At two short points in the video, the sound quality for Veronica experiences issues. Thank you for your patience with this as I work to ensure that this is not an issue with future interviews. 🙏 TIMESTAMPS 1:37 Veronica's ME/CFS onset 11:23 The quest for recovery 23:39 Veronica's experience with Ayurveda 28:36 Failed recovery attempts/Going into therapy 32:37 What finally helped Veronica fully recover 43:27 Becoming a different person 47:31 Veronica's advice for others facing similar conditions 52:11 How to reach/follow Veronica
The medical institution saying that CFS is incurable while not knowing anything about it is such an interesting insight she pointed out. If they don’t know why you’re ill how can they assure you you won’t recover? It shows a lot of arrogance (as you said), ignorance and sometimes just a lack of empathy.
absolutely, i'm so lucky to have ran into her channel before i got too deep into the hopelessness that is shown online, on facebook groups and in hospitals.
The mystery is much greater than that. If you ask literally any "health expert" in the world certain questions about how the human mind, the human emotions, or the human body function; then they will not be able to answer them directly. No one totally understands how the human mind, the human body, or the human emotions work in their totality. They are infinitely complex and paradoxical; immersed in a state of perpetual change.
Wow! What an incredible interview. I worked with Veronica for a few months and made a functional recovery very fast. She is the kindest coach you can ever have!
I do not have ME/CFS but something similar. After a series of very stressful events in the past year which included a family members death from Covid, a concussion followed by a C Difficile infection I began to decompensate. I now struggle with severe insomnia, anxiety and IBS like symptoms from a dysregulated central nervous system. I'm looking for my road to recovery. Your channel is giving me hope. Thank you. Congratulations to Veronica on her wonderful recovery.
You know Raelan, it’s somehow almost a legacy of your mum. (And nan) Because of the pain and struggle you saw her go through, when you got sick you had more determination than anyone in the world to find a way to recover and not live sick your whole life. Your work has given so many people the key and puzzle pieces to doing the same and in some wonderful way your mums life has helped many through you x
What an inspiring story! I’m a new subscriber, one year out from 2 Pfizer jabs and have been struggling with all sorts of side effects which I see now fit into CFS, PEM. I look forward to learning more in order to heal my body so I can get back to my life!! Thank you for this channel!
@@RaelanAgle Hi, thank you. My husband and daughters and most of my friends are very supportive. Doctors somewhat believe me but it’s difficult because this covid stuff is all so new and no one talks about the vax side effects. I’m in a great support group on fb and have learned a lot, researched on my own and came up with this diagnosis for myself as I’m a Nurse. Not sure if the vax can cause this but as my symptoms fit I’m going to educate myself on healing my own body because no one has any other answers and I like the answers I see on your channel and with your guests. My goal is to get my life back and be able to return to work in some form, I’m definitely changed from this experience so not sure what form work will take…. Kind of exciting!
I already had CFS/ME but after the Pfizer vaccine my health got significantly worse and hasn’t improved since. This was about 7 months ago after the second dose. I think CFS/ME most of the time is caused by a virus but could also be caused by vaccines.
Here is a good quote from a respected CFS recovery program - "Your body knows how to heal itself". It is incredibly intelligent. All you need to do is support your body so that it can recover.
"Your mind is writing checks that your body cannot pay" - yep, that's me 😂 how funny how we are so alike in this community, I sense that it may be that some personality types are just more prone to CFS/ME/long covid? Thanks for this great interview!
‘I am fine (without fearing)’ love it. I can totally understand your fear of going near anything you do with cfs/me after. It’s traumatising. It’s so good to hear you conquered that
I too was told that I never would get well, this Dr. diagnosed me with fibromyalgia. I refused to believe it. After 35 yrs I now believe I will get well using a brain retraining program. I just began and already I see a difference in my health. 👌🏿 The last 35 years has been like riding a roller coaster, my health went up and then down, over and over again. 😜
Thank you. I was feeling so much love for you both whilst listening to this. Veronica is very inspiring. And Raelan thank you so much for working so hard to bring hope to our community xx
My doctor also said, when my blood pressure was creeping up, to stop working from home. To start going back into the office. The extra stress of commute, school drop offs in time to get into the traffic etc Unbelievable.
It seems that we all have many different ways that we connect our body and our mind which is why everyone's journey to recovery seems so different. But the common thread through all of these recovery stories is that we are listening to our bodies and finding what they need to understand that we can and will recover.
This is an incredible interview but I am confused why you say this woman had severe me? Severe ME means you cannot endure light sound or human contact- but she could go to an retreat for treatment. I understand she couldn’t walk but to be able to go out and do things it seems she would be mild/high end moderate ME. I only say this as a person who is totally housebound and was bed bound for a year. And am now moderate. As members of the ME community it seems important to use mild moderate severe and very severe correctly. Love what you do for our community. Thank you for these videos
Dear Any, I could not walk or tolerate light or sound. The treatment felt like hell and I was taken everywhere in my husband's arms. I hope this clarifies.
In my health authorities description "Severe ME" means mostly bedbound. I was this way from 2009 - 2017, mostly in a darkened room but I had periods of improvement where I could sit up, tolerate listening to audiobooks etc. I could "endure" limited human contact, limited light exposure and very limited sound.
I cured my autoimmune disease with a strict nutrient dense anti-inflammatory diet and supplementation and eliminating all stress. I healed my gut and nervous system and got rid of systemic inflammation that was through my body and brain. It took 2 months for all symptoms to disappear.
@@RaelanAgle I'm stuck in my recovery . I was recovering finely in the last one and half month. I found the way of my recovery, everything was going fine. But..... My overconfidence made it down. When i started feel normal in the last month i eat everything like a normal person like wheat, noodles etc. I forgot that I'm in my recovery path,Though I was FEELING NORMAL but I'm internally not that much strong as like a normal person. That evening i ate much noodles(made of wheat) and that was my hyge mistake. I'm now 55% of recovery from 70%😔
Thank you for this video! So happy for you Veronica! I guess I missed the part where you mention the exact name of the therapy/method that helped you fully recover. Could you specify the name please? I’d like to learn more about it. Thank you so much 💕
From what i been hearing in these interviews so far it really does sound mental. It sounds like a nervous system dysregulation that you can re-regulate through mind work. Is that right Raelan?
(Not Raelan but) seems so, yeah. For me atleast I want to learn how to properly relax. To deal with my fatigue when it emerges. To get better sleep. This points me to some kind of meditation. I'm thinking Vedic meditation (the video with Sam was very inspiring) or Transcendental meditation. (But personally I might just have sleep apnea that I have to deal with since sleep feels like my biggest issue...)
It’s not “mental” but it is I’m the nervous system… The nervous system is physical. But yes, it is affected by thoughts, emotions, situations, behaviours etc
No, it's a mind body connection. There are physical problems, caused by a variety of issues, but the body cannot heal when in a stressed state. This is why calming the nervous system is essential.
I tried reverse therapy. I think it is the same or very simmialr to mickel and ask got no benefit. I think maybe it is more helpful for those whose symptoms are tied to emotional states or emotionally traumatic experiences. I remember getting so frustrated with the therapy as they get you to try and find the “hidden message” behind symptoms. My symptoms were primarily of view cause, worsened by covid. I already was emotionally aware, able to set boundries etc. physicall exertion triggered my symptom, there was no “hidden message”. Like all things, it will work for some but not others.
Unfortunately we all don't get better we have worse symptoms Like heart problems AFIB bone Loss some need breathing machines Like me so it's not that simple for everyone sorry
@@jenniferflower9265 there’s a little arrow on the right hand side, under the video, next to the title of the video. It’s a drop down menu with all the info. ( I just found it myself) 😀
At two short points in the video, the sound quality for Veronica experiences issues. Thank you for your patience with this as I work to ensure that this is not an issue with future interviews. 🙏
TIMESTAMPS
1:37 Veronica's ME/CFS onset
11:23 The quest for recovery
23:39 Veronica's experience with Ayurveda
28:36 Failed recovery attempts/Going into therapy
32:37 What finally helped Veronica fully recover
43:27 Becoming a different person
47:31 Veronica's advice for others facing similar conditions
52:11 How to reach/follow Veronica
The medical institution saying that CFS is incurable while not knowing anything about it is such an interesting insight she pointed out. If they don’t know why you’re ill how can they assure you you won’t recover? It shows a lot of arrogance (as you said), ignorance and sometimes just a lack of empathy.
absolutely, i'm so lucky to have ran into her channel before i got too deep into the hopelessness that is shown online, on facebook groups and in hospitals.
@@LeaFaye Me too, I’m definitely better than a year ago and I’m hoping for full recovery 🤍 Lots of luck with your health journey
@@andylopez6411 thank you andy, same with you
@@andylopez6411come india 🇮🇳 doctors better than your country ima omf
The mystery is much greater than that. If you ask literally any "health expert" in the world certain questions about how the human mind, the human emotions, or the human body function; then they will not be able to answer them directly. No one totally understands how the human mind, the human body, or the human emotions work in their totality. They are infinitely complex and paradoxical; immersed in a state of perpetual change.
I come froma family full of doctors. The entire system is so sure of itself and completely ignorant of its blindness. It's so brutal to hear this.
I never want a diagnosis for these reasons. The fear is enough to keep you stuck. So glad you made a full recovery ❤️🩹 xx
Wow! What an incredible interview. I worked with Veronica for a few months and made a functional recovery very fast. She is the kindest coach you can ever have!
Thank you 💓
❤️❤️❤️
Did you work with Veronica in person or online? Unfortunately I don't live near Nottingham - well, not even in the UK ;-)
I worked with her online
@@justbecauseican1410 Thank you for letting me know 😃
This video gave me tears of joy. What a powerful story. I really loved this Raelan. So inspired by your light Veronica, this was amazing.
Thank you Liz. ❤️🙏🏽
❤️❤️❤️
@@akashayogawithveronica.yog4095
Hi!
How can I come in contact with you?im very severe, bedridden.thank you
I do not have ME/CFS but something similar. After a series of very stressful events in the past year which included a family members death from Covid, a concussion followed by a C Difficile infection I began to decompensate. I now struggle with severe insomnia, anxiety and IBS like symptoms from a dysregulated central nervous system. I'm looking for my road to recovery. Your channel is giving me hope. Thank you. Congratulations to Veronica on her wonderful recovery.
How u doing now kathy 7 months later?
Hello! How are you feeling now?
I’m better than I was a year ago, but still have a way to go.
I’m better than I was when I originally posted but still have issues with IBS. I hope you are doing well.
@@kathy.7475 Thats great news, good for you :). Can you give some tips, what did you do? And thank you for your reply.
Just been recently diagnosed with CFS, this story brought tears to my eyes & gives me so much hope. I hope I can feel the way she does now one day ❤️
Mia, I'm so sorry to hear that you've been dealing with this. I hope you find all your puzzles pieces and can finally put this all behind you soon ❤️
You know Raelan, it’s somehow almost a legacy of your mum. (And nan) Because of the pain and struggle you saw her go through, when you got sick you had more determination than anyone in the world to find a way to recover and not live sick your whole life. Your work has given so many people the key and puzzle pieces to doing the same and in some wonderful way your mums life has helped many through you x
I appreciate that so much, Lu. Thank you ❤️
What an inspiring story! I’m a new subscriber, one year out from 2 Pfizer jabs and have been struggling with all sorts of side effects which I see now fit into CFS, PEM. I look forward to learning more in order to heal my body so I can get back to my life!! Thank you for this channel!
Hi Patty, I'm sorry to hear about all that you've been facing, I hope you have some support and are managing ok ❤️
@@RaelanAgle Hi, thank you. My husband and daughters and most of my friends are very supportive. Doctors somewhat believe me but it’s difficult because this covid stuff is all so new and no one talks about the vax side effects. I’m in a great support group on fb and have learned a lot, researched on my own and came up with this diagnosis for myself as I’m a Nurse. Not sure if the vax can cause this but as my symptoms fit I’m going to educate myself on healing my own body because no one has any other answers and I like the answers I see on your channel and with your guests. My goal is to get my life back and be able to return to work in some form, I’m definitely changed from this experience so not sure what form work will take…. Kind of exciting!
I already had CFS/ME but after the Pfizer vaccine my health got significantly worse and hasn’t improved since. This was about 7 months ago after the second dose. I think CFS/ME most of the time is caused by a virus but could also be caused by vaccines.
@@leftthatbehind6090 I’m sorry you are dealing with this too… it’s so frustrating…. Blessings to you!
Here is a good quote from a respected CFS recovery program - "Your body knows how to heal itself". It is incredibly intelligent. All you need to do is support your body so that it can recover.
"Your mind is writing checks that your body cannot pay" - yep, that's me 😂 how funny how we are so alike in this community, I sense that it may be that some personality types are just more prone to CFS/ME/long covid? Thanks for this great interview!
There do seem to be a lot of similarities, don't there Jessica! Glad you enjoyed this ❤️
Yes perfectionist s
‘I am fine (without fearing)’ love it. I can totally understand your fear of going near anything you do with cfs/me after. It’s traumatising. It’s so good to hear you conquered that
I too was told that I never would get well, this Dr. diagnosed me with fibromyalgia. I refused to believe it. After 35 yrs I now believe I will get well using a brain retraining program. I just began and already I see a difference in my health. 👌🏿 The last 35 years has been like riding a roller coaster, my health went up and then down, over and over again. 😜
Thank you. I was feeling so much love for you both whilst listening to this. Veronica is very inspiring. And Raelan thank you so much for working so hard to bring hope to our community xx
Our pleasure!
Thank you, as always, Raelan 🙏You did an amazing job interviewing her and you have such a great heart. Both of you are beautiful souls.
Thank you so much, you are so kind 💛
Absolutely amazing. And again I had to cry. Veronica and her story are just wonderfull
❤️
Wonderful inspiring story to give people hope. Thanks both of you for sharing this and for all your videos Raelen.
My doctor also said, when my blood pressure was creeping up, to stop working from home. To start going back into the office.
The extra stress of commute, school drop offs in time to get into the traffic etc
Unbelievable.
It seems that we all have many different ways that we connect our body and our mind which is why everyone's journey to recovery seems so different. But the common thread through all of these recovery stories is that we are listening to our bodies and finding what they need to understand that we can and will recover.
I really loved watching this. I love Veronica's joy, energy, kindness and the emotion shown in her interview! I feel very inspired!
💓💓💓
Please interview the therapist who recovered after 19 years.
Well that would be me! How about it, Raelan?
@@angelawilson4638 hello happy new year! how can I work with you????
@angelawilson4638 was it really? Because I need help asap if you can please?
This is an incredible interview but I am confused why you say this woman had severe me? Severe ME means you cannot endure light sound or human contact- but she could go to an retreat for treatment. I understand she couldn’t walk but to be able to go out and do things it seems she would be mild/high end moderate ME. I only say this as a person who is totally housebound and was bed bound for a year. And am now moderate. As members of the ME community it seems important to use mild moderate severe and very severe correctly. Love what you do for our community. Thank you for these videos
Dear Any, I could not walk or tolerate light or sound. The treatment felt like hell and I was taken everywhere in my husband's arms. I hope this clarifies.
In my health authorities description "Severe ME" means mostly bedbound. I was this way from 2009 - 2017, mostly in a darkened room but I had periods of improvement where I could sit up, tolerate listening to audiobooks etc. I could "endure" limited human contact, limited light exposure and very limited sound.
What is ME?
Wauw thank you so much for sharing your story. You give me hope and trust ❤️ lots of blessings and love to you and Raelan 💕💕💕💕💕
Thank you, Janna ❤❤❤
Beautiful Veronica what a delight you are ❤
Just fabulous. Thank you 🎉
Absolutely amazing and inspiring!
Love it. No payback. Inspiring
I cured my autoimmune disease with a strict nutrient dense anti-inflammatory diet and supplementation and eliminating all stress. I healed my gut and nervous system and got rid of systemic inflammation that was through my body and brain. It took 2 months for all symptoms to disappear.
Thanks universe and God she is fine , happy and healthy may everyone feels happiness
❤️
This gives me hope 😍💜
💓💓💓
Great video. Thanks to you too for sharing your recovery story 💐💐💐🙏🏻
Thank you as always, Kuldip 💓
@@RaelanAgle I'm stuck in my recovery . I was recovering finely in the last one and half month. I found the way of my recovery, everything was going fine. But..... My overconfidence made it down. When i started feel normal in the last month i eat everything like a normal person like wheat, noodles etc. I forgot that I'm in my recovery path,Though I was FEELING NORMAL but I'm internally not that much strong as like a normal person. That evening i ate much noodles(made of wheat) and that was my hyge mistake. I'm now 55% of recovery from 70%😔
@@kuldipChoudhuryVlogsdo you have gluten sensitivity Or is gluten not good to take during CFS?
Very interesting interview!
💓💓💓
Bravo Veronica!
Needed this ❤️
❤️❤️❤️
Inspirational!💙
❤️❤️❤️
Thank you for this video! So happy for you Veronica!
I guess I missed the part where you mention the exact name of the therapy/method that helped you fully recover. Could you specify the name please? I’d like to learn more about it. Thank you so much
💕
Me too.
Me too :)
me too
It’s called the MindBody Reconnect
💯🤍🤍🤍Very inspiring !
THANKS Sooooo MUCH !!!!😊💖
You are so welcome, Barbara!
Very inspiring video. Did Veronica share the woman who she did the 7 sessions of treatment with? Apologies if I’ve missed it! Thanks, Verity
Díky!
Thank you so much, Tere! ❤
What a wonderful girl! I never cease to be appalled and disgusted by the medical establishment! Their just drug pushers !
I"d love to know the name of the therapist she worked with? What was the name of the therapy?
From what i been hearing in these interviews so far it really does sound mental. It sounds like a nervous system dysregulation that you can re-regulate through mind work. Is that right Raelan?
(Not Raelan but) seems so, yeah. For me atleast I want to learn how to properly relax. To deal with my fatigue when it emerges. To get better sleep. This points me to some kind of meditation. I'm thinking Vedic meditation (the video with Sam was very inspiring) or Transcendental meditation. (But personally I might just have sleep apnea that I have to deal with since sleep feels like my biggest issue...)
It’s not “mental” but it is I’m the nervous system… The nervous system is physical. But yes, it is affected by thoughts, emotions, situations, behaviours etc
No, it's a mind body connection. There are physical problems, caused by a variety of issues, but the body cannot heal when in a stressed state. This is why calming the nervous system is essential.
What is the name of the lady who did the therapy to cure CFS with her? Does she still offer therapy?
It's through The Mindbody reconnect program - there's a link in the video description :)
Can you share more about the therapy
Hi Raeglan could you please share Veronica's details so that I can get her help.
Thank you
Hi Faith - her contact details are in the video description. Wishing you all the best 💛
My dx was in 1997..I still have good and bad days.
Me. To neurosthenia diagnosed.then.then CFS now more fybromyalgia
P.PS. Please add Dan Neuffer ,with Raelan and Daniel, to the paragraph ,four down!
So which program did veronica do?
“Unknown” ,near the bottom of this page, said it all!
Raelan, where can I get her information? BTW you are an amazing interviewer!! You cultivate hope!
You can see more details about Veronica in the description 💓
So beautiful 😍 you’ll rock ❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️❤️
Thank you as always, Sylvia ❤❤❤
Mind body reconnect is mickel therapy - i did 1 year of mickel therapy didnt work for me :(
Sorry to hear that Graham
Did you see any improvements during the therapy or was it 'useless'?
I tried reverse therapy. I think it is the same or very simmialr to mickel and ask got no benefit. I think maybe it is more helpful for those whose symptoms are tied to emotional states or emotionally traumatic experiences. I remember getting so frustrated with the therapy as they get you to try and find the “hidden message” behind symptoms.
My symptoms were primarily of view cause, worsened by covid.
I already was emotionally aware, able to set boundries etc.
physicall exertion triggered my symptom, there was no “hidden message”.
Like all things, it will work for some but not others.
Hi raelan i wanted to know what types of meditations are more useful than others
This seems to vary by person and preference from what I can tell 😊
Unfortunately we all don't get better we have worse symptoms Like heart problems AFIB bone Loss some need breathing machines Like me so it's not that simple for everyone sorry
❤️
P.S. two down! I’m referring to her website, but mainly the “ resources” sections! She is o.k. now, but where is our hope ??
Where do we find this theropy to try?
It's through The Mindbody reconnect program - there's a link in the video description :)
@@RaelanAgle 😊
@@jenniferflower9265 there’s a little arrow on the right hand side, under the video, next to the title of the video. It’s a drop down menu with all the info. ( I just found it myself) 😀
I never cease to be appalled and disgusted by the medical establishment! They are nothing g more than drug pushes! Shame on them!
Too hard to listen to sadly
If you mean that the sound is too low, I have the same issue on my laptop, but on my phone it's totally fine.
@@__OL__ thanks
how i contact you please help me suffering f4om cfs pls help
❤❤❤