Marina is so incredibly wise about this. I was always a fan (ever since Mowgli’s Road) and always suspected that she was probably a really wonderful, beautiful, clever person. And she is.

But she healed herself or is just to overcome the illness all the time ???

You are what you drink 💦?? Just saying 😂😂

Can this work for Fnd (Functional neurological disorder)?

I only look at you tube now as I deleted all my socials as its sooooo draining. Thanks for persuading Marina to come on and talk, My house is so moldy I am looking into trying to sort that out

Great conversation 🩵

I Follow Marina since 2011 she is great strong and very intelligent person emotionally keen on , surely she will came over from generic anxiety (her symptoms told me that ) chronic fatigue is currently how anxiety developed on her ❤.

Could we get the name of the facial reflexology lady please? 🙏 also, the 20 minute nervous system reset breathwork :)

Good intervju. Rashlin explains it so well. Nice to have you back in the erher Phil 😊

Apart from being the most gorgeous human on this planet she is incredibly intelligent, well spoken, and in tune with her emotions<3

Thanks 😊

THANK YOU ANGIE. And the interviewer. It feels like a blessing from the angels I found your interview. As I have the exact same diagnoses as you Angie (EDS hyper mobile dysautonomia mast cell disease) as has my mother sister and niece. I got so sick that I lost my job a few years back. Now I am trying to heal. But am on my own with no family or anyone to help pay for medical costs. So I am looking after myself and healing with any resources I can find on you tube and social media including support groups. And so without you both sharing your knowledge people like me, of who I know (from the support groups) there are many, would have no access to this information. Like you I trying qi gong. I am keen to learn about the nervous system rewiring techniques and could not afford the course you mentioned but I believe I could buy the practitioner’s book assuming she has one. Mast cells are causing blindness now and there is no treatment and I must work quickly to heal from this but I know that I can and your story gives me added faith. My friend also healed from lymphoma and believes I can reverse my eyesight with the right attitude. I do not want to be overly optimistic.I feel i am more like you. In that it is not that I am against this “think positive and you will get well”. However I have been trying that for 56 years and it hasn’t worked. Like you said, we need to do that AND also get our condition tackled at the root cause. Just ‘being a nice person’ and who “stays positive adn smiles a lot” is more for the doctors and friends. Not the patient! How many people like to say at the funeral: she always stayed positive putting other people\s needs ahead of her own right to the end.” Is taht really somethign to be celebrated? Perhaps that is why the person is to an early death. So, I am determined to learn to say no more often. I believe my health condition is linked to not feeling my feelings. That is whyI am keen to learn more about the nervous system treatments you mentioned from your program. Qi going is definitely working but I am having a lot of torn Tissues in my ribs since two frozen shoulders from the fibrosis. So it helps me mentally and emotionally and also with my breathing. But is tearing the tissue. I am more hopeful than ever after hearing your AMAZING story. Sending you my warmest and biggest wishes for your continuing strength to strength recovery. So AMAZING ❤❤❤ I feel so happy for your and so hopeful for us all !!!! ❤ I have been diagnosed EDS and mast cell disease and told it is “genetic” and “incurable”. The more I look into this the more this looks like bullshit. Yes, these conditions are VERY REAL!! But are they “genetic”? No evidence to really convince me of this. Are they “incurable”. NO!!!!!! Science has so many holes in it here !!!! There is no proof for any of this! I am keen to connect with other patients who like me are suffering immensely but being told there is nothing they can do to heal themselves. I personally feel this is really quite evil to allow people to believe their illnesses are incurable when there are so much we could be doing. Thank goodness for social media. For us patients it has literally been a LIFE SAVER. Connnecting with non-mainstream health practitioners and patients has opened my eyes to a world of self-empowerment Things women are routinely told when they are unwell: - you are lying - you are just making it up for attention - you are just being lazy - you have a bad attitude - you are stupid - you are a bad person Do they not understand that have these kinds of character attacks levelled, on top of already being sick, is only going to make the illness worse? We need love and compassion to heal. Our health system has cultivated neither of these and they are FUNDAMENTAL to healing. Build a world of hatred and watch more and more of us develop chronic disease. The link is VERY CLEAR. Hatred creates illness. Love heals.

Wow is the algorithm hiding you from people?? It makes me wonder. I have mast cell disease and the way our medical profession has responded to this illness, and me, has COMPLETELY shattered my illusions about our mainstream paradigms. Our medical system is completely dysfunctional and really in some respects somewhat evil (big pharma and government as their puppet is REAL). Watching with interest.

Just beautiful

What is the technique she says at 5:18, I can't quite make out what she says

What a great interview, thank you so much, both of you. And thank you Phil for not interrupting this lady and letting the interview flow❤❤

Moldy homes are a huge issues for a lot of UK and London homes and flats. And landlords just paint over it

I changed to a carnivore diet and it solved my health issues I lost weight and feel loads better.

Do you know who the FEFT practitioner was?

Thank you 😊

I wish I came across your videos when I was really sick and hadn’t learned about nervous system regulation yet! Thank you for making this content!! I know this information will really help people

I always wonder how these young people can afford to travel all over the place when they’re so sick oh I think I’ll move to Sedona do they have people giving them a lot of money do they have rich parents? I am much older but when I was in my mid 30s and doing very successful and couldn’t work I certainly couldn’t afford to travel wherever that I wanted to and pick and choose where I lived. Just curious not judging

This is phenomenal he needs to get a Ted talk show ASAP he’s smart he’s been where many of us have been or still are. I love when he figured it out that it was the nervous system he said so then I went to find another doctor and he started to laugh oh my God I laughed so hard I started to cry. I so know what he was feeling like what’s the point. I was also in my mid 30s when this all hit me CFS fibromyalgia interstitial cystitis, and I went to a gentle yoga class and I literally could not lift my arms just like you said. The teacher was looking at me like what’s wrong with you I put you in a really easy class I said I can’t do this why did you put me in advance class she said it’s not advanced I didn’t believe her. Lol. I said this is for experts in yoga she said no you’re just weak. excellent excellent talk Bravo 👏👏👏👏👍👍👍👍.

You work hard so what do you expect ? Your only human Marina. Best wishes tho' Mark Liverpool x

doing a lot of plane travel can mess with your health, via emfs, time zone shifts, bugs from other travellers etc. Add to that grief, stress, overwork, vaccines, poor diet, gut issues from over use of antibiotics and it's a perfect storm for CFS. I notice she listed a lot of these things. Except for the vaxes, which are not to be underestimated. Recreational drugs like cocaine, alcohol, meth etc. can also contribute.

Hello I’ve only discovered your channel briefly but am curious if you help others recover or if you give resources for recovery? Thanks

I'm a Marina fan already 11 years and I'm always getting so impressed her strength. I love you Marina speaking about health issues it's not a sign of weakness at all.

How do you lose blood from parasite cleanse? Unless something went really wrong... Omg 😳

What an incredible story! Thank you Angela for sharing 💜

There are few health challenges more frustrating than looking perfectly normal while feeling like the end is near. Anyone with Crohn's knows exactly the dynamics she is describing; healthy and exuberant looking, but feeling mentally, spiritually, emotionally and especially physically like the life force is being drained right out of them. Marina' assessment of social media is so spot-on that I had to back up the video and watch a second time. I bailed-out on social media in 2018, best decision I ever made.

Really happy that she recovered from all that, a very inspiring story. However, she mocks people who mask and take protective measures against viral infections. Disappointing since many of us in this community are disabled from infections and cant afford to get ill again.

All of these diseases, and I have all of them, are clearly genetic BUT it isn’t what doctors say or believe it is. I think we have to stop saying that only EDS is the genetic one. They all have a genetic root cause, however they only get triggered and sustained by massive nervous system dysregulation. Most of us have the MTHFR gene and methylation issues. I was healthy until less than a year ago when I was prescribed antibiotics and then had encephalopthy from it. I, like her, had shown some symptoms since I was a child. Belly pain, insomnia from a young age, some IBS stuff, etc. but I was a very active and healthy child overall. And an extremely active adult. Until I was given those meds that messed up my nervous system and then was literally tortured in psychiatry cause no one would believe or listen that I didn’t have muscles anymore (my connective tissues literally gave up overnight), I developed POTS, MCAS issues, and over all I now have 25 diagnosis and possibly more. That didn’t happen just like this. I would not have gotten sick hadn’t been all of these traumas to my nervous system back to back. I now have SEVERE EDS, when I had barely any symptoms before. My mom has endometriosis (which falls under mast cells activation syndrome), my cousin has tons of party tricks,. Etc. the thing is: I have done so much research and bloodwork and tests and, guess what? I now have: high homocysteine levels (methylation issues will cause that), we for the majority have: low b6, b9, b12 (all symptoms of poor methylation), we develop anemia, have low glutathione. ETC. these diseases have a genetic root cause. But it ISNT A HEDS gene. There is NO hEDS gene cause hEDS is a metabolic problem, not a collagen problem. And yes, we can heal once our metabolism is back on track. But like me, it got so severe, it will take time for my connective tissues to work properly again and in the meantime, it is scary.

Wow, such a young girl getting ignored by her parents it’s just so sad all of us have sad stories a little bit different but very similar in many ways. I hope parents are waking up to what’s happening.The majority of people don’t fake illness they have better things to do with their time and going to doctors no one wants to sit in a doctors office. This just saddens me that she was accused of faking it.

Yep Western healthcare has a long way to go...

Does this work with chronic pain his method? Has anyone succeeded with chronic pain I have 20 years of atypical trigeminal neuralgia caused by a dentist who did surgery on my bone when I was down with CFS and fibromyalgia. Now they tell Dentist don’t do any aggressive work such as implants on someone who is chronically ill. I also had interstitial cystitis a lot of those symptoms are better but not the trigeminal neuralgiaAnd I still have some Neck and back pain soul just wondering if anyone cured their pain with this type of method or DNRS anything that’s similar.

I just saw a podcast of a woman who was a ballerina and developed all of the horrific symptoms we know of who did LP she said it helped her up to a point but then she stalled, And had to move on with somatic tracking, somatic healing trauma release to truly get better. She has a book I’m sorry I don’t remember the name of the book her story was just released on helmuts KZbin

Loved this interview! I can also attest to healing from EDS being possible. I think it's criminal they tell people it's a lifelong, incurable disease (when really, they don't know that). Many are recovering. And often a significant part of that recovery involves letting go of limiting beliefs and the labels of diagnosis themselves.

Anyone have the link to the program they were talking about?

I just posted in her group regarding your podcast and it was removed. I tried again and it was removed because I mentioned your podcast. It's mad how you can be platform to share others but doesn't work both ways. Mad

She's a nut job!

So she healed her Ehlers-Danlos by treating her mast cell through neuroplasticity is that correct? Fascinating interview. Only thing I struggle with is she said isn't genetic. My daughter age 4 diagnosiled with eds symptoms include sublux, super soft stretchy skin, chronic fisures, bruises easily etc. How can 4 year old have nervous system dysfunction? Not challenging just interesting

I've been listening to Marina's music since 2021 and I've often wondered about some of her lyrics, or rather their source. After this podcast, her lyrics and herself are even closer to me. I admire her for her courage and perseverance and I hope she won't have to struggle with problems like this again. We love you Marina ❤

👏👍🙏

Much woo woo :)

great interview, good to see Marina on the mend, I had issues with fatigue in my mid 30's turned out to do with silent acid reflux causing gut issues, I was constantly tired.

14:51 oh my fucking god...🙎

Heartbreaking

the only artist I ever related to. Before my 38 or so, I just enjoyed what some music sounded like but it never struck home like dozens of her songs do. So brave to just call stuff out.

Brillant,honest and coherent conversation...luv it..well done both of you

Thank u for sharing, marina 💖💖