Monday, January 3, 2011
Sunday, December 12, 2010
Strep Throat
Hoping she is well soon....
Sunday, December 5, 2010
December is here!
Hi there! The Carter family is doing well! We have had fun the last week and a half with lots of family and friends.. Nana, Grandad, Memaw, Pa, extended family and so many fun friends! Neely celebrates his 36th birthday tomorrow and Christmas is right around the corner.
Kyla is doing well. School is tough this year but she again has a fabulous teacher that works with her and accommodates for her weakness and inattention. Laura is having a blast at the pre-k program at PCA. She enjoys school and making friends.
Neely and I find it hard to believe a semester of the school year is already gone!!!!
For all of our CMS followers and parents of CMS kiddos, I just want to say that I have struggled again with Kyla's disease and the affects it has on her life. Just when I think I have accepted what comes with this part of her life, I find myself getting bogged down again in the "what if's, why's and when will's...." She is such a trooper! Currently she struggles with remembering if she has or has not had medicine, pain in her ankles and legs, general weakness, and attention in school. We go to the neurologist this month for the annual visit and this year we have a few new concerns for him. Medicine dosage, physical therapy issues, etc.
Overall, we have such blessings to be thankful for. She has come so far and is able to voice her hurts and issues more clearly to us now.
Here is a little video from her church choir presentation tonight... Hope you enjoy...
Sabrina
Kyla is doing well. School is tough this year but she again has a fabulous teacher that works with her and accommodates for her weakness and inattention. Laura is having a blast at the pre-k program at PCA. She enjoys school and making friends.
Neely and I find it hard to believe a semester of the school year is already gone!!!!
For all of our CMS followers and parents of CMS kiddos, I just want to say that I have struggled again with Kyla's disease and the affects it has on her life. Just when I think I have accepted what comes with this part of her life, I find myself getting bogged down again in the "what if's, why's and when will's...." She is such a trooper! Currently she struggles with remembering if she has or has not had medicine, pain in her ankles and legs, general weakness, and attention in school. We go to the neurologist this month for the annual visit and this year we have a few new concerns for him. Medicine dosage, physical therapy issues, etc.
Overall, we have such blessings to be thankful for. She has come so far and is able to voice her hurts and issues more clearly to us now.
Here is a little video from her church choir presentation tonight... Hope you enjoy...
Sabrina
Saturday, August 7, 2010
Tuesday, July 6, 2010
Here and there...
Here are a few pics from the last few weeks...
The girls and I on the 4th of July
Just a note... I am always thinkning and muddling through how best to help Kyla with the challenges that she faces because of CMS, but it seems some seasons make me more intense for the search of community and help than others. I have recently made more contact with others who have CMS or their children have it through facebook. It is so comforting and rewarding to find others who are on this journey with Kyla.
Most recently our concerns with Kyla are her fatigue (late in the day), physical therapy issues (running and walking form), writing fatigue, inattention, and sleep habits.
We are trying to give her mestinon doses somewhat closer together to see if we can help her body adjust to the long summer days.
Just a note... I am always thinkning and muddling through how best to help Kyla with the challenges that she faces because of CMS, but it seems some seasons make me more intense for the search of community and help than others. I have recently made more contact with others who have CMS or their children have it through facebook. It is so comforting and rewarding to find others who are on this journey with Kyla.
Most recently our concerns with Kyla are her fatigue (late in the day), physical therapy issues (running and walking form), writing fatigue, inattention, and sleep habits.
We are trying to give her mestinon doses somewhat closer together to see if we can help her body adjust to the long summer days.
Monday, May 31, 2010
Kyla is 8yrs old!
Yes! Can you believe it, my baby turned eight Saturday! What a blessing. Kyla is tough. She is always thinking and dreaming. She loves to be "just a little different"... She is the queen of the one liners. Kyla dreams big and invites others to come along. She loves to read, but reading is really "making pictures and movies in your head." She is a fan of all things water. Kyla is sweet and concerned about others. She likes to joke and kidd around. She loves to eat ice cream and drink Chi Tea- hot of course. Tea parties, dress up, and games are a few of her favorite things. Happy Birthday, princess. Mom and Dad love who you are... Kyla Ann Carter.


Thursday, May 27, 2010
School Days, 2010
Kyla and Ms. Donna (school nurse) Thank you for always taking care of me!!!!
Great year --but super busy anf full of new experiences! Both Girls had a great year. Thank you to Mrs. Stokes and Mrs. Sharon. It is a mom and dad's greatest pleasure to see their children loved and cared for. Hats off to you!!! Now let the summer time begin... :)
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