Tenmilsokhet

Private equity buys UK fertility clinics. PE already controls social care, hospitals, GP surgeries, dentistry, child fostering. Usual business model. High debt, quality of care declines, prices increase, high profits. When things go wrong, NHS has to step in, PE doesn't pay.

UK lacks essential electricity transmission/storage systems. Billions paid to solar & wind turbine farms to switch off during periods of high sunshine/winds, expected to cost £8bn a year by 2030. National Grid pays dividends. What is the Govt doing? Watch the Minister's reply.

They are openly trying to fix voting in the USA.

It's Invisible Disabilities Week 🩷 For people living with GBS, CIDP and MMN, symptoms like fatigue, pain and weakness aren't always visible. #IAmInvisibleNoMore reminds us to listen, be patient and never judge someone's health by how they look.

Last chance to apply to be our new Operations Manager. Applications close on Sunday at midnight #CharityJobs #Charity

@talksport.com

Lucy is doing a skydive tomorrow for IN UK 🪂 Both her mum & brother have been impacted by inflammatory neuropathies, making this a very personal challenge. She’s already smashed her fundraising target, but there’s still time to help push the total even higher! 🔗 www.justgiving.com/page/lucy-kn...

MEATH COUNCIL: We were delighted to have commissioned interior designer Neela Sorensen to give Newgrange a well overdue facelift. The charred black wooden cladding well and truly takes the site into the 21st century. The €14 million project will boost tourism to the area.

🔴 More than four in five Britons (83%) believe wealthy individuals use political donations to influence the government in their own personal interests. Episode 2 of Democracy for Sale's new series with @transparencyuk.bsky.social on big money in British politics out now! youtu.be/q84jM1QHQkk?...

Seven people joined our latest local Get Together, despite the heat! ☀️ For one new attendee, whose husband is currently in hospital with CIDP, connecting with others who understand offered some much-needed reassurance. 🩷 We hope to see the group together again soon 🥰

Gatwick Airport has lost water supply. There are massive Data Centres within just 7 miles. They are going to put Billionaires useless AI above your thirst.

Huge thanks to Ali Stoneham for fundraising for Hope for POEMS 🩷 Please support if you can: www.justgiving.com/page/alison-...

CIDP Get Together this afternoon. 🩷 Come along for a friendly chat with others who understand.

The Kiltwalk is back! 🥾 Registration is now open. Walk for Inflammatory Neuropathies UK 🩷

Good luck Dan! 🩷 Taking on Yorkshire Tough Mudder on Saturday for Inflammatory Neuropathies UK

A huge thank you to Bobby for fundraising for Inflammatory Neuropathies UK. Read more about Bobby's story here: www.justgiving.com/page/bobs-vs-poems #Fundraising #CommunitySupport #POEMS

🎙️ IN Conversation is today at 12pm in our Facebook Group 🩷 Come and join the conversation! #InflammatoryNeuropathiesUK

🤩 Reminder: Our MMN Get Together takes place today. A welcoming space to connect with others living with MMN and share experiences. Details can be found here ➡ www.inflammatoryneuropathies.uk/get-togethers #MMN #InflammatoryNeuropathies

Reminder 📢 Our Advoca webinar is tomorrow at 2pm 🩷 Advoca is a free app created by doctors to help patients & caregivers navigate their health journeys. Join us for a walkthrough of onboarding and how to use the app. Register at us06web.zoom.us/meeting/regi...

CIDP Get Together this Thursday 🩷 Join us for support, conversation, and connection with others who understand. 📍Head to www.inflammatoryneuropathies.uk/get-togethers & click the second pink link 🕒 2pm #CIDP

Read our easy to understand blog at inflammatoryneuropathies.uk/post/what-is-cidp-chronic-inflammatory-demyelinating-polyneuropathy or scan the QR code. And while you are at it, please share this post so others can find out about #CIDP as well.

Join our Advoca Onboarding Session - Get Started with Confidence We're inviting members of our community to a free, friendly 30-minute online session to help you get up and running with Advoca, the free note-taker app built by NHS doctors to help get everything from your medical appointments.

Pal just shared this 😂

Are you living with CIDP? If so, take a look at this. Our partners in EPODIN (the European network of organisations supporting people impacted by Inflammatory Neuropathies) has developed Neuroquali, an evidence data platform that collects anonymised information from people living with CIDP.

This is Zoe Steele. Zoe is running the Hackney Half Marathon for us on Sunday. What a flipping star 💫 Wish her the best, and if you want to support her then head over to justgiving.com/page/zoe-steele-2

Most people won’t have heard of (let alone be able to say) Guillain-Barré Syndrome or #GBS until they are diagnosed with it. And that’s a scary thing to happen to anyone.

If you’d like to get involved head over to gbs-cidp.org/2026/04/gbscidp-awareness-month-this-may/

Did you know that Guillain-Barré Syndrome was first named and described 110 years ago. So, during GBS and CIDP Awareness Month our friends over in the GBS/CIDP Foundation International are looking to collect and share 110 stories about GBS.

Last week, Rich and Tansy spent some time at the Association of British Neurologists conference in Birmingham. Rich has written a blog to explain why we attended and what we got out of it for our Community – inflammatoryneuropathies.uk/blogs

This month we have a couple of extra special Webinar Sessions scheduled in. The first is on Tuesday 19th May at 12.30pm where we will focus on Benefits and Welfare. You need to register for the Webinar, and you can do that at us06web.zoom.us/meeting/regi... 1/2

From Wednesday this week Rich and Tansy will be over in Birmingham at the Association of British Neurologists Conference. The aim is to tell as many Neurologists as possible about Inflammatory Neuropathies UK, and to ask them to share our information with their patients. 1/2

Just £5 a month can help us make a life changing impact for people impacted by Inflammatory Neuropathies. Providing advice and information to one person costs around £10. An emotional health support session costs £85. A Local Get Together costs about £100 to run.

This month, during #GBS and #CIDP Awareness Month, we are asking you to #ShareandShout about your experience of GBS and CIDP. Put up a post on Social Media and tag us in @InflamNeuroUK, wear your Inflammatory Neuropathies UK T-shirt (you can get one at www.inflammatoryneuropathies.uk/shop) 1/2

Polls looking good for SNP and GREENS. BUT. And it's a MIGHTY BIG BUT. You still have to go out and vote. NOTHING is won until you actually vote. Do not think it's "In the bag." It's NOT. Not until you get out and VOTE. VOTE INDY.

Every year in May we take the opportunity to shout about #GuillainBarréSyndrome #GBS and #CIDP. It’s an opportunity to raise awareness about the conditions, share stories and experiences, and raise vital funds to support what we do here at Inflammatory Neuropathies UK.

Please read

Please read

Monarchy and the Church have always been in it together, ever since Christianity was designated the state religion of the Roman Empire. Emperors knew how powerful the idea of “one god up there, one king down here” was.

Remember, Israel has the right to exist as an independent sovereign state, but, Scotland doesn’t. That’s just how it is.

Sensational 😂😂

This amazing scientific advance may one day lead to either more effective treatments or dare I say perhaps a cure. This is why it is vitally important to fund basic scientific research. Scientists Discover Way To Reverse Chemical Process Linked With Alzheimer’s Disease share.google/Vm0hfSMfkGIc...

Paranodopahy. Anyone?? Medical peeps only🙏

Curse of Private Equity US evidence shows: When private equity incentives collide with clinical care, patients—especially those who are sicker, poorer, or harder to treat—are more likely to be killed or harmed. Yet UK handing more of the NHS to PE, enabling it to make profits.

Today is #RareDiseaseDay Through EB Research Partnership, families, scientists, and supporters are pushing research forward, pioneering progress in EB and helping reshape what’s possible for rare diseases. It’s not a matter of if. It’s a matter of time. 🦋 Learn more: ebresearch.org

Where can I buy that badge?

Totally tory

Seems Legit