This has been a fun post. We all hate listening to our own selves whine and keep it in our head so we have to come here because only our A.S. family knows what it is like to have A.S. and other things PLUS family, friends and other issues to whine about.

We have enormous things to be grateful for. I am grateful for all of you. Some of you I don't know very well but maybe you might have posted something that you had no idea affected someone else and made their day-mine!

It is not easy living with pain and Dr.s and Dr.s appt.s and bad Drs. and treatments and protocols and tests and waiting for tests but we can come here and get it off of our minds. It sure helps to know that there are others who "get it".

I just hope that you all know that I might not post back to everyone's questions and complaints because I am a tired unit but I want you all to know that at the end of the night, I pray for all of you because you all mean a lot to me.

Pea
Diagnosed with A.S. 29 year's ago.
Diagnosed with Fibro 10 year's ago.
Remicade, Intrathecal Pain Pump 2013