Funding directive needed for neglected and stigmatized conditions

What have you done this week for people living with ME/CFS, long covid, post-SARS, post-Lyme, and similar diseases? What have you done this week for under-researched diseases like ME/CFS, vulvodynia, and migraine? Did you know that NIH says that they need a directive in order to appropriately fund ME/CFS? In the midst of everything else, don't forget people who can't get good medical care due to institutional misfeasance in ignoring their stigmatized disorders, their gender, their ethnicity, their sexual or gender identity, their disability, etc. Please write and tell me what steps you're taking to address these issues. I look forward to hearing from you. All the best.