Phil P
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pprydderch.bsky.social
Phil P
@pprydderch.bsky.social
Dad of two | EVs | Born at 332 ppm CO2 | ME, FMS, POTS | @wrexham_AFC ex part-owner⚽️ | M.CIWEM | Flood Defence & Hydrometry 💧 | @PJPrydderch on X | Medium Blogs: https://medium.com/@prydd
Well done today @Wrexham_AFC v @crawleytown. 🙌

I had away tickets (thanks Kerry 🙏) for me, kids & wife as we live local, but unfortunately was too ill to go.

I hate chronic illness #MECFS. 😢

Great to see the new forwards in action & nick an important Away win! ⚽️ 🏴󠁧󠁢󠁷󠁬󠁳󠁿

#WrexhamAFC @WrexhamFX
February 1, 2025 at 6:39 PM
Gov petition website is open again. Thinking of creating petition for public inquiry into the scandal of ME/CFS treatment. Whether it does anything is another matter

I want to try to get the wording right to give it a chance

Here’s a first draft (will likely have mistakes!)

/1
November 27, 2024 at 8:09 PM
This is truly shocking from one of, if not the, leading UK #MECFS charity

I’ve been a supporter of @MEAssociation since I became ill in 2018/2019. My wife and eldest son fund raised for them, raising £2k on a charity walk.

This from their chairman is totally tone deaf… /1
November 18, 2024 at 10:17 PM
Being mod/severe chronically ill feels like we’re on pause, but life is carrying on around us. I’ve often felt if I miraculously got well, and tried to “rejoin” life, go back to my job (not that I could - had to ill health retire), my mind would be expecting to see all the people who were there../1
November 11, 2024 at 9:38 PM
Finally opened my BlueSky account. Twitter/X has become a cesspit since Musk took over and is getting worse. But it’s a good place for #MECFS & #chronicillness community, so it’s such a shame.

Hoping we can slowly recreate that here.

#pwME #MyalgicEncephamylitis
November 11, 2024 at 9:59 AM