#endometritis

[magicalaugirl]

To everyone being told their unbearable menstrual pain is normal

Today is endometriosis visibility day

To everyone being denied medication for menstrual pain when needed

Today is endometriosis visibility day

To everyone being accused of exaggerating when describing menstrual pain

Today is endometriosis visibility day

To everyone that had to go through outrageous numbers of ginecologists before being given a diagnosis

Today is endometriosis visibility day

To everyone that only found out they had endometriosis because they were trying for pregnancy and were infertile

Today is endometriosis visibility day

To all the scientist advocating and being denied funding for the study of endometriosis and women’s menstrual rights

Today is endometriosis visibility day

To every single person that up to this date have to take contraceptive pills because there is no treatment for endometriosis

Today is endometriosis visibility day

To everyone being denied medical leave by their jobs despite not being able to get themselves to work due to menstrual cramps

TODAY 14/03 IS ENDOMETRIOSIS VISIBILITY DAY

#endometriosis visibility day #endometriosis #period cramps #menstrual #menstrual cicle #women’s rights #menstrual rights #endometrium #menstrual cramps #menstrual cycle #infertility #menstruation #menstruation visibility #people who menstruate #menstruación #endometritis #uterus #people with uteruses #period rights #menstrual leave

[talkethtothehandeth]

Everyone with dysmenorrhea deserves a kiss on the forehead right nOW

#PLEASE #disabled #endometritis #pcos #dysmenorrhea #undiagnosed #chronic pain #chronic illness

[dabnyfantown]

so tired of being in so much pain every single day of my life

#chronic pain #chronic illness #endometritis #crps #fibromyalgia #ibs #back pain #everything hurts #i cant win #spine injury

[sparkles-and-trash]

If you enjoy my writing and want to see more of it and have the opportunity, I’d be forever grateful for your support as I am struggeling with my medical bills rn!

kofi - paypal

No pressure of course!

Reblogs helps a ton too!

I’m super embarrased to be doing this, but medical bills are stacking up once again, and I’m working as much as I can freelance, but to afford the treatmeant that keeps me able to write for both work and fandom, I need some help!

masterlist - ao3

#irl tag #personal #donation post #writer #fanfic writer #fandom writer #chronic illness awareness #chronic illess #lupus #lupusawareness #chronic migraine #scoliosis #chronic fatigue #CFS #endometriosis #endometritis #PCOS

[honeydew-wombat]

For the love of Jesus fucking Christ can people please stop telling me to be proud of my period to love it to think it’s some amazing thing. That my body is healthy for having one.

Like no. I have endometriosis and possibly from my last scan PCOS, I’m not fucking proud of that. Im in pain, I can’t move, I can’t walk, work or fucking function. Why would I be proud of this

Im 20, I have toasted skin because of my heat packs, strong pain relief doesn’t work and I just hate everything. I hate the way my body looks because of the toasted skin because I feel like it looks horrible, and I’ve finally found someone I want to have sex with for the first time ever and I’m currently getting my period every second week. And I don’t really want them to see me like this, with the pain, break downs or any of that

I hate everything about this disease, and I hate even more when people say that I should be proud of my period when that stupid thing makes my life so much harder then it needs to be

Fuck endometriosis and fuck anyone who tells me that I need to be proud of my period

#endometritis #fuck endometriosis #pain #chronic illness

[paddockbunny]

As if I get my period the very first day of my holiday 🫠💀

(Sorry if tmi but, it is what it is, hello world of pain from endo)

#endo #endo warrior #<I hate those hashtags but honestly if you could see me rn it would be justified #periods #end the stigma around periods #endometritis

[cemitadepollo]

I wish all people who blame my big clots of menstrual blood on a lack of water to shut the fuck up <33

It's fucking endometriosis, bitch. Wouldn't it be nice if it was just dehydratation.

#endometritis #endometriosis #hormonal problems #blood clots #menstrual problems #menstruation

[fertilityphoenix]

IVF and HHV6 in Pregnancy - A Group Study

IVF success rates were 20% for women with active HHV-6A infections in the uterus, compared to 60% for women who tested negative for HHV-6A in the uterus. There was no link associated between HHV-6 and endometritis (CD138). Endometritis, by CD138 positive

IVF Success Rates with Active HHV-6A Infection in the Uterus 2024 January 07 What is the Impact of Human Herpesvirus 6A on Pregnancy Outcomes? The impact of Human Herpesvirus 6A (HHV-6A) on pregnancy outcomes appears to be significant, potentially affecting the success rates of not only pregnancy but even In Vitro Fertilization (IVF). This conclusion stems from a collaborative study by Coppe…

View On WordPress

#CD138 #endometritis #HHV-6 #HHV-6A #ivf

[stuckys-babydoll]

Me: “Hi, I’m so sorry to bother you, but I’ve been waiting for 3 hours, and I really need the medication that will help me not want to take my own life.”

American Healthcare: “Just be patient omg you’re only 22, you can’t be in that much pain. Plus, you’re a woman so you’re probably just being dramatic.”

Some 70 year old white guy named Richard who just walked in: “Give me my Viagra!”

American Healthcare: “ofc here u go sweetie we also have a cookie for you on the way out have a nice day ily!”

#endometritis #feminism #healthcare

[photography-slut]

To My Future

After Finding Out I Could Have Endometriosis

When I was 4 I used to dream about owning my own house, singing and dancing with my partner and children, as the sun rises and sets, we were all happy. And without a care in the world.

When I was 11 I started my period, I remember naively being excited about it and the thought of becoming a woman. Meaning my 4 year old self's dreams were becoming more and more of a possibility.

When I was 12 my parents took me and my sister to Florida. I remember the pain of my 11th period. I collapsed in the hotel room's bath. And woke to my mother frantically trying to work out what was wrong.

We booked a trip to the doctors when we landed back in the UK. I was told to regular my painkillers and put a hot water bottle on it.

When I was 15 I was getting ready for my ICT exam. The pain getting worse as I was coming out the bathroom, I had just brushed my teeth. My nan found me passed out on the landing. Worried that something serious had happened she called my mother.

My mother took me back to the GP, they put me on progesterone contraceptive pills.

When still at 15 I was on holiday with my family in Devon, my crying woke my sister up. I felt depressed and suicidal.

My mother took me back to the doctors, told them about my pain, the pill that the previous doctor suggested to me and they put me on the combined pill.

At 17 I began to wonder why my back was sore.

At 18 I was knelt in front of the toilet profusely sweating thinking the pain I was experiencing was a result of wanting to throw up. Apparently it was a normal consequence of periods.

At 21 I was out having dinner with friends and they found me lying on the bathroom floor unable to move.

At 22 my mother heard someone talking about endometriosis on a podcast.

We went to the doctors.

The doctors told me it was normal.

My mum said we think it's endometriosis and that I needed to be referred.

Today I had a call with the endometriosis nurse, I'm on a 9-12 month waitlist. She told me there isn't a cure, just ways to make the pain tolerable.

And so now im sat in my thoughts wondering and thinking the possibility of having and raising and enjoying the moments of raising my own children are only thoughts.

#endometritis #uk healthcare #endojourney #i feel numb

[nospoonsbutknives]

Well I got to play Diablo 4 with some friends, it was awesome, and now I have nerve pain going off randomly. Probably because I was sitting weird trying to balance the controller and my phone. Why can’t we have all the nice things😭😂

#chronic pain #chronicpain #spoonie #disabled #endometritis #chronic illness

[keyboard-clicks]

So I need surgery to remove an endometrial cyst on my left ovary and after waiting two months to get in for a consult, it’s going to take a further 5 months to get me in for the actual surgery. Until then I just have to deal with the monthly bouts of nauseating pain that not long ago had me in the ER.

But we can’t have socialized medicine bc it would make the waits too long.

#endometritis #health #text post #tw surgery

[actualrealnews]

Why Does the Medical System Keep Failing People with Endometriosis?

Tracey Lindeman’s Bleed unpacks why the condition prevents people from finding meaningful care

Bleed is part memoir, part history, part investigative journalism—and all searing, acerbic prose. Lindeman includes stories of other people suffering from endometriosis, following each experience so closely that it feels like learning about a friend’s painful, secret second life. She skillfully connects their journeys with recent data on the costs and efficacy of and the trade-offs necessary to pursue pain medication, birth control, hormonal modulators, or surgery as treatment options. Along the way, she clocks the consequences of gatekeeping in medicine and of pharmaceutical-company corruption.

In a climate where abortion and contraceptive access in the United States are under more threat than they have been in fifty years—and at a time when nobody can afford to mince words about women having access to the care they need and deserve—Bleed arrives in full force, exposing the raw and isolating experience of living with a feminized disease in a world that doesn’t want to acknowledge women’s pain. Lindeman does a great service to her readers by showing them they are not alone in their struggles and by sharing everything she has learned about how best to navigate the health care system, but she stops short of giving false hope. “I wish I could tell you that being an empowered patient gets me respect or better treatment,” Lindeman writes, “but it doesn’t.”

sirce

#book review #news #women's health #endometritis #who run the world #further news of the stupid #tracey lindeman #bleed

[honeydew-wombat]

I’m so fucking mad

I’ve got endometriosis

I’ve had the surgery, I took the medication, I did the physio, I did the grounding techniques, I did what I was fucking meant to. Now 3.5 months post op my symptoms have come back with a vengeance. The pain is so bad and it hurts to breathe. What was the point spending 2k on a surgery then now being right back where I was 6 months ago.

#endometritis #fuck endometriosis #endo #endo warrior

[ssbhospital]

#Endometritis

[hotmess-exe]

my doctor prescribed me oxy for the next few days and I finally feel like the waking world is fucking bearable again

#that's nice #why is everything tylenol and ibuprofen like #i know Why #but i mean the kind of shit im recovering from involves so much inflammation and sharp acute pain #i genuinely dont understand being like here's aspirin and tylenol for it you should be fine -_- #anyway #not to complain about finally feeling better lol #altho i did also learn today that i have chronic endometritis 🙃🙃🙃🙃 #just thoughts