Orthotic Devices (part 2) Common Concerns

Orthotic devices are a part and the beginning of a new stage in the development of your child's mobility. Physically, orthotic devices aid in the child's activity, building strength and agility. They are absolutely beneficial in the child's therapeutic care. However, there are concerns of parents. Two particularly common concerns parents ask themselves are, What may people, peers, siblings say to our child? How will we pay for orthosis? Suddenly, feelings of guilt or anxiety for your child can arise. In this article, a review of these two common concerns will be addressed to help parents better cope with certain emotions that may surface along with this therapeutic stage.

Well, everyone has a bit of curiosity in them, especially children. Anticipation of what questions may surface at school or in public can bring anxiety. Together with your child, be honest and derive a brief explanation of what the brace is used for. We all are open to new learning. A good idea may be to have a show-n-tell or demonstration at school or at home for other siblings. This will make your child's, siblings, peers and teachers familiar with your child's orthotics. In addtion, it is important to include in your demonstration your child's abilities and need to be treated like any other child. Also, what orthotists may discuss with you is painting the brace a bright color or decorating the brace with your child's favorite cartoon character. This actually makes the brace more fun for children to wear. And what a conversational piece it will be!

The expense of rehabilitation, surgery, and the ongoing medical care, can put a strain on family finances. Insurance policies vary widely in terms of what are the required co-payments and benefits included in insurance plans. Usually, Most insurance companies only pay a certain percent of the costs of care involved. There is financial aid available. Such programs are children funded at either a state or federal level. Furthermore, financial assistance is available through local or national charities and foundations. The United Way, United Cerebral Palsy Association and the National Easter Seals Society are a few organizations that will guide you in the right direction.

Lastly, you and your family may consider participating in a parent support group. The organizations mentioned will also provide the names of various support groups in your area. Most support groups are led by parents or child psychologists. Support groups enable you to get advice and reassurance from others experiencing a similar situation. Also, these groups sponsor family fun activites, giving children the opportunity to play with other children who have similar disabilities.

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