My Battle with Endo ۶ৎ
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mybattlewithendo.bsky.social
My Battle with Endo ۶ৎ
@mybattlewithendo.bsky.social
130 followers 55 following 22 posts
📍AUS | NSW sharing my battle with Endometriosis, PCOS, Chronic Pelvic Pain, GERD + suspected Dysautonomia
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Reposted by My Battle with Endo ۶ৎ
Reposted by My Battle with Endo ۶ৎ
Reposted by My Battle with Endo ۶ৎ
Endometriosis is one of the most painful health conditions which affects more than 1 in 10 women in the world. More needs to be done for this chronic condition.

#EndometriosisAwarenessMonth #Endometriosis
Reposted by My Battle with Endo ۶ৎ
Endometriosis Awareness Month
Just as common as diabetes. But more than half of you don't know what it is.
Just sayin'
If you’re a cishet white man, I promise you that your experience accessing healthcare is far better than the rest of us.

We need diversity in research and medicine because women, minorities and LGBTQ+ people are more frequently misdiagnosed, gaslit and harmed

www.nature.com/articles/d41...
Exclusive: NIH to terminate hundreds of active research grants
Studies that touch on LGBT+ health, gender identity and DEI in the biomedical workforce could be terminated, according to documents obtained by Nature.
www.nature.com
It is important to note that each stage can manifest differently and the severity of symptoms does not always correlate with the stage of disease. Some can also be asymptomatic. 💛

#endo #endowarrior #endometriosis
#endometriosisawareness
#endometriosiswarrior #endometriosissupport
#endoawareness
SARCASM OBVIOUSLY. Don’t attack me.
Yes Marty Sheargold, the 14% of Australians diagnosed with endometriosis are faking their chronic disease. We simply lied about undergoing surgery and receiving a pathological biopsy of the tissue for a definitive diagnosis. How did you know?? 😱
According to a study held by Western Sydney University + Endometriosis Australia in 2021, 1 in 6 of those AFAB in Australia have lost their jobs due to managing endometriosis. 🤯💔

#endometriosis #endo
#endometriosisawareness #endoawareness #endowarrior #endometriosisaustralia #extrapelvicendo
PSA 🗣️
It’s not up to YOU to decipher who “looks” sick enough, so can we finally stop with the “but you don’t look sick” comments in 2025?!! Invisible ≠ imaginary.
Drop a reply sharing where your Endo was found down below! Mine was found in my Pouch of Douglas. 💘

Please note this is not a full list. Extra-pelvic Endometriosis is NOT rare.

#endo #endowarrior #endometriosis
#endometriosisawareness
#endometriosiswarrior #endometriosissupport
#endoawareness
So tired of this misconception! It’s a huge barrier in Endo warriors accessing appropriate treatment and care in Australia and takes us backwards :(
Reposted by My Battle with Endo ۶ৎ
It's time for the whole medical community to take a good look and see endometriosis as what it is: a systemic disease (and it's histological connections e.g. to fibrosis). Gynaecology is not the only place from which to tackle it.
#endometriosis #chronicdisease #femalehealth #endowarriors #fibrosis
More often than not we tend to be our own worst critics.. so this is your friendly reminder that these things are perfectly okay! 🫶

#endometriosis #endo
#endometriosisawareness #endoawareness #endowarrior #endometriosiscommunity #endometriosissupport #chronicillness #chronicpain #chronicallyill
In the same boat as you currently 🤧 sick to my stomach with how painful it currently is. Sending hugs :( ❤️‍🩹
Endometriosis has been found on EVERY major organ in the body. It is not a period or menstrual disease.

FYI this isn’t a complete list.

#endometriosis #endo #endometriosisawareness #endoawareness #endowarrior #endometriosiscommunity #endometriosissupport #endometriosisaustralia #endoaustralia
Reposted by My Battle with Endo ۶ৎ
I couldn’t agree more! Thank you for sharing with me 🙏