Jacob: 4 Years
These have been four fun years. He is still the sweetest boy I know. He is such a nice boy, he is always happy, and always excited to meet people. He is funny and has a great sense of humor too. He still has lots of hugs and kisses for us and loves his family and friends. He and Paige get along really well, with normal spats here and there. But he genuinely loves and cares for his sister. When she makes sad choices he is sad for her. Even when it is a sad choice at his expense. And I can't tell you how much he loves baby Eli. He is so good with him too. Always gentle and never misses a chance to give him a kiss or a hug. It is really sweet to watch.
He is a Daddy's Boy. He wants to do anything and everything he can with Daddy. I find the times he wants me over Daddy are times when he is hurt or really tired. Every night Travis puts him to bed and they pray and talk about Jacob's day. Travis ends with saying" I love J-A-C-O-B." (Spelling out his name.) And Jacob repeats back: 'I love T-R-A-V-I-S." It's so fun.
He finished his first school year and had a great review from his teachers. He is in PPCD (Preschool Program for Children with Disabilities) and has an Individual Education Program designed for his needs. His IEP last year had goals and action plans laid out for him and was designed to watch for regression of skills that might indicate a bigger problem. Depending on how much you remember about Jacob, he had a severe speech delay that halted his development by months. We saw several specialists and he was given a label of "Suspicion of Autism" diagnosis. Meaning he was too young to really be able to tell and he needs more time to see where his development goes. Doctors, therapists, his school, and his parents are all partnering together to help Jacob and find out if it's just delays or a diagnosis. His year at PPCD was going to help fill in gaps of where he fell on the spectrum if he even was on the spectrum. He had an education program mapped out, a special ed program mapped out, and an autism plan mapped out. Basically, he was in good hands.
We were so blessed and completely blown away with all that his school year gave him last year. His teachers were wonderful and the program was fantastic. He achieved all his goals and was praised not only for his class work but also for his peer interaction. He loved all his classmates and has a genuine care for their well being. It was wonderful to hear the praises. And, they never had to implement anything from the autism plan. He never regressed. He only excelled.
He also sees his developmental pediatrician this coming month and I am excited to hear her feed back on his progress too. All that to say, while it is looking good for his suspicion of autism, I constantly remind myself that Jacob is and always has been exactly who God made him. Whenever I would get anxious about Jacob's development or a label I remembered Psalms 139: 13-14- " For you created my inmost being; you knit me together in my mother's womb. I praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well." AMEN! I will be ready to rule out or accept whatever label a doctor or school needs to give him, and in the mean time I am thankful for his progressing development and the hard work he has done.
Jacob is still very smart. Delay aside, we never questioned his intellect. He loves spelling and is always asking how do you spell this or that. He loves puzzles and is very good at them. Check out this 100 piece puzzle he did all by himself tonight.
He loves movies and likes to recite their lines at random times. He uses them appropriately too. Which depending on the line is not always a polite thing.He is doing wonderful with speech and OT. He is ready to be released from OT and he is at his peer level with speech. A huge praise and improvement from his "severe delay" diagnosis he got when we started two years ago.
He is very active. Loves running, climbing, just about everything a playground has to offer.
We are working on food, and I will say it's getting better. He still doesn't have the biggest appetite and that's okay.
His allergies have improved and we are hoping that one day as an adult he will be nut allergy free. But in the mean time still no PB & J and we keep an epi-pen with us at all times. Thankfully we have never used it.
His doctor stats today were: Height- 43 inches (95%) (Yes! He can ride Soarin' at Disney now!) Weight- 39.75 lbs (80%). He had to get 4 shots and it was very sad. Not a fun check-up at all.
He still loves his trains and can name them all and spell most of them.
I could go on and on but will wrap it up with how thankful we are to be his parents. We love him SO much and could not imagine a world without Jacob. Our Buddy. Our sweet boy.
Labels: jacob 48m






































