Thank you, Project Lyme! As a patient and advocate for Morgellons disease (MD), I can't adequately express how much it means to hear the mention of MD in this video. Thank you for spreading awareness about Lyme, co-onfections, and including Morgellons disease. It's so important! Your service to humanity is beautiful 😍
not just doctors, but parents that ignore symptoms. I was abused and made fun of with symptoms I had and suffered for years. Now I have chronic Lyme because my complaints were ignored and I thought all I was going through was normal.
I had an accident and lost half my vision in one eye. Diagnosis NAION. Three months later my other eye went. Very unusual to have more than a few days between eyes. My wife told her rheumatologist and he wanted to test my for lyme disease and others like that. Came back positive for Bartonella! Bartonella attacks the optic nerve. The dr thinks the event of losing half by blood weakened my immune system and let Bartonella activate.
Thank you. It's been rough. I got myself tested and it came negative I was ready to see it a negative result upon research. However my medical physician is ill equipped to help treat me. I'm doing it by myself. Thank you this helps. I am grateful for your research and experience. 🙏
Yes, that would be really helpful. English is not my native language, and I didn't study medicine. So it would be a great help if I could have the text, and Google some of the terms that are being used.
Anyone do SOT for Bartonella with success? I understand it's hard to test for because it doesn't stay in the blood? I did the Vibrant Test this past summer and it was positive for Bart., barely. But I'm thinking my true numbers are probably higher since this was a blood test and Bartonella is probably hiding.
Did SOT for Bart E. If it was effective for Bartonella Elizibethae then it triggered other co-infections to activate. No Silver bullet, Not sold on SOT.
@@zackjones7183 So are you still treating? Does Bart Eliz. come from a certain country? I have the Bart H. I heard if you knock down some infections and not treat others that can happen. My clinic advises to do ozone as well as SOT. Just because of this. Ozone will keep everything tapped down. I also added methylene blue taking daily. The clinic also added IV silver infusions for me. So I'm doing SOT, ozone sporadically, MB and now silver. It's never a one treatment disease. Can't be that easy you know. And I had already treated it seems for 4 years after diagnosis in 2016. Wasted a 1+ year on all types of herbals not getting anywhere. Then LymeStop (alternative magnetic therapy) but never gave me any pain relief. Just jacked up my autoimmune system. Then I did ozone (one-pass) for 1.5 years. It's a battle, a marathon, hang in there and try multiple treatments.
Sorry when I read Morgellons I can barely take this man seriously anylonger - do not get me wrong, I do have Bartonella from a tick bite and have a big collections of documented rashes - but this "Morgellons" is such a unscientific BS.
@@ivooMD I dug into Morgellons 15 years or so ago due to my work as a psychiatrist with one of my outpatients and I confirmed also that it seemed to be a delusional illness. But in just now googling it again all these years later, up pops this article from the journal Clinical, Cosmetic and Investigational Dermatology (2018; 11: 71-90. Published online 2018 Feb 9. doi: 10.2147/CCID.S152343) which was archived on the NIH National Library of Medicine site, which indicates it's a real thing that is related to spirochetal infections.
I appreciate that you have your own experience with Bartonella and rashes, but I respectfully disagree that Morgellons is 'unscientific BS.' It's a real condition that many people are struggling with, including myself, and it deserves to be taken seriously.
Thank you, Project Lyme! As a patient and advocate for Morgellons disease (MD), I can't adequately express how much it means to hear the mention of MD in this video. Thank you for spreading awareness about Lyme, co-onfections, and including Morgellons disease. It's so important! Your service to humanity is beautiful 😍
Thank you. We need more attention on children. They’re suffering because very few “Lyme” Dr’s will help them.
not just doctors, but parents that ignore symptoms. I was abused and made fun of with symptoms I had and suffered for years. Now I have chronic Lyme because my complaints were ignored and I thought all I was going through was normal.
I had an accident and lost half my vision in one eye. Diagnosis NAION. Three months later my other eye went. Very unusual to have more than a few days between eyes. My wife told her rheumatologist and he wanted to test my for lyme disease and others like that. Came back positive for Bartonella! Bartonella attacks the optic nerve. The dr thinks the event of losing half by blood weakened my immune system and let Bartonella activate.
Who is the Dr that helped you?
I'm in San Diego. Most rheumatologists can test for bartonella.
Thank you. It's been rough. I got myself tested and it came negative I was ready to see it a negative result upon research. However my medical physician is ill equipped to help treat me. I'm doing it by myself. Thank you this helps. I am grateful for your research and experience. 🙏
Thank you for the info.
Thank you for this important information!
Awesome video!
How did the Dr differentiate between Cancer/Lymphoma and Bartonella?
Great info! Volume is super low, but worth the strain.
How to find a doctor that will work with you.
Ya, how? I’m there too.
And finding one as skilled as Dr. Burrascano.
Hello, Project Lyme offers a known provider database on our website: projectlyme.org/providers-landing/
Great Presentation
I wish he would post his slide show so I could print and take notes
Yes, that would be really helpful. English is not my native language, and I didn't study medicine. So it would be a great help if I could have the text, and Google some of the terms that are being used.
@@ramram21 use the RUclips transcripts function. It shows you what is said for the hearing impaired. This might help you a bit.
Are ‘tracks’ always present with bartonella?
No
No.
The tender nodules under the skin sounds like Lipedema.
Have Bart. Cant tolerate abx..severe blurry vision... on mino and tinadozole
Yeast infections start anywhere IN THE BODY, fueled by high carb high sugar diet !! Sakes dude 🧐
Anyone do SOT for Bartonella with success? I understand it's hard to test for because it doesn't stay in the blood? I did the Vibrant Test this past summer and it was positive for Bart., barely. But I'm thinking my true numbers are probably higher since this was a blood test and Bartonella is probably hiding.
Did SOT for Bart E. If it was effective for Bartonella Elizibethae then it triggered other co-infections to activate. No Silver bullet, Not sold on SOT.
@@zackjones7183 So are you still treating? Does Bart Eliz. come from a certain country? I have the Bart H. I heard if you knock down some infections and not treat others that can happen. My clinic advises to do ozone as well as SOT. Just because of this. Ozone will keep everything tapped down. I also added methylene blue taking daily. The clinic also added IV silver infusions for me. So I'm doing SOT, ozone sporadically, MB and now silver. It's never a one treatment disease. Can't be that easy you know. And I had already treated it seems for 4 years after diagnosis in 2016. Wasted a 1+ year on all types of herbals not getting anywhere. Then LymeStop (alternative magnetic therapy) but never gave me any pain relief. Just jacked up my autoimmune system. Then I did ozone (one-pass) for 1.5 years. It's a battle, a marathon, hang in there and try multiple treatments.
HAHA you will get it and change your tune.....
Bartenella lol!????
Sorry when I read Morgellons I can barely take this man seriously anylonger - do not get me wrong, I do have Bartonella from a tick bite and have a big collections of documented rashes - but this "Morgellons" is such a unscientific BS.
You don't know what you are talking about, so best to keep fingers off the keyboard.
@@lou-nc4rc Keep calm and dig in your pseudo-science.
@@ivooMD I dug into Morgellons 15 years or so ago due to my work as a psychiatrist with one of my outpatients and I confirmed also that it seemed to be a delusional illness. But in just now googling it again all these years later, up pops this article from the journal Clinical, Cosmetic and Investigational Dermatology (2018; 11: 71-90. Published online 2018 Feb 9. doi: 10.2147/CCID.S152343) which was archived on the NIH National Library of Medicine site, which indicates it's a real thing that is related to spirochetal infections.
@@ivooMD is what you are doing "science"? I don't think so. Where's your data?
I appreciate that you have your own experience with Bartonella and rashes, but I respectfully disagree that Morgellons is 'unscientific BS.' It's a real condition that many people are struggling with, including myself, and it deserves to be taken seriously.