My Endometriosis Story

Hello my friends, today I wanted to share with you my endometriosis story. I hope you enjoy!
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For more info on my chronic illnesses check out the links below!
POTS (Postural Orthostatic Tachycardia Syndrome)/ Dysautonomia: kzbin.info/www/bejne/jKDLd5aOr7N8ftU
Hashimotos: kzbin.info/www/bejne/pnzIpGp6pc9qZ68
Fibromyalgia: kzbin.info/www/bejne/o2LTg5qvd92hoc0
CFS (Chronic Fatigue Syndrome): kzbin.info/www/bejne/e6WsYqCLhtKhatE
SIBO (Small Intestine Bacteria Overgrowth): kzbin.info/www/bejne/aWTSaqJqYq-ge6s
IBS (Irritable Bowel Syndrome): kzbin.info/www/bejne/d5O7Z2eiq7Sbq5o
Leaky Gut Syndrome www.health.harvard.edu/blog/l...
Chronic Migraines: kzbin.info/www/bejne/kJ6YgoSNmpunY6c
PCOS (Polycystic Ovarian Syndrome): kzbin.info/www/bejne/q6apqp6Agqxmaac
Endometriosis: kzbin.info/www/bejne/kF65nWdpZ8qagck
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[@Quit3Cut3]

I’ve been dealing with endo pain since I was 10. No one ever took me seriously, and back then endo was never talked about. I’m 34 and finally having surgery and it sounds like it’s pretty severe. My pain brings me to my knees and I can’t walk. I puke from the pain. My husband had to wheel me into the ER twice last year. And now the only reason I’m being taken seriously now is because I’m trying to get pregnant. They think I have stage 4, I have 2 endometrioma chocolate cysts, my right Fallopian tube is blocked, and he’s pretty sure it’s on my bowels and I’ll need a bowel resection. It needs so much more awareness, ridiculous no one takes us seriously for years!! I use naproxen, heating pads, muscle relaxers, a tens unit, sometimes only narcotics help.

[@olisaprice9870]

Is Endometriosis Pain worse then cramping pain

[@brookebeck3367]

I don’t understand how waiting to remove it benefits you in any way; it just grows in the process and makes whatever surgery you do have more involved with more possible complications with more endo tissue possibly not removed and able to come back. Why do we not have surgery to remove it WHEN ITS SMALL AND PREVENT LARGER ISSUES

[@Quit3Cut3]

@@brookebeck3367 it wasn’t my decision, no one believed my pain for years. Til I finally took matters into my own hands and saw a specialist. The pain became unbearable.

[@Quit3Cut3]

@@olisaprice9870 worse than childbirth from what I hear. There are days I can’t walk.

[@georgiabeardsley4013]

I think I have it, it’s so fucking painful

[@AuthenticallyAshley]

Birth control sucked for me too! I tried mirenna, nuva ring, pill.. made me sad and angry. And like you said every year it got worse. I’m close to going for a laparoscopy soon! Hoping everyone reading this finds the peace they need. You are valid

[@LATX1388]

I have endometriosis, I've had excrutiating cramps during my period since I was 14. Been to the ER a few times, used birth control for most of that time and currently am again. However it isn't working anymore. I have been bleeding for 9 months every single day and am in pain even on it. It used to be the one thing that calmed it to where I could function. Now we are talking about having a baby which obviously means getting off of birth control. I am absolutely terrified. The pain is indescribable. Muscle relaxers, prescription pain medication, heating pads literally won't even touch the pain. I have memory loss I'm in that amount of pain. I'm convinced it's worse than childbirth pain because I can't humanly imagine anything worse. It sucks that I've seen 12 different obgyns and no one has helped me other than here's narcotics and birth control have a great day. I want to try for a baby more than anything but after 4 years no luck before this, I fear how many of those painful periods I'll have to experience to maybe even get a shot at conceiving. 😔

[@Aimee_Esther]

I am so sorry you have been dealing with all that! It is so hard! Thank you for opening up and sharing that with me. I wish I had the answer for you. Sending you prayers of healing.

[@ma0987]

Try to go to an endometriosis specialist. Normal obgyns are often undereducated on endometriosis.

[@Embraceyourcurls24]

I can fully relate to this, I also have endometriosis, extra long cycle and I can’t handle birth control.

[@olisaprice9870]

Great video on your story about endometriosis story Time

[@kirtisoma3211]

I was misdiagnosed many years ago my gynae ran blood tests as my symptoms do not meet the criteria of PCOS.

[@amymiller1782]

Thank you for sharing your story! Love your channel!

[@Aimee_Esther]

Thanks for watching!

[@AstroGirl_draws]

This is a rather personal question , but did you ever find you had pain during intimacy with pcos or endo

[@mariahdavies4232]

I have both and yes for me

[@aoifemccarthy2299]

Thanks for sharing 💕

[@kianaraynee]

We are so alike 😅 you got this

[@Aimee_Esther]

Thank you! Glad someone understands!

[@Thesouthlandfamily123]

I just got in medical school at age 13 year old I started since 12 year old I started easy lesson then I did them all of the all the courses all I just did all of my courses but I am completely 55% of medical school I now I am a medical student again The first ever HMX fundamental Immunology that my fist ever degrees Then HPX Gynecologist then HMX nephrology Then HMX urologist HMX cardiologist HMX encronologist HMX fundamental oncologist Then other CPX final Nephrologist Then HOX obstetrician Then HPX Endocrinologist Then HPX fundamental Otolaryngologist Then t try hen HPX pulmonologist Then HPX fundamental ophthalmology APX osteopathic medicine Then OPX gastroenterologist Then PMX final Nephrologist again Then MPX final Neurologist Is too many I will talk about later in my video

[@nompumelelomahlangu360]

I have suffered a lot because of Endo😢

[@olisaprice9870]

Hello there

[@Aimee_Esther]

Well Hi!

[@Dress_to_fuck_n_dlz]

Im.crying😢😢😢 someone can relate my sittuation now...i have endometriosis and i have nonstop period...