Thanks Dr Younger! You are making more sense than all the other doctors (and quacks) that I have been to and read research from. I am a 41 year old male that has been suffering with Fibro/CFS/ME symptoms for the last 11 years. About 3 years ago my doctor had me taking B12 injections. Those shots took away about 75% of my daily muscle pains. My B12 blood work was never low but he convinced me to try it. I have not taken B12 shots in the last 6 months and I still don't have the muscle flair ups (Crashes) like I did before. I still have low energy, insomnia, IBS, etc. I am now taking Lithium capsules and trace mineral liquids daily and I have found these seem to help with some energy and concentration. LDN did not help me any and I didn't like the side effects. Turmeric never seem to help either. Brain inflammation makes a lot of sense for me. Ever since this started I have had a sore and stiff neck/back of head area, ringing in my ears, tension in my temples, etc. I would like to be in your research group if possible.
I appreciate the closed caption at the bottom. That helped a lot for me, someone with the usual ME/CFS cognitive impairment. Thank you for sharing this video for all the ME/CFS patients too sick to attend
YES!!! It definitely is helpful. Hearing and cognitively impaired here. I wish all of the medical speakers would. Jarred is a great speaker. He gets it out there.
At approx the 9:25 playback location, Jarred mentions a drug that calms down microglia. I am not understanding the name and the closed caption is not showing it. Does anyone know what drug they are looking at?
Thank you all at Emerge Australia and Dr Jarred Younger. You all are way ahead of present day doctors and clinicians who think ME CFS is psychological. This video should be seen by every so called Doctor who think GET and CBT will cure this
What are the 3 organic substances that had an effect? I saw a recent study with positive results using Pycnogenol. Did you research French maritime pine bark? Thanks
Well, i think we all know deep down what is causing the inflammation...I would say a complete elimination of inflammatory foods is the only cure. A carnivore diet based of organic grass fed animal products and wild caught fish and organic eggs when tolerated. Time for us to see the truth and take responsibility for our own health..
@@HaleyHolt it's the same thing but there are two parts of Naltrexone a left and a right part dextro part is what we're looking for, but like I indicated is only available two veterinarians perhaps it can be compounded but I'm not sure on that. Good luck in your research.
@@HaleyHolt I do not know what your condition is if you never heard of dr. Jared younger he is doing a research on people that have me/cfs and fibromyalgia he is funded by NIH I would also check out doctor Stephanie seneff of MIT she believes a many of The Chronic illnesses today all because of GMOs, glyphosate at and other pesticides used in our food supply of course there is no research being done on this this is her Theory I believe it's a very good one...
Dr. Jarred Younger, Calcification look for Eagle Syndrome with proper CT Images Contrast also look on x-rays & even Panoramic Dental x-rays countless with ME/CFS now have Eagle Syndrome & measure request these bones from Radiologist otherwise they will not measure them...Missed in MRI's Scans
Dr. Younger is a hero. THANK YOU SO MUCH!
you are a real hero and a Gift for Humankind.
I love Jarred Younger so much
Hi I’m Shay, would you mind telling me more about your journey with MECFS?
Thanks Dr Younger! You are making more sense than all the other doctors (and quacks) that I have been to and read research from. I am a 41 year old male that has been suffering with Fibro/CFS/ME symptoms for the last 11 years. About 3 years ago my doctor had me taking B12 injections. Those shots took away about 75% of my daily muscle pains. My B12 blood work was never low but he convinced me to try it. I have not taken B12 shots in the last 6 months and I still don't have the muscle flair ups (Crashes) like I did before. I still have low energy, insomnia, IBS, etc. I am now taking Lithium capsules and trace mineral liquids daily and I have found these seem to help with some energy and concentration. LDN did not help me any and I didn't like the side effects. Turmeric never seem to help either. Brain inflammation makes a lot of sense for me. Ever since this started I have had a sore and stiff neck/back of head area, ringing in my ears, tension in my temples, etc. I would like to be in your research group if possible.
I appreciate the closed caption at the bottom. That helped a lot for me, someone with the usual ME/CFS cognitive impairment. Thank you for sharing this video for all the ME/CFS patients too sick to attend
YES!!! It definitely is helpful. Hearing and cognitively impaired here. I wish all of the medical speakers would. Jarred is a great speaker. He gets it out there.
At approx the 9:25 playback location, Jarred mentions a drug that calms down microglia. I am not understanding the name and the closed caption is not showing it. Does anyone know what drug they are looking at?
Chris Frates dextro naltrexone?
@poodleriffic UA-cam now does this automatically as well. You can enable it on any video using the gear icon in the lower right.
Thank you all at Emerge Australia and Dr Jarred Younger. You all are way ahead of present day doctors and clinicians who think ME CFS is psychological. This video should be seen by every so called Doctor who think GET and CBT will cure this
This makes me so hopeful!
What were the botanicals
What are the 3 organic substances that had an effect? I saw a recent study with positive results using Pycnogenol. Did you research French maritime pine bark? Thanks
Well, i think we all know deep down what is causing the inflammation...I would say a complete elimination of inflammatory foods is the only cure. A carnivore diet based of organic grass fed animal products and wild caught fish and organic eggs when tolerated. Time for us to see the truth and take responsibility for our own health..
So what do we do about it?
Dextro Naltrexone is used by veterinarians right now that would be a good place just start why can't this being prescribed for people?
Wow! I need to google, I had no idea.
Is this the same thing as regular naltrexone?
@@HaleyHolt it's the same thing but there are two parts of Naltrexone a left and a right part dextro part is what we're looking for, but like I indicated is only available two veterinarians perhaps it can be compounded but I'm not sure on that. Good luck in your research.
@@HaleyHolt I do not know what your condition is if you never heard of dr. Jared younger he is doing a research on people that have me/cfs and fibromyalgia he is funded by NIH I would also check out doctor Stephanie seneff of MIT she believes a many of The Chronic illnesses today all because of GMOs, glyphosate at and other pesticides used in our food supply of course there is no research being done on this this is her Theory I believe it's a very good one...
Dr. Jarred Younger, Calcification look for Eagle Syndrome with proper CT Images Contrast also look on x-rays & even Panoramic Dental x-rays countless with ME/CFS now have Eagle Syndrome & measure request these bones from Radiologist otherwise they will not measure them...Missed in MRI's Scans