TIMESTAMPS 3:26 Valerie's illness onset 6:10 How Valerie processed what was happening to her 7:55 Live Cell Blood Test 9:57 Living With ME/CFS For 30 Years 19:35 What finally helped Valerie achieve her full recovery 24:07 What it felt like to recover so quickly 27:16 Valerie's advice for others facing similar conditions 29:07 A cute puppy
Thank you Valerie. At the end when when you said :"anybody can recover" , I started crying Valerie , and I am a tough cookie don't cry easily at all , but you see you have given me hope. I have CFS , spend most of my time in bed , (2 years now) , and now after watching you I have decided : I will get well !!!! Thank you thank you Valerie , you touched something in me !!
Raelan and Valerie...There are no words to say how much I appreciate this...I am walking in Valerie's shoes...but with two decades behind me. Thank you for being brave enough to share your story Valerie.
Loved Valerie and her story. I’m 34 years with CFS so she was very helpful. And I’m 73 so I got CFS also when they didn’t know what it was for 20 years. Thank you again Raelan, you are so hopeful.
I only just found this, it was posted two years ago, Valerie thank you so much for sharing your story and what got you well, thank you also to You Raelan for your channel, for helping us all. I have had ME/CFS for 5 1/2 decades I am now 68. I have no family or friends for support, no savings or assets as I have never been able to hold a job for long enough due to my ill health, so it makes doing a recovery course impossible. I have gained a bit of knowledge from RUclips and what others are sharing, I’m trying to piece it together to help myself, only this week did I find out about brain training and self soothing. listening to Valerie story has given me a little bit more hope that I may recover. My love to everybody else that is suffering with this debilitating illness.♥️
Raelan, her recovery seem quicker because when she took the lightning program, she had already worked on the other three pillars so the brain retraining/lightning program was the last piece of the puzzle. She had been working from the bottom up for years.
I cried after hearing this. She is telling my story. My heart breaks weekly cause ‘Mom, can’t go. ‘ Thank you so much for sharing your experience! I have hope!😭😭😭
Thank you! Thank you! I can’t tell you how much that helps me to see someone my age recovering. It has given me renewed hope. Would love to see more stories like this.
Dear Valerie, I’m so happy for your recovery. Enjoy you life now. If you work or study, be careful and don’t overdo anything. Listen to your body, your brain, rest. Greetings from Sweden 🇸🇪
That was a wonderful interview for me. I am 71 years old and have had CFS for22yrs. Have tried all sorts over the years and had resigned myself to never recovering. It has given me hope and I will give it another try. Think I’ll google the lLightening Process. Thanks Raelen for all your amazing interviews. Cheers Trish
Thank you Valerie and Raelan. I’m 68 and in a similar position I also have done the LProcess. However, it still continues to be a struggle. I experience fatigue and migraines, so concentration and lack of energy were a problem and in the end I gave up LP. However, I am trying to persist and this interview has renewed my hope to keep doing the process regardless of how many times a day I do it and not feel discouraged when I forget.
Krysia, I'm so sorry to hear that you've been dealing with this for so long. I hope you find all your puzzles pieces and can finally put this all behind you soon ❤️
I am 57, nearly 58. I have been ill with cfs for 22 years . I did a 3 day course based in TLP...I felt good after the three days but once home could not sustain any wellness. I don't know why. I gave up. My friend did it, she was much younger, but she got well in abt 3 months, and never looked back. I was told to do the technique 100 x day if I had to, I found this completely unsustainable and fatiguing It was just all too much . I don't know why it did not work. I know of a woman older than me, who after decades of cfs, booked herself into a rest home and just stares at the wall. She has completely given up. I have gone back to the brain retraining , but for me, I seem to need a lot more than just this brain stuff. I am still working at getting well, but sometimes I do think I can't do this anymore.
Please keep your chin up, Jacqui! ❤️ Sending you all the best vibes on your health journey.❤️ I hope you find exactly what you need to get through this.
What an incredible story. Thank you so much for sharing Valerie (and Raelan) It’s renewed my hope. So good to hear of a recovery from a very long termer ❤️ x
For the first time almost after 1 year i played badminton for 20 minutes two days ago. I can't explain how good i feel. I will try to introduce all the activities one by one very slow and gradually. After introducing a new activity i will give rest my body to adjust it. Because adjustment period is also important. When i feel down or lonely i come to your channel & Miguel's channel... seriously,it gives me much strength. Thanks for your hardwork for us 😊. Much love from india again ❤️❤️❤️❤️❤️
I love when the lightning process works for people. I did it and gave it everything and wanted it to work so much but it didn’t end up working for me. There really is no one path out of ME/CFS
I wrote my will at 36. I’m 41. I got there and then got shingles. Then lost my ability to breath. Then seizures. Then arthritis. And on. Blah. I will. I can. I will. Ty x
As a follower of your videos I was so impressed listening to Valerie's recovery story. I've had CFS/ME for what seems forever, about 12 years, following a brain injury. I did consider the 'Lightening Process' as I've tried other therapies/treatments, but I'm still sat on the fence. I would like to know the clinic she used (in London) for this form of treatment. I live in the UK. Thank you so much Raelan for all your good work in putting out video's - I watch them all....and live in hope!!😊
Oh my goodness!! Thank you I've had this for 10 years and now having given up working at 53 feeling super tired exhausted. Similar history and at last your are both providing light at what seemed dark place. Thank you!
Really grateful for this video. I am 6 months into ANS rewire and experiencing a setback. Its discouraging. It's tempting to try LP but i think i just need to stick with ANS and trying my best with diet changes. I really needed the inspiration to continue. Thank you. Btw one of the biggest things with the program and diet changes is perfectionism. I feel down on myself that i am maybe not trying hard enough and thats why it hasn't worked yet, and then cynicism battles hope and tells me it wont work for me. Thats why i need to keep watching inspiring videos like this
try watching Dan Buglio and Jim Prussack on youtube, TMS approach which is related to the LP / ANS Rewire etc x helping me to make bigger improvements x videos are short so good to watch daily to keep you on track x
Thank you, an older person! Your’e the best Raelan.I’m 68, with two fibro kids! What hope do I have?? My wife works, and we are poor,and I am in bed. Yeh,the single,wealthy, living with parents,and few responsibilities, yep,let’s here a few honest replies!! From people in my position!,all that being said, you do such great,great work Raelan,thank you !
I did the LP years ago. Neither I nor the other 2 people on my course recovered. I do believe in brain retraining modalities, and am now doing ANS Rewire, but I believe that it will take time to lay down new neural pathways so am in it for the long haul! I would say though, that there is absolutely no reason for the LP course to be as expensive as it is. I'm glad it worked for Valerie though-it must be amazing to have your health back!
I bought one of his books. "Get the life you want" ....IS this book pretty much the same as the LP or does the LP have some hidden teachings in it.? ..thanks. ....12CFS now and hoping it over now. So many of these probgrams could be written in a $20 book but now a days they just make a program and charge thousands which especially CFS like us cant afford.
Thank you for your positivity. Thank you for spreading hope. I am 20 years in with my me/cfs. If you search online it doesn't give any hope for a complete recovery. I wanted to apologize. I left a possibility distressed/negative comment I was trying to locate it to delete it. I was having an exceptionally bad night. I hope you deleted it. I truly hope I am healed. On this side of heaven.
I'll try and have hope again. I'm more on the FM side w/ a side helping of CFS, and chemically sensitive. The worst is the depression though. Some manage not to have that, but I seemed to have it before the environmental illness developed. Of course depression got much worse when I couldn't work or feel normal and do much of what made others so happy. It's been around 25 years. I'm in my 50's and just resigned. It's hard not to feel like it's for anyone else.
Thanks for sharing Valerie and Raelan. What an incredible story Valerie. I’m so happy you found what worked for you and you recovered. I loved hearing your insights and wisdom ❤️
You won’t see the process anywhere for free. It’s basically brain retraining stopping fear thoughts about the illness - unfortunately didn’t work for me
@@lindapayne1429 Thank you for your answer. I’ve heard about several training programs out there and no one seems to share their techniques for free. I don’t think that is the right thing for me either though, but when I hear about all these people that “miraculously” have gotten well, I’d like to know. What has helped my health a bit so far is partly bio resonance/frequency therapy and anti infection diet/spices, etc. Started parasite cleanse…
@@annahallgren1055 I am trying ANS rewire as I the theory makes sense to me. It’s main component is brain retraining but also includes other strategies - it’s cheaper too. I definitely think the body needs to be in a relaxed state to heal. For me it’s a long slog my brain seems to take a long time to take stuff in. I wish you all the best.
My words exactly ! A Dr repeated to me over & over that there’s ‘No cure ‘ which to me said never recover ! & I love massively telling ppl if it comes up usually it’s someone sad about their Mum or Daughter & the younger the more likely they have children so their maybe getting less of their Whose ever it is ( usually it’s a female ) ( is there something in this ?) . Don’t stop these videos . I couldn’t do much at all b4 I descovered your Videos ! Love u Xxxxx
So very happy for you Valerie, being also in my sixties you do wonder if you will ever get well. I also did the lightning process a few years ago and it was sooo incredible that it “ blew my mind”, and unfortunately I became very anxious, was continually dancing around like a mirranet . It was like someone had thrown me a life line and I was hanging on for dear life. So what I would like to know Valerie did you suffer from any anxiety doing the program, particularly with the speed of recovery and if so how did you handle it ? Wishing you and yours all the best 🥰
I would love to know what the lightening process is/ the one minute process. I've been working for 23 years to hear "fibromylagia" that turned neurological with optic neuritis/nerve damage 16 years ago-numbness, weakness, twitching/jerking, insomnia, neuro band on head, heart palps etc. I have no autoimmune diagnosis. I'm doing DNRS . I could write a novel on all the extreme diets, detox, amalgams out, mhbot, mexico treatments, homeopathy , supplements, yoga/meditatio, qi gong etc etc etc I've done over the many years ( Type A). Very sensitive to pharma, vaccine, surgery etc which all triggered disabling neuro attacks for me. Now I've developed GERD. Over the years I was also diagnosed hypthyroid, endometriosis, high BP . I find myself mostly couch bound -still walking each day/yoga and trying not to lose hope. Catching all my thoughts-it's challenging. I so want to heal and live life.
Hello. Have you had your B12 status checked. You need to do an Active B12 test with no b12 supplements at least 4 weeks prior to test. Your symptoms are very typical of a B12 deficiency. Best wishes.
I just checked out the Lightening Process website and it looks like there are different protocols. I would love to know which protocol Valerie used as I have all the exact same symptoms as her!!
Thank you Valerie, I've been walking in your shoes for 30 years. I'm much better now but fatigue after a couple hours of doing chores. I'm 81 and did survive all these years. I'm sure I had Epstein Barr but my doctor told me it was elevated because of allergies.
Thank you for this interview! Valerie congratulations 🎊🎈 you are free now ! Go and live the life of your dreams ! I have a doubt that it’s difficult to find an answer. Imagine that you are taking psychiatric medication that injured your brain but you still have to taking it because it will take lots of time to wean off. Does the brain retraining still works ? Does the brain can get to homeostasis while thanking the insulting drug ? I don’t know if anyone feels like this , I find my case very complex because involves extreme brain sensitivity, and this feeling of fight or flight in my head with very loud tinnitus especially when my hormones shifts . I basically know how I’m going to feel everyday of my monthly circle. Depending the hormones I’m more or less depress lots of adrenaline in my ovulation and crashes every hormonal shifts . I started with a little brain retraining but I’m not sure if I should follow another route since I’m still taking this meds and have Lyme as well. Anyone here with a similar experience that have recovered with brain retraining ? I feel my brain it’s broken 😞
I’m having a similar experience. My big onset was due to a psychiatric medication. I’m continuously highly nervous and experience many symptoms like tinnitus, insomnia… I became highly sensitive to many things, including my own hormones. I have spoken to a woman who experienced something similar and was able to fully recover, although it took her many years. As a complicating factor, I have PCOS, so my hormones have very abnormal levels too. I would love to hear a recovery story too, as I’m working on it but am only making very slow progress.
@@lingeske exactly the same my hormones are out of wack . And I don’t know if it’s from antidepressants or cfs or Lyme … the issue now for me is that I was polydruged again so I can’t see an end of sight. Because our brains need to heal without the meds, and if it’s from antidepressants it can be taking years but I wouldn’t mind if I got better and cfs was only part of the process … nice to meet someone with same issues , although I wish we didn’t have to deal with this …
@@clarissericardo2313 I’m at the moment tapering a benzo for hopefully the last time and then I would be off everything. If I succeed, it will have taken me 4,5 years from when I unfortunately first started polydrugged medications. Let’s hope that nature is kind on us and heals us well. I already had the hormonal issue since I was a teen. It’s not related to the medication or CFS. Although they do influence each other a ton, I’m sure.
Oh my gosh , this is soooooop me! 35 years with this , I just turned 61. Any possibility of having a way to connect with Valerie ????? I would love love love to be able to talk with her ‼️ Please let me know if she has an Instagram or a Facebook or a website or someway to connect to her.
Wow, Valerie, as a fellow 65 yr old going on 20 yrs with CFS which started with Epstein Barr, you have probably given me the final push to the lightening process. Was it hard to get thru 3 days straight though? I’m grateful for your interview. Thanks to you and Raelan !!💖💖
So many people who have been homebound disabled for decades with CFS/ME and obviously living on very little income because of this situation. Wouldn't this Lightning Process thing be shared for free? No life and no earning a living means a segment of people who need to be helped in any way possible. I'm not against those earning a living helping others. My only point is that we're talking about a predominantly very poor population from being disabled and help needs to reach them. I am one of them and living on $14000 per year and lucky I have that much to live on.
Could it be that those with cfs that's been affected at a biological / cellular level that recovery using brain training is unlikely or more challenging? What I mean by that is those with cfs and other issues such as arthritis, osteoporosis, ehlers danlos, lupus, bone loss in jaw, sevsre gun disease etc etc these individuals don't respond so well to brain training? What I see is recovery stories of people who have cfs and just cfs no biological damage at any level.i could be wrong. Regardless its nice to see this lady recovery after a very long time of being unwell
It may be possible, BIT brain reteainong can only help bc it calms the nervous system down, whoch then allows the body to heal. Its can only be helpful if you do it, but perhaps if its something biological, it may not get you 100%, but again, biologixal things have time to heal when the system is calmed down..
Kelsie is right. Nothing happens without homeostasis. Homeostasis requires a balanced nervous system. Calming down that danger response is the first step. The more time you can spend in homeostasis the more things will change, but calming down is the very first thing that gets you on the path. For most it won't be overnight. The less time I spend getting spun up by the internet about this stuff the better I do. It's gradual.
TIMESTAMPS
3:26 Valerie's illness onset
6:10 How Valerie processed what was happening to her
7:55 Live Cell Blood Test
9:57 Living With ME/CFS For 30 Years
19:35 What finally helped Valerie achieve her full recovery
24:07 What it felt like to recover so quickly
27:16 Valerie's advice for others facing similar conditions
29:07 A cute puppy
0
This is a year late, but new to me. Thank you. You are a great person
Thank you Valerie. At the end when when you said :"anybody can recover" , I started crying Valerie , and I am a tough cookie don't cry easily at all , but you see you have given me hope.
I have CFS , spend most of my time in bed , (2 years now) , and now after watching you I have decided : I will get well !!!! Thank you thank you Valerie , you touched something in me !!
Hope you are feeling a little better ❤
Hi. I hope you are better. I need something
How are you?
Raelan and Valerie...There are no words to say how much I appreciate this...I am walking in Valerie's shoes...but with two decades behind me. Thank you for being brave enough to share your story Valerie.
Yes, same 💜 and same 🕊️ this is hope
Loved Valerie and her story. I’m 34 years with CFS so she was very helpful. And I’m 73 so I got CFS also when they didn’t know what it was for 20 years. Thank you again Raelan, you are so hopeful.
I only just found this, it was posted two years ago, Valerie thank you so much for sharing your story and what got you well, thank you also to You Raelan for your channel, for helping us all.
I have had ME/CFS for 5 1/2 decades I am now 68. I have no family or friends for support, no savings or assets as I have never been able to hold a job for long enough due to my ill health, so it makes doing a recovery course impossible.
I have gained a bit of knowledge from RUclips and what others are sharing, I’m trying to piece it together to help myself, only this week did I find out about brain training and self soothing.
listening to Valerie story has given me a little bit more hope that I may recover.
My love to everybody else that is suffering with this debilitating illness.♥️
Raelan, her recovery seem quicker because when she took the lightning program, she had already worked on the other three pillars so the brain retraining/lightning program was the last piece of the puzzle. She had been working from the bottom up for years.
I cried after hearing this. She is telling my story. My heart breaks weekly cause ‘Mom, can’t go. ‘
Thank you so much for sharing your experience! I have hope!😭😭😭
My story too, same sentence weekly! We are strong moms Melanie, we will figure it out one day and recover🙏🌈💪
Hi I know what you mean. How are you now? What have you changed?
Thank you! Thank you! I can’t tell you how much that helps me to see someone my age recovering. It has given me renewed hope. Would love to see more stories like this.
❤️❤️❤️
Dear Valerie, I’m so happy for your recovery. Enjoy you life now. If you work or study, be careful and don’t overdo anything. Listen to your body, your brain, rest. Greetings from Sweden 🇸🇪
this gives hope to so many. What a beautiful soul.
That was a wonderful interview for me. I am 71 years old and have had CFS for22yrs. Have tried all sorts over the years and had resigned myself to never recovering. It has given me hope and I will give it another try. Think I’ll google the lLightening Process.
Thanks Raelen for all your amazing interviews. Cheers Trish
Recovery in 5 days amazing!! Im so glad. Brain is so powerful
Valerie's Story was a Gift... It truly is a Blessing Raelan to here these stories.. Can't Thank You enough for doing these videos..♥️
Thank you Valerie and Raelan. I’m 68 and in a similar position I also have done the LProcess. However, it still continues to be a struggle. I experience fatigue and migraines, so concentration and lack of energy were a problem and in the end I gave up LP. However, I am trying to persist and this interview has renewed my hope to keep doing the process regardless of how many times a day I do it and not feel discouraged when I forget.
Krysia, I'm so sorry to hear that you've been dealing with this for so long. I hope you find all your puzzles pieces and can finally put this all behind you soon ❤️
I am 57, nearly 58. I have been ill with cfs for 22 years . I did a 3 day course based in TLP...I felt good after the three days but once home could not sustain any wellness. I don't know why. I gave up. My friend did it, she was much younger, but she got well in abt 3 months, and never looked back. I was told to do the technique 100 x day if I had to, I found this completely unsustainable and fatiguing It was just all too much . I don't know why it did not work. I know of a woman older than me, who after decades of cfs, booked herself into a rest home and just stares at the wall. She has completely given up. I have gone back to the brain retraining , but for me, I seem to need a lot more than just this brain stuff. I am still working at getting well, but sometimes I do think I can't do this anymore.
Please keep your chin up, Jacqui! ❤️ Sending you all the best vibes on your health journey.❤️ I hope you find exactly what you need to get through this.
Thank you for the encouragement Valerie, God bless!
What an incredible story. Thank you so much for sharing Valerie (and Raelan)
It’s renewed my hope. So good to hear of a recovery from a very long termer ❤️ x
Glad you enjoyed it, Emma!! ❤️
Thank you! Both of you have saved lives with this video!
For the first time almost after 1 year i played badminton for 20 minutes two days ago. I can't explain how good i feel. I will try to introduce all the activities one by one very slow and gradually. After introducing a new activity i will give rest my body to adjust it. Because adjustment period is also important.
When i feel down or lonely i come to your channel & Miguel's channel... seriously,it gives me much strength. Thanks for your hardwork for us 😊. Much love from india again ❤️❤️❤️❤️❤️
Kuldip, this is amazing!!! I'm so happy to hear about all the progress that you've made. Great work!
@@RaelanAgle Thank you raelen. Keep making videos for us. 😊
How are you now?
When my hope wanes, I know I can listen to Valerie and life blooms. Thank you Raelan.
Thank you, April! 💖💖💖
I love when the lightning process works for people. I did it and gave it everything and wanted it to work so much but it didn’t end up working for me. There really is no one path out of ME/CFS
I wrote my will at 36. I’m 41. I got there and then got shingles. Then lost my ability to breath. Then seizures. Then arthritis. And on. Blah. I will. I can. I will. Ty x
Please don't give up ❤
As a follower of your videos I was so impressed listening to Valerie's recovery story. I've had CFS/ME for what seems forever, about 12 years, following a brain injury. I did consider the 'Lightening Process' as I've tried other therapies/treatments, but I'm still sat on the fence. I would like to know the clinic she used (in London) for this form of treatment. I live in the UK. Thank you so much Raelan for all your good work in putting out video's - I watch them all....and live in hope!!😊
Oh my goodness!! Thank you I've had this for 10 years and now having given up working at 53 feeling super tired exhausted. Similar history and at last your are both providing light at what seemed dark place. Thank you!
Really grateful for this video. I am 6 months into ANS rewire and experiencing a setback. Its discouraging. It's tempting to try LP but i think i just need to stick with ANS and trying my best with diet changes. I really needed the inspiration to continue. Thank you. Btw one of the biggest things with the program and diet changes is perfectionism. I feel down on myself that i am maybe not trying hard enough and thats why it hasn't worked yet, and then cynicism battles hope and tells me it wont work for me. Thats why i need to keep watching inspiring videos like this
try watching Dan Buglio and Jim Prussack on youtube, TMS approach which is related to the LP / ANS Rewire etc x helping me to make bigger improvements x videos are short so good to watch daily to keep you on track x
@@seffie4363 thank you i definitely will start watching
How are you now?
Congratulations Valerie ❤️ bless you and enjoy your new life! 💫 🎉 🥂 love to you and Realan 😘❤️🙏
Love to you as well, Janna! ❤️
Thank you, an older person! Your’e the best Raelan.I’m 68, with two fibro kids! What hope do I have?? My wife works, and we are poor,and I am in bed. Yeh,the single,wealthy, living with parents,and few responsibilities, yep,let’s here a few honest replies!! From people in my position!,all that being said, you do such great,great work Raelan,thank you !
I did the LP years ago. Neither I nor the other 2 people on my course recovered. I do believe in brain retraining modalities, and am now doing ANS Rewire, but I believe that it will take time to lay down new neural pathways so am in it for the long haul! I would say though, that there is absolutely no reason for the LP course to be as expensive as it is. I'm glad it worked for Valerie though-it must be amazing to have your health back!
I bought one of his books. "Get the life you want" ....IS this book pretty much the same as the LP or does the LP have some hidden teachings in it.? ..thanks. ....12CFS now and hoping it over now. So many of these probgrams could be written in a $20 book but now a days they just make a program and charge thousands which especially CFS like us cant afford.
@@Truehoon capitalism causes alot of CFS fybromyalgia to one way or another yes terrible what they charge
How are you now?
Thank you for your positivity. Thank you for spreading hope. I am 20 years in with my me/cfs. If you search online it doesn't give any hope for a complete recovery. I wanted to apologize. I left a possibility distressed/negative comment I was trying to locate it to delete it. I was having an exceptionally bad night. I hope you deleted it. I truly hope I am healed. On this side of heaven.
Thank you so much Valerie. And thank you as always raelan. So grateful for both of you.
💓💓💓
I'll try and have hope again. I'm more on the FM side w/ a side helping of CFS, and chemically sensitive. The worst is the depression though. Some manage not to have that, but I seemed to have it before the environmental illness developed. Of course depression got much worse when I couldn't work or feel normal and do much of what made others so happy. It's been around 25 years. I'm in my 50's and just resigned. It's hard not to feel like it's for anyone else.
Thank you both 💕🙏
Thanks for sharing Valerie and Raelan. What an incredible story Valerie. I’m so happy you found what worked for you and you recovered. I loved hearing your insights and wisdom ❤️
💗💗💗
Could someone PLEASE share a video on the techniques, HOW to use your brain/thinking/whatever that helped people with ME/CFS to get well, please.
You won’t see the process anywhere for free. It’s basically brain retraining stopping fear thoughts about the illness - unfortunately didn’t work for me
@@lindapayne1429 Thank you for your answer. I’ve heard about several training programs out there and no one seems to share their techniques for free.
I don’t think that is the right thing for me either though, but when I hear about all these people that “miraculously” have gotten well, I’d like to know.
What has helped my health a bit so far is partly bio resonance/frequency therapy and anti infection diet/spices, etc. Started parasite cleanse…
@@annahallgren1055 bio resonance/frequency therapy sounds interesting. What is it?
@@annahallgren1055 I am trying ANS rewire as I the theory makes sense to me. It’s main component is brain retraining but also includes other strategies - it’s cheaper too. I definitely think the body needs to be in a relaxed state to heal. For me it’s a long slog my brain seems to take a long time to take stuff in. I wish you all the best.
@@lindapayne1429 that’s to bad. Did you do LP?
Amazing story! 0-60 in 5 days. Wow! Wow! Wow!
True! 💓💓💓
Valerie can you send us the link for the lightening proces. Thank you for sheering your story.
Nice regards from Europe❤
My words exactly ! A Dr repeated to me over & over that there’s ‘No cure ‘ which to me said never recover ! & I love massively telling ppl if it comes up usually it’s someone sad about their Mum or Daughter & the younger the more likely they have children so their maybe getting less of their Whose ever it is ( usually it’s a female ) ( is there something in this ?) . Don’t stop these videos . I couldn’t do much at all b4 I descovered your Videos ! Love u Xxxxx
💖💖💖
So very happy for you Valerie, being also in my sixties you do wonder if you will ever get well. I also did the lightning process a few years ago and it was sooo incredible that it “ blew my mind”, and unfortunately I became very anxious, was continually dancing around like a mirranet . It was like someone had thrown me a life line and I was hanging on for dear life. So what I would like to know Valerie did you suffer from any anxiety doing the program, particularly with the speed of recovery and if so how did you handle it ? Wishing you and yours all the best 🥰
Thank you for taking the time to share this, Nola 💛
I can’t find the lightening program online. And , can Valerie receive emails? I would love to ask her questions
What an inspiring interview,! Well-done to both of you!!
Thank you, Carolyn! 💓💓💓
Great interview!! Thank you to both of you!
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I would love to know what the lightening process is/ the one minute process. I've been working for 23 years to hear "fibromylagia" that turned neurological with optic neuritis/nerve damage 16 years ago-numbness, weakness, twitching/jerking, insomnia, neuro band on head, heart palps etc. I have no autoimmune diagnosis. I'm doing DNRS . I could write a novel on all the extreme diets, detox, amalgams out, mhbot, mexico treatments, homeopathy , supplements, yoga/meditatio, qi gong etc etc etc I've done over the many years ( Type A). Very sensitive to pharma, vaccine, surgery etc which all triggered disabling neuro attacks for me. Now I've developed GERD. Over the years I was also diagnosed hypthyroid, endometriosis, high BP . I find myself mostly couch bound -still walking each day/yoga and trying not to lose hope. Catching all my thoughts-it's challenging. I so want to heal and live life.
Hello. Have you had your B12 status checked. You need to do an Active B12 test with no b12 supplements at least 4 weeks prior to test. Your symptoms are very typical of a B12 deficiency. Best wishes.
Great interview. Thank you both 🙏
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@RaelanAgle did you go through a particular program? I'm new to your channel. Binge watching tho 😌 great at what you do
Such a lovely lady 💜
So inspiring and uplifting. I was wondering what Lightning Process practitioner Valerie went through?
Also interested to know
hi raelan where is the video that you interview who recovered by using curable app?
Hello, I believe it's this one (although it wasn't just the app) ruclips.net/video/as7I55hY29k/видео.html
Thank you so much Valerie. I have all the exact same symptoms and have also been wearing a continuous glucose monitor. You have given me hope. ♥️🙏🏻
I just checked out the Lightening Process website and it looks like there are different protocols. I would love to know which protocol Valerie used as I have all the exact same symptoms as her!!
@@misselle3049 following
You got this 💓
@@RaelanAgle Thanks Raelan. ♥️
@@misselle3049did you get an answer? Ty
Thank you Valerie, I've been walking in your shoes for 30 years. I'm much better now but fatigue after a couple hours of doing chores. I'm 81 and did survive all these years. I'm sure I had Epstein Barr but my doctor told me it was elevated because of allergies.
Thank you for this interview! Valerie congratulations 🎊🎈 you are free now ! Go and live the life of your dreams !
I have a doubt that it’s difficult to find an answer. Imagine that you are taking psychiatric medication that injured your brain but you still have to taking it because it will take lots of time to wean off. Does the brain retraining still works ? Does the brain can get to homeostasis while thanking the insulting drug ?
I don’t know if anyone feels like this , I find my case very complex because involves extreme brain sensitivity, and this feeling of fight or flight in my head with very loud tinnitus especially when my hormones shifts . I basically know how I’m going to feel everyday of my monthly circle. Depending the hormones I’m more or less depress lots of adrenaline in my ovulation and crashes every hormonal shifts .
I started with a little brain retraining but I’m not sure if I should follow another route since I’m still taking this meds and have Lyme as well.
Anyone here with a similar experience that have recovered with brain retraining ? I feel my brain it’s broken 😞
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I’m having a similar experience. My big onset was due to a psychiatric medication. I’m continuously highly nervous and experience many symptoms like tinnitus, insomnia…
I became highly sensitive to many things, including my own hormones.
I have spoken to a woman who experienced something similar and was able to fully recover, although it took her many years.
As a complicating factor, I have PCOS, so my hormones have very abnormal levels too.
I would love to hear a recovery story too, as I’m working on it but am only making very slow progress.
@@lingeske exactly the same my hormones are out of wack . And I don’t know if it’s from antidepressants or cfs or Lyme … the issue now for me is that I was polydruged again so I can’t see an end of sight. Because our brains need to heal without the meds, and if it’s from antidepressants it can be taking years but I wouldn’t mind if I got better and cfs was only part of the process … nice to meet someone with same issues , although I wish we didn’t have to deal with this …
@@lingeske are you still on meds ?
@@clarissericardo2313 I’m at the moment tapering a benzo for hopefully the last time and then I would be off everything. If I succeed, it will have taken me 4,5 years from when I unfortunately first started polydrugged medications.
Let’s hope that nature is kind on us and heals us well.
I already had the hormonal issue since I was a teen. It’s not related to the medication or CFS. Although they do influence each other a ton, I’m sure.
Danke!
Thank you so much, Nathalie! I really appreciate it 💛
Thank you Valerie and Raelan! Very inspiring.
Thank you, Tanya 💓💓💓
Thank you what an incredible story!!
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Oh my gosh , this is soooooop me! 35 years with this , I just turned 61. Any possibility of having a way to connect with Valerie ????? I would love love love to be able to talk with her ‼️ Please let me know if she has an Instagram or a Facebook or a website or someway to connect to her.
Great interview! What dietician did you use?
Hi Raelan, thanks for this!
Have you found any cases of older women who recovered and were also somewhat overweight? I have not spotted any yet...
Good question - some that were mildly overweight, yes
@@RaelanAgle Thank you very much for your reply. I just noticed that all recovered were rather slim and that kept me thinking.
How can i find this lightening process thing?! Im willing to do ANYTHING and EVERYTHING to get my life back.
Just for those that don’t know Lightning process is another form of brain retraining- with a stop process
Thank you
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Proverbs 23:7. As a man thinketh in his heart, do is he.
V certainly is the new 55 emphasizing joy filled life
vs defined by age
Thanks
Thank you so much, Graham! 💓
Wow, Valerie, as a fellow 65 yr old going on 20 yrs with CFS which started with Epstein Barr, you have probably given me the final push to the lightening process. Was it hard to get thru 3 days straight though? I’m grateful for your interview. Thanks to you and Raelan !!💖💖
You got this!!!!
You got this💓
@@ceciliamac4283 encouragement is so valuable, thank you!💖
@@RaelanAgle Thanks for all your encouragement!😍
Please update us on how the program goes! I’m also looking into it. 😊
I don't know if others have trouble hearing you but I find your sound is very low. Valerie is fine.
thanks for the feedback!
Good stuff!
Valerie, I would dearly love to send you a private message if that is at all possible. Thank you.
So many people who have been homebound disabled for decades with CFS/ME and obviously living on very little income because of this situation.
Wouldn't this Lightning Process thing be shared for free?
No life and no earning a living means a segment of people who need to be helped in any way possible.
I'm not against those earning a living helping others. My only point is that we're talking about a predominantly very poor population from being disabled and help needs to reach them.
I am one of them and living on $14000 per year and lucky I have that much to live on.
The cutest puppy!!
Blue is the cutest! 💓
You can do it online???
Could it be that those with cfs that's been affected at a biological / cellular level that recovery using brain training is unlikely or more challenging? What I mean by that is those with cfs and other issues such as arthritis, osteoporosis, ehlers danlos, lupus, bone loss in jaw, sevsre gun disease etc etc these individuals don't respond so well to brain training? What I see is recovery stories of people who have cfs and just cfs no biological damage at any level.i could be wrong. Regardless its nice to see this lady recovery after a very long time of being unwell
It may be possible, BIT brain reteainong can only help bc it calms the nervous system down, whoch then allows the body to heal. Its can only be helpful if you do it, but perhaps if its something biological, it may not get you 100%, but again, biologixal things have time to heal when the system is calmed down..
Kelsie is right. Nothing happens without homeostasis. Homeostasis requires a balanced nervous system. Calming down that danger response is the first step. The more time you can spend in homeostasis the more things will change, but calming down is the very first thing that gets you on the path. For most it won't be overnight. The less time I spend getting spun up by the internet about this stuff the better I do. It's gradual.
@@FreshAgenda thanks 😊
I know so many in their 60s who are healthier than many 20 year olds!
They didn't have social media better food less stress in the while when younger this is why more and more are getting CFS fybromyalgia
How can u do it at 20%...
What is the one minute secret?
I also have Epstein Barr Virus. Thank you for telling your story.
So then Valerie was cured by The Lightening Process?
Let me guess without watching. She used LP or similar thing and recovered overnight?
In three days, after being ill for 33 years
After already doing a lot of work with diet etc.. i dont think its always possible to be thats fast, but its a true story, makes you think!!
Can you recover from parkinsons?
A carnivore diet gets good results with Parkinson.
Check Dr Ken Berry.
Wow!!!!! Beautiful interview. Beautiful lady
Both ladies. Not just the interviewed lady. The dark hair one too.