Can you please write those 2 names?

Well i am about to start my ID rotation part of training and we follow chronic lyme disease patients. And its part of my family medicine training. So i will always follow my chronic lyme disease patients. Not living in the US though. 😅

Thanks, Dr. Ducharme. That was a great summary of the AcuDart test!

Where r u located?

Please inform me how about taking Inmunocal ? Saludos desde México !!! Gracias

Thank you so much for sharing this information! I have been working with Dr. Jules at Restor Medicine for several months now. I have Lyme disease, Mycotoxins, and Mast Cell Activation. My treatment at Restor has really changed my life. I was crippled and unable to walk for nearly 6 months and I can walk again now. I've gained 20 lbs and am excited to start using semaglutide in the next week for weight loss, inflammation, and many other benefits. I feel the need to eat every 2-3 hours and cannot wait to be alleviated from that burden! Thank you so much for the amazing life changing work you and your staff are doing at Restor Medicine! ❤🤗

We always should prefer nac and glycine (glynac) for glutathione compare to pure glutathione because with precursors, body can make only the glutathione that it needs

I take 500mg glutathione capsule and 600mg NAC for maximum glutathione.

Taken at night, LDN is the difference between me wanting to live instead of die with LC. It’s not a panacea. I have to do all of the other things. It does reduce pain, fear, and anxiety.

I did urine test last year and since then I’m completely bed bound to this day

I was planning to see infections disease to treat co infections

Having horrible symptoms; have moved out of our home; just made appointments with you…🙏🙏

In a nutshell you didn't explain how SOT works because you barely understand it yourself.

We can just inject glutathione ourselves. that’s what we do. We buy gluten from peptide sciences, reconstituted ourselves, and use it once a week just to maintain health.

Four months in, Chronic fatigue and all its side effects, I’m markedly improved. No side effects that I can tell. It took a while before I began to really improve, at least two months, but after much experimentation with dosage, I have settled approximately on 3.5 ml before bedtime. I do shift work, at sea, 6 hours on 6 hours off, and when I’m doing this I take 3 ml before each sleep break, so that’s 6 ml per day in 2 doses. That’s the best for me. Mood is much improved, aches and pains are mostly non existent, energy is vastly improved, so good.

Kind of interesting: The one gentleman mentioned a symptom like walking on glass. Plantar fasciitis is one of the very first symptoms (other than a lot of mucus in my throat at a young age) and it turned out I have huge antibody titers of EBV and CMV. I had my first SOT today. I've been miserable for 18 years since I had a Shingles vaccine (Zostavax) which completely ruined my immune system (and my life). For the last three months I've had heavy metal chelation treatments which are really helping. I'm hoping that the SOT treatments will be the coup de grac' so I can get my life back. It's been a very rough road. All the best to you folks!

I have hand arthritis that came on out of nowhere. Positive for bebesia, h pylori, sibo, mold. None of it appears to be a large positive 🤔🫣. Hand, fingers & wrist pain, swelling and stiffness but not sure what the cause is. Is this doctor a good place to get checked out? Thanks

Any sexual side effects in men that you’re aware of ?

Thank you. Fantastic information, the best I have come across.

Because it’s made up

Has anyone tried oxytocin spray for calming down the body?

❤

Good talk . Thank you

How long before I see results?

We are so fortunate you followed your passion. I've read most your books and it helped me understand so much about my condition. You have quite a gift for articulating medical concepts most regular doctors don't even understand.

Please add the links to the documents you mentioned you'd put into the chat; thanks so much! 😊

The screen of the conference update is not in focus

IFS (Internal Family Systems) therapy has been HUGE for me. It's similar to EMDR but a little more gentle on the system, so may be better for Lyme patients. The book "No Bad Parts" by Richard Schwartz explains it well. Highly recommend IFS!

Nicola I think you made some mistakes in this video...there's no bio and you said it starts Aug 22.

Ok?...no bio, no link...

Good video ladies, thank. you.

Include some case studies of chronic Lyme sufferers where nothing else worked until they did SOT please.

Can you do SOT if you are on Skyrizi?

The S in SOT stands for scam.

what do you do about swollen lymph system in the legs Nicola?

thanks nicola

Well done!

What’s a good digestive enzyme with high proteolytic enzymes?

Great news! Thanks for sharing - I've passed it on to the San Diego Lyme and Mold group :)

Hi :) Which food sensitivity test are you currently recommending/using?

😋 'promo sm'

Hello there :) do you have any thoughts on the topic of reinfection? People who are going through treatment for late stage Lyme + co who are then reinfected by a new tick? Have you seen that happen before?

There haven’t been too many studies on this. Is there a reason why? Does RGCC plan on sharing their findings openly? They aren’t that transparent on their website as to how they create the serum etc. Also with Bartonella it’s usually always in tissue and rarely in blood, so how do they create the SOTs for Bart?

Great video~ yes, ILADS search database is how I found my doctor, I also searched the database for the American Association of Naturopathic Physicians and she was on both lists. Before I started getting treatment under her care, I saw an infectious disease doc who was the most condescending, arrogant and sexist doctor I’ve ever met. Not the first, but the worst. I explained my 35+ symptoms and travel history/ timeline. I went to see him because I had a fungal sinus infection (that was only one issue out of many)- that is 100% within the scope of practice. After I explained my exposure and symptoms he looked at me and said: “You do not have a disease. You do not have an infection. What you have is a psychiatric disorder.” No tests. At all. No referrals. He lied on the visit summary and said I had NO symptoms. For diagnosis he wrote “Somatic Symptom Disorder”. I had enlarged lymph nodes, fever, chills, sweating, shortness of breath, headaches - these are obvious signs of infection. The anger I feel about this is immense. I went to the ER the next day, and the ER diagnosed a kidney infection. 1 month later, I discovered that I have 3- I repeat-3 strains of Lyme (American European Asian), Bartonella, Babesia, Anaplasmosis, Rickettsia, HHV6, Epstein Barr reactivation, Parvovirus 19, CMV, Toxoplasmosis, and f*cking TULAREMIA. Plus Candida parapsilosis, Candida krusei, Aspergillus colonization and Black mold. My PCP recently referred me back to the same infectious disease department since my Tularemia diagnosis. Different doctor on request. We will see how this goes…..

www.drnicoladucharme.com/transformational-healing-academy

Hello Dr. Is it true that if we take Liposomal Glutathione it would only get absorbed about 5% into our body ?

Does this cause skin rashes?

Yayyyy! The Cavallo-Rholl family is SO excited that you are bringing SOTs to RestorMedicine! You may be hearing from us soon. ;)

Brain frog first, couple weeks later, sick, couldn’t concentrate, then swollen turbinates and clogged nose, fever after fever and llergies, now sinusitis, and then antibiotics 3 times during the whole thing. Now a year later trouble breathing all the time, nose always clogged and dry, can’t smell or taste for most of the day, trouble sleeping panic attack and anxiety, and the ent just keeps trying to give me antibiotics, a spray and stroids and nothing changes

I’m a proctor