I had my post-op yesterday and was given my first round of Lupron. I am very thankful and lucky that insurance covers the
add-on pill, which is suppose to lower side-effects.
After surgery, Doug supposedly told me that the doctor wanted me to go on this therapy-but of course anything you tell anyone after surgery usually doesn't work since the person who just had surgery is still very out of it. So when the nurse called me the following day, after surgery, to tell me how everything went and how the doctor wanted me to go on this injection for the next 3 months, I was overwhelmed. The nurse said I would have to talk with insurance since they have to verify I want to go on this therapy, and every month I will have to verify to send the medicine to the doctor. I did my research and joined a support group, most women who have gone through this didn't end up liking it very much, but I still haven't found someone (from the support group) who has done this therapy with the add-on pill. From what I gathered from research, what the doctor told me, and from other women is this-the medicine has these side-effects: bone loss (will have to take calcium supplements), mood-swings, depression, hot flashes, won't be able to sleep (like tonight), and makes women angry (advice was to go to the gym and often).
The reason for this route, is because since my endometriosis is at a level/stage 3 (with level 1, being not severe/easily treated and level 4, being very severe/hard to treat), this medicine will stop my cycles and lower my levels of estrogen. Endometriosis is when endometrial tissues that lines the uterus, grows outside the uterus, this irritates the body, causing pain. Because the lining grows outside the uterus, on the ovaries, fallopian tubes, etc; the bleeding produced by the growths (same as menstruation), causes the body to react and surrounds the blood and tissue with scar tissue, causing more pain and infertility. By lowering my levels of estrogen, it should stop the tissues from forming/growing and will stop my ovaries, why it will "trick" my body into a menopause state.
When I went in to my post-op, I wasn't sure if they would have gotten the Lupron, since I talked to insurance about 4 days prior to my appointment-but sure enough, they had it (and I was very glad, since I hate having to make multiple appointments a month at their office since they don't allow children-due to respect towards couples who are having issues with conceiving). I had a million questions for the nurse and doctor and was pleasantly surprised that the nurse knew almost everything about this injection and gave me a few brochures about Lupron therapy and the side-effects. When the doctor came in to do the post-op examination, he seemed very (happily) shocked I had agreed to do this since the side-effects scare women off of doing this drug. But because I trust this doctor and I truly believe he is looking out for me and believes this will help me in the long-run, I agreed. I can't say enough how much I love this doctor. After the experience I went through with my last doctor, who was always too eager to open me up and not tell me anything-especially annoying when I was pregnant, I am so thankful for this doctor who tells me like it is, talks me through my issues and gives me options. Dr. Alfred Rodriguez is amazing. Anyway, after my exam, he talked with me about the medicine and told me that women under his care (who take the pills along with the injection), usually don't have severe side-effects, so that makes me hopeful. He told me that since I just had surgery and he took out as much of the endometriosis as possible, he strongly believes that I only need 3 months of this medicine-but the effects of the medicine will last 6-7 months and not to expect to TTC for 8 months. So what will happen is I will go in every month, for 3 months to get the injection. Two weeks after my third injection, he will do another exam and figure out if I will need 3 more months (6 months is usually the rule with women like me, but again just had surgery and am pretty cleaned up on the inside). Because endometriosis can occur quickly, we have no clue if I will need 3 extra months of this therapy. After the doctor left, the nurse had me turn around, as she didn't want to scare me with the size of the needle, and although the injection hurt just a tad, I joked with her saying it couldn't be worse than the epidural and we both laughed.
After reading the booklet the nurse gave to me it seems that the first 2 weeks will be hard. Pain might be severe and the symptoms of endometriosis might increase. After that, it is a guessing game when the side-effects and pseudo-menopause will kick in. Nurse said it could happen immediately or it could take as long as the third injection to appear.
My next scheduled injection is for Dec. 19.