EndoPcoSOS @ENDOPCOSOS
Connecting with women with diagnosed or suspected endometriosis and/or PCOS for support, sharing and collective action #deedsnotwords United Kingdom Joined November 2021-
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It's hard to listen to people tell you not to get angry about an issue that doesn't affect them.If the healthcare system actually worked for those with conditions like PCOS or Endo, I'm sure I'd be able to 'chill out' too... this is why community & allyship is so important!
Endometriosis Reminders ✨ - Not everyone can afford surgery - Not everyone has supportive partners/family - Not every medication works for everyone - Self-care is essential, not selfish - Your pain is valid, even if others can’t see it - You’re not alone 💛 #endometriosis
#Endometriosis also causes hideous hormonal migraines, and I am experiencing a fierce one today. I gave myself permission to rest, and spent the day on the sofa. Listen to your body. It's taken a long time for me to learn this, but your body will always tell you when it needs to…
Finally, some sense! And on this subject...Shout-out to the PE teacher who ripped up a note my mum wrote when I was in agonising pain & said loudly so others could hear: 'Periods AREN'T a reason not to do P.E.' 🤯 theguardian.com/education/2024…
Period pain policy reversed as school apologises bbc.in/3zXk7dd
What a compassionate message ❤️
What a compassionate message ❤️
“Maybe if you didn’t think about your illness, it wouldn’t effect you so much” I wish it worked that way! Unfortunately, chronic illness doesn’t take a break when I’m not thinking about it.
Get your #PCOSMerch & help raise awareness whilst supporting Verity’s work in fighting for better outcomes for all 💜💜 pcosmerch.com
That moment when someone close to you, who never quite seemed to fully believe your symptoms actually sees you during a flare up... #Endo #PCOS #WomensHealth #Endometriosis #Heavyperiods
The fact we still 16 years on from when I was dismissed & ridiculed at times in school for my painful periods (which was later diagnosed in stage 4 severe endometriosis), & we are still no further forward is beyond me
People + healthcare + profit = a broken system where vulnerable people get taken advantage of #healthinequity #womenshealth #healthcare #healthempowerment #PCOS #Endo #peopleoverprofit
The healthcare system does a great job of keeping women feeling small...because there's not enough money invested into women's health conditions, we're still mostly using models based on the male body etc. It's 2024. It's about time things changed. Women are being failed.
The Healthcare System Doesn't Work For Women And This Needs To Change Now #womenshealth #healthinequity #PCOS #endo #endometriosis
Women Deserve To Be Treated With Respect Especially When It Comes To Healthcare #Womenshealth #healthinequity #PCOS #Endo #Endometriosis And that's the tweet!
Waited months for private gynae referral. Ask to be referred to a nutritionist to support natural management of symptoms.Get told they don't know any specialists and that 'there's loads of nutrition advice for PCOS on social media.' People pay up to £220 for these consultations!
Recording available: PCOS at Work, a webinar in our Menstrual Health at Work series about PCOS at work. In this webinar, with @veritypcos, we explain what PCOS is and how employers can support staff with the condition. Available at: endometriosis-uk.org/webinar/pcos-w… #PCOSAwarenessMonth
📢 A N N O U N C E M E N T 📢 @veritypcos & @cardiffuni are so excited to announce the official launch of our @LindAlliance Priority Setting Partnership for #PCOS. The #JLAPCOS PSP will create the Top 10 research priorities for PCOS in the UK. 📷 Some of our steering group
YES Demi! So inspired by you opening up about your endometriosis on #loveisblinduk. Great interview too! Now where do we get more amazing and empowering specialists like Dr Nitu? ❤️ #endometriosis #endo #womenshealth youtu.be/E7o-9PWMBqw?si…

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