Tag: ThereForME
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New Zealand GP Group Disavows Lightning Process Endorsement; BBC’s Con or Cure Takes Skeptical Look at LP
“A small step in New Zealand” Sometimes there is modest good news. In this case, the good news is all due to the diligent efforts of Nina Steinkopf, who writes the always useful blog MElife (MElivet). Steinkopf, who was diagnosed with ME in 2010, mostly covers goings-on in Norway and across Scandinavia. That means she…
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Some Things I’ve Read Recently…
Lisa McCorkell leaves Patient-Led Research Collaborative after five years… Way back in 2020, when it became clear that some people were experiencing prolonged symptoms after an acute bout of COVID-19, Lisa McCorkell helped found the Patient-Led Research Collaborative (PLRC). The organization grew out of an online health-related support group, which published the first survey on…
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Interview with Karen Hargrave, Co-Founder of #ThereForME
Karen Hargrave is co-founder of an advocacy campaign called #ThereForME, which was launched this past summer to draw public awareness to the UK’s lack of care and treatment and to call “for an NHS [National Health Service] that’s there for people with ME and Long Covid.” The campaign has drawn significant media attention, especially in…
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UK Health Care Professionals Appeal to Health Secretary for Quick Action on Poor ME Care
Tuesday, September 17th, was World Patient Safety Day. (I didn’t know that either.) In the UK, more than 200 physicians, nurses and other health care providers and professionals marked the occasion by issuing an appeal—in the form of a letter to Wes Streeting, Secretary of State for Health and Social Care since–about the dire state…