Endometriosis

What a cool site, thank you for sharing. On Dec.11, I had my 7th laproscopic surgery for this. My doctor finally removed my last ovary, so I am currently on the Climara patch. Unfortunately, the only thing my doctor could reassure me was the fact that I wouldn't be bothered by the pain of the ovarian cysts. As I am now on the estrogen patch, my chances of the endometriosis recurring are still there as this is a hormone fed disease. For those of you who suffer from this, or those of you who have a close relation who suffers from this, my heartfelt hugs to you. People who do not have this condition do not understand the constant pain this brings...
 
My heart goes out to you, and anyone who suffers from this. I've watched my sister-in-law battle endo for three years, and it never gets easier for her. I hope a cure will be found someday. Thank you for providing the link, Mrs. NS. I'll tell my sis about it.
 
shut the fuck up about it all ready. in fact just shut the fuck up totally. what is that? 41 threads about how bad your fucking belly hurts? like the rest of feel great all the time. have some cheese with your whine, maybe you will feel beter.
 
I hope you feel better soon and the docs figure out how the heck to fix it.
 
sigh said:
shut the fuck up about it all ready. in fact just shut the fuck up totally. what is that? 41 threads about how bad your fucking belly hurts? like the rest of feel great all the time. have some cheese with your whine, maybe you will feel beter.


You know I might just buy you some crackers to go with that cheese and wine of yours....


If you don't like what I talk about then don't look at my thread...

LICK IT PUT A STAMP ON IT AND MAIL IT TO SOMEONE WHO GIVES A SHIT:p


THE WIFE
 
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