Andrew Gifford
@andrewgiffordphoto.bsky.social
2.9K followers 1.2K following 2.9K posts
Hello, welcome :) This Invisible Illness: my first long form documentary photography project, about ME/CFS a complex & challenging health condition - like Long Covid. https://linktr.ee/andrewgifford.photography Bristol, UK. 335.42 ppm. He/him/oi.
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andrewgiffordphoto.bsky.social
Here but not here - from my ME/CFS photo project

glass.photo/andrewgiffor...

ALT: Colour photo of a caucasian adult male's head just about visible through foggy blue-grey glass, as he peers in through the murk

#DocumentaryPhotography #pwME #MECFS #LongCovid
Here but not here:
Andrew Gifford on Glass
glass.photo
andrewgiffordphoto.bsky.social
Making sure to name 'Sir' Simon Wessely as a bad actor in the Action4ME survey.
Reposted by Andrew Gifford
dpcarrington.bsky.social
Record leap in CO2 fuels fears of accelerating global heating

- CO2 in the air hit new high last year, with scientists concerned natural land and ocean carbon sinks are weakening
@wmo-global.bsky.social

#climatecrisis
Story by me
www.theguardian.com/environment/...
Record leap in CO2 fuels fears of accelerating global heating
CO2 in air hit new high last year, with scientists concerned natural land and ocean carbon sinks are weakening
www.theguardian.com
andrewgiffordphoto.bsky.social
I'm absolutely not a Capa expert, so please forgive me if a new understanding of his work at this time and death has since come to light (I made this photo in 2010).
andrewgiffordphoto.bsky.social
Robert Capa's camera at the American War museum, Hanoi, Vietnam

The documentation says he was killed while seeking to make photographs of farmers trying to grow rice under the pressure of war.

#Photography #RobertCapa
Colour photograph inside the American War museum in Hanoi, Vietnam. Grey walls are lit by flourescent strip lighting. Adult tourists browse the hung photographs and documentation. An adult female Vietnamese citizen reads the caption beneath a large back-lit photo of Robert Cappa's 35mm film camera, which has a hole ripped through it, likely from the shrapnel which killed the dedicated war photographer.
Reposted by Andrew Gifford
funkishen.bsky.social
"...If you really want to know about the most serious health challenge facing our planet, one that still has not been recognized, be sure to watch these videos and then demand the change that is so desperately needed.”
Leonard Jason, Ph.D.
andrewgiffordphoto.bsky.social
Reasonably sure it is a contravention of our human rights for the UK Gov to: systemically back quackery, under fund effective research AND under pay on welfare. 400,000 people impacted, nearer 1.3-2 million including Long Covid. If Gov wants us productive asap, it should better support us meanwhile.
andrewgiffordphoto.bsky.social
I've never seen a single ME/CFS or Long Covid advocacy group or org fighting for this realignment in expenses we face. It would make such a difference, as we can each make some improvements in both health and quality of life, while awaiting medical breakthroughs which could be years and years away.
andrewgiffordphoto.bsky.social
A whopping two thirds of my welfare goes on fighting the disease - drugs, supplements, therapies, accommodations - without this I'd be much worse and likely worsening. I could not afford this were it not for being in a relationship.

DWP must double PIP immediately, back-dated to date of diagnosis.
andrewgiffordphoto.bsky.social
IMHO the commonest practical problem is the expense of ME/CFS. It's really fucking expensive, as you cannot work once at moderate level.

DWP's paltry PIP and ESA 'welfare' in the absense of ANY clinical support from the NHS means poverty while trying to stave off a worsening of the disease.
wamesmecfs.bsky.social
Dr Nigel Speight writes that ME families are still encountering charges of FII (Fabricated and Induced Illness) formerly called Munchhausen Syndrome by Proxy. In the UK he believes the current paediatric guidelines regarding FII need to be changed.
tinyurl.com/44c4zykd
Current problems facing ME families in the UK
The commonest recurring problems ME families are encountering in the UK at present stem from current paediatric guidelines regarding FII. (Fabricated and Induced Illness) This was formerly called M…
tinyurl.com
Reposted by Andrew Gifford
carolecadwalla.bsky.social
My colleagues & I have taken a huge gamble to set up @thenerve.news We’re trying to build a new independent publication from the ground up. Social media is our only distribution for now.

Sharing this article in your networks would make a huge difference. Thank you! 🙏🙏🙏
carolecadwalla.bsky.social
NEW: The British politician, his Russian intelligence handler & a Kremlin plot against the US & Ukraine.

My new piece about Nathan Gill and Nigel Farage for @thenerve_news in which we ask:

Why, even now, is no-one asking questions?

t.co/BUTtpK9C4S
Reposted by Andrew Gifford
minstronemonster.bsky.social
#neisvoid #me/cfs #longcovid folks, can anyone point to research on exercise post covid? I know 'six weeks rest' is the anecdotal suggestion, but are there any actual papers on this?
Reposted by Andrew Gifford
emmahaslett.bsky.social
This is a huge story but massively under the radar in the UK.

A US Christian legal org called the Alliance Defending Freedom (ADF) is working to roll back abortion rights here using the same playbook it used in the US: briefing politicians, watching, waiting.

www.nytimes.com/2025/10/13/w...
They Helped Topple Roe v. Wade. Now Their Sights Are Set on Britain.
www.nytimes.com
andrewgiffordphoto.bsky.social
In my own case, iirc, none of my NHS blood tests have suggest low blood volume. I'm sure it would have been flagged if so.

I would love to peruse any papers around electrolytes and ME or Long Covid. I'll dig around tomorrow.
andrewgiffordphoto.bsky.social
Mmmm, chips.

Adult daily recommended amount of salt is 6g (NHS website). We're already at double this. I wonder how much further we should go as pwME. Seems bloating is the main sign of too much intake; www.webmd.com/diet/ss/slid... (this is NOT medical advice etc.)
Telltale Signs You’re Eating Too Much Salt
Learn about the telltale signs of too much salt in your body, and how you can keep your sodium levels in check.
www.webmd.com
andrewgiffordphoto.bsky.social
I see, thanks Kati, sounds like I'm much the same re scenario and intake. Do you suspect low blood volume btw? Have you tried a higher intake of salt and any observations?
andrewgiffordphoto.bsky.social
Thanks Margo, good points all.
andrewgiffordphoto.bsky.social
Pre my ME developing from Mild to Moderate and worse I would get a dry mouth from salty foods but, thinking about it, this hasn't happened in 15 or so years. I don't crave salt nowadays, but my pallete/body seems to be finding more seems better, going by taste. But, I don't know sweet spot.
andrewgiffordphoto.bsky.social
My Q prompted by a Patrick Ussher podcast ep where he talks about low blood volume in ME. My GP hasn't tested me for this and I've no idea if/how the ME-addled results would appear via NHS methods/scale. podcasts.apple.com/us/podcast/p... (has his own podcast, and YouToob, too)
Patrick Ussher, author of Understanding ME/CFS and Strategies for Healing
Podcast Episode · The POTScast · 10/07/2025 · 1h 7m
podcasts.apple.com
andrewgiffordphoto.bsky.social
Nope! I do have a meter, but I really don't like monitoring or apps, recording shit - I generally detest admin. I did test for a few days and was a little low on blood pressure, but my OI improved with salts and so I didn't bother retesting.
andrewgiffordphoto.bsky.social
My mid Moderate ME body almost never asks for water, I'm almost never thirsty. This seems odd. I do get a headache if dehydrated, but never thirst. I have to drink to a rough schedule, rather than a sensed need.
andrewgiffordphoto.bsky.social
Salt/electrolytes, how much should pwME consume? How to find the sweet spot?

I take 5g mineral salts daily, plus 5g sea salt with food. Has resolved orthostatic intolerance, but I'm not sure how much more I may need nor the signs of 'too much'. I don't know if I have low blood volume.

#MECFS #pwME