I’m a physio and work part time. I have endometriosis and generally cope quite well with the condition but my flares ups have become more frequent lately, throughout the month not just on my period.
My role is physically and mentally demanding and over the past few months I’ve noticed that increased stress at work is correlating with worsening flares. I think it’s the nature of the job, I used to work in a bank which was relatively stress free and I didn't struggle like I am now .
I’ve talked it through with DH and I think I’d cope much better if I reduced my hours further to around 3 days a week. We could manage financially but I’m worried about the response from my line manager (she isn’t overly supportive) and my team. Our work culture is very work focused.. everyone else is full time and it’s kind of expected to just get on with it.
I feel I’d come across as work shy or lazy if I requested this, it might impact future progression too but right now I feel I need to prioritise my health . I’m torn because I know so many people are burnt out and I feel I should just be grateful that I already have part time hours and accept it.
Has anyone with endometriosis found they are ok up to a point but then work stress or hours noticeably worsen symptoms? Did reducing your hours help? How was asking to reduce your hours received?
Thank you x