Well…
Last night was Peyton’s first night off of his baclofen in
preparation for his surgery in a few weeks, which means; it was not a
good night sleep for dad. Due to Peyton's spasticity he gets
severe muscle spasms, pain and stiffness throughout his lower body,
more so at night. His orthopedic surgeon prescribed baclofen and valium that he usually takes at night to help combat the spasms and let him rest.
Most
people are familiar with baclofen as it is a muscle relaxer and an
anti-spastic agent. It is used to treat muscle symptoms such as:
spasms, pain, and stiffness. To read more on this drug and its uses
you may visit: http://www.drugs.com/baclofen.html.
It
is going to be a very difficult few weeks for Peyton but having him
off the anti-spastic medicine will provide Dr. Park with the ability
to isolate the ventral rootlets in the spinal cord that are
causing the spasticity. If Peyton is still taking baclofen, it could
interfere with the readings, making it appear that he is not as
spastic; therefore, making more difficult for Dr. Park and his team
to identify the rootlets that need to be cut.
We
are still able to give Peyton his valium, but that is just not enough
to help him as valium will relax him, but the spasms that are usually
dulled by the baclofen overpower that causing extreme discomfort, as
demonstrated last night by his waking consistently every 90 minutes.
We
feel so bad for him and wish there was more that we could do for him,
but at the same time we understand the need to be off of the baclofen
until the surgery and will continue to get up with him and console
him the best that we can. We pray he catches a break and can get a good night sleep. If he is anything like his daddy, when he doesn't get sleep he gets sick...and we DO NOT need that right now!
Hi!
ReplyDeleteI just wanted to connect with you and let you know that we have a 9 year old son with Spastic Diplegia CP. He is a preemie (29 weeks, has a twin sister and is 9 years old. We have alot in common!!! He has some huge surgery issues to face this summer! I tried to leave a message on fb for you. We live in Pueblo West, Colorado. It would be great to hear from you. We could share some stories! Anyway
I will keep your son in my thoughts and prayers. Will keep up with his progress! Tamrt1
Hello,
ReplyDeleteWhy yes we seem to have abit in common. You mention your son has some huge surgery issues to face this summer. If you don't mind me asking what are they? Have you known about your son's diagnosis for a long time? How does he manage to get around?
I am glad to see you on here and thanks for your message. I wish you guys nothing but the best and the most opportunities you can offer your son!! Please feel free to message me with any questions you may have or just to chat thats ok too!
Mel :)