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My ME/CFS expert, Dr. Susan Levine, said she is very excited about fecal transplants (FMT) being a promising future treatment. I have been very interested in trying this for a while given I also have IBS and my ME/CFS started with GI symptoms. I know FMTs are something that has been talked about and tried in ME/CFS for a while, but the field is continuing to grow every year with a better understanding of what a healthy microbiome should look like. Dr. Levine said it is crucial to get an excellent donor, which can be a very hard task, but this should get easier in the future. Maybe this is why she considered it a "future treatment."
Does anyone have experience with this and know where to try it? I understand you can either do it at a clinic or diy. I think diy is too risky for me and it would be really hard for me to find a "perfect" donor that makes up only 0.1% of the population. I am willing to pay a fairly large amount of money for a very reputable clinic/donor, and if anyone has any information please share!
One last note: Dr. Levine, who has been treating ME/CFS for decades, told me she is very excited and optimistic about the future of ME/CFS treatments currently! Who knows what information she has that we don't, but I thought I would share this.
Does anyone have experience with this and know where to try it? I understand you can either do it at a clinic or diy. I think diy is too risky for me and it would be really hard for me to find a "perfect" donor that makes up only 0.1% of the population. I am willing to pay a fairly large amount of money for a very reputable clinic/donor, and if anyone has any information please share!
One last note: Dr. Levine, who has been treating ME/CFS for decades, told me she is very excited and optimistic about the future of ME/CFS treatments currently! Who knows what information she has that we don't, but I thought I would share this.