|
|
|
Hydranencephaly Resources in caring for a Child with Hydranencephaly Physical Care of a Child with Hydranencephaly Difficult Times
Pt. 1: Taking Care of You Book: Caring for Your Child With Hydranencephaly Printed Materials |
Orthopedic Considerations: What I’ve Learned
Unfortunately, no matter how much therapy and positioning we do with our children, they most likely will end up with some orthopedic problems. In this section I’m giving you some basic information on the more common ones and what can be done to prevent or treat them. Remember; I am not a physiotherapist or Dr, merely a parent. I am not promoting any particular treatment, just providing you information based on my experience and what is available on the internet. What I’ve learned: Well, with Kayda I tried, and managed to prevent most of the severe deformities or problems, but not all. Along the way I learned a lot. Remember; these are my opinions only. One of the things that you will be
working against is a reflex called the Asymmetrical Tonic Neck Reflex. . The
asymmetrical tonic neck reflex is a normal pattern of infant In this section I’m giving you some articles explaining the technical aspects of orthopedic problems and their treatment. First though, I’m going to give you a list of some things that I’ve learned. 1. Do not let your child sit in a windswept position. 2. Avoid “lounge” chairs that allow your child to sit twisted. 3. Get any splints or braces recommended for your child; afos (ankle foot orthotics), hand splints, abduction brace, back brace, whatever 4. Do “stretches” daily as much as you are able. These are range of motion exercises, which will be demonstrated by your child’s physiotherapist. 5. Use a stander!!!! This is one of the most important things you can do to prevent your child’s hips from dislocating. This chapter gives you the technical explanations for hip socket formation. I’ll give you a layman's’ description: When born the hip socket is fairly flat and shallow, it becomes cupped and holds the femur in place by bearing weight. Every minute in a stander helps to form a firm socket. It’s not too late to start the standing after hip surgery either. 6. If a dr tells you that your child needs to have the tendons at the top of her legs (adductors) snipped, do it. As long as the hip is still in place or only partly out (subluxed) surgery is called soft tissue and is relatively simple taking only about an hour and a half followed by 4-6 weeks in a cast. Once the hip is dislocated it becomes ‘bony” surgery (described in detail in this chapter) and is much harder on your child. My daughter had to have both hips reconstructed and it was awful. No one told me about preventing the hips from coming out by having the adductors snipped. Now I tell everyone. 7. Watch your child’s spine and how they are sitting. Make sure they are always positioned upright rather than hunched and try to make sure they don’t twist to one side. Scoliosis & Kyphosis are real enemies for our children. Not only are they uncomfortable but both conditions can compress the lungs and compromise your child’s breathing abilities. 8. From what I’ve read; 95% of children with severe disabilities develop osteoporosis, which leaves them very vulnerable to fractures. When I heard this I was really concerned and wrote to a physio and a Physiatrist that I know. Their responses on preventing this were; prevent contractures (wear splints, position carefully), weight bearing (stander) and adequate calcium intake. 9. The more your child uses a particular limb the tighter that limb will become-sort of a double-edged sword. With Kayda we could really see that as her hand use increased. There’s not much you can do about it, it’s just something to be aware of. 10. Bones grow, muscles don’t. For this reason, every time your child has a growth spurt their limbs/muscles will get tighter. “Stretches”, standing and splints will help loosen them up again. I know that it’s hard to picture how these small steps can make a difference. With Kayda, at one point it appeared that she would need surgery to release her hamstring muscles. At the time she was still recovering from her 3rd hip surgery when she had nearly died so I was willing to do anything to prevent her from needing surgery. The physio mentioned previously suggested a soft splint by Medi Kids (address is at back of this book) worn at night and standing to lengthen the hamstrings. In only a few months she went from a contracture of –40 degrees to only –5 degrees. Just from those 2 strategies. She wore the soft splints each night and stood each day in her stander. Other pages in this section:
|
|
Subscribe to the
Hydranencephaly Mailing list
August 16, 2001- January 12, 2005 This website is funded in loving memory of Jason S. by his mother Kammy The information on this site is provided by families, caregivers, and professionals who are or have been caring for a child with Hydranencephaly. Please report any broken links or missing photos to angelbearmom@shaw.ca
|