Wahoo!!!! You got a Big Give!!!Wish I could help out with this one, but until income taxes come in- we can hardly deal with the bills, much less my desire to give all my husband's income away.
I
doing the Gives, it makes my heart happy- and I know that's why I have not been hanging out as much on the dis lately..... because I know I can't do anything.
But our time is coming. I wish I could sew still.... maybe one day I will be able to get my machine fixed and learn! I would love to be able to make some of the great stuff I see all the disers make! My kids would flip too- Hope you get some great stuff!!!! And I told you- we all lurk. lol
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I found your thread through the BigGive and I just read your whole PTR and so sad what you and your family has to go through![]()
How about the colorectal team too? Maybe get a consult with them while you are here. Dr Levitt is wonderful. They have a bowel management program where they can prescribe a daily regimen. They will take xrays daily to see what works best for her.
Ty is hanging in there. Alot of pain today. But he has also sat up in a chair more today so he is making progressI can't wait till he can get off the morphine. It makes him pretty grumpy and the halucinations are awful.
Now we get it compounded into a syrup, but before that, we used to give it to her in pill form. The pills are tiny, tiny, and once you figure out exactly how to do it, they split pretty easily. Crushing them still works (that's how they gave it to her during her colonic manometry), but it causes a lot of cramping. The syrup is great because it makes it so easy to adjust the dose.
Does Kylee have a tethered cord? Or would this be an initial spinal MRI? The thing that stinks about mito is everyone wants to attribute everything to the mito. We were flat out told that kids with birth defects do not have mito (and vice versa), which is why it took us so long to get a diagnosis. I would think that if Ali had the mito dx before the other things were dx'd, they never would have found her laryngeal cleft, tc, etc. Ali is a patient in the motility program at Children's Hospital Boston, but I have heard good things about Cincy, too.
Prayers that tomorrow goes better than expected and that a solution can be found to help your
Pretty Princess!
Hi Kris,
I'm following along with your PTR! I just PM'd you. Let me know what you think.
Hope things go well with Kylee and the doctors will be able to figure out what medication her body needs!
Looks like GKTW will have their hands full with Mito Kids. Looks like we will be there the same time as you guys!!!
How did things go today? Been thinking about you guys. *hugs*
Oh no, not again. I hope you guys are out of there quick. I'll keep her (and you too) in my prayers.We are here at the hospital. Thankfully we had a direct admit and didn't have to go through ER. We are here for a clean out, but unfortunately Kylee caught some bug and now has a 102 fever. She just looks so pitiful. Just praying this is not a long stay like the last time. Tomorrow she will get her PICC line.
Thank you Lisa for coming by. I can't say enough how special all you ladies are. What you all do to make a family feel special
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We are here at the hospital. Thankfully we had a direct admit and didn't have to go through ER. We are here for a clean out, but unfortunately Kylee caught some bug and now has a 102 fever. She just looks so pitiful. Just praying this is not a long stay like the last time. Tomorrow she will get her PICC line.
We are here at the hospital. Thankfully we had a direct admit and didn't have to go through ER. We are here for a clean out, but unfortunately Kylee caught some bug and now has a 102 fever. She just looks so pitiful. Just praying this is not a long stay like the last time. Tomorrow she will get her PICC line.