Editing Huntington's disease (section)

===Education===

The families of individuals, and society at large, who have inherited or are at risk of inheriting HD have generations of experience of HD but may be unaware of recent breakthroughs in understanding the disease, and of the availability of genetic testing. Genetic counseling benefits these individuals by updating their knowledge, seeking to dispel any unfounded beliefs that they may have, and helping them consider their future options and plans. The Patient Education Program for Huntington's Disease has been created to help educate family members, caretakers, and those diagnosed with Huntington's disease.<ref name="PEP">{{cite journal |vauthors=A'Campo LE, Spliethoff-Kamminga NG, Roos RA |title=The Patient Education Program for Huntington's Disease (PEP-HD) |journal=J Huntingtons Dis |volume=1 |issue=1 |pages=47–56 |date=2012 |pmid=25063190 |doi=10.3233/JHD-2012-120002 |url=|doi-access=free }}</ref> Also covered is information concerning family planning choices, care management, and other considerations.<ref name="lancet07" /><ref name="OxfordMonographtesting">{{cite book | vauthors = Harper P|chapter=Genetic counselling and presymptomatic testing |veditors=Bates G, Harper P, Jones L | title=Huntington's Disease – Third Edition| publisher=Oxford University Press| location=Oxford| year=2002| isbn=978-0-19-851060-4|pages= 198–242}}</ref>