Thank you for sharing your story. Feeling seen over here. You’re not alone in it. Praying all these stories really take traction and turn the tide in the medical world for the next generation of lyme+co generation.

Lyme’s Disease is a worldwide epidemic 😱😱😱 There are millions of individuals who have been undiagnosed and/or misdiagnosed & have fallen through the cracks of the medical system 😰😰😰 I was bitten 6 years ago by multiple ticks, and as a result, contracted Lyme’s Disease along with 12 other Co-Infections 😖😖😖 My story has been horrific as well 😰😰😰 The pain that it cause was excruciating 😰😰😰 Pharmaceuticals were entirely ineffective 😰😰😰 I was tested for Lyme’s Disease ( CDC ) twice & the results were both negative 😳😳😳 In my desperation, I sent my blood to the Armin Lab in Germany for an accurate analysis and received the results within a few weeks 👍👍👍 I’ve been on a modified version of Stephen Buhner’s Protocol along with several supplements 🥹🥹🥹 I’ve also had to drastically alter my diet as I had developed severe food allergies at the same time 😖😖😖 I’ve been currently pain free for 1 year now 👍👍👍 I hope that this info will help other victims 🙏🙏🙏 God Bless

Osha root, fringed sage, and lomatium root cured my lyme

Ever heard of cfs, chronic fatigue syndrome? I've been wanting to try sot therapy myself. Atleast test for everything that could be corrected with sot. As I feel it could help in my fight with cancer. Unfortunately much like the possibility of Lyme. Drs never addressed the tumor they messed up and left in me for right about a decade by the time I self diagnosed.

Methylene blue has been working for me.

So you feel the mind/body training and drawing safety into the body has been the missing piece? My story is similar but EBV vs lyme. Dx w MEcfs POTS FND etc etc. I have connected the pelvic pain with trauma (specifically whenever i deal with my mother, interestingly! Also connected my migraines to her) and the psoas muscle. I actually typed that before you even said psoas lol. And yes! Thanks for mentioning cell danger response

I hope you get more shooting stars of hope across your dark sky. I see you! I know the dark pit and just wanting to be done. I hope you can find that moment by moment hope. Also doing some brain retraining and it is nearly impossible to do in those dark pits.

Thanks for sharing, 15 yrs in hell for me and I am on my first dose of antibiotics after found lyme .. I have been so alone on this journey but one day at a time and keep fighting 💪

Holy cow, I have been experiencing nearly exactly the same psychological symptoms for about the same period of time! I got diagnosed with Lyme about 9 years ago, and while treatment did help, my mental health declined for no discernable reason. Zoloft did help to pull me out of it, but I always spin out of control after I'm off SSRIs for several months. I am also dealing with a lingering Bartonella infection (most likely). I and my naturopathic doctor suspect MCAS (Mast Cell Activation Syndrome). I'm sure you've heard of it. The immune system can get in a stuck state even if there isn't much danger. I am currently doing LDI (Low Dose Immunotherapy) to help retrain my immune system to stop attacking my brain and giving me needless anxiety/panic/doom. I didn't watch the whole video, just skimmed parts of it, so I don't know what else you're taking to help manage, but here's what I've found helpful: - Quercetin supplements (There's a good quercetin + bromelain supplement on Amazon), eating foods with quercetin is not enough, we need a clinically higher dose with this condition - MAGNESIUM: Our bodies churn through a ton in this overactive state. If you're not taking supplements, I highly recommend it. I am using two brands: ReMag Liquid Magnesium, and Magnesium Extended Release from Mother Earth Labs. I just started on the latter a couple days ago and it's making a world of difference. I also take two packs of LMNT per day. - I have found Qigong to be helpful for moving that energy that constantly builds from the racing mind. Doesn't work all the time, but it can be more effective than standard meditation. - Gut microbiome is a big player as well. It can be helpful to do stool testing to see the state of your gut, but regardless of testing I have found that drinking raw kefir daily to be a stabilizing factor. It's easier to tolerate with a dash of maple syrup or vanilla extract. Also, if you have leaky gut, an Akkermansia Muciniphila supplement can help restore the lining. If you're in to DIY stuff, there is a beneficial bacteria called L. reuteri that produces oxytocin which can have a naturally calming effect. I make special L reuteri yogurt weekly and it has also made a difference. There are plenty of good tutorials on KZbin. If I remember anything else, I'll add to this. Calling it hell is no exaggeration. I feel you. There are truly no words for this depth of suffering. Brain retraining can help, but I think that's for a later stage when the nervous system will be responsive to that type of treatment. It's only good for after we get a handle on the excessive inflammation. Still it's good to keep trying it for those times when it does help. The Joe Dispenza stuff works if the body has enough support from other areas. Regardless of how it feels, it is certainly a display of power to persevere and share your journey with the world. I salute you from within a similar pit of hell.

I also suffer from Lyme so I appreciate you using the little energy you have to share healing information with other people with this disease. The more I research Lyme, the more heartbroken I feel because too many people are suffering from this agony. Your message resonates with me. I also suffer from PTSD and I've suffered emotional hardships and betrayals during my life.

Would you say that SOT didn't really do anything?

Hi Gabrielle, I’ve been following your channel & tuning in for a while now. I feel you. Relate in so many aspects. Our journey is immense. I discontinued the sot route & took a leap/changed my approach. Completed Sanoviv’s 2 week program in February. I’m still working with a naturopathic dr back in the states getting eboo/plaquex/peptides, but just wanted to let you know Hyperthermia with iv abx really moved the needle for me. Post 3 months, I’m in a much better place mentally, physically & spiritually. Retesting in June to see where I’m at with all of this. But yes, you need both mind & body. We are holistic beings. Treat the physical but take care of your mental/emotional & try your best to address nervous system retraining. I love primal trusts program & it is a reasonable monthly membership with anytime cancellation. Her first module goes all in depth as to what you’re talking about.. cell danger response, polyvagal theory, limbic system impairment, etc. Think it’s interesting how you mention the Pelvic area/psoas being connected with fight flight & insecurity. That’s Lyme in a nutshell. It is heavy on our nervous system, doesn’t necessarily matter where in your body it is but yes I have issues with neuropathies in my hips & at one point couldn’t even walk when I was at my worst point undiagnosed & unknowingly living in mold. But anyways, the whole concept of nervous system rewiring is to utilize your conscious mind to reprogram your subconscious & all of the chronic stress loops that have developed over this period of time being so ill. To bring your body back to a calm state & allow your body to help itself heal. I still have neuropathies in shoulder, back, hips & knee (which have improved). All the other symptoms that were suffocating my soul & keeping me bed bound, however.. the anxiety, depression, brain fog, fatigue, gi distress.. has very much dissipated since hyperthermia. It doesn’t work for everyone, but it sure as hell worked for me & am so glad I did it!! If that’s something you are interested in knowing more about feel free to ask me about my experience. In honor of Lyme awareness month, I just want to say thank you for sharing your story. I see you & I hear you 💚 Sincerely, Anna :)

Not sure why but your video was on my recommended page so I just clicked on it. I'm so sorry to hear about your struggles. I'm sure all your friends/family/internet strangers have given you "all the advice" but I am currently on a low carb diet and watch a lot of carnivore testimonies. There have been many folks who have cured (or nearly cured) their Lyme by going full carnivore. If you type in carnivore lupus you'll see some of their testimonies. Just throwing it out there as a last resort!

Hi Gabrielle you symptoms are exactly what I'm dealing with. Please do a follow up on your progress. I need to look into SOT. Keep fighting the fight. It's terribly hard I know.

i think it's important to get on some type of mood stabilizer before trying to kill lyme. It will destroy you mentally if you don't.

How are you doing now? I've used herbal therapy, some antibiotics, and some ten pass ozone. Feel like I've lost some ground. I might have to look into the SOT idea. I had a weak pos igg via igenex, a neg thru LabCorp and MDL. It's all confusing.

you mentioned ozone therapy. was that Direct IV Ozone gas directly into the vein?

Covid can reactivate Epstein bar, which I believe you said you have. Have you ever thought about getting an ENT treatment for that virus.?

Please talk more about the money aspects.. insurance.. ect??

I’m sending you love and prayers for complete recovery and wholeness. It’s possible to completely recover. I’ve walked that journey with a different disease. Keep moving forward. You can do this. ❤️♾

Did u go to Tennessee or San Diego Ca?????🫶🏿

How are you now?

Where do you get your methylene blue from?

I was a Genesis patient for 18 months 22’-23’, followed their antibiotic/antiviral protocol until I was dry heaving all day when standing up or walking and had to stop. They didn’t find out I was positive for Babesia until post SOT which got me very upset, their poor attention to detail on my SSRI medication was the final strike for me. I see a new co-infection doc tomorrow, I plan on a retest on everything and if anything else was missed, I’m late chronic 15 years. I’ve been plagued with meningitis symptoms the last couple years. With the high risk for brain damage/Alzheimer’s, I’ll be requesting a MRI. I’m about 80% better physically but mentally I have not recovered. I was also very low on testosterone (test I requested), might be worth checking and your estrogen levels. 💚

I AM WITH YOU,I AM VÈRY ĎESPERATE..

Hi you need to go on green juice diet you need to stop feeding Lyme in your body get ozone therapy and hyperbaric oxygen and vit c in dripp for 30 days drink green juices for 12 months to starve of the infection dis is like.no.other bacteria

I did emdr therapy n this helped me Theres an app by mark grant that’s awesome

Thanks so much for sharing This could be my story. Could you let me know approx how much it cost? Would you do it again?

What is s.o.t??

Thank you for sharing - I am sorry it’s been so hard! But you’re willingness to share even the hard parts is so meaningful!

Relate more than you know. Sending you strength.

Hi Gabrielle! Everything you say is so relatable to me. I feel what you’re going through.. the mental, physical & spiritual challenges this experience puts us through is very much real. I like you I am human & have had very dark moments on this healing journey, but choose to see this as an opportunity for growth & personal enlightenment. I just wanted to let you know I completed 8 sots. Last year I was at a good place after my first round of sots & weekly ozone one passes for months. But then like you, I hit a plateau. So this year I decided to retest & get more sots. It seems over time sot therapy has reduced my infections based on my reports, but it hasn’t gotten me remission & when I stopped the ozone I even started to decline. After so many sots, I feel I have given this modality a fair shot. So now I have been changing my approach. I’ve been doing hyperbaric oxygen therapy which has helped get me in a better place again (hit another low point in the winter after multiple colds, more mold exposure, really bad herx reaction to my babesia sot & reducing the frequency of one passes ozone’s I’d get), but still no remission after a couple months of it & hit a plateau. So now I have just recently received 200 million embryonic stem cells in hopes to allow the body to regenerate enough so to the point my immune system can reduce the infections on its own & repair any damage they have caused. I also have heard of a very effective version of ozone called eboo. I’ve yet to try but may be worth looking into as it sounds you do well with ozone. I should know by mid December if embryonic stem cells worked for me. Hang in there. Hope this insight helps & I will keep you posted!

Thank you for sharing. I'm so sorry that you're struggling right now. " Acceptance " of chronic illness is incredibly difficult, but it eventually saved me from my crippling health anxiety. I've fallen into the depths of darkness and spent way too long there. No matter what condition that you are in, it's always better to accept the moment and stay mindful than to worry about what is coming. Try not to anticipate anything. Bad or good. The future is completely out of your control. It doesn't mean that you shouldn't plan and fight with everything that you have and explore every option available to you. It's simply releasing the burden of your situation and the outcomes of your efforts to the universe. You're not in control. I know that you understand all of this, but I can relate to what you are going through, and I wish i could help. 😘

Sorry you are not fully better! What did the genesis center say as to why the SOT has not worked? It sounds like the SOT was working then COVId messed it up. Curious what they said needs to be done next? My blood is at RGCC and waiting on my SOT now. 🙏

Sorry you got covid. That was a big fear of mine but I am a big believer in medical ozone so I bought an ozone generator years ago. I learned how to do BOOO (breathing ozone through olive oil) and I suggest learning that. No one can take your ozone generator from you and will help you in the future. Learn to do other at home ozone therapies because they are cheaper. LymeStop did not help me. I went there August 2017. He claimed I had Lyme plus everything. I had previously done the test DNA Connextions--it was positive for Lyme +Bart. I had already tried all the herbals possible for 1.5 years with no pain relief. So I opted for LymeStop. So did Mr. Smith's magnetic treatment and I was incredibly sick for 4 months, never had any relief and went back for that checkup. As I stood there is pain, in my whole body, nerve pain down my entire leg, he claimed I was cured. It was surreal. That he could say that to my face. I cried all the way home. I did HBOT about 20+ times with no improvement. Then sought out a local ozone clinic. Decided to do weekly IV ozone treatments and I hexed horribly the first week. Proof Mr. Smith did NOT cure me. I continued the weekly treatments and felt ill every time. I went for aprox 1.5 years, missed a couple months, had great improvements but couldn't get to normal. No further help from those NDs at that clinic. So I'm going in circles again. Tried LDI from two different NDs, it didn't work for me. Long story, short, still at it, looking for relief from ongoing chronic lower back pain, nerve pain in left foot since 2015. Went to yet another clinic that offers ozone. The young ND fresh out of school, suggested I test again and told me about SOT. I agreed to the test and it was Vibrant testing. I was still positive. Maddening but it made sense. I did my 1st SOT for Lyme last week. Preying this gives me life back. I'm also going to do some more ozone as there's a couple co-infections, bartonella being one still on the border of concern. I believe it's been in my body for 50 years. What a nightmare. My health took a nose dive about 10 years ago and I haven't been able to get better. I hear ya. Thank God I didn't get covid but I had my BOOO kit handy and did it for prevention.

Can you give us an update ? :)

I'm very proud of you and this is a very good and beneficial series.

Any update on how u feel now with SOT? I have had Lyme for 9 years and been treated by LLMD for 8 years and while better I still suffer and thinking of doing SOT. I am looking into going to TGC in Georgia which is where I guess you are going. Are you happy with them? Please any info would be greatly appreciated!

Covid, can you take zinc. Great for colds floo. Can you say the clinic?

You look better

Thank you for this! I'm getting ready to start my treatment.

How are you know?!

6 month update?

Thanks for making these videos. The covid stuff reminded me of book I'm listening to on audible. A bit of an inflammatory title but it's just series of eyewitness testimony of what people went through with covid. Has good info on covid treatment. May consider microdosing nicotine for vagal tone. Book is entitled rise of the fourth reich. Another good book is Bitten which is about origins of lyme.

Im sorry that you have to go through this. You have to be a strong woman especially as painful for you as it is him and he tolerates pain well. Not this type of pain. My husband is a tree climber and we been dealing with ticks daily mostly during the summer for the past 20 years. It was like a normal thing checking for and pulling ticks off sometimes there would be a bullseye and sometimes not. About two yrs ago my husband was sick flu sick we thought then the next day he was like paralyzed in so much pain it was awful. We went to a dr and he was diagnosed with chronic late stage Lyme he got a antibiotic and that was it out the door we went. No info no follow up. Can u point us in the direction you choose? He just went through another episode. It’s so sad. There has to be something more research. It shocks me there isn’t or very little research done. How do we look into SOT?

lots of good research on the value of optimizing Vitamin D levels. this really helps our immune system to minimize the effects of Covid, shots, etc.. Take Vitamin D along with Vitamin K2 & Magnesium! Your vitamin D levels need to be at least 60-80 ng./ml. check these levels ( via a blood test) at least once year... ideally twice/year. Magnesium will help calm things down. A magnesium bath before bed will help with sleep! There are many forms of magnesium. I recommend alternating between Epsom salt baths ( magnesium sulfate)( inexpensive!) & magnesium chloride baths. When you go to bed, make sure the room is completely dark and the room is cool/chilly. You will sleep better. Cheers!

Sincere thanks for putting your lyme story out there. I've been fighting it for 3+ years. The symptoms are unreal, multisystemic, and often difficult to describe. Validating for me to hear others describe their symptoms, treatments, and ultimately, improvement. Much appreciated.

How long was you real bad? Did u have blood pressure issues

Thank you sweetheart your so nice.

Hey Gabriella, when I got the first covid vaccine, it caused my symptoms to increase. I was just wondering if anyone else experienced that. I'm struggling to live everyday. Just started antibiotics for the first time 3 weeks ago, so far, no progress. Been on suppliments for about 4 months, and there is no progress either. Thanks for your video. It helps to know others are out there.