
#ThereForME is a campaign founded by Karen and Emma, two carers for partners with very severe ME/Long Covid. #ThereForME is calling for an NHS that's there for people with ME and Long Covid. Follow our Substack to stay up to date with the latest.
| Platform | Pricing | Only free issues | Publishes | Weekly | |
|---|---|---|---|---|---|
| Issues | 84 | Founded | 2 years ago | Last Issue | 2 months ago |
| Active | |||||

We’ve been a little low on capacity lately at #ThereForME HQ. Between busy day jobs, complex home lives and health challenges, you may have noticed that lately we’ve been a little less active than usual.
This week, we’re celebrating the am...
Today’s guest blog is from friend of #ThereForME Tessa Munt, the Liberal Democrat MP for Wells and Mendip Hills (in Somerset). Since election in July 2024, she has been an active advocate for people with ME. Recent activities include securi...
January 22nd marked six months since the publication of the government’s new Final Delivery Plan for ME. What progress has been made? Are there signs the plan is making a difference? Today we’re taking a whistlestop tour of the latest devel...
Today’s guest post is from #ThereForME co-founder Karen Hargrave. Karen is a carer to her husband James, who lives with very severe ME.
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It’s been a while since our last update. Some of you may have noticed that we’ve been a little quiet lately - we’ve been working on a little something behind the scenes which we are looking forward to being able to share with you. As you’ll...
Subscribers, engagement, traffic and sponsorship for #ThereForME.
| Subscribers | Engagement | 76 | Monthly Web Visits | ||
|---|---|---|---|---|---|
| Accepts Sponsors | Estimated Cost per Ad | ||||
The writers behind this newsletter.
Living with and writing about myalgic encephalomyelitis (ME).
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