
Skylar's increased pressures on her bi-pap and cough assist have really helped her out, but we're battling one ill side-effect. Because of the high bi-pap pressures at night, she's either swallowing air or the muscles aren't strong enough to resist the air from getting into her belly and she's getting really bloated. She'll wake up at least once during the night and cries because she's in pain... I've gone in there in the middle of the night to see her belly looking like a balloon that's just about to pop and it's hard as a rock. The Gooden Family taught me a new way to release some of the air in her belly because the vent bags on the IV pole were not working. Right now, we're just trying to figure out the best balance of pressure and bloating. If we lower the pressure, she doesn't breathe as easily the following day, but if we raise it, then we bloat her and she doesn't sleep well (and I don't sleep well either). Hopefully, we'll figure it out soon!
Great news - hospice is providing a CNA (certified nurse assistant) to help me bathe Skylar twice a week. The woman is super sweet and gentle and helps me get Skylar back in the tub! That's right, we're back in the tub :) I had been giving her "sponge baths" for a while because I was unable to move Skylar back and forth with all of her equipment when she wasn't stable. Now that she's stabilized, Skylar seems to enjoy the time in the water and I have an excuse to turn the heat on, lol. I thought Skylar's legs were not able to move anymore on their own, but she tries so hard to bend at the knee when she's in the water and every now and then I'll see them wiggle.
What else... Oh yeah! The van! We had our first outing in our minivan last week for Skylar's pulmonologist appointment. Despite having to wait three hours (one whole hour in the waiting room packed out - my worst nightmare for Skylar) before we saw a doctor, the appointment went really well. The doctor said Skylar's lungs sounded nice and clear, she looked good, and was doing well all things considered. The only downside is that our doctor seems to think we've reached the max pressures for Skylar's body to handle so if she tanks again, there may not be much more we can do. Anyway, the ride itself was great - Skylar could see out the window which she seemed to really enjoy and we had Finding Nemo playing in the background. It's really nice to have and hopefully we can get out as a family soon when we get the right power hook up.
When Kyle was out of town this past week for work, my cousin from Indiana flew down to stay with me and help out. It was so much fun to see her and have some quality one on one time together.


No word on the home makeover... and I have to assume that we did not get it because I think we would've heard by now. Oh well - it was a long shot, but fun to think about. We're going to try and hold onto our property as long as we can, but we have other priorities. Medicaid is still a nightmare and we need to get that sorted out before the new year when we have to start paying out our deductible again. There's always something...
Children's Scottish Rite is hosting an SMA conference for doctors and nurses in GA the second week of November and I am very honored and excited to be on the parent panel for the day. I will be speaking along with Ashley Manross and Stephanie Miller to try to help the doctors and nurses who attend learn more about SMA, how to care for our children, and answer any questions they have to help them understand the disease on a personal level as well. In addition to speaking, I'll have information about our GA Chapter of FSMA. We'll be having a member drive soon, so if you're interested in getting involved with our GA Chapter, please let me know! We have plenty of volunteer opportunities with fundraisers in the works for 2011.
Last, but certainly not least, I'd like to introduce you to the newest member of our household:

So that's all the excitement in the Jones' house these days... Have a great week! Peace.