God bless you, Dr. Davis! And God bless all the researchers who have chosen to study this awful disease! I know there isn't any money in it, so that makes us that much more grateful to you all! ❣
I discovered Ron Davis 9 years ago after I got sick from CFS. I have much hope in Ron and his team and others and have been following the research for these past nine years. I'm 75 now and still hope that there will be a cure before all my time runs out. Thanks Dr. Davis.
Thank you so much for your dedication and research to find a cure not only for your son but for all of us. To say I’m grateful for all that you are doing doesn’t seem like a big enough word. I pray for more funding for this research, I think once you find the cure for ME/CFS this will also be a cure for Long Haulers Covid patients as well. Bless you Mr Davis, stay well.
Thank you for your dedication, Dr. Davis! Long before C*VID, my geographic area had several outbreaks of "unknown" "really tough" viruses, so labelled by our small town doctors. These monsters began like mild upper respiratory illness and in about 48 hours the GI tract, mostly intestines, were attacked. Neurological symptoms followed for some and those who had neurological symptoms had difficulty recovering or never fully recovered. Such patients were then labelled mental which is a fairly common procedure in the U.S. No one knows how many people drag through life, or who have given up on life because of ME/CFS or other sequelae from extremely nasty, unidentified viruses.
Thank you for your tireless efforts! We’ve all seen the stat that if you’ve been severe for 5 years, you’re not likely to improve. I’ve been severe for seven years now and continually deteriorate further. My (little 😅) brain is trying to comprehend how that scenario fits with these theories? I was very severe at initial onset twenty-three years ago, relatively mild for fifteen years (with some brief moderate to severe episodes during that timeframe), now apparently permanently severe, homebound, almost entirely bedridden, and miserable. My return to severe about seven years ago was triggered by Hashitoxicosis. No idea if I could have rested my way out of this return to severe, as I didn’t get an accurate diagnosis until two years ago and didn’t realize how critical it was not to try to push through. I desperately wish I’d have known, and desperately wish for a cure. You all have my prayers and whatever financial support that I can manage.
God bless you and your son, my son is in the same medical state as your own son and has been for 18months now, most UK NHS services telling him the same old fashioned "get out more" "you need CBT". Thanks for all your doing and giving us hope.
I remember Dr. Robert Phair's presentation in 2018, which was about IDO2. Now, we're looking at IFNa/Itaconate. It's frustrating that, despite donations to OMF, we're still in the hypothesis phase for understanding these metabolic traps. I had hoped we'd be doing small clinical trials like those with JAK-STAT inhibitors etc. While I'm disappointed with the lack of progress, I appreciate the researchers' hard work. Funding is crucial for scientific advancements, and we can't expect quick results without it.
I am bedridden too due to CFS plus other symptoms like neuropathic pain in both arms and legs, too drowsy during the day and insomnia at night, extreme food and supplement or even RX sensitivities, joint pains, brain fog/memory loss, etc. For me it started when I took multiple antibiotics for extended periods of time like couple of years for Lyme, Sibo, lung and bladder infections. Holistic medicine says that antibiotics kill not only bad bacteria but also good ones and somehow it’s true for me as I don’t have lactobacillus and Bifido strains. Also, this caused leaky gut or increased intestinal permeability causing autoimmune diseases. The problem is if it’s severe, people are unable to tolerate probiotics due to Mast Cell Activation or histamine intolerance. Those who tolerates probiotics at therapeutic strength are able to get better or cured. I hope you could also look into this and ask Functional MDs regarding this. Thanks
Thank you for your work on this, it doesn't go unnoticed. Have you ever considered that traditional plant medicines might be helpful in breaking the above immune response loop that you described? Thank you 🙏
I am recovered from ME/CFS but when I was ill, I used to get bad allergies. Now, I don't get any allergies. I think there must be a correlation so something is happening in the immune system as one of the things gone wrong.
Cptsd, trauma, can cause it as well. I had it and healed myself. It can heal. Part of my healing was not to have crashes, i had to develope my day to what was sustainable with out a crash. Id do that for a few days, then id up my game the fourth day, just a tiny bit. Sometimes id do my routine for up to 15 days before id increase my activity just a bit. This was alot of trial and error until i found my pace. I started mostly bed bound, today, im a yoga teacher amd weight lifter.
Наука
God bless you, Dr. Davis! And God bless all the researchers who have chosen to study this awful disease! I know there isn't any money in it, so that makes us that much more grateful to you all! ❣
Thank you
Thank you for the work that you do. You are a true hero, and are keeping hope alive for so many. ❤
A big Thank You to Dr Davis and all the rest of the team!
I discovered Ron Davis 9 years ago after I got sick from CFS. I have much hope in Ron and his team and others and have been following the research for these past nine years. I'm 75 now and still hope that there will be a cure before all my time runs out. Thanks Dr. Davis.
Thank you so much for your dedication and research to find a cure not only for your son but for all of us. To say I’m grateful for all that you are doing doesn’t seem like a big enough word. I pray for more funding for this research, I think once you find the cure for ME/CFS this will also be a cure for Long Haulers Covid patients as well. Bless you Mr Davis, stay well.
Words seem insufficient to convey how much I wish to thank you Ron for your tireless work. May your funding increase ten fold.
Thank you for all of your hard work Ron
Thank you so much to all involved.
Great video thank you Dr Davis and everyone involved. This gives me real hope.
thank you to all involved.
Thank you. I can't tell you how much you and your work mean to me and my family
Massive thanks to you, your family and your team. Hate to think where we'd be without you.
God bless you and reward you
Thank you Dr. Davis ❤
Thank you so much for the hope! I'm so sorry you know this misery so intimately. Keep researching and fighting the good fight for so many of us.
Thank you Dr. Davis, you give me hope 🙏
Huge thank you to Ron Davis and all the other researchers who are working to find a cure for us!
God bless you. Thank you, Doctor
Thank you Ron and team ! If anyone can figure it out, it’s you !! Words can’t express our gratitude
Thank you for your dedication, Dr. Davis! Long before C*VID, my geographic area had several outbreaks of "unknown" "really tough" viruses, so labelled by our small town doctors. These monsters began like mild upper respiratory illness and in about 48 hours the GI tract, mostly intestines, were attacked. Neurological symptoms followed for some and those who had neurological symptoms had difficulty recovering or never fully recovered. Such patients were then labelled mental which is a fairly common procedure in the U.S. No one knows how many people drag through life, or who have given up on life because of ME/CFS or other sequelae from extremely nasty, unidentified viruses.
Thank you!
Thank you for hope ❤
Thank you for your tireless efforts! We’ve all seen the stat that if you’ve been severe for 5 years, you’re not likely to improve. I’ve been severe for seven years now and continually deteriorate further. My (little 😅) brain is trying to comprehend how that scenario fits with these theories? I was very severe at initial onset twenty-three years ago, relatively mild for fifteen years (with some brief moderate to severe episodes during that timeframe), now apparently permanently severe, homebound, almost entirely bedridden, and miserable. My return to severe about seven years ago was triggered by Hashitoxicosis. No idea if I could have rested my way out of this return to severe, as I didn’t get an accurate diagnosis until two years ago and didn’t realize how critical it was not to try to push through. I desperately wish I’d have known, and desperately wish for a cure. You all have my prayers and whatever financial support that I can manage.
God bless you and your son, my son is in the same medical state as your own son and has been for 18months now, most UK NHS services telling him the same old fashioned "get out more" "you need CBT". Thanks for all your doing and giving us hope.
Thank you for helping us! ❤️
Thanks for all the hard work!
Thank you. God Bless you Dr. Davis. I hope you find a cure soon. 💕
Thank you for all this explanation!
I remember Dr. Robert Phair's presentation in 2018, which was about IDO2. Now, we're looking at IFNa/Itaconate. It's frustrating that, despite donations to OMF, we're still in the hypothesis phase for understanding these metabolic traps. I had hoped we'd be doing small clinical trials like those with JAK-STAT inhibitors etc.
While I'm disappointed with the lack of progress, I appreciate the researchers' hard work. Funding is crucial for scientific advancements, and we can't expect quick results without it.
We all know this...this guy is a total champ!
🙏🙏🙏🙏🙏🙏🙏
I am bedridden too due to CFS plus other symptoms like neuropathic pain in both arms and legs, too drowsy during the day and insomnia at night, extreme food and supplement or even RX sensitivities, joint pains, brain fog/memory loss, etc. For me it started when I took multiple antibiotics for extended periods of time like couple of years for Lyme, Sibo, lung and bladder infections. Holistic medicine says that antibiotics kill not only bad bacteria but also good ones and somehow it’s true for me as I don’t have lactobacillus and Bifido strains. Also, this caused leaky gut or increased intestinal permeability causing autoimmune diseases. The problem is if it’s severe, people are unable to tolerate probiotics due to Mast Cell Activation or histamine intolerance. Those who tolerates probiotics at therapeutic strength are able to get better or cured. I hope you could also look into this and ask Functional MDs regarding this. Thanks
Me too!!!
Thank you 😍😘
Thank you for your work on this, it doesn't go unnoticed. Have you ever considered that traditional plant medicines might be helpful in breaking the above immune response loop that you described? Thank you 🙏
My man!
Thank you for keeping going with this. Hoping you get the answer and results we are all looking for soon . 🙏
SELF TREATMENT: Can someone explain what one should take to self treat? I can’t wait for the years. It will take to have treatment available.
pacing and do everything to love yourself!
I am recovered from ME/CFS but when I was ill, I used to get bad allergies. Now, I don't get any allergies. I think there must be a correlation so something is happening in the immune system as one of the things gone wrong.
What helped you
❤
Cptsd, trauma, can cause it as well. I had it and healed myself. It can heal. Part of my healing was not to have crashes, i had to develope my day to what was sustainable with out a crash. Id do that for a few days, then id up my game the fourth day, just a tiny bit. Sometimes id do my routine for up to 15 days before id increase my activity just a bit. This was alot of trial and error until i found my pace. I started mostly bed bound, today, im a yoga teacher amd weight lifter.
Lots of he says she says here. I hope you had some actual facts. Appreciate your time. I don’t have a life because of this disease.
Thank you!