Hello All,
I hope everyone is well..
Just going to post and share something spontaneous as have not posted in a while.
I have had really strong HPPD for 28 years now. It has been been quite a journey and battle.
At the end of the day, I'm feeling frustrated that more action is not being taken sooner to find an actual cause, treatment or cure. I know that some study's are being conducted although with Covid 19 it has slowed things down temporarily.
I feel like people in general would have no fucking clue what having real HPPD is actually like, and likely could not handle it. I have learned to accept it mostly, live and get along despite all symptomologies although it really takes its toll especially over the long term.
I wish we could do more, like more sufferers banding together to fight for whatever needs to happen to accelerate research. Like I feel enough is enough.
Cheers