stevelassiter
"Have been dealing with alot of joint pain and onset of returning psoriasis.I am new to this site,but have been dealing with PSA for 20 years now.I also have CP which increases the joint pain severally.Winter is coming and I will probally end up back inside a emergency room to deal with this .Sorry to sound like a downer,but having PSA is physical,and mental and unfortunately having to fight for Disability for the last 3 years has taken a toll on me.Thanks for letting speak."
@stevelassiter, we hope you will come here anytime you need to. I hope this winter is a mild one for all of us (winter is often so tough). Where are you with your SSDI application process?
A very warm welcome,
-Victoria, Community ModeratorHi Vicki.I am glad someone is actually listening.There are people out their.THANKS.I am currently on my 3rd appeal at the Richmond VA SSI on Main St .My judge is Deborah Foresman.My case has been mishandled and not taken serious.I know that you and any person with any common sense would see that I am in need of Forever medical assistance and the court system has delayed me to the point of not being able to afford my doctors visits or my necessary medicine for my PSA.Last time I went 4 months without my medicine and ended up in the hospital.I have to go every year to the emergency room due too the intense pain.I told the Judge I was at a 8.5 out of 10 in pain,that is from sun up till I crawl and cry myself to sleep.No Joke.Thank you again for taking the time to read this.Any support and help is a true Blessing.God Bless.Steve
I really hope there are better days on the near horizon for you, @stevelassiter. Keep on fighting. We know how hard this is, but we are stronger together!
-Victoria, Community Moderator