It has been a long time since I've found myself any time to sit down and actually write something, though I have been needing to for a while. Writing my thoughts, my feelings and my worries is like the best therapy for me, and I'm finding I need that more than ever right now!
First, I'd like to update on Jaxson.
He is almost 2 years old! He is 24lbs, 32inches long and he's growing and learning a little more each day! The doctors all say he's going to be a short guy when he grows up....But, He's got some pretty big shoes to fill - Have you seen his daddy?! (Biiiig guy!)
Health wise, it has been a very hard year and a half, full of never ending appointments, therapy, questions and fears. I know a lot of our family and friends either do not know what is going on with Jaxson, or are very confused - which we get, Josh and I are also very, very confused..... so I thought this blog with be a great opportunity to explain some of what we've been going through.
Very Mild Spastic Cerebral Palsy
Jaxson has had an in home physical therapist since he was born. Around 7 months of age, we started noticing that Jaxosn's left foot turned in when he was in his high chair and when he was being held. He started to have spasms - called clonus in this leg when I was feeding him a bottle. Since he was so young, We've all opted for a wait and see approach. When Jaxson first started to crawl (he was 11 1/2 months old), his therapist noticed that his left hand was curled in when he did so, his thumb tightly pressed into his palm. Again, We decided to wait and see for improvement. By the time Jaxson was 17 months, He was not standing on his own, he would hold onto furniture, but he would not let go. He preferred to crawl to get around and would resist to being walked with his hands. This raised some red flags to our therapist and to our neurologist. They suggested an SMO braces for Jaxson to support his ankles. He was walking on the side of his ankles and he was weak and would fall. He was hyper-reflexive on the left side. By this time we had started constraint therapy on his hand, and he started to use his left side a lot more - we caught it at the right time! When Jaxson's SMO's came in, He was 18 1/2 months old and still not standing on his own. With ONLY 2 weeks of the braces, he was able to stand on his own, and took a few wobbly steps. Now at 23 months old, Jaxson is walking. Walking slowly he does well, but is very wobbly and turned in when he tries to run. He likes to go on his tippy toes when he does not use his braces. Due to some other issues, which I'll discuss later, our Neurologist suggested that we do an MRI.
|Left hand in fist, left leg hanging out behind him, left eye (psuedostabismus)|
It hurts sometimes when people say "I don't see anything wrong with him, he's perfect!" Honestly...I hope you don't see it, I'm glad you don't. I don't spend 3 days a week at therapy so you could. But it is real, and it is there... as is my fear, and worry for his future.... All real. However,We are so incredibly blessed that it is mild...
Jaxson was just recently diagnosed with Epilepsy on August 22nd from a Neurologist in Boston. Epilepsy often goes hand and hand with CP. We have started on Keppra (and He's really had a horrible time on this medication....Long story and I wont get into it here). We started noticing around Easter that Jaxson was having these starring spells, though at first we thought they were just normal tuning out, anxiety ect...until they started increasing in duration and he started to lose consciousness, excessive drooling, and he would also lose his blink response often. We have had 2 different testing for this, one in the doctors office and another was a 3 day hospital stay (also the MRI). Developmentally Jaxson is struggling. He is not hitting many milestones that he should for even his adjusted age. Firstly is Speech (We see a speech therapist 2 x a week) Currently, He has 1 consistent word and that is "sit". Though he babbles, and we hear words such as Mama, Dadda, Nana, he is not consistent with them and does not use them directed at us or objects at all. We use sign language. He signs "Bottle" and that is his sign for all things eat or drink. He also can sign "all done" but that has currently been lost. As far as communication - it is hard, frustrating, but we guess and play "choices". Although He has had some words and signs before- many of them have regressed from time to time and he goes months without remembering them, forgets them. Sometimes they come back but some have yet to come back. Regression is never a good thing. The neurologist in Boston said there are some rare disorders that could be causing this, (that I was not given the names of), It is possible that its all linked to seizures or this could be a sign of autism spectrum (though Jaxson is so incredibly social, He does have signs/flags and we have that appointment next week, though they will likely want to see how he does on Keppra) Early intervention is the key for most everything here. He has some abnormal behavior concerns.There are a lot of different things of development that is of concern for Jaxson...Too many to write, if you want to know more about this, please ask me because I would be more than happy to talk about it.
Jaxson suffers from chronic fever of unknown origion. He is always between 100.6f to 101F. I consider that his "normal" temperature. When he is sick (as when he had Lyme disease, his temps reach in the high 103's to 104.8, and even something as simple as teething, it cannot be brought down with NSAIDS or tylenol). The heat of the environment also effects this, so there has been times its felt completely out of my control. He has had this for over a year, and we have gone to infectious disease, immunology, ENT, and Neurology for this. We have gone through about 20 thermometers. We do not have any answers. We do not know if its related to the seizures other than the high fever is a trigger to the seizures We are going to see a specialist this week for his ears/adenoids but this most likely isn't the cause, since his fever does not respond to antibiotics. (but another thing we have to investigate) I am not sure what happens after Keppra and the adenoids are ruled out. They spoke to me about genetic syndromes....I don't know. We had to give up on our Summer. We tried to do things and even risked the Fourth of July Parade but he got a dangerously high fever, glassy eyes, had a seizure so instead of being with our family and having a normal cook out that afternoon, we had to stay inside by ourselves with the A/C, as we have had to all Summer. Honestly it was really hard, it still is. It is lonely. We play outside in the early morning and in the late evening. We do not go for car rides when its hot. We do our errands in the evening. Prevention has been the best key for him, since I cannot effectively cool him. I'll let you know more on this as we continue to learn...its a weird one and he puzzles everyone with this!
I guess those are the biggest concerns... I am sorry for those who didn't have this information and really needed it. Some days I feel like I have failed as a wife, as mother, as a daughter, as a daughter in law, as a sister, as a friend...I know that I am not the kind of person that I want to and should be to those people...Not like I use to be before all of this. Most days I am consumed by this, and spend whatever time I can with my husband and Jaxson. Most days we just focus on doing fun stuff with him, because we are just so emotionally exhausted and scared. Maybe it seems like we are always busy...and I guess honestly we really are. I love you all, and I appreciate the love and support you give us. Please be patient with us...We are in the unknown, and it is hard. Love us even if we make mistakes. Love us even when we are crazy. Hug us when we are scared...because we are SO scared....Please try to understand...Please be patient....We love you all so much.