Its amazing what services are out there to help people with special needs children. I generally feel kind of bad like I'm taking a handout whenever my husband and I both are blessed with wonderful jobs and can pay for trips to the hospital. Anyways, a lady from the help desk of Nationwide Children's Hospital called me and asked if we'd like to have a donated hotel room for our visit next week. I was confused at first, because I hadn't asked them for "help" or a room, they just called me, set it up and sent us the reservation information. She said its just something that local hotels do for families of children visiting their hospital that have to drive farther than 3 hours. Crazy huh?
Well we also found out that we have been approved to have our meals paid for on this trip and our mileage through another program that our EI told us about. Its pretty crazy, but really is a blessing. Of course now we kind of feel bad for the restaurants we normally go to on our trips - its not like we want to have people paying for us to eat at P.F. Changs or anything. So we are going to behave and eat at much cheaper places. :)
Tuesday, June 30, 2009
Tuesday, June 2, 2009
Tuesday, May 19, 2009
CDCSP Approved
We found out that the other assistance program we applied for (CDCSP) actually accepted our application - so we have in essence a medical card for the next year! So that is great. Having two insurances has been wonderful, but this is going to be sooooo good. It sure takes the stress off. Well at least until next year. :)
Wednesday, May 13, 2009
Waiver Denied
We got our denial for the Waiver application we had filled out for Isaac. MR/DD Waiver would give him a medical card to pay for his medical expenses. Since growth hormone isn't free, we were really hoping to get it so we wouldn't have to worry about keeping 2 insurances all the time.
Apparently PWS "is not an approved waiver diagnosis."
Of course its not. It is in a bunch of other states, why would WV be one of those enlightened states?? This is one of those situations that the rarity of it all becomes very very frustrating. Just like we did in the beginning when the doctors were clueless around here as to what was wrong with Isaac, we wish we lived somewhere else today.
Oh well, I believe we'll get it eventually. We just have to work a little harder for it. Go figure. :)
Apparently PWS "is not an approved waiver diagnosis."
Of course its not. It is in a bunch of other states, why would WV be one of those enlightened states?? This is one of those situations that the rarity of it all becomes very very frustrating. Just like we did in the beginning when the doctors were clueless around here as to what was wrong with Isaac, we wish we lived somewhere else today.
Oh well, I believe we'll get it eventually. We just have to work a little harder for it. Go figure. :)
Friday, May 8, 2009
We've been sick :(
Since last wednesday Isaac and I have been fighting a nasty cold. Poor little Isaac sounds so pitiful, coughing and sneezing. The pedi said to elevate him, use the aspirator and saline drops, and just generally pamper the little fella. He is still in a good mood - I just hope he gets better soon! He doesn't like to eat all that much when he's stuffy and congested.
Happy side note: We did get a cool new highchair (FP Precious Planet) and that kid goes WILD in it. You could sit 50 toys on top and he will not rest until he's grabbed each one. He is holding his head so well and really reaching and working it. :)
Happy side note: We did get a cool new highchair (FP Precious Planet) and that kid goes WILD in it. You could sit 50 toys on top and he will not rest until he's grabbed each one. He is holding his head so well and really reaching and working it. :)
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