Hi Ladies,
I am 22 years old and just started birth control last April/May because I started getting my period twice a month. My obgyn put me on a low dosage of Lo Loestrin Fe. I had a visit with my obyn yesterday because I've been having issues with my period again and I want to have it changed since it is no longer effective and I think it is impacting my blood work that my GI doctor has been ordering.
I started feeling sick right before going to my fall semester of school and emailed my GI doctor instead of calling her. She never received it and since it wasn't completely urgent so I waited until October to email her again. I was feeling sick and it was hard for me to bring myself to eat. My GI doctor called me finally and had me come in for an evaluation. I had stool samples collected and blood work done. My blood work came back abnormal for my lipase which was almost at 300 but I wasn't experiencing symptoms of pancreatis and I read online that birth control can have an affect on lipase levels but she just thought it was pancreatis and told me to avoid alcohol (which I only drink occasionally). When my stool studies came back, I was positive for C-Diff and she put me on flagyl and cipro (i hate flagyl so much). Besides the cold I recieved from my weakened immune system, I was feeling better after my course of antibiotics. I'm finally going in for my endoscopy and pouchoscopy on Thursday to see if there is anything else going on in my body. It is my first time having a pouchoscopy since I had my surgery in June 2011.
In October and November I missed both of my periods and I randomly got it last week when I wasn't supposed to have it. I went in to see my Obgyn yesterday since it is no longer correctly regulating my period. I gave her a copy of my most recent bloodwork. She said the only way we can know if its my birth control affecting my blood levels is by coming off birth control for the next three months. She tried pushing me towards the alternate options of an IUD which I have been always been very skeptical of and especially now that I have a jpouch. One option she gave me was Skyla which is inserted by her and provides you with 3 years of BC and lighter periods. As I was reading the pamphlet it says people who are prone to infections and weakened immune systems shouldn't take it which was a red flag to me. The second option was nuvaring which I would have to insert and remove every month. My problem with this is that after my pouch surgery everything is so tight and it hurts sometimes to even put a tampon in. I don't think I would be able to handle doing this and I suffer from bartholin cysts every now and then which are painful as well. I don't think she is very familiar with jpouch patients and I think I might look into finding somebody who works with patients like us.
I would rather just go back on the pill after my 3 months are up but on a different one since it is the least invasive. Are there pills that any of you suggest and what are your thoughts on IUDs and having a jpouch?
Any advice at all would be helpful!
Thank you!
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