so much Fiona and the Living Proof team.💕 I am struggling now and am excited to look into the Curable app and find other motivational stories like these.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 8 หลายเดือนก่อน

      Thank you for your comments - we are delighted you found the film empowering. Lots of resources and recovery stories linked on our website (including a 6-week free trial to the Curable app): www.livingproof.org.uk/list-of-resources. We wish you all the best with your recovery, you can do this.

  • @athollgow7981
    @athollgow7981 10 หลายเดือนก่อน

    What an inspirational young lady you are. Your story will hopefully help others to look outside of medication and try and find what is right for them. You have given everyone a great start to helping them find their way through the fog.

  • @VividYouth
    @VividYouth 10 หลายเดือนก่อน

    Not here for it

  • @rachellewidmann3621
    @rachellewidmann3621 10 หลายเดือนก่อน

    What is the programme though? What are the steps? The work involved is so abstract in a way. If its got clear and concrete steps, even if the process for an individual is as varied as eaxh mind is... It may seem possible if you still hold hope, even if its only a glimmer, as i do. I have been living with ME CFS for at least 22 years... Starting the decent sometime shortly after being 10 years of age... I have known for a while that i can probably find a way out through a mindbody approach. Its hard to do without concrete attainable clear steps when your existence is complete and utter exhaustion, even if you believe its possible, even if you have hope. So... HOW?

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 10 หลายเดือนก่อน

      Hi Rachelle, sorry to hear you have been unwell for so long. The specific programme that Fiona followed was the Curable app. It is a fantastic app with a clear programme to follow, but it does have a cost attached. There are also many other resources available, many of them at a lower cost. More info on our website: www.livingproof.org.uk/list-of-resources. Very best of luck - thousands are now recovering with this science.

  • @rg1869
    @rg1869 10 หลายเดือนก่อน

    Hello! What program did Fiona do to get better? Please share. Thank you so much!

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 10 หลายเดือนก่อน

      Hi there - the specific programme that Fiona followed was the Curable app. It's a great app but there are also lots of other resources available, many at a lower cost. More info here: www.livingproof.org.uk/list-of-resources

  • @JMJ4444-f2n
    @JMJ4444-f2n 11 หลายเดือนก่อน

    This is so wonderful to read & so promising! 😢❤ Thank you for sharing!

  • @charlottebest1122
    @charlottebest1122 11 หลายเดือนก่อน

    I cried watching this, god bless you Fiona x

  • @reneebueckert9882
    @reneebueckert9882 11 หลายเดือนก่อน

    Hi Charli Thank you so much for sharing your story! My son is dealing with TMS (widespread pain and tension) and he has a question about something you said in the video. Can we contact you directly?

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 11 หลายเดือนก่อน

      Hi there, we are sorry to hear your son is struggling with such symptoms. Please feel free to contact us at Living Proof with any queries: www.livingproof.org.uk/contact

  • @jl2006
    @jl2006 ปีที่แล้ว

    Bless you - good news.

  • @johnathanabrams8434
    @johnathanabrams8434 ปีที่แล้ว

    Rich, first world, privileged pain is not the same as persistent pain

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 10 หลายเดือนก่อน

      Hi Johnathan, thank you for your comment. We do hear you. Our organisation Living Proof has been established as a social enterprise in order to try and bring this science to everyone, regardless of their background or financial circumstances. Our colleagues at Flippin' Pain are also doing great work in bringing this science to people of all backgrounds: www.flippinpain.co.uk/. Anyone can see improvement from this approach - but it is an uphill struggle getting the word out to all communities when there is not yet widespread buy-in from the NHS. It is coming though and over time, more GPs and other healthcare practitioners will start to learn about this and be able to support their patients towards improvement or recovery. We are doing what we can - all on a voluntary basis, so please bear with us.

    • @angelm6497
      @angelm6497 3 หลายเดือนก่อน

      I'm sorry but one person's story of discovering stress management is not science. Just a poor reflection of a failing NHS and inflated Ego's. And Johnathan, I am inclined to agree with you.

    • @johnathanabrams8434
      @johnathanabrams8434 3 หลายเดือนก่อน

      @@angelm6497 The Effects of Racial/Ethnic Minority Status on Sleep, Mood Disturbance, and Depression in People with Fibromyalgia Fibromyalgia syndrome (FMS) is a musculoskeletal disorder that is characterized by persistent and widespread pain.1-5 It is most commonly diagnosed among middle-aged White women.

  • @rockerchick4368
    @rockerchick4368 ปีที่แล้ว

    Watching again!!! This has been very helpful for me . I perform a little better at work. I go for walks in the Forest. SHINRIN YOKU ❤❤❤❤❤❤

  • @RaelanAgle
    @RaelanAgle ปีที่แล้ว

    This is incredible! Thank you for this beautifully inspiring and informative video ❤

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      Thank you so much. I love what you're doing with your channel so it's great to see your name pop up here (Fiona)

  • @stephenhocking9467
    @stephenhocking9467 ปีที่แล้ว

    The problem is that this kind of stuff isn’t replicated in any observable or clinical setting. All of the evidence for this kind of stuff was reviewed by the National Institute for Clinical Excellence and was found to be of very low quality. The problem we have as group of patients is that people who are sadly mentally ill do find their way into our ranks. Because we don’t currently have an easily reproductive biomarker we are the disease that these people end up mistakenly thinking they have. Being cured of our often lifelong and real issues by an app is just a good way of discovering that you never did have ME/CFS in the first place. I’m glad that Fiona is feeling better but assuming that her story means we are all similarly mentally ill just doesn’t make sense. Like I say I’m glad she is better but suggesting that she has found the answer to a disease that has confounded medicine is just not a productive thing to do.

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      I think the really sad thing is the ME community doesn't realise how comments like these make them look. When I was ill I never wanted people saying things like this in my name. It's a terrible comment to write and actually inaccurate in that the NICE guidelines haven't considered what helped me actually recover

    • @stephenhocking9467
      @stephenhocking9467 ปีที่แล้ว

      Being gaslighted by someone who mistakenly thought they had ME for 14 years is the cherry on top for my experience with ME. I personally don’t believe that childhood trauma can give you a post infection associated disease. You’re the one I feel sorry for. It must be difficult to make sense of why and what led you to this state for so many years. Mistakenly believing that you had ME and then buying into this nonsense is a kind of extreme form of self punishment/revenge on your former self. I can tell you that having REAL ME is infinitely worse than you can imagine.

    • @stephenhocking9467
      @stephenhocking9467 ปีที่แล้ว

      And btw insisted that Brain Training or CBT have not been reviewed by NICE is utterly false but I’m not surprised that you would say something like that. Just because it is packaged differently doesn’t make the principles any different. Curable £100 per annum 500k subscribers = £50,000000 per annum!

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      You have no idea how badly you're coming across. This is only harming the community 😔

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      Ah I realised you are the man who spent over 24hrs being aggressive on my Twitter. Funny to claim to have M.E then have the energy to relentlessly attack someone over the course of a couple of days. You are a bully and that is all there is to this.

  • @wildgardens
    @wildgardens ปีที่แล้ว

    I did the curable app and ANS rewire and Im still sick. I got covid 3.5 years ago and have been totally housebound this whole time. Ive read enough neurorplasticity stuff and done the whole mindset thing which only caused me to overexert myself and have terrible crashes. Seems to me that there is a group of people who perhaps only have the dysregulated ANS part and maybe that can be alleviated by positive thinking, meditation and calming thoughts, stopping negative thoughts, elevating emotions etc. But for those of us with elevated inflammatory markers and more complex pathophysiology going on this approach just does not work. Hopefully in the future there will be better phenotyping to figure out all these different subsets as this illness clearly exists on a giant spectrum.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi - sorry to hear you are so sick. For information, a dysregulated ANS can cause all of the biological/physical issues you mention; those are examples of how the dysregulation manifests. We wish you all the best for finding a resolution soon 🙏🏻

    • @wildgardens
      @wildgardens ปีที่แล้ว

      @@livingproof-storiesofhope6314 Maybe? but also a lot of other things could such as viral reactivation/persistence, endothelial issues, mitochondrial problems, microclots, autoimmunity etc, there is still lots of research going on finding various pathologies. That is why it is so important we get the phenotyping right with biomarkers so we can get individualised treatment. I think for some of us our underlying pathology is more complex so simply calming down the nervous system to feel safe is just not sufficient. If someone can recover from these dreadful symptoms using these simple practises then good for them, certainly no harm in trying!

    • @sneakypress
      @sneakypress ปีที่แล้ว

      @@livingproof-storiesofhope6314 @wildgardens post has valid points. If Fiona (in the video) tried this approach five or ten years earlier, it probably would not have helped much, as her body may not have recovered enough from the prolonged resting period. Also, her caring and supportive parents, have no doubt made a big difference (in helping her recover).

    • @sneakypress
      @sneakypress ปีที่แล้ว

      Also, you can see from / in the photos at the beginning of the video, the terrible state that Fiona was in years earlier. Years of rest, has allowed this mind-body approach to help. It was Fiona’s time to recover considerably.

    • @reiniweigel3070
      @reiniweigel3070 11 หลายเดือนก่อน

      I'm also someone having done lots including ANS rewire, Curable, reading many books, podcasts etc.... 20 years of illness!! ANS rewire, started to give me hope 5 years ago with it's mind body techniques. I still believe it will work, but the healing environment needs to be set and mine has never been good enough to recover. But it will. I've seem glimbses. I continue to adjust new bits and pieces. There is so much involved! Changing your personality traits and rewiring all those fearful thoughts, behaviours and attention to symptoms...and true rest, not lying down and ruminating... It is really a huge job for most with CFS or Fibromyalgia. But it has worked for many and why not for me. And you?

  • @Healingispossible1313
    @Healingispossible1313 ปีที่แล้ว

    I have healed too after 10 years of suffering. It’s absolutely possible. I healed with natural therapies, meditation and brain retraining. My testimonial is on my channel. Thank you for sharing so happy for you ❤

  • @susanWilder2175
    @susanWilder2175 ปีที่แล้ว

    Such joy!

  • @nanyaverey
    @nanyaverey ปีที่แล้ว

    CFS is not a thought and it's absolutely real. I'm glad emotional work was enough for you, but it's not enough for majority of people suffering with this condition. My CRP is usually 10 to 20, and I can't make it less with my willpower - my body is making an inflammatory reaction in itself. I have a cold intolerance, exercise intolerance, sensory overload can make me crash, and I can't meditate myself through it - it's something my body is choosing to do, when I'm the least prepared for it. I do write down symptoms etc. to not feel so helpless. But it is a physical condition, not a purely mental one, often caused by some virus or a major strain to body like that. I'm feeling very sad today and I was looking for a real recovery story to cheer myself up, instead I have to watch this mumbo jumbo narrated by a person who may not even have the same illness as me, who involuntarily gaslights all the people who can't get better with just some emotional work.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi - sorry to hear you are struggling with CFS; it is indeed a miserable condition. Best of luck with it.

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      Hi, I just saw this comment and wanted to respond. I hope you know we think M.E is 100% real and absolutely it is physical. I also had consistently high inflammation markers (across years), crashed from things like sensory overstimulation and temperature extremes etc. My condition also started after a series of horrible viruses. I was ill enough that I was unable to have children. Did meditation cure me? Absolutely not. It is your choice but I would hope you'd look more closely at the techniques that helped me recover, even if just to rule them out. I started using them also thinking they were rubbish but they gave me back my life. It is absolutely up to you though, it has to be your choice. Anything about John Sarno's theories is worth looking into. Wishing you well as it's clear things are tough for you right now. I know both Penny and I are always happy to answer questions and there are so many free resources out there too. X

  • @christinaallison1448
    @christinaallison1448 ปีที่แล้ว

    You are the epitome of “if there is a will, there is a way.” You’re right, how could all of this pain be individual and not connected? I love that you know yourself enough to dig in and dive deeper. Your desire to understand the mind body connection in your body is only going to catapult your progress forward. Your story is helping people charli. I can’t wait to hear testimonials from the many people you have helped open there eyes! This is amazing.

    • @angelm6497
      @angelm6497 3 หลายเดือนก่อน

      Actually no, did you ever consider that she never had chronic pain at all, she was just suffering from stress. Rather misleading actually, but I agree a very sad representation of a failing NHS, who misdiagnose conditions all the time she should be thankful they didn't kill.het!

  • @rockerchick4368
    @rockerchick4368 ปีที่แล้ว

    I refer back to Fiona. It's very helpful for me. I'm working part time, without restrictions. THANK YOU! I also can walk up Hills, now. 😊😊❤

  • @alysonwong818
    @alysonwong818 ปีที่แล้ว

    What is the name of the Mind Body Programme used?

  • @annevaleriesaez6159
    @annevaleriesaez6159 ปีที่แล้ว

    @Fiona, did you continue pacing while trying the app? Thanks.

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      Sorry not to see this until now. I did! I very much felt that the change had to happen from the outside in. I couldn't risk pushing myself and then crashing.

  • @annevaleriesaez6159
    @annevaleriesaez6159 ปีที่แล้ว

    I have ME too, just dwl the app. But I'm very hopeful about this. 🤞 Thanks for the inspirational video. 😊

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Glad you enjoyed the film Anne. Lots of other resources on our website too: www.livingproof.org.uk/list-of-resources

    • @jocelynalfante3524
      @jocelynalfante3524 ปีที่แล้ว

      ​@@livingproof-storiesofhope6314It is such an inspiration. I want to try what Fiona did. Where can I find the method? Where can I find the app to download? I'm hoping it will help me.

  • @toneyfree7179
    @toneyfree7179 ปีที่แล้ว

    To all of you suffering from this illness, you are not alone, you are strong, don't give up hope I pray for all of you 🙏 ❤️

  • @lessons9745
    @lessons9745 ปีที่แล้ว

    7 years in and I would love to have remission. I ve tried 4 different mind body programs over the years too. 😕

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      Which ones have you tried? (sorry for only seeing this comment now)

    • @lessons9745
      @lessons9745 ปีที่แล้ว

      @@fionasstory6126 DNRS, CFS Unravelled, Gupta and another one that no longer exists. 😊

  • @Ivar1231
    @Ivar1231 ปีที่แล้ว

    That hill was her mountain. I’m still struggling after 22 years

  • @DorienFlowerDesign
    @DorienFlowerDesign ปีที่แล้ว

    Thank you very much, I am new with this approach and hope it will help me with the migraines for o er 40 years 🙏🙏

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi Dorien, we are happy you have enjoyed our films. Yes, this approach can help you - you have already achieved the first step just in being open to it. We are a volunteer-led non-profit aiming to help people like you, have a look at our site for more info and resources: livingproof.org.uk. Good luck, you are on the right path now 🙏🏻

    • @DorienFlowerDesign
      @DorienFlowerDesign ปีที่แล้ว

      @@livingproof-storiesofhope6314 thank youuuuuuu very much ❤️🙏

  • @DorienFlowerDesign
    @DorienFlowerDesign ปีที่แล้ว

    What a beautiful great story !!! Tears of hope tears THANK YOUUUUUUU 🙏❤️🙏❤️

  • @cherylallis2458
    @cherylallis2458 ปีที่แล้ว

    Thank your family for their concern, then send your family this youtube video in response: th-cam.com/video/THCZac4Yz7s/w-d-xo.html "Defective Energy Metabolism in ME/CFS" and ask them for suggestions as to how to correct this defect. Do try to give them the benefit of the doubt. They may just want to see you well again and they don't know how to help.

  • @cherylallis2458
    @cherylallis2458 ปีที่แล้ว

    I never tried this program. I was bedridden for years. I can do a lot of daily activities now, but my energy envelope is still quite small if I don't want to suffer "payback." Once, I thought I was cured (2007) Lived for 6 months like a normal person. Then had a severe relapse that left me with neuropsychologist diagnosed dementia, bedridden, living in a darkend room- for YEARS. ME/CFS is a very complex issue. Things that help one person may not help another. For example- electronic lymph treatments have been a game changer for me. Instead of physically feeling misery, I actually feel good many days. I had Hakomed treatment for pain- no longer need pain medication. Found a chiropractor who specislizes in training my brain not to go into "fight or flight" mode due to triggers like light, sound, slerping positions, drinking cold liquids, EMF's, etc., etc, (Dr Wentworth at Advanced Chiropractic in South Carolina) I'm also doing biofeedback clearing of allergies to foods, chrmicals, metals, etc. at Perfect Balance Natural Health in South Carolina. Will the combination of these things cure me? I don't know. But they improve my quality of life.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Living Proof - Stories of Hope 5 days ago Thanks Cheryl and sorry to hear you are still struggling with ME symptoms. This approach is first and foremost about understanding the theory and the science, then applying the tools within that new context and mindset. The tools alone without the mindset shift will only take you so far. This science won't necessarily help everyone but many are recovering. It sounds like your chiropractor is on the right track which is great news. You may find some of the resources on our website helpful for understanding more about this theory: www.livingproof.org.uk/list-of-resources

    • @MackLee23
      @MackLee23 ปีที่แล้ว

      Cheryl, my name is Cayla and I would love to correspond with you if possible. I live in Virginia but may be willing to travel to see practicioners like the ones you described. I've never heard of a couple of the therapies that you mentioned and am interested to learn more.

  • @lightofall
    @lightofall ปีที่แล้ว

    I've done years of meditation and all these exercises don't allow me still to exercise without many days in bed sleeping after

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi there. Sorry to hear you are struggling with symptoms. This approach is first and foremost about understanding the theory and the science, then applying the tools within that new context and mindset. The tools alone without the mindset shift will only take you so far. You may find some of the resources listed on our website helpful for understanding more about the theory, if of interest: www.livingproof.org.uk/list-of-resources

    • @lightofall
      @lightofall ปีที่แล้ว

      @@livingproof-storiesofhope6314 thanks but I have a great mindset :) I was studying volunteering and travelling and living overseas. It isn't my mindset, it is physical exhaustion and autoimmune related with the cells literally attacking themselves. Do tell me how you think my mindset is stopping me from walking when I want to be exercising having children and meeting the man of my dreams?? I've lost 10 years to this illness. If it was mindset that is the issue many more people would recover.

    • @Lena.9
      @Lena.9 ปีที่แล้ว

      @@lightofall You are right. It’s not the mindset for many of us. I am calm, happy for the majority of the time. Still declining slowly over the years. I do some nervous system exercises to activate the parasympathetic nerve. Because I believe the illness itself is a stressor for the body, but we cannot remove it unfortunately. But the exercises slightly reduce stress and give me better / deeper sleep. But that doesn’t have resulted in more energy unfortunately.

  • @lightofall
    @lightofall ปีที่แล้ว

    The world is unsafe lol

  • @lizzieh5284
    @lizzieh5284 ปีที่แล้ว

    I am in my 60s and have had ME/CFS for many years. I had a traumatic childhood and teenage years. believe it is my body living at a high state of anxiety for many years plus viruses.I have tried supplements, alternative therapies and private clinics. The only thing that helped a bit was aromatheraoy massage. I am now in a very good place mentally after many years of therapy and work on myself. I use meditation/mindfulness, writing my feelings down, good diet, yoga and stretching (when i can manage it). I am also less of a perfectionist than i was but still get the exhaustion. Thankfully any pain I have I can manage. I have niw accepted that this is as well as i'll ever be, there is no miracke cure. I am managing the condition thd best I can. Perhaps younger people will be helped by this advice but I see nothing in it that I am not already doing.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Thanks Lizzie and sorry to hear you are still struggling with ME symptoms. This approach is first and foremost about understanding the theory and the science, then applying the tools within that new context and mindset. The tools alone without the mindset shift will only take you so far. This science won't necessarily help everyone but many are recovering. Age isn't relevant :)

    • @fionasstory6126
      @fionasstory6126 ปีที่แล้ว

      I would echo this. What helped me recover looks simple on the outside and it is but you need an understanding of the science along with the tools. It sounds like you're doing so well but it's really worth diving into Sarno's theories fully. They might well help you further

    • @thedancingdivaofdaviestree2320
      @thedancingdivaofdaviestree2320 5 หลายเดือนก่อน

      Without doubt, you are right, Lizzie, about your traumatic childhood causing your symptoms, as your nervous system goes into Fight or Flight, which floods you with stress chemicals and hormones helpful when you're running from a bear - but harmful when it becomes long term. I too had a traumatic birth and was bullied as a child. A trauma counselor told me that trauma gets trapped in the body. Using Peter Levine's pioneering techniques for trauma release has helped me hugely, and then discovering somatic and neuroplastic work has helped me recover enormously, even after suffering with it for 54 years. It can take longer for those of us who had it for decades, particularly if you have a lot of major stresses in your life. But I'm learning new ways to manage them, and my pain has reduced MASSIVELY, and my energy increased. As someone who was mostly housebound and bedridden for years, I'm thrilled to be dancing, writing, performing and socializing again. And I AM in my late 60s - so you don't have to be young to recovery from ME/CFS -- even if you've had it for over half a century, as I have. I wish you the best of luck, and DO understand - I thought for years I would never recovery any further myself. But I kept at it, kept learning, changing, and growing - and it's finally paying off. Thanks, Fiona - what a wonderful story and SO inspiring on days when I feel like the fibro is kicking my butt! But I keep creating safety and doing somatic tracking, telling my overactive crocodile brain I call "Croco Pops" - 'We're fine and perfectly safe. This is all harmless, and I WILL heal." And it's working. I hope one day to be on top of that mountain with you, fully recovered! But I'm still thrilled I've recovered by 80%, and got my life back.

    • @thedancingdivaofdaviestree2320
      @thedancingdivaofdaviestree2320 5 หลายเดือนก่อน

      @@fionasstory6126 Dr Howard Schubiner's videos and book and Alan Gordon's book The Way Out are also helpful. For me, they had new research that added onto Dr. Sarno's work I found particularly helpful for ME/CFS and Fibro pain.

    • @lizzieh5284
      @lizzieh5284 5 หลายเดือนก่อน

      @@thedancingdivaofdaviestree2320 thank you so much for telling how you have managed your ME/CFS and how your life has chhanged for the better. It is so inspiring to hear of an older person whose health has improved. It gives me hope. 😊

  • @cath9621-x3f
    @cath9621-x3f ปีที่แล้ว

    Love this! I’m watching again and again. I’m using the mind-body approach to recover from Post-Covid POTS. Thank you for making this video. Please make more if you can! The music is really calming too.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi Catherine, thanks for your comments, we're delighted you are finding the film helpful. And yes we love the music too :) Good luck as you continue on your recovery journey.

    • @cath9621-x3f
      @cath9621-x3f ปีที่แล้ว

      Thank you! The mind-body approach is awesome.

    • @monnmar1
      @monnmar1 3 หลายเดือนก่อน

      did you make a full recovery ?

  • @cath9621-x3f
    @cath9621-x3f ปีที่แล้ว

    I think this is the same Fiona from the Curable ‘Like Mind, Like Body’ podcast?

  • @AmandaSmith-77777
    @AmandaSmith-77777 ปีที่แล้ว

    My CF is from mold and water damaged buildings. Getting out of the moldy building was the first step. Garlic helps somewhat, but I'm in bed today watching this

  • @sarahs5340
    @sarahs5340 ปีที่แล้ว

    Oh my goodness, I relate to her so much.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi Sarah, thanks for your comment. Hope this can help you on your road to recovery ❤️‍🩹🙏🏻

  • @rockerchick4368
    @rockerchick4368 ปีที่แล้ว

    I'M watching this again. It's extremely helpful. Unfortunately, I got Bronchitis in the beginning of winter. Set back! I do manage to work just part-time . I do manage to pay my rent. HAVE TO.

  • @irynadz1894
    @irynadz1894 ปีที่แล้ว

    Sorry, but what exactly books, techniques, sources did you use ? Thank you.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi - the specific programme Fiona used was the Curable app. But there are lots of different options and resources listed on our website: www.livingproof.org.uk/list-of-resources, you can see what might suit you best.

  • @jessicanilsson2437
    @jessicanilsson2437 ปีที่แล้ว

    Hi Fiona ! I had/have like you ! High anixety/lots av toughts , burning pain in my head and body ! Im lost 😢sick since 7 years ! How did you get your brain safe ? All my life unsafe in my body , perfektion , high performance etc How I do ?

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi Jessica, thanks for your message. Please have a look at our website www.livingproof.org.uk for more information and resources on how you can try this approach yourself. Good luck, you can do this :)

  • @LitGyal
    @LitGyal ปีที่แล้ว

    Any advice for me on how to recover? I have severe light and sound sensitivity.

    • @livingproof-storiesofhope6314
      @livingproof-storiesofhope6314 ปีที่แล้ว

      Hi Aneesa, thanks for messaging. Feel free to have a look at our website www.livingproof.org.uk in the first instance, there is lots of information and resources there on how you can try this approach yourself. Best of luck, now you know it is possible.

    • @tempestblack3840
      @tempestblack3840 ปีที่แล้ว

      I dramatically improved my symptoms (but eventually hit a ceiling) with an essentially Paleo diet, tailored to my needs over a long period of experimentation. Overnight I quit all potential problem foods, including sugar, casein, gluten, and processed food. Within a couple weeks my brain fog lifted dramatically, my daily crashes got less severe, my headaches and sore throats lessened in frequency and severity, and my energy picked up a little. After about six weeks, the improvements stopped coming, but I was happy enough with the results that I've never in 9 years gone back to eating the way I used to. I eventually figured out that I am intolerant to nightshades and high-FODMAP foods. (I was able to reintroduce FODMAPs after successfully eliminating a harmful bacterial overgrowth in my guts.) Quitting sugar was very difficult for the first few weeks, but 10000% worth it and eventually the cravings went away completely. I am very happy eating the way I do. www.drmyhill.co.uk/wiki/Category:Your_very_good_health!