It’s day 1 of #GastroparesisAwarenessMonth! With more #awareness we can spread the word, help others, and find a cure for #Gastroparesis. Help spread awareness by sharing with everyone you know. Someone may be suffering symptoms and not even know how to approach their situation.
I dealt with my symptoms for 7 months before I found a doctor that could diagnose me correctly I spent an additional 5 months suffering through symptoms, different medications, and side effects before I had a pacemaker placed. Then 2 more months until I am where I am today– finally being able to eat on my own again. I still have good days and bad ones but without that doctor’s help I would be under 100 lbs and slowly #starving to death. It sounds dramatic– but that’s because this #invisibleillness can become extreme if not correctly diagnosed and managed. Help spread the word. Thanks! #CureGP
greyskiesandsunshine 
Thank you for sharing this info. I didn’t know what Gastroparesis was! Like you, I live with an “invisible illness.” So important to support each other and bring awareness to others…
LikeLiked by 1 person