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Petitions and activism

Please sign this petition re the lack of care for lipoedema patients

73 replies

bringonthecrumpets · 12/03/2026 08:06

Lipoedema is a chronic condition with no cure and the only treatment is surgery. NHS won’t cover, neither will any private insurance.

https://petition.parliament.uk/petitions/758164?fbclid=IwdGRjcAQepQpleHRuA2FlbQIxMQBzcnRjBmFwcF9pZAo2NjI4NTY4Mzc5AAEeVIB3zqR2hsGOwlFAOuDPGlZ0a-FKGxfTNktvatsehXSkVqkl0zf2LOm15_Q_aem_YLsvXZex_AstbEsCXG-W1g

Petition: Review NHS lipoedema care

We ask the Government review the NHS approach to diagnosis, referral and treatment of lipoedema. This should include GP training, access to conservative treatments, and clear pathways to specialist care.

https://petition.parliament.uk/petitions/758164?fbclid=IwdGRjcAQepQpleHRuA2FlbQIxMQBzcnRjBmFwcF9pZAo2NjI4NTY4Mzc5AAEeVIB3zqR2hsGOwlFAOuDPGlZ0a-FKGxfTNktvatsehXSkVqkl0zf2LOm15_Q_aem_YLsvXZex_AstbEsCXG-W1g

OP posts:
TinyRebel · 19/03/2026 00:54

@Piknik I used to have it many years ago when I lived in a different part of the country. I remember her doing one leg and seeing the difference it made when compared to the other - was really striking. She was newly qualified in the Vodder method and I think had found the course and its intensity quite gruelling and I was her first patient. Seeing those results spurred her on to keep going with it!

Kdobelda · 19/03/2026 01:06

bringonthecrumpets · 18/03/2026 19:52

We are slowly getting up to 4,000. Please continue to sign.
In a nutshell:
lipoedema is a chronic / progressive condition
There is no cure
Fat cells are diseased and cause inflammation as your body tries to fight them
your legs / bum will be bigger than the rest of your body
No diet or exercise will make a difference
You will be permanently covered in bruises
Your legs will swell up all the time
The NHS will not treat you
Surgery is the only option
In the uk it will cost you approximately £11k per surgery - most people need more than one
In Europe it will cost you about £6k plus travel costs
if you can’t afford it you just have to live with it.

Can you please PM me with some information about your surgery, where it is and cost etc? Thanks. If pm-ing is still possible on MN

bringonthecrumpets · 19/03/2026 06:53

@Piknik I had a few sessions with a suit (before I knew I had lipoedema) and I felt amazing after it. I will have a couple on the run up to my surgery (recommended by the surgeon). Lots of people in the lipoedema Facebook group had it regularly.

OP posts:
wyntersky · 19/03/2026 07:08

Signed

bringonthecrumpets · 19/03/2026 07:15

More signatures!! Thank you 😍

@Kdobeldasent you PM :)

OP posts:
fartoomuchtoblerone · 19/03/2026 07:20

Signed and bumping! Thanks OP

bringonthecrumpets · 19/03/2026 13:04

Lunchtime bump. Please sign

OP posts:
bringonthecrumpets · 19/03/2026 19:17

Anyone else willing to help us?

OP posts:
bringonthecrumpets · 20/03/2026 17:34

We’ve gone over 4,000 now. We still need to get to 10,000 for someone to listen to us. Please sign

OP posts:
Piknik · 20/03/2026 18:10

OP might be worth posting the link in 'Chat' for more traffic

TheAutumnCrow · 20/03/2026 18:19

This condition predominantly affects women, doesn’t it? And is associated with the hormone oestrogen (notably during biological hormonal changes that only affect women) and is rare in men?

Sounds like a clear case of discrimination to me by the NHS, butting up against the protected characteristics of sex, pregnancy & maternity, and disability.

fartoomuchtoblerone · 20/03/2026 19:59

Adding another little bump

bringonthecrumpets · 20/03/2026 20:24

@TheAutumnCrowyes it is hugely affected by hormonal changes and as far as I know it’s 99% women who are affected. I’ve read more stories about gps telling people to walk more and lose weight and their legs will look and feel better. It’s very sad really. In the US at least private health insurances cover it. That’s not the case in the uk either.

OP posts:
bringonthecrumpets · 20/03/2026 20:25

@Pikniksomeone said you’re not allowed to post petitions elsewhere?

OP posts:
bringonthecrumpets · 22/03/2026 09:50

Bumping this for the Sunday crew. Please help us and sign our petition. Thanks.

OP posts:
Piknik · 22/03/2026 15:15

@bringonthecrumpets I've definitely seen petitions in Chat. MN HQ may move them at some point (I'm not sure) but you might get a good few sign ups and shares before they do....

indiecisive · 22/03/2026 22:03

Thanks so much for sharing this @bringonthecrumpets

NerdyBird · 22/03/2026 22:32

signed!

bringonthecrumpets · 24/03/2026 19:22

We are close to 5,000 now. Please keep signing. I’ve read more stories of women being fobbed off and told their legs “don’t look too bad” so it can’t be lipoedema. Those with no means to pay privately for surgery are being left in pain.

OP posts:
TheAutumnCrow · 24/03/2026 19:30

Did you know about about Mumsnet's campaign, @bringonthecrumpets?

I wonder if you email Justine at MNHQ she might be able to assist?

https://www.mumsnet.com/talk/mumsnetcampaigns/5507431-medical-misogyny-women-are-being-systematically-dismissed

bringonthecrumpets · 24/03/2026 22:27

Thank you. I didn’t know about it. Will message them.

OP posts:
bringonthecrumpets · 20/04/2026 07:54

Bumping this again in case you haven’t seen it. We’ve gone over 5k now so more than halfway. Please help! Sign and share. Thanks

OP posts:
feedmechocolatenowplease · 20/04/2026 09:51

Signed!

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