One of the downsides to a condition like endometriosis is the fact that your doctor will try you on every type of contraceptive pill going to see if that will ease the side effects of the endo. What I found when I was being given various pills and tablets from the doctor and very little information. This is where I feel as a blogger I can make a difference in the world (even if it’s just to one or two people) and share information from around the web that I wish I’d been able to find when I was looking for info rather than the horror stories which was what I actually found.
When I was being given new pills I’d always have a list of questions for the doctor:
- Should I expect any side effects?
- What are the side effects I can expect?
- Is there an alternative if this doesn’t work for me?
- Any other advice for me?
My advice
One of the most important things I learnt from the time I had endometriosis and now being a few years post op is that you are the one that knows your body. Not the health professionals – you! Feel that the drugs aren’t doing what they’re meant to or that you just don’t feel quite right then go back and tell them. Make a diary or take notes with you so you don’t forget anything and if you know what treatment you think will be right for you then push until you get what you want. It took me years to get the operation I wanted and I hate to think what state I would be in if I hadn’t pushed for what I knew was right for me.
Does the pill work for you or do you have a question about endometriosis?




