Having A Baby With Gastroparesis

Sara Nesti

My story is different but this time I hope to help some people. I had many problems with my stomach and after many times that I had nasogastric tube, I had my surgery Iatoplastic and fundoplication.

I had a baby but for me, having a baby is dangerous! In fact when my son was born, I had an intestinal infection that made me near death. I again had to have a nasogastric tube and I was in the hospital for a month. I want another baby despite all the difficulties because I don’t give up. After the birth of my son and having all the problems, I’m here! I’m a survivor and I want to help other people.

This picture for me means a lot. It’s a picture with my son when I was in the hospital when he was born. This is my different story but i want to help all people that have and had digestive desease as me because nobody is alone.

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About the author: Gastroparesis: Fighting For Change Admin

We created this website to provide the public with additional information regarding Gastroparesis. It is our goal to connect users with our Facebook advocacy group, “Gastroparesis: Fighting for Change.”

Our Gastroparesis: Fighting for Change Facebook group was formed to unite people with Gastroparesis and other digestive and motility disorders to work for change. It is not a typical GP support group, as we do not discuss personal medical issues. Rather, we established this as a place where members can discuss ideas regarding our mission, vision, goals, needs, services, and resources to work toward solutions. So if you want to make a difference for our GP community, we encourage you to share your ideas! Additionally, we need you to help us fight for changes in legislation! Also, you can help raise funds! Finally, you can help spread awareness! Please join our main group. We would love to have you!

You can find links to our Community Page and our Advocacy Group on our Resources Tab.

In order to accomplish our goals, we will be sharing many ways you can get involved on our Campaigns Tab.

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