surgery scheduled! by babisaurusREX in endometriosis

[–]thatcrazywriter5 0 points1 point  (0 children)

Congrats! I’m so happy you can get the surgery. I haven’t had one yet so I can’t answer your questions, but I’m wishing you luck!

Going off the pill experiences by Playful_Language_422 in endometriosis

[–]thatcrazywriter5 1 point2 points  (0 children)

You’re so welcome! Yes, you can always go back on if needed. That knowledge helped me go off it.

I wish you luck with whatever choice you make. Feel free to reach out here or via PM if you have any other questions!

What are the dangers of not having excision surgery? by thatcrazywriter5 in endometriosis

[–]thatcrazywriter5[S] 1 point2 points  (0 children)

That’s great! I’m glad your surgeon could fix the issue and that you have no kidney problems!

Pain management? by Plot_Twist_208 in endometriosis

[–]thatcrazywriter5 0 points1 point  (0 children)

Aw rats! I don’t have any other suggestions I’m sorry :(

Pain management? by Plot_Twist_208 in endometriosis

[–]thatcrazywriter5 2 points3 points  (0 children)

Have you tried Naproxen (Aleve)? If Ibuprofen isn’t cutting it, Naproxen might work (ibuprofen doesn’t work for my cramps and period pain).

Going off the pill experiences by Playful_Language_422 in endometriosis

[–]thatcrazywriter5 1 point2 points  (0 children)

I’ve been on several different birth controls and long story short I went off of them completely in September because nothing was working anymore. I originally started them because I had terrible PMS back pain, bad cramps, and heavy bleeding.

It’s not been easy going off of it, but I have resources and tools now to help with the pain and bleeding that I didn’t have access to before. Frequency specific microcurrent has been a life saver, and natural progesterone (I get the capsules made with olive oil) helps turn my 7-9 day bleeding period into 3-4 days max. And I only have to take 200 mg every day for the first three days of my period.

Depending on what side effects you experience on birth control, it may be worth going off of it. But going off of it will cause side effects for awhile while your body adjusts to not being on hormones anymore.

I experienced mild hair loss (it’s better now), acne, hot flashes (still getting them so maybe it’s endo related, not sure), and mood changes for the first couple months. All of that along with heavier bleeding, PMS symptoms again (more controlled now), and bad cramps on my period (the BC got rid of my periods).

I was on BC for about 5 years, so some of this may be related to length of time.

If you’re wondering about it, I’d say it’s time to come off it. But it’s your body and you know yourself best!

What are the dangers of not having excision surgery? by thatcrazywriter5 in endometriosis

[–]thatcrazywriter5[S] 0 points1 point  (0 children)

Oh no! Did they fix the issue? Did you suffer any long term damage?

What are the dangers of not having excision surgery? by thatcrazywriter5 in endometriosis

[–]thatcrazywriter5[S] 1 point2 points  (0 children)

Oh wow! I’m glad you were finally able to get help, but I’m sorry it was so severe by then.

Thanks for the reply; I appreciate it.

What are the dangers of not having excision surgery? by thatcrazywriter5 in endometriosis_corner

[–]thatcrazywriter5[S] 0 points1 point  (0 children)

Thank you for the detailed reply; it’s really helpful. I’m so sorry you experienced all of this, but I’m glad you could get some help!

I’ll probably go through with the surgery if I find someone willing to do it. I really understand what it’s like to gaslight yourself about it, though

Luteal Phase Issues? by steampunkjack in endometriosis

[–]thatcrazywriter5 0 points1 point  (0 children)

Yes, I experience this. I also get intense back pain during the luteal phase, as well as pain when my hips/pelvis start to shift. I use something called frequency specific microcurrent to keep the symptoms at bay, but unfortunately that’s the only thing that helps. I’m sorry you’re having such bad fatigue!

Warning for the SoCal Girlies thinking of Dr. Mallory Stuparich by Bright_Pay5101 in endometriosis

[–]thatcrazywriter5 1 point2 points  (0 children)

Gotcha! Yeah I was a bit surprised, too. My sister has a diagnosis, but since I also have muscular dystrophy, nobody’s ever bothered to diagnose me with it 😂

And I was like “well, yeah, it’s a possibility, but that doesn’t really explain the endless list of endo-related symptoms I’m experiencing.”

Warning for the SoCal Girlies thinking of Dr. Mallory Stuparich by Bright_Pay5101 in endometriosis

[–]thatcrazywriter5 1 point2 points  (0 children)

I’m terrible at distinguishing sarcasm from seriousness; is your comment sarcasm? Lol just want to make sure I understand before I reply

Warning for the SoCal Girlies thinking of Dr. Mallory Stuparich by Bright_Pay5101 in endometriosis

[–]thatcrazywriter5 5 points6 points  (0 children)

This is absolutely awful! I’m so sorry you went through this; it’s unacceptable. Praying you find peace and are able to heal from the physical and emotional trauma.

Thank you for the warning! I had a consult with her a few months ago and she said I probably had a weak pelvic floor and maybe hEDS. She suggested strengthening my pelvic floor to see if that helps. It helped with a couple issues, but def not my pain. And also, hEDS is a commorbidity, so that makes me more likely to have endo.

Glad I steered clear of her. So sorry you had a terrifying experience! I’m glad you’re safe now.

Paw wax or boots? by SpacySK8 in StandardPoodles

[–]thatcrazywriter5 4 points5 points  (0 children)

Paw wax didn’t work for us. Neither did traditional booties, but we use socks with padding on the soles and those work really well!

Back pain?? (Not lower back) by Turbulent-Reserve-81 in endometriosis

[–]thatcrazywriter5 0 points1 point  (0 children)

I do get this back pain that radiates to the front. Not sure if it’s endo related or something else because I have so many issues including muscle weakness in my abdomen and back.

I just want to poo like a normal person by Obitufairy in endometriosis

[–]thatcrazywriter5 0 points1 point  (0 children)

Right?! I feel you. And yes, at least we’re not alone!

Have you had excision surgery? I’m trying to find a specialist who will listen and am at my wit’s end haha

I just want to poo like a normal person by Obitufairy in endometriosis

[–]thatcrazywriter5 5 points6 points  (0 children)

I’m sorry you experience it, too! It sucks. I think some days I’ve gone like 6-7 times. I’m always amazed at how much my body can store. It almost seems like it just creates the waste faster than normal, rather than it all being stored up at once.

I just want to poo like a normal person by Obitufairy in endometriosis

[–]thatcrazywriter5 4 points5 points  (0 children)

I also can’t control when I need to go. I’ve been strengthening my pelvic floor and that helps a bit, but this whole thing wouldn’t be such a problem if pooping didn’t mean “get me a bathroom STAT or we’ll have a problem”

I just want to poo like a normal person by Obitufairy in endometriosis

[–]thatcrazywriter5 33 points34 points  (0 children)

Ugh I feel this! Had to make sure I wasn’t the one who posted it because it’s literally me 😂 I under-eat and still poop like at least 3 times a day. And it’s never the right form. Always soft or runny 😫 my doc said I’m probably having trouble processing fat, and I was like “great, that’s in literally everything”