People describe their Endometriosis | Living with Endometriosis, diagnosis and symptoms 🌸
Thank you so much to those who got involved and shared their stories with us today Here are the questions incase you’d like to …
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Episode: Monday, September 27, 2021 Guest: Puma ••••••••••••••••••••••••••••••••••••••••••••••••••••••••••• We appreciate you joining The … source
David speaks with Curtin researcher and chemical engineer, Professor Neil Foster, and Chief Operating Officer of Little Green … source
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Hey sweethearts! I hope you enjoyed this video as much as I loved making it as these are my fave types of videos to make!! Please let me know what you'd like to see in this series thank youuu xxxx
my apologies, i dont want to come across as ignorant, maybe i am used to a different reality. in my country women usually go to a gyno at least once a year (check up, report back on period, symtoms and smear test). if you notice symptoms with a pattern why would you ever go to a GP and not to a gyno? ladies, for real, stop going to your GP unless it is needed to get a referal to a gyno in your local health care system.
Thank you so much Jess and all the people in this video, I’ve recently had a pharmacist suggest I might have endo after being told it was just painful periods for 12 years. I didn’t know what I was experiencing wasn’t normal, because the professionals led me to believe it was. This video really encompasses what I’m going through right now and is really validating for me. Thank you!
As someone who has been trying to get a diagnosis for ten years this video really helped me. I pass out from my periods and they are debilitating. And to be told you’re fine or you’re healthy makes you feel invalid or like it’s all in your head. Or that your pain tolerance sucks or something, it’s exhausting and you eventually give up and just try to live with it. Every month when your period is coming which isn’t the same ever sometimes it’s 6 weeks you’re terrified because you don’t know if you’ll make it home to die alone with the pain. I’m
Sorry for anyone who has to feel this way but we are valid and it is real
Pain.
As someone with endo this video meant a lot to me. Thank you for using your platform to talk about this 💛
Awesome video Jess 😊 Thanks to all the participants. I'd love to see people describe their Nuerodiversity.
<3
Seems like your channel (or at least this video) has restrictions put on it. I tried writing a comment but immediately it got automatically removed..
I don’t have endo but I do know how damaging it can be to have healthcare professionals mistreat and gaslight you.
Thank you for covering this topic<3
My heart goes out to these participants and everyone suffering with endometriosis.
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VOR.RED
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No le entiendo nada pero la amo