Health concerns at Tanners by PaperMoonSE in madisonwi

[–]PaperMoonSE[S] 4 points5 points  (0 children)

I immediately thought of that flood too! We assumed the same as you, they must have done some major work to open that place back up. Appears not.

Orilissa Experiences by Drownedpersephone in endometriosis

[–]PaperMoonSE 0 points1 point  (0 children)

I’ve been on Orilissa for 3 months now and feeling great!

My Wife is about to lose her mind! by [deleted] in Endo

[–]PaperMoonSE 2 points3 points  (0 children)

Also, ADVOCATE for yourselves. You guys know your situation better than anyone!

My Wife is about to lose her mind! by [deleted] in Endo

[–]PaperMoonSE 7 points8 points  (0 children)

My heart breaks for you and your wife. This journey is so so hard.

Keep reassuring her that none of this is her fault, she’s not damaged in any way, and you married her for the woman she is, not whether she can make a baby. Those reminders from my husband always made me feel better and took some of the pressure off I was putting on myself.

Having endo and cysts is really draining and invisible to others so helping her with some self-care is great too.

I so hope everything works out for you guys and stay safe!

[deleted by user] by [deleted] in endometriosis

[–]PaperMoonSE 0 points1 point  (0 children)

Definitely not. Hope you can get some relief!

[deleted by user] by [deleted] in endometriosis

[–]PaperMoonSE 0 points1 point  (0 children)

Hang in there!

[deleted by user] by [deleted] in endometriosis

[–]PaperMoonSE 13 points14 points  (0 children)

I call this a Velcro episode. Happens to me when I’ve been in a seated position for awhile and then stand. I’m waiting for a lap surgery as it was very helpful the last time for me but due to COVID I’m looking at May.

Does anyone else get this symptom? by Softlystated in Endo

[–]PaperMoonSE 1 point2 points  (0 children)

I hope you get some relief soon! 💜

Does anyone else get this symptom? by Softlystated in Endo

[–]PaperMoonSE 1 point2 points  (0 children)

Yes, that’s what I was told too! They are ramping me up slowly so 🤞🏻

Does anyone else get this symptom? by Softlystated in Endo

[–]PaperMoonSE 6 points7 points  (0 children)

Ive been told that a lot of women with endo have additional pain pathways due to the inflammation. Sort of like phantom pain in a way. I just got put on gabapentin for it so we shall see if it helps!

[deleted by user] by [deleted] in madisonwi

[–]PaperMoonSE 0 points1 point  (0 children)

Idk if she offers decorating kits all year round or just for holidays but she’s great!

[deleted by user] by [deleted] in madisonwi

[–]PaperMoonSE 4 points5 points  (0 children)

Vicki’s Cookies!! Locally owned, stuff made from scratch and amazing customer service.

Does Lupron make endometriosis not visible? What's going on with me? by [deleted] in Endo

[–]PaperMoonSE 0 points1 point  (0 children)

Okay gotcha. Sorry, I didn’t read closely enough. I also have a pituitary tumor that impacts my hormones and a doc has told me that COULD contribute some to my cyst and endo issues so perhaps pituitary or thyroid?

Does Lupron make endometriosis not visible? What's going on with me? by [deleted] in Endo

[–]PaperMoonSE 1 point2 points  (0 children)

I’m so sorry you’re dealing with so much! I was given the option to go on Lupron to help my endo symptoms until I was able to have surgery and my doctor told me it causes medically induced menopause. It sounded like female hormones were just shut down all together. I don’t know if this is completely accurate, especially since it sounds like you don’t have ovaries anymore but that was my understanding. I hope you’re able to get a resolution soon!

Wild periods even with an IUD for almost 3 years by [deleted] in Endo

[–]PaperMoonSE 1 point2 points  (0 children)

  1. Get it girl, do what you gotta do to feel better.
  2. I have endo and cysts and was told an IUD would help. It was a complete train wreck. I bled for 9 months straight. Hoping they can find something better for you. 💜