Endometriosis Awareness Month

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Endometriosis Awareness Month
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Do you or someone you know struggle with endometriosis?

I've been struggling with Endometriosis since I am 13 years old. Please share your story if you can relate!

anchor.fm/thewellnessprojectwithdes/episodes/89--Endometrios...

#Endometriosis #Endo #EndometriosisAwarenessMonth #mentalandphysicalhealth #MentalHealth #podcastepisode #Sharingmystory

89. Endometriosis Awareness by The Wellness Project with Des

Welcome to my podcast, The Wellness Project with Des. On today’s episode, I talk about my own personal struggles with Endometriosis in hopes of spreading awareness.  Join my mailing list and get your free printable 7-day Gratitude Journal: https://www.subscribepage.com/k6p4b2 Become a part of my facebook community: facebook.com/groups/accordingtodes If you liked this episode or have enjoyed any of my past episodes, please leave me a review on iTunes! I would really, really appreciate it! https://podcasts.apple.com/us/podcast/the-wellness-project-with-des/id1477570126?utm_source=newsletter&utm_medium=email&utm_campaign=lets_talk_about_a_taboo_subject&utm_term=2022-01-27 And make sure you share this episode and tag me on social media @the.wellness.project.with.des
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110%

I feel like I’ve given EVERYONE in my life 110% of myself, making sure that they were okay, that they knew I was there for them, I would be the shoulder, the ear, the advice giver, I’d be everything for everyone. Just to make sure I didn’t lose any part of them.

NO ONE. && I mean NO ONE seems to care if they lose a part of me.

Why is it so hard to do what is best for me?
Why is it so hard for people to do the same for me?
Why am I like this?

#helpme #HypothyroidismUnderactiveThyroidDisease #Endometriosis #PolycysticOvarySyndrome #EndometriosisAwarenessMonth #ChronicDepression #ChronicMigraines #ChronicPain #BipolarDisorder #Anxiety #PTSD

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Hoping for answers soon #Endometriosis

I’ve been having issues with my women’s health for many years now. All women on both sides of my family have a history of fibroids and endometriosis. All of the women in my family have had a hysterectomy and went into early menopause because of it. Yet it’s taken me more than ten years to be heard by doctors. I have a specialist appointment in June and I’m hoping that I’ll get some answers.

Endometriosis affects 1 in 10 women, yet it can take an upwards of 10 years to be diagnosed. Endometriosis isn’t just a bad period, and pelvic pain isn’t normal.

It might be the end of Endometriosis Awareness month but that doesn’t mean we don’t keep fighting for advocacy and fighting for our doctors to listen to us. Sending love to all Endo warriors out there and all others who are trying to find answers about their women’s health, keep fighting.

(Artwork done by myself on IPad Pro)

(Pic ID - shot of Amelia’s stomach and pelvic area with a striped shirt on and black pants. With a drawing over the top of a uterus)

#EndometriosisAwarenessMonth #ChronicFatigue #WomensHealth #Disability #Hysterectomy #PolycysticOvarySyndrome #Adenomyosis #Infertility #InterstitialCystitis

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#EndometriosisAwarenessMonth

I am an RA and I am planning to make my bulletin board themed toward Endo Awareness Month. I want to create a program for the women in my community who also suffer with Endo, PCOS, and other reproductive issues to gather together and provide information on their experience. Anyone have ideas about the programming or another concept??