“Unkie Jots” came to visit on his way down to Phoenix. I was so happy to be able to get these super cute photos of Josh and Regan. I only snapped these three and was happy to stop at perfection before either of these boys were done posing. They were so good to humor me and my photo taking obsession. We hope Josh had a lovely vacation, and we hope to have another visit from him soon.
And now for a Regan update:
We had our appointment with the pediatric Gastroenterologist. He asked LOTS of questions. Which was good. He then decided that we should try a different formula for a couple of weeks. It’s even more broken down and so it smells so much worse. Poor Regan doesn’t really like it. I don’t blame him the smell makes me gag. Pre-digested ick! But hopefully it will do the trick. Dr. “K” also ordered a test for Cystic Fibrosis (CF). He said it was possible that Regan may have CF. We are praying that the test has a negative reading and that Regan does NOT have CF. Jon is going to get the test scheduled ASAP. However if the test comes back negative and the new formula doesn’t help, our poor Regan will most likely have to get the scope and biopsy done. So that is where we are at……
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Great pictures and I know that Josh had a great time at your house because
he told me so.!!
I think I told Jon that Jerris had these problems when he was a baby. He was
a very sick little boy and so skinny…….But but had all the tests for CF and just took
time to get the right eating formula. So I’m praying the same with be with Regan.
I believe most of Shawn’s kids thrived on Goats milk. And I think Sharice along
with Chelsea had to take the “expensive” powdered milk. Don’t remember the name
of it now….Seems like at the time it was 25 or 35 dollars a can. So having good thoughts
about Regan………..(Shawn even had her own Goat to milk)
Love,
Grandma Sapp
I’m certain Regan will be ok. Hang in there. It is sad that Eden officially weighs more than Regan now… She hit 15 lbs at her sick apt. At Kael’s well child check they asked if we had a family history of cystic fibrosis. Kael’s weight is lower so that’s why they asked. So we have another apt in 3 mo to check Kael’s weight. I think all will be ok though. 😉 Hang in there. Sick kiddos are no fun!