Hey everyone. Sorry that it has been so long since I have last written. However, I do still read all of the comments that come through and try to respond as much as I can. (Even if it is super delayed. Will you believe me if I say that the GP elves take me hostage? No? Well, it was worth a try!)
It still boggles my mind how a little blog that was made as nothing more than a creative outlet for everything I went/go through with Gastroparesis has developed such a following. There are still new likes and followers each week. I’m glad that my writings have helped so many people not feel alone.
Lately, I have been battling my Endometriosis more than my Gastroparesis. I have also really missed writing and having the creative outlet. As such, I decided to create a new blog that is a catch all of everything. There will still be Gastroparesis stories, but there will be many other things as well.
Please hop on over and check it out. http://www.anomalyadventures.com
Happy Tummies!
~Millie
Adventures with Gastroparesis 
Great post. My husband has GP and it is so aggravating at times. And he sweats! Like yesterday at church, my son had to take him home to change clothes because he had an attack and he was literally soaked to the skin…We never know when it will hit and when it does it is usually at the wrong time. Nice to be able to follow someone else who understands!