@Silas33@kimisgubbed@MaritSkotheim "I feel that I have looked down the barrel of the ME/CFS gun and disarmed it." He implies that it is risky to his own health to listen to those who have not recovered. He may feel more invulnerable if others join his personal crusade? https://t.co/Me08M60njl
@Naomi_D_Harvey I think people recommend inosine because inosine pranobex (Imunovir) is expensive and difficult to obtain. Discussions ongoing here, for many years:
https://t.co/4nULvvKXQq
@davidtuller1@JanetDafoe@TimesONeill Beautifully written, David. Your heart shines through in everything you write. So thank you for enduring for the sake of Maeve and so many others. ๐น๐
@GayKiwiDan @aparachick It's natural to feel that way when the institutions you have relied on fail you. Sadly, people rarely understand anything that doesn't affect them personally. Govt. will always claim they don't have money to help. People living with M.E. know exactly what you mean. ๐๐น
@SerpinaLonghaul@exceedhergrasp1 Dear Healthy People who are paid to understand the condition you are researching. Try harder to do so. Take a break if you need to. We have been waiting decades for you to understand that your break schedules break us.
@JuliaCTaylor@darrenabrown@history_physio ๐นHope you don't feel too discouraged ๐We do have Long SARS people in the M.E. community but there are no doubt Long SARS people who recovered and went on their way, so we don't hear from them again. ๐คทโโ๏ธ