Yes, many organizations and support groups offer resources, networking, and emotional support for families affected by NPB and other lysosomal storage disorders.
Are there any support groups for families dealing with Niemann-Pick Disease Type B?
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About the Author: Staff Writer
World Eyecare Foundation staff writers are experienced eye care providers, researchers, academicians, industry leaders and practicing ophthalmologists and optometrist from around the world. Content may be generated by AI and is reviewed by the editorial team and specialists in the areas of publications.
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