Caleb was born with two rare syndromes, CHARGE and DiGeorge. Caleb is the 6th person in the world born with both syndromes. CHARGE is a multisystem-effecting syndrome which can cause several severe anomolies. DiGeorge prevented Caleb from developing an immune system. He spent over a year straight in the hospital, had multiple surgeries with a possibility of having more in the future. This blog details his heroic journey and story. God Bless Caleb!!
Ephesians 3:20 "Now to him who is able to do immeasurably more than all we ask or imagine, according to his power that is at work within us"
Thursday, April 21, 2011
Eye Appointment Clarification and Just a Note
Also, I just wanted to make a small note. It made me sad to once again come across how ignorant some adults are. I have always been very sensitive to the respect handicapped and disabled indivuals deserve from others, as I think most of us are. I saw a comment on FB yesterday, followed by more disrespectful comments regarding a handicapped individual. These comments came from 'adults'. It makes me sad that people behave like this. These are parents, professional individuals, etc. I just don't understand what goes through people's minds to believe that the rude things that come out of their mouths regarding another HUMAN BEING are justified. I am sick to my stomach about it and it has bothered me. Sorry just waned to share my experience. If you hear someone making rude comments about a handicapped/disabled individual remind them we are all HUMAN! I really hope those individuals realize how hurtful their comments can be!
God Bless you all!!
God Bless Caleb and Camryn!!
Wednesday, April 20, 2011
More Talking, Feeding Sissy, and an Eye Infection
Well two quick updates!
So this past Friday it was nice here so Bri and I and the kids were outside. Bri and I both did some yardwork and at one point I found a worm and took it over to Caleb to show him. This is kind of how it went:
Me: 'look Caleb a worm'
Caleb: 'aterpillar'
Me: 'no not a caterpillar, a worm. Worm. Worm' (repetition works well for him to hear) 'do you want to touch it?'
Caleb: 'no'
Me: 'oh come one, yeah you do'
you could see him hesitating but he finally touched it and then so excitedly he turned to Brian and screamed 'I TOUCH IT!' It was so great to see how excited he got and to hear him put together a sentence-ON HIS OWN!
Lastnight I was doing the dishes and turned around and saw this:
When I saw it, I teared up and stood and watched. Not only was he doing a great job but he took it on his own to go over to the table and get her food to feed her. They were giggling. He was so good at it.
Well, Caleb has another eye infection and the Ocularplastic Surgeon told us if he should get another one to call her or take him to the Children's ER. So I called her this morning and she did not have office hours but agreed to come in to see him to see how his eye handles an eye infection (this has nothing to do with the 'lazy eye'). So she thinks from what she can see that he possibly has puncta that they may just not be in the typical place that you or I may have them-she said she will know better when she sees him in the OR when they re-do his nose from his cleft. But she said the encouraging news is she does not think there is anything wrong with the tear duct (not to be confused with the puncta-the hole that drains to the tear duct) so she was very happy she got to see him. There was even another doctor who looked at him too and gave the same opinion. So he is on an antibiotic and hopefully that will help and then we can use it as needed when his eyes act up. I really like this doctor, what a great person to make the time to come in and see what is going on.
So this is where we are!
Thanks for checking in!
God Bless you all!!
God Bless Caleb and Camryn!!
Thursday, April 14, 2011
Easter Bunny and Welcome Sissy Camryn to Blogger
Wednesday, April 13, 2011
Social Security Waiver and Verbalization
Well I filled out the second appeal for the overpayment on Caleb's SSI. Now it's another waiting game. Let's just hope this time it is handled a little more appropriately and expeditiously.
Caleb has really been doing well talking lately. Even though it isn't sentences..IT'S WORDS! I have really been pushing him to talk here at home and his school aide told me this morning when I was dropping him off at school that he is saying more in the classroom. He's awesome! It's so neat. We will even be driving down the road and if he sees something he will yell the word. For those of you who know Apollo. There commercial was on this morning and I started singing it right in front of Caleb as it is, what I think, an easy jingle/song for him to learn and HE SANG IT(well the spelling of the word, with my help)! It was awesome!
Well just a quick little update!
Have a great day everyone!
Oh, found a cool quote today thought I would share:
'When the grass looks greener on the other side of the fence, it may be that they take better care of it there.' -Cecil Selig
Well have a fantastic day!!
God Bless you all!!
God Bless Caleb and Camryn!!
Monday, April 11, 2011
Eye Appointment
However, we have just noticed that every once and while Caleb's eye seems to be having some 'lazy' characteristics to it. I called his Optometrist at Children's today to tell her what is going on and that I am concerned. I asked her if this could be related to the other eye issues and she doesn't think so but wouldn't be for sure until she sees him. So I then asked her if it isn't related what is it. She said some kiddos around this age develop a lazy eye and if needed can be treated with glasses or an eye patch. ay yai yai-I really don't see him leaving either on and feel bad for him that he would need either. He's got enough to contend with for Pete's sake!
On a positive note, the weather here yesterday was gorgeous and we spent the whole day outside on the deck. Brian and I were in awe at how much more Caleb did yesterday compared to what he did last summer. It was very awesome to see his progress. We had a great day as a family!
Well I am off to write an appeal for his SSI overpayment and to apply for the MRDD Waiver for Caleb.
Thanks for stopping by!
God Bless you all!!
God Bless Caleb and Camryn!!
Friday, April 01, 2011
Darn Winter Germs
So here we go..
SSI:
Well, it is not what I wanted but our appeal was denied but we are appealing the denial and the overpayment. So please pray that the appeal is approved! This also means that Caleb's medicaid card was not reinstated. Some states have a provisional medicaid card and I believe unfortunately WV is not one of them. So I have begun the application process to try to get Caleb MRDD Waiver, which is insurance based off of Caleb's disability. It is not the easiest application, but if granted it could really help us. Down side, the waiting list is one to two years. He could get approved a week or so after the application is complete, but the coverage would not be optimal.
Eyes:
Despite the insurance issues, we have to get Caleb's eyes checked. He pushes on his one eye constantly to help it drain and we just need to get him some relief. So we will be seeing the Oculoplastic and Reconstructive Eye Surgeon on Tuesday. I hope we can get him some help, unfortunately this will probably mean yet another surgery.
Bugs:
We have been fighting many bugs in the house this winter. GI bugs, respiratory bugs, RSV, pink eye, sinus infections, you name it. I am hoping the warm weather comes soon and gets rid of the nasty bugs in the air.
School:
Can I just say how smart Caleb is?!? HA HA spoken like a true mom right :)
He continues to do well in school. Following directions and participating more. Actually, today he doesn't have school and I have been able to really get him to talk today, so I walked around the house with him and pointed to things and said what they were and he repeated them! AH, what a great feeling. I even pointed to his sister and asked him if he knew her name and he said Amryn his version of Camryn! It was so cute! I hope he continues to talk more. This would be great! Caleb has also been able to tolerating sitting in a regular chair, here at home and at school. The chair at our dining room table is a little low, so we will have to modify it so our big boy can sit in a chair.
Article:
An article has been written about Caleb in a magazine. I am supposed to be getting a copy of the magazine in the mail. As soon as I do I will share for all of you to read!
I also, wanted to continue to thank you for the email I receive with suggestions on how to deal with SSI. Some of the feedback I have gotten was via the comments section, and I know some of you gave some personal info and that is why I did not post your comment.
Also, if any of you are on facebook, I do post updates on his facebook page to 'Caleb Hlebiczki is a Fighter'. So check us out there too. I am able to put photos on there easier than here as blogger is not that photo friendly for me!
Okay well I think Camryn is waking up from her nap.
Thank for stopping by and check back for updates!
God Bless you all!!
God Bless Caleb and Camryn!!