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Wow! Glad that guy found you! I had a live B. Mycroti and was put on antimalarials. I was SO sick! I can’t imagine being told it can’t be live in the blood! That poor person! Thank you for stepping in with your knowledge!

Thank you. It seems people are woefully unaware of the dangers of Lyme disease as well as other tick borne diseases. Fast and total treatment is necessary ❤

Hi Dr Cameron, Thanks for this post! Would you please share the Zithromax and Malarone regimen you used that helped this patient? I too have been through various treatments Two rounds of Doxy and also IV Rocephin for 6 weeks and felt good for 2 or 3 weeks after but then symptoms came back.

Thank you for informing the public and practitioners about Lyme and co-infections. These diseases do not behave like others most know. Bodies react differently to it. A massive continuing education effort is in order. Thank you for all that you do, by standing with people suffering from long Lyme Dr. Cameron.

Thank you for the great content, Dr. Cameron. Could Chronic Lyme Disease be treated 10 years after the bite (no proper treatment right away)? And what are the best strategies (10 years later) for reducing the symptoms, especially knee pain? I am asking regarding a young person who loves sports but can't currently do them because of intense knee pain. I would really appreciate a video on this.

Thank you for the great content, Dr. Cameron. Could Chronic Lyme Disease be treated 10 years after the bite? And what are the best strategies (10 years later) for reducing the symptoms, especially knee pain? I am asking regarding a young person who loves sports but can't currently do them because of intense knee pain. I would really appreciate a video on this.

check out the work of dr eva sapi and bee venom

Good luck trying to find a cure to the most insidious bioweapon that ever crawled under the gates of plum Island. Glad they moved it to the interior of the country. I can't think of anything that could possible go wrong on a global level.. Good luck bro seriously wish you luck, that plague has destroyed both my mother and brother and though I've never been tested pretty sure I have it too

After I garden, I feel kind of sick snd lately have an itchy scalp when I come inside. Is this from sensitivities from Lyme, like fungal allergies, etc. it seems I’m allergic to everything now!!

I have tonic clonic seizures but they only happen when I have extreme stomach pain that comes in 3 ways. So by the 3rd worst pain than I pass out. Not sure what that is and doctors can’t figure out what’s wrong with me. I have a thyroid condition.. and other health issues so not sure what could be the cause.

This is where my medical model gaslighting began, “You can’t have all those unrelated symptoms.” - Making yourself sick - Seeking attention - Too much Dr. Internet searching! And more. Practitioners, continue your education about Lyme disease and the many co-infections.

I like the way you fight the silly tik tok and youtube shorts because too many people put up shorts that are normally a waste of time to watch.

i have had a nerve conduction test and the diagnosis was”idiopathic neuropathy” still no concrete diagnosis or treatment after 8 years. diagnosed with lymes 7 months ago and treated no change in the neoropathy😢

The only Lyme rage I have is being absolutely furious at incompetent people and an incompetent system that put me in a psychiatric facility and force fed me antipsychotic medication for months after a tick bite... Then not being able to get proper lyme diagnosis and treatment in Australia because the stupid people in government refuse to acknowledge foreign bacteria and viruses exist..

CDC, NIH and FDA are just now acknowledging chronic symptoms from Lyme. There are only 2 major diseases from spirochetes in the USA, Lyme spirochetes and syphilis spirochetes. Spirochetes are The Great Imitators. Unacceptably, 50 years it is still being ignored or disparaged. Even though "juvenile arthritis" in Lyme, CT was found to be from Lyme spirochetes. For some reason, the doctor from Yale only acknowledged Lyme as a easily cured disease, not acknowledging the chronically ill and so Lyme and coinfections is now epidemic. CDC estimates 500,000 cases/yr of Lyme spirochetes. In addition, coinfections occur in 1/3 of ticks and these are not recognized For ex: Bartonella causes mental illness, babesia causes multisystems and takes months of antibiotics too. Inflammation from infections/toxins/cytokines triggers amyloid plaques from our immune system protecting us per Tanzi at Harvard. Covid, EBV, Lyme, HSV, toxins are likely the underlying inflammation that triggers amyloid plaques in Alzheimer's disease, autoimmune responses and many mental illnesses. I advocate for gov't to host a national research and education Brain Day on infections, toxins causing brain inflammation to raise awareness quickly and to recognize chronic Lyme symptoms and prevent children's suffering.

I know this all too well with my son and I both having Lyme.

Thank you from Finland🇫🇮 ❤

Please discuss the role of biofilms and the tendency for the infections to resurface after a course of treatment.

Thank you for the video. How is this patient doing know? I have these symptoms but with a heavy head and circadian symptoms so thought it was a CSF leak. A doctor now thinks it's Lyme. Have you seen Lyme patients who say their head is too heavy to hold up? Thank you.

Can you post a video on Reducing Cytokines during Lyme Treatment to reduce symptoms during herbal treatment? Thanks.

B!!

Silly study, since the rash is not the problem. And “preventing” it has nothing to do with the pathogens launched into the host.

I am so addicted to sweets!! 😢

B

😂😂😂😂😂 ❤

This was me last night. 😂😂😂😂

what medication was used to treat her Lyme Disease?

Beautiful. Thank you.

Disulfiram can cause psychosis

can you have chronic psychiatric lyme without any fevers?

The fibers are lint that gets caught between the skin and fungal waxy/ scaly coating on skin. They pull it out seems like it is within its just on the outer layer

I am diagnosed with babesia duncani. I live in Arkansas, US and have had no out of state or country travel. I feel my Dr. has no idea how to help me. My family doesn't understand how severe the symptoms are for me. My quality of life has drastically changed.

Its netherlands we have nobody...psychiatrist treat us like crazy so we do euthanisia..like your video's but wish u would advise souls who dont have medical support..🙏

I had a reaction like this recently and not taking antibiotics or medication. I am having a flare up from having Lyme 20 years ago. One local hospital St Peter's in Ny near Albany refused me care from one of their infectious disease doctors. Where can i go to get help

I never had a tic but have pots…

Any recommendations on how to start looking for a provider?

Boy, This is SO true! It’s SO misunderstood and dismissed, unfortunately, for so many people who have no idea what’s going on with their bodies! I’m trying to spread the word, but most people have no clue what Lyme disease is all about. At one point, my sister told me I had a nervous breakdown! The other sister said she thought it was strange that two people in one family had Lyme. I did have a breakdown last year from CPTSD, because of the 21 year battle with chronic illnesses and the medical system lying to me (I had a live Babesia Mycroti Protozoa and several other Lyme infections including Bartonella plus viruses that resurfaced. I was SICK!). My own former fiancé dismissing it as “an insect bite”. My 38 year-old son’s Lyme rage gave us both PTSD. He’s in a lot of pain and has huge neuropsychiatric problems, and no one can stand to be around him. It’s so debilitating and tears families apart and the losses are great! 😢🩷🙏

I actually got that! Also, can be a vaccine injury causing POTS

Thank you Jennifer and Dr. Cameron for sharing this journey of struggle and hope.

Thank you doc ... you are appreciated. I have had chronic Lyme for 4 years and am with an LLMD but just seem to continually be going downhill over this time. I guess we are all a little different and all respond differently to the meds. So far I haven't found the right "cocktail" needed. I'm thankful for your commitment to the Lyme community and bringing awareness to all. God bless

I have 2 antigens for Lyme disease .they won't treat me for lyme will not treatment. I have been sick . Rash cant go in the sun . My skin feels strange. I ache etc . This has been going on 10 years ...help

Ah, hypertension is "C".🎉

Génial ! Merci

Thank you Dr. Cameron. Too many have been accused of “lingering”. Either intentionally or due to mental illness labels such as Munchousen Syndrome- intentionally making ourselves sick to get attention. What doctors don’t know yet, I urge all to approach with curiosity rather than assumptions.

It took until 1996 to find out about Babesia? Wow! I’m glad they have the testing now because I had an active (alive, but forget what it’s called), plus various other Lyme infections like Bartonella. I was told ivermectin probably had decades of Lyme.

💖

😮

Thank you for sharing this! And also for educating people about lyme disease and the treatment for that. It is much appreciated!

Thank you for being a doctor who supports their patients, rather than dismissing them.

what about cancer patients or people going through addiction? they don't keep you up at night? ppl are suffering