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Thank you for sharing your testimony Rachael. It is very encouraging for anyone going through chronic illness to see you recover so much and keep your faith in God in the process. In 2016 developed severe nerve pain in my knees which spread to my legs and arms,at first I though it was an injury, but there was no event to cause it and imaging did not identify anything other that inflammation without a clear cause. I have inflammation, allodynia, and symptoms similar to reflex sympathetic dystrophy. After multiple surgeries and a lot of research my doctor, physical therapist and my psychologist all agree my symptoms are being generated by my nervous system a result of PTSD from work. I feel like is the first time in 7.5 years I have answers that makes sense. I am seeing the beginning of improvement with brain retraining and it is the first time I have felt confident in a treatment plan. To our Christian brothers and sisters out there, keep the faith, remember Job, James 5 10-11, 1 Peter chapters 4 and 5. And if you are not a Christian I recommend picking up a Bible and giving it a read, ESV and NASB are great English versions. Here is a link to a free download. YouVersion. app.bible.com/FCPc/ilyCM8GCtC?add_friend_id=201171919

I went to caring medical as well. Dr. Hauser is the best. ❤ I do wish I would’ve started primal trust prior to doing prolo/prp. I had multiple vasovagal responses after treatment which was terrifying and had to get a lot of treatments. Many more than you. It has helped me immensely on its own, but I truly wish I would’ve started primal trust prior to prolo. I know I would’ve faired far better. Love the birds chirping in the background of your video 🥰

I haven’t experienced much progress with prolo but I have never considered the impact that a dysregulated nervous system could have on its effectiveness. Thank you for sharing that tidbit! Definitely an a-ha moment. I greatly admire what it must have taken for you first to go through with making this video and then editing it and putting it out there. I hope you are celebrating its completion! You deserve to.

I had the PICL procedure 2 months ago and am hoping to avoid fusion. I have been following “the steady coach” and “Christina Choy” on here and the neural retraining videos are so, so helpful. Thank you so much for always sharing your story.

You’re beautiful! Inside and out! You’ve helped me with my CCI route so much. Xox I document my journey with regen and carnivore soon. CCI is an absolute beast

Hi! My body is diagnosed with CCI and also recently severe dystonia with swallowing and issues walking. What helped most with the dystonia? Thank you

Yesterday i had c1 and c2 fusion today is the second day my neck is painful 😮 im still laying in hospital bed .i can wait to get up and walk again

Thank you for sharing your experience. I have also started the carnivore diet, done prolo therapy, and done many other therapies. I am a year and a half post prolo. I love dr Hauser and Caring Medical, I feel like they gave me a year of amazing life, I however cannot afford to go back every year for tune ups. I am now completely destabilized again and back in the neck brace almost full time and using my wheelchair again. I am at a last resort for help again. I am considering the surgery. I am grateful for another opinion and shared experience to give me more to consider. I am so glad you are getting better and healthy. Ps my name is also Rachel Elizabeth lol

Thank you for sharing your story! It’s very brave. I had a total colectomy when I was 19 (before I knew all the healing modalities I know today) and I used to always wish I could go back too and not get all that intestine out bc as you know we realize it is all completely unnecessary. BUT our bodies are miraculous and are honestly way ahead of us and your body will continue to move to a new normal that is beneficial. I am 35 now and even though I’m missing 9 FEET of intestine, I function surprisingly normally. So don’t have fear about “what could be” ,our bodies know what we want and how we want to function. These bio suits are really incredible! You’ll get better and better each year and eventually a decade down the line you may even forget anything was ever done to you. Visualize your ideal outcome for yourself. I always thought that sounded hokey when I was really sick but it truly works. I wish you the best. You are doing amazing ❤

I had an artificial disk replacements on my neck C4-C6. Even though I didn’t have any serious complications I wish I had tried other treatments first. Thank you for sharing your story ❤.

My other question for you is how could have you cured yourself if you really needed decompression for the chairi?? I don’t understand how that would have been possible.. maybe there was a delay in your healing but as they told me after surgery you gotta put IN THE WORK TO GET BETTER! So idk very interesting your story..

I came see Dr bolognese and his people and as the neuropsychologist told me it’s not a cure but it can help you. Thing is we don’t know what percentage looks like for everyone. Everyone is a different case.. I did everything for 2 years and I still can’t get to a place where I wanna be my neck just hurts so bad from being unstable so I believe I’m making the right decision.

Rachael, you are the reason that I revisited brain retraining after writing it off for a couple of years, and it has given me so much more quality of life and hope. And that definitely a God thing. Thank you for being so vulnerable and putting yourself out there. God used and is still using you in my life and in countless others, I am sure. Keep being your beautiful, authentic self❤

One thought: I had a craniocervical fusion, Chiari decompression, and tethered cord release in February 2021. The next 3 years were extraordinarily tough with a chronic csf leak, immune problems, severe leg weakness around 2 years post op. But I had done brain retraining and physical therapy before the surgeries, and never saw the benefits that I am seeing now from brain retraining and physical therapy (including lymphatic drainage massage). My pcp really is convinced that 3 years post op I'm finally seeing benefits from the surgery. I really think that the anatomical changes have allowed me to benefit from pt, brain retraining, ivig, etc in ways that I didn't pre surgery. I identify with a lot of what your saying, particularly getting sicker post surgery. But at least for me, it has allowed me to benefit from other treatments in ways I didn't before.

What an amazing honest video , Rachel ..!!! I wish i could meet you in person and hug you.. You are amazing and beautiful. ❤❤❤❤

I know you’re better now and working on myofunctinal therapy. I’m not sure if in your search you ever came across LVI dentistry? TMJ/TMD PHYSIOLOGICAL POSSIONS group. They are dentists specials trained to change your bite. Not just your bite but your curve correction and air way will open better with this approach. Less invasive than fusion for those who have not heard of it.

Hey Rachel, thanks for sharing. Glad to see you're still doing so well :) I have hEDS, POTS, and gastroparesis. I've been doing pretty well though sticking to a mostly animal based diet, but one of the limiting beliefs I struggle with is knowing no.matter whay I do, I will always be hyper mobile. Like I can bend my fingers back to touch the back of my hand 😂. And I think some of that hypermobility in my spine is a cause of a lot of my dysautonomia. (Though again, I've Eben doing better animal.based and working out alot.) Sorry for the long ramble. What I was wondering was, when you say carnivore brought your body more stability, and you no longer meet eds criteria, do you mean you actually are no longer hypermobile? Thanks again!

Thank you so much for sharing! Do you feel the stent surgery helped your intracranial hypertension? Or was something else more helpful for that? I would love to try the carnivore diet, especially after hearing about your healing on it. I'm completely bedbound with similar issues as you suffered from. But my kidneys are failing due to medication I'm on to save my eye sight from intracranial hypertension. I'm not allowed much protein due to kidney issues sadly.

Thanks for sharing..🙏

A retired orthopedic surgeon said he never saw one spinal fusion patient that didn’t end up with more problems above and below the fusion. Spinal fusion is not a cure.

Thanks very much for sharing this Rachel. I can tell it was difficult talk about. I really appreciate you sharing your experiences, your channel has been helpful to me in my journey wirh CCI.

Thanks for your honesty Rachael! It is so helpful and glad you are healing :)

You are so Lucky to hace been able to have this surgery... ( Thanks GOD )... Im dying from severe AAI / ICC with several respiratory pauses during for jours, its pure hell... The worst synptom !!! With swalowing matters, simili paralysis, Heart and tension matters, vert sévère dysautonomias... sévère pain, bedbound 23h55 / 24h since several yesrs etc etc etc But unfortunately, im unable to afford even only one surgery... Im glad you recovered enought to enjoy Life a minimum

You are so Lucky to hace been able to have this surgery... ( Thanks GOD )... Im dying from severe AAI / ICC with several respiratory pauses during for jours, its pure hell... The worst synptom !!! With swalowing matters, simili paralysis, Heart and tension matters, vert sévère dysautonomias... sévère pain, bedbound 23h55 / 24h since several yesrs etc etc etc But unfortunately, im unable to afford even only one surgery... Im glad you recovered enought to enjoy Life a minimum

so uplifting and encouraging. GREAT video

Thank you for the video. I have mine scheduled for 5/20/24 and as the date gets closer I am starting to get really scared. Your video helped calm those nerves a bit. Thanks again.

Are you still taking LDN?

Thank you for your updates! I love your content!

Awesome ❤ have you ever read We Want To Live By Aajonus Vonderplanitz

Hello 👋 much love from Cleveland Ohio ❤️ have you ever read We Want To Live By Aajonus Vonderplanitz 📚

I hear what you are saying and I know you’ve spoken about all the treatments for all the PHYSICAL barriers you’ve had but I think it’s so misleading in these short videos like this where you don’t mention your de-compression surgery, fusion or prolotherapy. I really feel you should mention this every time you make a statement about the nervous system being the be all and end all because so many people are actually dying and need treatments and to have people like you with the same conditions kind of act like you’ve done it all yourself from healing your mind is a bit unfair. I’m sure you didn’t feel like you could heal yourself at the time you decided to go ahead with all of your major surgery’s…

Your thyroid is in good shape right?

Just curious if you’re following Paul Saladino for the animal based diet. I discovered him at the end of last year and it has been life changing.

I've been using you visualizations regularly! Thank you so much for doing these and confirming the brain retraining work I'm doing is important after cronic health issues 🙏

Migraine-like pain is another big symptom!

I got lyme in 1978, DONT GIVE UP! Look into the Buhner protocol. It is long but if you learn about the organisms, confections, & your physiology will empower you!! Also lcheck out chi gong! I have been using these for years. You are awesome in my prayers1❤❤❤

@Healingwithrachel Why low histamine meats? Why is histamine important? I am experiencing some issues, and i see when i drink anti histamine medication it has some impact, but i just connect it to polen. From your experience, how is this connected to CCI

Were you bedbound for an extended period of time?

Take heme iron supplements for management. They made all the difference for me. Women are constantly loosing iron (and men too in case of surgeries fe)

Thank you! That is very insightful and helpful.

I like watching ur content

Amen! There is always something that we can do right now in this moment to begin the process of improving our well-being, health, and experience of life!

This is so helpful, It has calmed my nerves about going. I've had low iron for 3 years, finally getting an infusion and my doctor thinks it could be Celiac Disease. Hope you feel better now.

Hi Rachael! Do you supplement with vitamin c? I also have hypermobility and other issues, like eosinophilic esophigitis and am currently healing🥰

LDN is not known to be toxic like other drugs and has been used (and studied) for at least a couple of decades for numerous diseases - the list is quite impressive. I suspect it is effective because it gets little press, it is simple to use, and inexpensive. The patent has run out. I asked a pharmacist about it who has customers who are prescribed it and he stated as I recall that their cancers were in remission. But if you are healthy and don't need it it's not a loss and the body and mind were created to heal itself if the right conditions are met (e.g. Dr. John E. Sarno/ TMS & , Dr. Ryke Geerd Hamer /"German New Medicine", Dr. Arnold A. Hutschnecker "The Will to Live", Dr. Joel Wallach "Epigenetics - The Death of the Genetic Theory of Disease Transmission") which begin with peace of mind/rest, clean air/water, and healthy food plus the will to live. The widow of Dr Bihari (spelling) uses it as a cancer preventive as I recall. Interestingly she stated her late Husband would first ask his patients what happened to them 6 months prior to their illness. In other words, some event took place that affected them emotionally and was the catalyst that began the cycle of disease.

leafs fall in april? 😅

Oh my goodness you’re doing so well!! You have to do a video on how you get your breakfast eggs to look that way 🥺 they look so good lol I can never get mine to look that way

Chickens rock! Does he also eat carnivore or keto?

DNRS didn’t work for me.

I've always been looking for an answer to this. Thank you for posting this video. I have chronic Epstein barr virus and am hoping brain rewiring helps with this, but I also have a spinal fluid leak, which is totally structural. Blood patches have failed, and my next step is surgery. I just don't want to go forward with surgery right now, since EBV has flared and is making me quite ill. I really don't know if brain rewiring could help a csf leak though? My leak was caused by an epidural needle. I just feel like this might be an exception where brain rewiring can't fix the problem, but I know that is such a limiting belief! So hard.