Things You'll Need:
- Internet access
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Step 1
Diagnosis
Many orthopedic doctors don't see a single case of Fibular Hemimelia or other similar limb defects in all their years of practice. Getting an appropriate diagnosis can be difficult in and of itself. Asking your pediatrician too suggest someone is a good first step but may not get you far in terms of diagnosis or treatment. Local doctors may not have experience with rare limb deformities. -
Step 2
Once you have a diagnosis (or if you still need one) research treatment options (for limb defects in general if you do not have a diagnosis). If you have access to a college library in which you can read scholarly journals that is great (although they can be hard to navigate). Most of us do not have access to medical journals so the good old world wide web will do. In the case of limb defects like Fibular Hemimelia the treatment options may include amputation, limb lengthening and reconstructive surgery.
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Step 3
Once you have an idea of the treatment options available you are ready to find a doctor to consult with. I would suggest finding a doctor who has had success treating each individual option. It will not be hard to find a doctor familiar with amputation because that is still considered the standard treatment for many limb defects. Finding a doctor with experience in limb lengthening can be difficult. I suggest finding support groups or forums where parents who have a child with a condition like yours write about their experience. Hospitals web sites often have information on the treatments they offer and the experience they have in doing so.














Comments
xrayness said
on 7/22/2009 Very good article...thanks for sharing.