Fiona Wood
mewarrior1.bsky.social
Fiona Wood
@mewarrior1.bsky.social
Wife, mum, Severe ME, 💙✝️♿️Fibromyalgia
Observe small things, don't rush, love & forgive
#loveyourself #loveothers ❤️
#chronicillnesswarrior1 on X & IG
Opinions are my own 🤓
2/

This bill risks creating a two-tier system for disabled people.
Disabled voices must be heard, not sidelined.

Vote with principle on 1 July.

#PIP #DisabilityRights #Labour
June 28, 2025 at 11:54 AM
2/

rushed through without consultation.

@JessicaToale -my MP
@areyoflight

Please share & tag your MP and anyone who should know about this!
Thank you 💙

#WelfareNotWarfare
#TakingThePIP
#ReformNotRevenge
#ProtectLCWRA
June 28, 2025 at 11:38 AM
June 28, 2025 at 11:06 AM
Please watch the Instagram post below. It reflects the real fears and voices of disabled people who will be directly affected by this bill.

We need leadership that listens, not legislation rushed through without consultation.

instagram.com/reel/DLaa3V6I9…
June 28, 2025 at 11:06 AM
2/
for whatever reason whether you knew them or not. Perhaps sit quietly for a minute of two to think of them & their families 💙

#WeRemember 🤍
a blue candle with the words always a hero on it
ALT: a blue candle with the words always a hero on it
media.tenor.com
May 12, 2025 at 12:20 PM
It is definitely relative 💯
Even during my current severe stage it’s changed within it. I can do far less now than two years ago.
I do my best not to look at what others can or can’t do, & not to compare myself to myself even a few months ago.
Our illness journey is not linear.
May 9, 2025 at 1:28 PM
I found this hard to answer.
Intrinsically I am still me, as in my nature. In many ways that has increased bc I have more time, but then my memory loss can inhibit me 😂
I’m more confident in who I am as a person bc I’ve had to learn how to stand my ground with doctors!
Practically, nothing left!
April 27, 2025 at 9:53 AM
Great video! Loved that they were all living together! Love your commentary too Chris!
April 27, 2025 at 9:41 AM
Our two dogs go to my husband or carer around 11am everyday for their morning treat 😂
April 27, 2025 at 9:38 AM
🙋‍♀️ I want one even if I don’t go anywhere other than hospital but they definitely need to see it!
January 26, 2025 at 6:26 PM
Thank you 💙
January 21, 2025 at 1:29 PM
It’s really good. May we use it? X
January 21, 2025 at 1:13 PM
2/

think that means we can’t be proud of the UK 🇬🇧

However, Musk was so incredibly enthusiastic to the point you’d think he was the new president 😂
I wonder if that’s his agenda?

x.com/AutismCapita...
x.com
x.com
January 21, 2025 at 1:12 PM
Good luck 👍
January 21, 2025 at 11:19 AM
2/
the exercise until you have returned to a mild baseline.
I exercised for 3 years after onset of ME but wasn’t diagnosed. It slowly & surely made me more ill having more severe PEM. Eventually I stopped bc I couldn’t do it.
Please take care of yourself especially whilst still symptomatic
💙
January 21, 2025 at 11:13 AM
1/
Hi Bobby
I have severe ME and been ill for over 15 years, last 8 severe.
You mentioned you have PEM. Have you been diagnosed with ME as PEM is the hallmark symptom of ME.
Graded exercise is not seen as a treatment for ME or LC and can be quite dangerous for you.
If you are in PEM please forget
January 21, 2025 at 11:13 AM
Totally empathize! I miss cleaning 🤷‍♀️😂
Desperate to sort my cupboards, but I’m bed bound & for some reason crashing even more. Could be the UTI. Two weeks of antibiotics now finished and UTI has now gone according to my dip stick this morning.
Understand your frustration 💙
January 21, 2025 at 10:58 AM
Please take your medication ie, histamines because you need a constant dose to help block the mast cells.

As for eating high histamine foods, I cave in too. Christmas was horrendous, but (almost) getting my head around it again as from Saturday!

It’s done & tomorrow is a new day 😉 💙
January 21, 2025 at 10:53 AM