Hey Miguel and Team! I have a question regarding autoantibodies in the blood of some CFS sufferers. Have you included such people in the program? Is it possible to get this under control with the baseline training?
Oh my,! This was such an inspiring story and gave me hope that just maybe I too can recover after 38 years of having chronic fatigue. I got finally diagnosed in 1996 with CFS. I have spent a fortune and decades trying all sorts of treatments and therapies. But the number of symptoms and severity has been increasing over the years. I have had insomnia for well over 20 years. Now I think I may also be getting dementia, which i am sure due to constant lack of sleep or sleep medications I have to use. So much of your story resonated with me. I also feel i only get about half an hour of energy in the morning and just drag and push myself for the rest of day. It feels my body is stuck in an alarm mode. Instead of making energy, repairing and healing it is in alert mode. I have come to realise that nutrition, supplements and exercise do nothing until mental stressors are addressed. I have had stress and traumas since childhood. Since i have come across this brain retraining stuff it has given me new hope. So my heartfelt thanks to both of you for sharing the story and for the chanel.
I'm touched by your words, and I'm so glad the story resonated with you. 💕 Your journey is unique, and the hope you're finding is a powerful force. Keep believing in the possibility of recovery, and take small steps each day. 🌟❤️ You're not alone, and there's a community here to support you! 🤗
Wow.... i knew I had to listen to this one. I am Dutch, and my son Jeroen is about your age. Seemed to call to me. Ive had CFS for 30 years and know how you feel. I hope you will get back to 100%. Im doing a braintraining also with good results. But I picked out a few golden nuggets from you and will listen to this one again. Hou je haaks! Je kan het! Erna
Goed bezig Jeroen 🙌 This is the first recovery story I listen to and it’s truly inspiring and motivates me to fill another day with respecting my body. “Don’t take my energy!” I fully agree, let’s get it back 😊
What a beautifully inspiring story Jeroen 😊well done!! All your hard work is paying off. Miguel your smile near the end says it all😁 you truly are an angel that gives us hope and our lives back ❤
At the moment I am in a crash and my nervous system is running wild. I have a lot if negative thoughts which are hard to ignore. After having watched this interview, I feel a lit better. Thanks to the rwo of you.
So I was suffering off and on with CFS but last spring I got sick with sinusitis. Now I have the effects of it like clogged Eustachian tube in ear. So, I have some vertigo or slight dizziness. Wears me out so I have chronic fatigue with a touch of vertigo. I push and struggle. Forgot to include herniated disc pain . Tender achey pain and my legs easily get tired and feet ache. Forgive my grammar. I’m tired.
Sounds similar to the symptoms I had. Mold and EMF created my CFS. I moved from the exposure and feel 50% better in 7 weeks. Still a journey ahead but I struggled for 4 yrs until I seriously looked into my environment. My 13 yr old son developed the same symptoms at the same time. We are both now recovering quickly.
Hi. So sorry to hear about your health issues. Just a thought about vertigo after the bout of sinusitis. A similar thing happened to me and my Dr diagnosed me with Benign Paroxysmal Positional Vertigo (BPPV). The home Epley maneuver is a type of exercise that can help if you do have BPPV. There's information available online about it all. Best wishes. I hope you feel better soon.
Miguel, did you ever have trouble communicating with people? Everytime I even say one word my body immediately heats up and my head starts vibrating. I’m barely able to tell my family what I’m feeling
You are not alene. Many with cfs experience that. I have had a lot of body vibrations. Also in the head. Its a responce to stimuli becouse our nervousystem is hypersensitive. And it can be very challenging to talk to and be with "normal " people. Take it slow, pull back and learn about cfs. Its almost impossible to explain this state to family, friends or others who have no experience with this. Maybe you can show one close family member etc a video where miguel explain. ? Just a thought. Wishing you well ❤
Perhaps you've made a video on this already, but I am very interested in practical tips to stay consistent in recovery since this is one of the key (and perhaps hardest) components for getting healthy again.
Sure! Here are some videos I Made related to staying consistent during recovery: ua-cam.com/video/S8_DzAkm7PQ/v-deo.htmlsi=s43VD_epIo7IbojT ua-cam.com/video/WfpnXQkA_m8/v-deo.htmlsi=Mdx5lx-G8ft7VAFT ua-cam.com/video/6-dC6mg1wCw/v-deo.htmlsi=JP4WMqfBp_1pOSmK ua-cam.com/video/BNZYLK9vDlw/v-deo.htmlsi=oGh1tTbaVhxGbA6a I hope these helps! 😁🙌
Miguel i have overcome lots of my body pain But i want to know that how to overcome this zombie like feeling and brain fog It's unbearable i am not sure I'm thinking everytime like I'm an alien
I've had it for 17 years, like the woman you mentioned. I think the hardest part is not the symptoms but feeling like I've missed the healthiest years of my life (started when I was 11). I really hope I can recover before my youth is over 🤞
In terms of the cost, it really depends on access to me and I have to see if we can even help you first. I always recommend going through the questionnaire and if you qualify, booking a strategy call to see if you're a good fit for the program! www.cfsrecovery.co/apply
WANT TO SPEED UP RECOVERY? APPLY FOR OUR RECOVERY JUMPSTART PROGRAM ⬇
www.cfsrecovery.co/apply
Hey Miguel and Team!
I have a question regarding autoantibodies in the blood of some CFS sufferers. Have you included such people in the program? Is it possible to get this under control with the baseline training?
20years of cfs!... these ppl r the real heroes in the world who survived the hell for decades ❤
Agree 💯💯💯
Oh my,! This was such an inspiring story and gave me hope that just maybe I too can recover after 38 years of having chronic fatigue. I got finally diagnosed in 1996 with CFS. I have spent a fortune and decades trying all sorts of treatments and therapies. But the number of symptoms and severity has been increasing over the years. I have had insomnia for well over 20 years. Now I think I may also be getting dementia, which i am sure due to constant lack of sleep or sleep medications I have to use. So much of your story resonated with me. I also feel i only get about half an hour of energy in the morning and just drag and push myself for the rest of day. It feels my body is stuck in an alarm mode. Instead of making energy, repairing and healing it is in alert mode. I have come to realise that nutrition, supplements and exercise do nothing until mental stressors are addressed. I have had stress and traumas since childhood. Since i have come across this brain retraining stuff it has given me new hope. So my heartfelt thanks to both of you for sharing the story and for the chanel.
I'm touched by your words, and I'm so glad the story resonated with you. 💕 Your journey is unique, and the hope you're finding is a powerful force. Keep believing in the possibility of recovery, and take small steps each day. 🌟❤️ You're not alone, and there's a community here to support you! 🤗
There are a number of different recovery programmes out there - hope you find one that suits you ❤
Wow.... i knew I had to listen to this one. I am Dutch, and my son Jeroen is about your age. Seemed to call to me. Ive had CFS for 30 years and know how you feel. I hope you will get back to 100%. Im doing a braintraining also with good results. But I picked out a few golden nuggets from you and will listen to this one again. Hou je haaks! Je kan het! Erna
Goed bezig Jeroen 🙌 This is the first recovery story I listen to and it’s truly inspiring and motivates me to fill another day with respecting my body. “Don’t take my energy!” I fully agree, let’s get it back 😊
Thank you so much! 😊❤️
What a beautifully inspiring story Jeroen 😊well done!! All your hard work is paying off. Miguel your smile near the end says it all😁 you truly are an angel that gives us hope and our lives back ❤
Thank you so much for your kind words ❤️😊
Jezus 20 jaar lang, zit net op twee jaar en gaat steeds beter met mij gelukkig. Super dat je nu beter aan het worden bent!
Thank you so much! 😊❤️
At the moment I am in a crash and my nervous system is running wild. I have a lot if negative thoughts which are hard to ignore. After having watched this interview, I feel a lit better. Thanks to the rwo of you.
I feel you. Please check this video I made about this and hoping it'll help you out: ua-cam.com/video/DNg7ipW5uNM/v-deo.htmlsi=C-RccrJWDPA6PfO7
Wow, quite the journey Jeroen, all the best getting to the finish line asap.
Thank you for your encouraging words! ❤️😊
Great interview!🎉 thanks!!!!
Thank you so much! 😊❤️
Thanks for sharing your story
Thanks for watching! ❤️
So I was suffering off and on with CFS but last spring I got sick with sinusitis. Now I have the effects of it like clogged Eustachian tube in ear. So, I have some vertigo or slight dizziness. Wears me out so I have chronic fatigue with a touch of vertigo. I push and struggle. Forgot to include herniated disc pain . Tender achey pain and my legs easily get tired and feet ache. Forgive my grammar. I’m tired.
Sounds similar to the symptoms I had. Mold and EMF created my CFS. I moved from the exposure and feel 50% better in 7 weeks. Still a journey ahead but I struggled for 4 yrs until I seriously looked into my environment. My 13 yr old son developed the same symptoms at the same time. We are both now recovering quickly.
Hi. So sorry to hear about your health issues. Just a thought about vertigo after the bout of sinusitis. A similar thing happened to me and my Dr diagnosed me with Benign Paroxysmal Positional Vertigo (BPPV). The home Epley maneuver is a type of exercise that can help if you do have BPPV. There's information available online about it all. Best wishes. I hope you feel better soon.
Please watch this and hopefully it helps:
ua-cam.com/video/0a5jCFGVPck/v-deo.htmlsi=7bpEWhO1AyNK2rq4
Miguel, did you ever have trouble communicating with people? Everytime I even say one word my body immediately heats up and my head starts vibrating. I’m barely able to tell my family what I’m feeling
You are not alene. Many with cfs experience that. I have had a lot of body vibrations. Also in the head. Its a responce to stimuli becouse our nervousystem is hypersensitive. And it can be very challenging to talk to and be with "normal " people. Take it slow, pull back and learn about cfs. Its almost impossible to explain this state to family, friends or others who have no experience with this. Maybe you can show one close family member etc a video where miguel explain. ? Just a thought. Wishing you well ❤
I did have trouble communicating with people, social interaction was too stimulating for me many times during my journey.
Perhaps you've made a video on this already, but I am very interested in practical tips to stay consistent in recovery since this is one of the key (and perhaps hardest) components for getting healthy again.
Sure! Here are some videos I Made related to staying consistent during recovery:
ua-cam.com/video/S8_DzAkm7PQ/v-deo.htmlsi=s43VD_epIo7IbojT
ua-cam.com/video/WfpnXQkA_m8/v-deo.htmlsi=Mdx5lx-G8ft7VAFT
ua-cam.com/video/6-dC6mg1wCw/v-deo.htmlsi=JP4WMqfBp_1pOSmK
ua-cam.com/video/BNZYLK9vDlw/v-deo.htmlsi=oGh1tTbaVhxGbA6a
I hope these helps! 😁🙌
Miguel i have overcome lots of my body pain
But i want to know that how to overcome this zombie like feeling and brain fog
It's unbearable i am not sure I'm thinking everytime like I'm an alien
Please check this video out: ua-cam.com/video/Z2e4qHOQP_k/v-deo.htmlsi=w-Zl9hDZwjJ2hZVG
20 years ??? I read some women had it 17 years. How did they get through that? And he still has his hair
I've had it for 17 years, like the woman you mentioned. I think the hardest part is not the symptoms but feeling like I've missed the healthiest years of my life (started when I was 11). I really hope I can recover before my youth is over 🤞
Please check this link. I hope it helps! ua-cam.com/video/AnCtJ10o28k/v-deo.htmlsi=GbJof3jAhmutNOG8
How much is this course ? Ive been sick for over 20 years ...its a life sentence of hell
Urine therapy has helped me
@@Mike-mh5rlhow long have you done it? I'm doing UT hasn't done anything
@@howtoskatewithanfour6889 what’s up bro. I got a UT therapy protocol that works. Hit me up if you want to know more
@@howtoskatewithanfour6889 I got the protocol from someone that works with urine
In terms of the cost, it really depends on access to me and I have to see if we can even help you first. I always recommend going through the questionnaire and if you qualify, booking a strategy call to see if you're a good fit for the program! www.cfsrecovery.co/apply