Bluebonnet08's Posts | DailyStrength

Status: Closely following the research out of The Open Medicine Foundation Website: https://www.omf.ngo They just found a biomarker for ME/CFS. The lives of many, including myself may soon be changing for the better!!

Mood: Horrible

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New Research (2019 Symposium)

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Hi Everyone- Hope you are hanging in there. This disease can be so terrible :( I just wanted to post some updates on the current research for ME/CFS. For those that missed it, the 3rd symposium held by The Open Medicine Foundation was on...
ME/CFS Symposium (Available Online)

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If anyone is near Stanford in California this would be an awesome symposium to attend. The best and the brightest will be there for ME/CFS research. The price is discounted for ME/CFS sufferers and caregivers. It will also be live streamed and...
Harvard & Stanford working on ME/CFS

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Scientists from Harvard and Stanford are now working to solve and understand ME/CFS. It's very exciting to see researchers working on this disease. I think they are gaining some...
Poems of HOPE written by those with ME/CFS

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These are absolutely beautiful poems/art by ME/CFS sufferers and caregivers. Worth a read. You can vote on your favorites. They are making the top winners into a video. https://www.omf.ngo/poetry-submission/
New Research- Close to finding a biomarker & test!

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This is what I received in my email from The Open Medicine Foundation - a new research study has just been published on Red Blood Cells and ME/CFS. I have attached the synopsis below. It is VERY exciting! It looks like they may have a...
A message of hope from Dr. Ron Davis

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https://www.youtube.com/watch?v=VScir4Dfk58A message of hope & optimism from Dr. Ron Davis
Newest Research - Potential Biomarker

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The newest research out of The Open Medicine Foundation.. a potential biomarker for CFShttp://www.bloodjournal.org/content/132/Suppl_1/4874?sso-checked=true
Funding for Research

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The Open Medicine Foundation has been making a lot of progress into a possible root cause and cure for ME/CFS. As a result of the latest symposium, 2 anonomous donors have stepped forward and agreed to TRIPLE any donations recieved for the next...
More research updates

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A blood test that is 84% accurate in testing for CFS:https://www.medicalnewstoday.com/articles/322414.phpThe newest research - a must...
CFS research updates

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The latest updates in the CFS research by Dr. Ron Davis:https://www.youtube.com/watch?v=WmI5Ri0V51U&t=1993s
Update

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Just a little update - I had a round of lab tests. It was found that I had very low levels of B-12, Vitamin D, Ferritin (Iron Stores), & Iodine. I've now gotten them all within range and feel it has helped a bit with certain symptoms (anxiety,...
OMI-End CFS

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Does anyone else follow the research out of the Open Medicine Institute? https://www.omf.ngo/the-end-mecfs-project-2/I am hopeful that they will find a cure & treatment!!I am seeing a doctor from the institute right now. I am starting some...
Interesting- Low Ferritin & CFS

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Thought this was an interesting article:http://www.vitality101.com/health-a-z/Cfs_fm-treating_low_blood_volume_and_heartI will say the saline IVs have helped me. I am also now taking steps to address my ferritin levels which were bottomed out at...
Saline IVs

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Just wanted to post this:https://www.healthrising.org/treating-chronic-fatigue-syndrome-mecfs/drugs-for-chronic-fatigue-syndrome-mecfs-treatment/iv-saline-solution-for-chronic-fatigue-syndrome-mecfs/The IVs have helped me. Before I was pregnant,...
23&Me

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Has anyone done the 23&Me genetic testing? If so, did you find anything interesting or useful from it? I've been looking at it for a long time, but not sure if it's worth the money. Thanks :)

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