Fibro and Me/cfs Info Carleton

Fibro and Me/cfs Info Carleton Fibro Info - Southport has now moved to Carleton Poulton-Le-Fylde Lancashire. With a hope that it may help people live a better life with their illness.

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A Community Support Group and helpful information service for Men and Women, Young Adults with FM/ ME/CFS. Fibro & ME/CFS Info Southport has now changed name and address to Fibro & ME/CFS Info Carleton Poulton-Le-Fylde Lancashire. We are a community support group and information service based in Carleton ran by Freddie (Frederica) - a Fibromyalgia and Chronic Fatigue /ME sufferer who volunteers to help give some positive assistance via supporting others within a support group environment. This page aims to assist not just members of our support group but also spouse's, relative's, friend's or just an acquaintance's who would like to have more understanding of things that may help the sufferer of these misunderstood conditions. The aim is give out some helpful information and some direction to other drop in services. All information on this page is provided by the credited sources. Fibro and Cfs/ME Support Group - drop in, is online via ZOOM MEETINGS. Please contact me for detail's. Hoping to get in my new Community in the near future. email me at fibrofreddie@outlook.com

Please note: I am a volunteer with close contacts to other valuable self help groups, however, due to my chronic illness I may not be able to run the support group some weeks. Please contact me via email or check page for information. Thank you. CREDITS: to my loving daughter for helping me run and maintain this page. Thank you Jessica. DISCLAIMER: Any guidance, Alternative Complimentary Activity, Tips, Paper Information or Signposting by Fibro & Cfs/ME Info Southport. Is not intended nor recommended as a substitute for medical advice, diagnosis, or treatment. Always seek the advice of your own medical Doctor or other qualified health care professional regarding any medical questions or condition. Any alternative complimentary activity undertaken is done at the participants own risk.

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28/11/2025

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People frequently waiting years to be 'taken seriously', postcode lotteries for access to care and a general lack of knowledge are among some of the key findings from a University of Aberdeen investigation into fibromyalgia care.

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24/11/2025

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That’s right — today’s 🖼️ Open Monthly Session – Online Art as Therapy, is happening this morning from 10:00 to 11:00am on Zoom!
Here’s a quick recap so you’re all set:
🎨 What to Expect
Creative art activities
Gentle mindfulness exercises
Friendly conversation
Sharing experiences
🕙 When: 10:00 – 11:00am today
💻 Where: Zoom (camera optional)
🔗 Register / Join: https://buytickets.at/fmauk/1865544
If you haven’t registered yet, make sure to do so soon — the Zoom link is sent automatically after registration.

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23/11/2025

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Yesterday, MPs gathered in Westminster Hall to debate government support for people with ME and what needs to change. We’ve pulled together a summary of the key points, actions, and commitments discussed, using AI to assist in summarising the Westminster Hall debate transcript.

Thank you to Tessa Munt for her continued commitment to the ME community, and to all the MPs who attended. We were pleased to hear MPs referencing points made in our briefing.

👉 Read the AI summary here: https://www.actionforme.org.uk/ai-summary-of-westminster-hall-debate/

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19/11/2025

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Evidence for spinal disinhibition as a pain-generating mechanism in fibromyalgia: https://journals.lww.com/painrpts/fulltext/2025/02000/evidence_for_spinal_disinhibition_as_a.16.aspx

A study published in Pain Reports shows spinal disinhibition, the disruption of the spinal cord’s inhibitory systems that modulate pain signals in people with fibromyalgia.

To measure spinal disinhibition in the new study, researchers used the Hoffman reflex (H-reflex) rate-dependent depression (HRDD) as a biomarker. They applied nerve-stimulating electrical pulses to the calves of 31 patients with fibromyalgia and 20 healthy control volunteers.

With normal spinal inhibition, the H-reflex response should have become smaller with repetition as the spinal cord regulates nerve activity and sensory information. However, people with fibromyalgia, especially those early in the course of their disease, had impaired HRDD. The H-reflex response did not decrease as it did in healthy control volunteers.

Reference:
Marshall, Annea,b; Burgess, Jamiea,b; Goebel, Andreasa,c; Frank, Bernharda,c; Alam, Uazmana,b,d,e; Marshall, Andrewa,f. Evidence for spinal disinhibition as a pain-generating mechanism in fibromyalgia syndrome. PAIN Reports 10(1):p e1236, February 2025. | DOI: 10.1097/PR9.0000000000001236

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19/11/2025

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A big thank you to Tessa Munt MP for leading today's Westminster Halll Debate and speaking so powerfully about the plight of people with ME, the urgent need for research funding and a service for severe ME. Please join us in thanking her.

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Poulton Le Fylde

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