Paddy Richmond
paddyrichmond.bsky.social
Paddy Richmond
@paddyrichmond.bsky.social
Living the dream, shame it's a nightmare.

M.e / fibro patient, politics nerd and bad mtg drafter
@nixostorme.bsky.social I've got a new haircut, have my gay powers been restored?
July 14, 2025 at 3:12 PM
Reposted by Paddy Richmond
Today is #InternationalMEawarenessDay 📣

We catch up with @investinmeresearch.bsky.social LunaNova Fellow Dr Krishani Perera who studies ME/CFS through a microbial lens 🧪

Read more about her research ⤵️
Research exploring the role of viruses in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome; Introducing Dr Krishani Perera’s fellowship - Quadram Institute
Dr Krishani Perera studies ME/CFS through a microbial lens. We catch up to learn if and how microbes contribute to the debilitating condition.
buff.ly
May 12, 2025 at 11:05 AM
Reposted by Paddy Richmond
Today is #MEAwarenessDay
🐋 Let's take a deep dive into what ME is
and
😇 Why allyship is so important
1/15
May 12, 2025 at 11:06 AM
I love you're work @electionmaps.uk. Do you have a spreadsheet for the local elections by any chance? I would very much like to see what parties are finishing second but I can't seem to find a full data set anywhere
May 7, 2025 at 9:04 AM
Quite possibly the best inclusion in a political article ever, "Davey then ate two scones, one with cream on top and one with jam on top, to celebrate gains in both Devon and Cornwall, where fierce debate rages over the best way to make a cream tea."
May 3, 2025 at 8:49 PM
Reposted by Paddy Richmond
It’s one insane thing after another with RFK Jr….now it comes out that HHS planning to cut the National Suicide Hotline’s program for LGBTQ youth that gets 2,100 contacts per day….cruelty is the point with this heartless bastard www.motherjones.com/politics/202...
April 22, 2025 at 7:41 PM
Reposted by Paddy Richmond
Trump has deported a four-year-old US citizen with a rare form of metastatic cancer without medication or consultation with their doctor.
Trump Has Now Deported Multiple U.S. Citizen Children With Cancer
Two families who had lived in the United States for years, including a child with cancer and a pregnant mother, were deported by ICE on Friday.
www.rollingstone.com
April 27, 2025 at 12:56 AM
Reposted by Paddy Richmond
This Monday, orange is the new black.
April 7, 2025 at 1:27 PM
This is well worth ten minutes of your time
Millions of you, around the world, have put the lessons I wrote in #OnTyranny in late 2016 to good use. It has been humbling to learn how from courageous and creative dissenters, protestors, and oppositionists. I was honored when John Lithgow volunteered to read them aloud.
Here is my best guidance for action, rendered beautifully by the great John Lithgow. I first published these lessons more than eight years ago, in late 2016. They open the twenty chapters of "On Tyranny: Twenty Lessons from the Twentieth Century."
snyder.substack.com/p/twenty-les...
March 30, 2025 at 9:44 PM
Reposted by Paddy Richmond
But not corrected before the grossly inaccurate figure was circulated and picked up by national media. Another Govt created hostile environment, this time for disabled people.
DWP has made a stealth edit to a page on GOV​.UK, removing a claim that there has been a 319% rise in people claiming out-of-work disability benefits www.gov.uk/government/n... vs webarchive.nationalarchives.gov.uk/ukgwa/202503...

HT www.disabilitynewsservice.com/dwp-refuses-...

#govcomms #opengov
March 18, 2025 at 12:23 PM
@mrjamesob.bsky.social it's a rather interesting, if worrying, conservation about PIP today. I would love to call you to talk about it but having an m.e/fibro flare up so unable to do so. This is part of the can/won't chat. Keep up the good work.
March 11, 2025 at 12:11 PM
@lewisgoodall.com just listened to your excellent podcast today and you wanted some ideas on alternative political history. There was a moment in the brexit years when there were rumours that Ken Clarke might be Prime Minister. I wonder if that's a good one? I can provide a voice not if required
December 11, 2024 at 7:16 PM
Ruby Daring Tracker from woe please
If you quote this post with the name of a card in a recent format (but not FDN), I'll give you the three cards with the highest pairwise synergy.

At least for the next few minutes.
Using @17lands.bsky.social data, I have a measure of pairwise card synergy which is, essentially, "how much more often are these cards played together than we would expect by random chance?"

Here is Writhing Chrysalis and the three cards in MH3 with which it had the highest synergy.
December 4, 2024 at 11:21 PM
@xabigazte.bsky.social
Hello Xabi, I would like to say that your art for Helpful Hunter is my new favourite. It's too cute. Are there going to be playmats of them? I need it in my life
December 2, 2024 at 8:33 PM
Reposted by Paddy Richmond
A worrying pattern of behaviour that suggests the outlet may be succumbing to the long warned about and damaging pseudoscientific dogma that pretends ME is not a biological but behavioural illness. @bmj.com must do better
November 30, 2024 at 4:48 PM
Reposted by Paddy Richmond
In 2022 @BMJ.com unreasonably criticised a treatment for micro blood clots that permanently improved my long covid/ME (www.bmj.com/content/378/...), while this week it's published a frankly feeble paper supporting the long debunked and potentially harmful CBT + physical activity as a LC treatment.
November 30, 2024 at 4:46 PM
Reposted by Paddy Richmond
This is not what many people would like to hear I suspect but is important to take on board:

"The majority of research funding [in general] comes from charities, with only a small percentage coming from the government for other diseases"

From:
www.youtube.com/watch?v=W3Ji...

#MEcfs #CFS #PwME
Who Funds Research? | Why The Charity Sector is Vital For Long Covid & ME/CFS
In this conversation, we discuss the importance of funding for research in the charity sector, specifically for ME, CFS, and long COVID. The majority of research funding comes from charities, with only a small percentage coming from the government for other diseases, hence the need to emphasise the power of an established and reputable organisation in the charity sector. The example of the Cystic Fibrosis Trust is an inspiring case of how focused efforts and resources can lead to significant improvements in a niche illness. We compare the fundraising efforts for ME/CFS with other diseases like MND and Parkinson's, noting the disparity in funding despite the lower number of people affected by ME/CFS. Hopefully this provides an overview of why the charity sector is so important, and inspiring that even diseases with low numbers of people were able to drive such huge change! Apologies that my camera dies right at the end of the call, but Peter wraps up the discussion for us. Hope you enjoy! TIMESTAMPS 00:00 Intro 03:15 Importance of Funding for Research 04:13 Sources of Funding for Medical Research 09:02 Funding for Parkinson's Disease Research 11:10 Funding for Cystic Fibrosis Research 15:22 Funding for Motor Neuron Disease Research 23:31 Funding for ME/CFS Research 26:07 Need for Fundraising and Driving Cash into ME Research 30:14 Harnessing the Engaged Patient Community 32:15 Comparison of Fundraising in ME Charities 34:23 Sources of Funding 35:11 Legacy Giving and Challenges 36:35 Spending on Fundraising, Support, Research, and Advocacy 37:57 Comparison with Other Diseases 40:46 Fundraising Strategies and Professionalism 44:12 Importance of Fundraising Spend 46:05 Lessons from Successful Charities 48:16 Overcoming Stigma and Misconceptions 51:48 Long-Term Trends in Income 56:09 Challenges and Overlapping Issues 58:47 Learning from Other Disease Charities 01:02:21 The Impact of Legacy Giving 01:06:58 Targeting People Close to Those with the Disease 01:08:24 Engaging Community and Faith Groups 01:09:38 Involving Community Groups in Fundraising 01:11:12 Engaging Companies and Offices 01:14:40 Learning from Other Charities: Parkinson's UK 01:15:28 Customer Journey: First Awareness of the Disease 01:16:13 Customer Journey: Joining the Charity 01:17:18 Customer Journey: Getting Involved 01:18:23 Search Engine Optimization and Visibility 01:23:42 The Customer Journey 01:32:19 Key Takeaways OTHER LINKS: 💌 Newsletter - https://harryboby.substack.com/ 🐦 Twitter - /harryboby4 🎤 TikTok - /harryboby2
www.youtube.com
March 29, 2024 at 1:20 AM
Reposted by Paddy Richmond
May 12 is ME/CFS Awareness Day. Speak with other people about ME/CFS today. Reject invisibility and stigma, build awarenesss and support.
May 12, 2024 at 9:23 AM
This is what we are up against. I want to be taken seriously and listened to by health care professionals and politicians alike. I fear we may yet have more hurdles to clear on that front
📺Phenomenal video by @abrokenbattery.bsky.social

Facts - Evidence - Damning

If you don't follow Adam please do, his is vital work 🔥
New Video: @georgemonbiot.bsky.social describes the treatment of #MECFS as "The Greatest Medical Scandal of the 21st century". The video explores the impact of ineffective & harmful treatments & how they were defended by the scientific & media establishment.

youtu.be/RiwX9Y0NbiQ?...
November 23, 2024 at 9:04 AM