Tuesday, September 29, 2009

Ramp and Switch Toy Fun!


Since the seizures have decreased, Kendall has been playing like crazy. She wants to be engaged pretty much ALL the time. She absolutely loves her switch toys. Its great to see her having fun on her own too. Our new OT has been great for Kendall. She told us to scrap the old hand splints and she's creating new ones for her. Having OT twice a week has been great and we're seeing huge benefits from it. Kendall will even hold her sippy cup on her own (and drink from it!) just for this OT!

The ramp Poppy made was a bit frightening for Kendall at first. I think she's warming up to it now though. We had to decrease the incline to prevent her from sliding down it! Now, she has to work a little bit harder, but she will (with the help of gravity) scoot down it. She gets very proud of herself when she does. She just has to be in the right mood.





Feeding continues to be an issue. She has been getting her calories...it just takes a while.

Nursing has worked itself out and I'm getting used to it. We have a delightful nurse who is so kind and compassionate with Kendall (and me!) She comes on Tuesdays, Fridays, and some Saturdays. Hopefully we will be able to continue having her. She cooked a wonderful Lebanese dinner for us tonight (yes, she cooked and I watched! Totally not in her job description, but I think I scarred her last week when she watched me make a meat loaf...she probably thinks I need help...but I'm open to free cooking lessons!) She's fluent in German (guess that doesn't really have anything to do with anything...I just think its cool!), and really clicks with Kendall. She gets her to eat, and also participated in therapy today. She's definitely an answer to prayers. I think we make a pretty good team during the day!


My mom has started her treatments, and she has been very run down and ill. This is just the beginning, so please send some extra prayers her way. I know if anybody is tough enough to live through this its my mom...I just hate to think of her feeling badly all the time. I'm sure there will be good days and bad days. Hopefully more good than bad.

6 comments:

Éimí said...

I'm glad to hear that Kendall is playing and engaging so well. And thrilled that y'all have found an OT that is working so well for you, and are getting somewhere with the nursing. Your mom will be in my prayers as well as you and your family as always! *hugs*

TMI Tara said...

Those pix of Kendall with her switch toys are too cute! Chloe loves switch toys, but she just holds them down to make them make noise non-stop, so they got on my nerves pretty quickly. Especially one -- the bus -- it plays 'It's a Small World' very loudly. Aaahh!!!

I'm sorry to hear about your mom. She is definitely in my thoughts and prayers (as are you). {{hugs}}

Jennybell said...

I'm fairly new to your blog. My daughter has seizures and my dad has cancer. I'm assuming your mother does too and you're talking about chemo treatments?
My dad is on chemo treatment #4 of 6 and it hasn't been as bad as I feared. Chemo has changed a lot and he isn't sick. He did shave his head, but small price to pay. Still has an appetite, only side effect he's had are hiccups on the day of treatment and the night after a treatment it's like he's had a double shot of caffeine and can't sleep. But after that it's fine. Hope your mom has a similar experience :)

therextras said...

Alles ist gut!

(Except of course that your Mom is sick. Sincere get well wishes.)

Barbara

Ellen said...

Hi. I am sending prayers your mom's way. You're so spirited—I'm sure you're keeping hers up, too.
ALL of those photos are great! So cool to see her on the ramp. Oh, and I left you an award on my blog tonight. You so deserve it.

Cjengo said...

WOW, I am so impressed, and that is all so wonderful!!!!

Jude starts at Baylor Our House today, I will let you know how it goes.