LIVING

With EoE, Allergies, Asthma and a G-Tube

Helping hands

The evening I had posted my last post, about finding a new church, I received an unexpected phone call. It was someone from the church. It was a very important person from the church, the Pastor’s wife and children’s ministry director. Completely caught me off guard. Through the grapevine she had heard about my post and read it. She felt it in her heart to call me right then. Let me tell you, I really felt grateful for that phone call.

She didn’t need to call me.

She could have ignored the whole situation.

She wanted to know our story and wanted to help. They wanted to make their church a safe place for my kids.

As you know, I am a HUGE advocate for my kids. However, I’m not one to walk into someplace new and say hey you need to change this and this just for us. So I did feel a bit awkward explaining what my kids can and can’t be around. When we were finished talking I felt so much love, hope and excitement that they wanted us to come back. More importantly they wanted it to be safe for us. They really wanted us to give them another chance. I knew in my heart that it was the right thing to do. The very next Sunday we went and this is what I saw. wpid-20150927_120025.jpgAs a matter of fact there is now no food allowed in the room Tinleigh is in. I could have cried. They didn’t need to go out of their way to make changes for us, but they did. That’s just HUGE! We’re just some little allergy family trying to find a new church home.

A number of times during the week the Pastor’s wife and I messaged about things that are okay and things that are off limits. I would smile every time I saw a message from her. Warmed my heart. I am enjoying sharing my knowledge that may help them to keep another allergy child safe in the future. I even had another mom that attends the church reach out to me who’s son also has a feeding tube. It’s nice to make those types of connections with people who know a little about what life maybe like for you.

I spoke with a number of people in charge of different positions at the church when we were there on Sunday. They all knew of our situation and all wanted to help us feel comfortable. They did. I felt so at ease and also excited, because I had helped a whole new house understand our allergies and how to help keep my kids safe.

I have learned a huge lesson through this, the hard way.

I’ve learned that I can’t just say she’s allergic to everything. That’s way to vague and leaves everyone wide open for disaster.

I’ve learned Tinleigh is VERY allergic to wheat. Those small reactions I’ve seen while she plays with play-dough could end up very bad. Wheat will probably be a food she never gets to eat again. I’ve also learned that a food she once wasn’t allergic to can become a huge allergen for her. Probably holds true for Gage and Charlie as well. SCARY.

I’ve learned that it’s okay to say “Hey, while we’re visiting today would you mind making a few changes?” People do want to help, they do want to keep my kids safe. I’m not being out of line by asking. If they don’t try to accommodate, then we’re probably in the wrong place.

I’ve learned there are still many people out there that want to help and do care.

wpid-20150928_132811.jpg

Please pray for Gage and Tinleigh this Thursday. We will be making a trip to see the GI doctor and they will be getting scoped to see if we have things under control enough to move forward with food trials. Gage had to remove sweet potatoes and broccoli. We also started him on a medication for reflux. His last scope numbers were as bad as right before he got his feeding tube. If he’s not better this time then we have a big problem and his disease is out of control again, which will mean we have to start removing foods we thought were safe. Tinleigh got to keep sweet potatoes and oranges. She also started a medication for reflux. If her biopsies are bad then she looses sweet potatoes and oranges. This is one of those huge scopes that I am so worked up about. My nerves are about shot. I worry so much about how it will effect them, especially Gage, mentally. He wants to move forward SO BAD. EoE sucks, we hate it. Please pray for a cure. wpid-20150823_184703.jpg

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September 28, 2015 - Posted by | LIVING | , , , , , , ,

1 Comment »

  1. Praying for a cure and for you & family.

    Like

    Comment by Jen | September 28, 2015 | Reply


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