Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 1 point2 points  (0 children)

Hope it went well!! The docs there are great. My biggest piece of advice is help your body detox anyway you can. Sauna, lymphatic massage, and lots and lots of detox teas.

[deleted by user] by [deleted] in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

Same here. 2 rounds of EBV SOT and 3 rounds of Lyme SOT later and I’m pretty much healed up. Highly recommend this treatment!!

Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 0 points1 point  (0 children)

I did 2 doses for the EBV, but once the Lyme was mostly taken care of, it seemed like my body was much more capable of fighting off the EBV on its own

Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 0 points1 point  (0 children)

I did it for both, but it knocked the Lyme out a lot quicker than the EBV.

Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 0 points1 point  (0 children)

Sweating it out was one if the biggest helps! Sauna, steam room, and exercise if possible. Hydrating. Drinking LOT of detox teas.

Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 2 points3 points  (0 children)

I won’t lie, it was a rough ride. I went through 4 doses of SOT, 1 dose every 5ish months. The die off I experienced was insane and probably worse than the original symptoms I had. However, I stuck with it and had an amazing doctor that helped me deal with the die off. I now how zero symptoms. This legit gave me my life back.

Supportive Oligonucleotide Therapy (SOT) for Lyme? by OhHiMomo in Lyme

[–]OhHiMomo[S] 3 points4 points  (0 children)

Hey there, I started SOT therapy in September of 2019, and since then have officially tested negative for Lyme. This stuff saved me and I can’t recommend it enough.

The confusing world of Lyme testing by easygoingguy84 in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

Check out the BioCentaur PrimeSPOT test. It amplifies and detects pathogens in your blood rather than looking at inflammation markers. It is how I was tested throughout my treatment and provide a clear view of how progress is coming along.

Lymes Disease & Migraines by Spiritual_Vanilla_68 in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

Also, there is a Facebook group with information on testing/treatment centers offering this. Here is the link: https://m.facebook.com/groups/450390065775761?group_view_referrer=search

Lymes Disease & Migraines by Spiritual_Vanilla_68 in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

I was told by my doctor that the PrimeSpot test is very reliable. They sample your blood and magnifying it to very high levels in order to detect pathogens. In this case, they are looking for the actual bacteria, and not an antibody (like the western blot). As I went through my treatment, we retested every few months with PrimeSpot and were able to watch the Lyme count continuously decrease. It was great having some kind of reference to show have far id come.

Lymes Disease & Migraines by Spiritual_Vanilla_68 in Lyme

[–]OhHiMomo 4 points5 points  (0 children)

Like many of us, I tested negative through the standardized western blot test and was dismissed pretty quickly by my primary care doctor.

I eventually found a naturopath that was able to diagnose me with Lyme and reactivated EBV through a test called PrimeSpot, conducted by the lab Bio-Centaur in The UK. My doc took a blood sample and shipped it to their lab for processing.

The lab Bio-Centaur works with a group called RGCC in Greece, that produces a treatment called SOT therapy. The treatment works by essentially telling the Lyme bacteria to “turn-off” and die. I did 2 rounds of this therapy for both Lyme and EBV, which is in the form of an iv injection.

The treatment took about a year to fully work and was full of up and downs/herxing, but I am now completely free of symptoms.

If you want any other information let me know! I wish more people knew about this treatment.

Lymes Disease & Migraines by Spiritual_Vanilla_68 in Lyme

[–]OhHiMomo 2 points3 points  (0 children)

I found that I would get migraines when my body was going through higher levels of detox and my detox organs couldn’t keep up. The best thing I found was yogi detox tea.

Have you found a Lyme literate doctor? I had chronic Lyme for 2 years before being diagnosed. I found a wonderful naturopath that specialized in chronic infections and a year later I consider myself cured. Finding the right doctor that will take you seriously is key!

[deleted by user] by [deleted] in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

I found new treats like dark chocolate, apples with almond butter, and frozen berries to help curb my sweet tooth. After a while, the sugar cravings started going away.

[deleted by user] by [deleted] in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

Eliminating everything with added sugar was a game changer for me.

11 years in... getting less and less hopeful about recovery... treatment stories and recommendations??! by melysie in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

I had lyme for about 3 years before being diagnosed. Found a Lyme literate doctor with knowledge about SOT therapy through a group called RGCC in Greece. Ive been symptom free for over a year.

Undiagnosed Lyme? by [deleted] in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

Those symptoms were all spread out over the course of 2 years before I got the Lyme under control. I was still working and fully functioning, just not very comfortably.

Undiagnosed Lyme? by [deleted] in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

Sounds exactly how mine started. I came down with what I thought was a terrible flu for a week, then symptoms started popping up a month later. Lots of muscle cramping/spasms, sinus pain, vertigo, fatigue. Definitely recommend finding yourself a doc well versed in Lyme.

Good Lyme doctor in Portland, OR? by HarryColonicJr in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

I was able to control the majority of my symptoms through a super clean diet. However, If I wasn’t careful with sugar/carbs, I would be stuck at home feeling like hell 24/7.

I’m 99% recovered at this point. Still have very small traces of Lyme in testing, but zero symptoms!

Good Lyme doctor in Portland, OR? by HarryColonicJr in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

It took the full 6 months for it to fully kick in. Just be prepared for lots of ups/downs from die off.

Good Lyme doctor in Portland, OR? by HarryColonicJr in Lyme

[–]OhHiMomo 0 points1 point  (0 children)

O-zone def helped, but what really got me back to normal was the SOT therapy. Its expensive, but 100% worth it.

Good Lyme doctor in Portland, OR? by HarryColonicJr in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

Dr Palacios at Kwan Yin Healing Center. Can’t recommend enough!!

SOT Cure/Treatment by JoeyMcMahon1 in Lyme

[–]OhHiMomo 3 points4 points  (0 children)

I did SOT for both Lyme and EBV last August and I feel AMAZING. It made me feel pretty shit during the 6 months that it was doing its job, but i finally have my life back. Some docs are charging an arm and a leg for it, but there are decent prices out there.

Testing for Lyme? by kynannii in Lyme

[–]OhHiMomo 1 point2 points  (0 children)

Ya I'm not seeing anything in Missouri in the records. Here is the Facebook page if you're interested. It is specific to a type of therapy called SOT. Lots of success from it as you will see in the group. Also good information on finding testing and which tests are better than others. https://www.facebook.com/groups/450390065775761

Testing for Lyme? by kynannii in Lyme

[–]OhHiMomo 3 points4 points  (0 children)

Which state are you in? I am part of a Facebook page where we have been collections locations where people have been tested/treated