We discussed sending Kenny to 2 day a week therapy school...I really think that would be great for him. They would work on his PT/OT and Speech/feeding...and he'd be around other kids like him. Like I said, I think it would be great for him, but I am nervous to send him because his lungs are so bad...and he is always getting sick...I guess it is time to really talk to his doctor about this. It's almost a no win situation...see...if we send him somewhere for PT/OT and the other therapies...he will get sick...if we don't send him...he wont excel in his development...not to mention how sick he has been...and what he has missed just from being sick.
I cant take him to preemie clinic, because he has been so sick, yet he really needs to go...it's just a continuous circle of events that wont stop. Now Gina is starting to get up on her knees and spin around in circles, scoot (backwards), hold things with both hand...and it shows me just how far behind Kenny is with things. Yes, he is making great progress for what he has been through, but it gets to me. I feel bad for him...that he is struggling with everyday stuff while it is supposed to come natural for babies. Isn't it bad enough that he went through so much when he was born...and those long 4 months in the hospital....losing his twin brother, whom shared a special bond with inside of me, being near death several times?! I am at a loss for all the options of what kind of therapies are good I know he needs speech and feeding therapy...but from who? Where? He is almost 22 months old and still not cruising against furniture...when will he start walking? Will he ever be able to walk? I am so scared for him and what the future holds. He is so precious and pure...when he looks at you, his eyes see right through you...almost to your soul...its kind of a peaceful, calm look that he gives. I just pray that this world is good to him throughout his lifetime because his everyday tasks may be harder for him to do, he may not be able to hear very well, or even talk, have horrible lungs which require oxygen at night, walk or eat solids, but he is still our family's miracle. And we all will love and protect him till eternity because that is what family is all about!
I want to give a short shout out to my sister Andrea, who is turning 38 today! Woo Hoo! Have a very Happy Birthday sis! Love ya much!
