Zoey with her friend Adric...he is 4 weeks younger and super cute!
Tuesday, September 6, 2011
May 2011
Zoey with her friend Adric...he is 4 weeks younger and super cute!
Wednesday, May 25, 2011
Bone Age
2 months ago Hannah had a bone age scan which showed her bones to be that of a nine month old when she was 18 months. She is short in stature so this is could be a good thing. It will allow her body to grow over a longer period of time.
Saturday, April 30, 2011
I am 39 weeks pregnant and I go in on Monday for a c-section. We are really excited! After tearing my house apart a month ago I am pleased to say that as of last night it is all in order and clean again.I love a clean home!
Ricky has been staying busy with work, church, being super dad, and an amazing husband! He is the best :)
Caleb is so much fun! He is the best little boy ever. He amazes me every day and find my self wondering when he got to be so big. He will do or say something and I don't even know where he learned it. He loves to play outside and has become a pro at riding his bike.
We were able to attend an event for our local TARC where they had tons of fun activities for the kids one being taking a ride on a horse or pony. I thought for sure Caleb would freak out once he got up and change his mind but he didn't, he loved it! One of those moments where I stop and realize just how big and brave he is getting. He plays soccer on Saturday mornings, he is so fun to watch. He has been potty trained since the first of April.. I am loving it! We tried on and off for quit some time but he just wasn't ready.... we decided to try again one weekend and he has been in underwear since. Love it!
He has such an imagination! He will go from being a dog one day to a super hero the next. He cracks me up! He has been asking for a small dog, the answer is no but he keeps asking. I wonder when he will figure it out ;) He makes me laugh everyday! He reminds me to be kind and loving towards all... he has the sweetest, purest spirit! Hannah! Where to begin? She has been through a lot lately and is still making leaps and bounds of progress! We are blessed by this sweet girl who always keeps us close to the spirit. She also got to ride a pony and was smiles the entire time. We are going to see if we can get her into hippo therapy. It is supposed to help her balance. We also started water therapy with but have not really been able to go much due to her surgeries and how busy we have been. That to should help her balance as well.
We decided in February to go ahead and start the process of opening her right nasal passage so she could breath better, eat better, and have more stamina overall. We scheduled the 1st surgery in March knowing that there would be a few more to follow but somewhere communication was lost and we failed to really understand how closely spaced the surgeries need to be. We thought 3 months apart...nope more like 3-4 weeks apart. What a mess! The 1st one was so hard on her body and we were there for 5 days. The second went great, and the third I canceled due to how much we had going on and the baby coming. So pray that the hole will stay open and she will only have to have one more surgery :)
With love,
Sam
Wednesday, April 27, 2011
Thank You
Thank you to all for supporting Sweets for Hannah. We had a successful bake sale at Wal-mart on Saturday where we raised over $900. We baked about 90 dozen cookies for the event, which was extremely exhausting, but well worth it. We sold almost everything except for some snicker doodle cookies (which are Ricky's favorite).
Between the two fundraising sources we were able to raise a lot more money than we had ever expected, $2,700 in total. We will treat this money with great respect and appreciation and we will make sure that it will be used for its intended purpose.
One thing that is critical when caring for a child like Hannah is that parents need to be proactive instead of reactive. We have already seen a huge improvement in her overall health because of our efforts. Her vision is a great example of why we need to be proactive. She has one weaker eye that use to wander a bit, but because we noticed it and worked with her ophthalmologist we were able to correct this potential impairment with daily eye patching of the stronger eye. Her balance (vestibular dysfunction) is much more complicated, and it will take a lot more work to help her live with no sense of balance. Because we learned about her vestibular dysfunction early on we have been able to start early with certain therapies to help her walk and cope with this impairment. If we can manage these two impairments properly then her abilities to learn and receive a normal education will be extremely high. Many people hear the word “syndrome” and correlate mental development issues, but that is not the case with CHARGE and that is why we are working so hard with Hannah in these early years. We have no doubt as parents that she will surpass all other expectation and have a higher than average learning ability.
CHARGE Syndrome affects each CHARGEr differently and has numerous possible physical and health disabilities that accompany the syndrome. Some of the funds will help us attend the International CHARGE Syndrome Conference. This conference brings together many of the professionals that research and work with CHARGE Syndrome to teach parents about the advances that have happened over the last two years. This is still a fairly new syndrome and there is a lot happening in the field of CHARGE. It wasn’t diagnosed as a syndrome until 2004 when they discovered a gene that plays a major role in why many of the symptoms of CHARGE occur in a child.
You have made a great difference in Hannah’s life! We feel so grateful and overwhelmed by the generosity and love from others!
Thank you!
With much love,
Ricky, Samantha, Caleb, & Hannah :)