Hello,
I had a recurrence last year after being in remission for over 6 years. I was diagnosed as being a 3C and am BRAC2.
I did really well with the chemo and now I have been taking Olaparib for a little less than 3 weeks. It's been rough especially at the beginning. They had to wait a few extra weeks to give me the medication as my neutrophils were too low. They came back up and my bloodwork was good. Just before that, I had caught for the first time COVID and had to deal with that as well.
I don't feel the best I must admit but the nausea has gotten a lot better. I did not take the anti-nausea medication because they cause constipation and I didn't want to deal with nausea and constipation.
My bowell movements were OK at first but not as great as before and then a few days ago, I started getting constipated and needing to strain a lot. I read online that this can be a side effect of the medication. My entire eating schedule has changed since I started taking the PARPS and it seems like my digestive system has slowed down. I was only able to go a little bit but with the help of Restoralax. I have only been taking it the last few days but I tend to panic and not wait long enough for it to work which means straining. I am by nature a nervous person.
Can you tell me your experience about being on Olaparib. Seems more people have diarhea than constipation. I am in Canada and I am followed by a nurse who takes care of the patients on PARPS. I haven't had the chance to speak with her because of the holidays.
I don't feel too good when I haven't had a decent bowell movement in a few days and I am scared that the medication will stay in my system too long and become toxic.
Just looking for advice. I know the first few months can be tough on PARPS.