What are they like? Are they helpful? I’m thinking about trying.
I know the facilitator. I am nervous driving to new places though.
What are they like? Are they helpful? I’m thinking about trying.
I know the facilitator. I am nervous driving to new places though.
I was an outcast when I went after I was honest about my diagnosis. They asked so I told them.
If I ever go to another meeting I won’t say my diagnosis.
That said, every group has its own dynamics and therefore your experience will be different from mine.
You’ll be in because you know the facilitator anyway
Interesting!! Thanks for the advice @LilyoftheValley
I will not share my diagnosis if I go to the meeting even though I know the facilitator. I don’t know her that well on a personal level, you know? So I won’t share my diagnosis.
That’s smart. People don’t understand this disease were diagnosed with and it scares them
I’ve been to groups. @LilyoftheValley is right. Most people there have depression or anxiety and those are accepted to state for yourself.
On the other hand if you want real help for a specific problem, I have stated my diagnosis and gotten specific advice for it. Of course there was a girl there with DID and we bonded. It depends on your audience.
I’ve been a facilitator at NAMI Connections support group and it really varies a lot on who shows up each time. Sometimes it’s the same people, and sometimes we get random new people who come to one meeting then never come back. Still, i enjoy the process, it makes me feel like my advocacy work is successful.
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