Thoughts about my sick leave

I’ve been on sick leave since 5th of January 2015, meeting with my doctor with about a 3 month interval for years now. It began with the severe panic attacks back in mid December 2014 when I was told that the gynecologist had found “something strange” in my ovaries (more on that story here) even if I’ve been on sick leave because of my depressions a few times before this major episode.

Now, I usually don’t write about me being on sick leave that often because there aren’t that much to say about it. I get a set amount of money each month from the government and I have my administrator at the Swedish Social Insurance Agency (Försäkringskassan), like most other Swede’s have in my situation. My psychiatric doctor are in touch with the agency and feeds them information on how my case is progressing roughly once every 3 months. I usually have a meeting with the agency once every six months or so as they like to stay in contact, even if nothing really changes.

I’ve tried going back to a regular job but with unsatisfactory results, my depression and anxiety levels flared up something bad. Therefore, everyone around me from agency administrator to nurses and doctors settled into the fact that it would probably be best if I was just left alone for some time. But, a lot of time have passed by and I’ve been trying to recuperate for years by now and so they are starting to reconsider my case. My doctor have recommended that I’d be considered to switch from the temporal sick leave to disability pension instead, which is a more permanent solution. It would mean I’m not under any pressure to apply for or have a every day job in the traditional meaning.

My agency administrative isn’t happy at all about this, this option is usually reserved for the ones who are never going to be able to handle a regular job ever again. But after several tours back and fourth she recognizes that the attempts to get myself back into a job always have ended badly. I’ve always been set back severely and needed a long time to recover from it. My doctor knows this and it’s the main reason she have put down such a suggestion. My doctor and agency administrator are trying to set a date for a meeting where all this’ll be discussed between the parties that are concerned.

My personal thought though? After discussing it back and forth during the summer T and I both agree that I have a need because of my diagnoses, psychological and physical. I break easily when I’m put under pressure and are exposed to stress. If going on disability pension is the key for my well being, I’ll go down that route. It would mean that I could take things in my own pace and keep all the routines and stability that I seem to need.