So once or twice a month, our little group of EndoSisters gets together for food, drinks, hugs, laughter, tears, and support. Tonight was one such meeting. And they’re always amazing, regardless of how many, or how few, people are able to attend.
One of my EndoSisters brought up an incredible question this evening, which inspires tonight’s blog:
Why isn’t there more info out there about life AFTER Lupron Depot? There’s plenty out there about life before and during, but not after.
So, I’d like to create an ongoing and open “testimonial” area, so to speak, for women who have been on Lupron Depot to write about their lives now. How long did it take to leave your system? Do you have any residual side effects? Has it changed your life for the better? The worse? Did it make one lick of difference? Would you ever go on it again?
Interested in submitting? Submit a comment below and I’ll post your experiences on this page. Be as detailed as you want. Let it all out…there’s no judgment here.
Interested in reading other people’s experiences after Lupron? Scroll down and read.
Feel free to share your experiences. We can only learn if we share. I thought I was the only one who had tingly, sensitive skin until a brave EndoSister brought up here own continuous skin sensitivities.
It’s not the harmless medicine our physicians lead us to believe.