I suffer from D.P.D which is Depersonalization/derealization disorder. Trying to get the rite help sucks cause no doctor where I'm from is familiar with it.

Just no your not alone and I'm here to talk if you need to

Thank you. The same for me. You can talk to me too. It is hard for certain individuals to understand what a person is going through living daily differently from others.

You'll find great support here.

Thank you. It is nice to find a place where individuals may understand what you are faced with daily.

hi pink raindrops
people on this site will know what you are talking about, but it can be slow in responses at times.
i would recommend joining other groups on DS a long with this one, in case you are having a rough day, then you have more support if one of the groups is slow or empty that day.
there are groups for anxiety, recovery, PTSD, all sorts of ones. double up and make some new friends!

Hi welcome to the site!

Thank you for the advice. I will be sure to add more groups. I would love to make new friends.

Thank for welcoming me ,all, I hope the day is going well for all of you.

hi PinkRainDrops, welcome to the group.

Thank you for welcoming me.

I've been living now with all of my personalities since 2015. An illness caused me to meet Anne , and many of my consciousness fully, living with DID , I've come to terms with it, but what makes it hard for me , is when someone makes it about them.
My mother made what I'm experiencing about her. Then in her negativeness she want to place demands on me. So in the end my consciousness as a group decided that we shouldn't converse, because she was unhappy with being around us , and talking to us.
I hope everyone in a positive place today.

I joined group today. Recently diagnosed DID. It’s so hard and weird. I now use the term unique. No family member knows. A few friends I just share I have a dissociation problem. ( like I might walk right past them and not notice as an example. )

Me too. I was blessed to find an excellent therapist that was trained for DID. I thought it would be comforting to connect with others that have this challenging and unique disorder. I haven’t told anyone yet . Any advice on thst?