When I refuse to go to appointments my pdoc comes to my house. Intellectual disability team = more holistic.
Oh, that sounds wonderfully convenient. I wish!
I’m from a small town… Intellectual disability services are small. My IBS tends to play up when they are trying to put me on a community treatment order (CTO) they then come to my house with AAMP.
I’d feel very uncomfortable if my pdoc made house calls.
I just see her via telehealth sessions.
I’m fine with this.
No, never.
Before the pandemic I would go to their offices. During the pandemic it has been phone calls.
@Wave I was wondering why you feel uncomfortable with a visiting pdoc?
I live in a group home so have a separate office on the complex. I would never let a pdoc in my bedroom.
My house is a disorganized mess, I wouldn’t want her seeing this.
But I’m glad it’s working out for you @bobbilly.
Maybe I’d get used to it.
@Wave my bedroom is a complete mess. On the depot and sleeping 16 hours a day don’t give me too much time to clean or motivation. I’m lucky that the staff clean downstairs or it would be worse.
I don’t think I would like that.
@Wave I like how your avatar is really distinctive when your replying. The colours are good.
With Covid I’m uncomfortable with people coming over the house.
I don’t feel comfortable with my case manager coming over.
With Covid they are being very careful.
I stay in touch with them over the phone.
Thanks @bobbilly
@Wave I have 24/7 support and staff wear masks when with services users. They don’t like this but management insists they wear them or they can get a disciplinary if caught with out them.
Yeah when I see my case manager she’s always wearing a mask.
@Wave How you coping without the face-to-face support?
Better than I thought I would.
But I kind of miss the face to face interaction.
@Wave you seem very resilient. Have you got much support off the online community . ie SZ forum, Has here helped?
here has helped me much. I can’t talk to many people in the group home about SZA related matters.
Yes coming here sure does help.
I don’t feel as alone.
@Wave same here.