{"id":12946,"date":"2024-05-13T09:46:33","date_gmt":"2024-05-13T08:46:33","guid":{"rendered":"https:\/\/www.familyfund.org.uk\/?post_type=organisations&p=12946"},"modified":"2024-06-10T10:26:21","modified_gmt":"2024-06-10T09:26:21","slug":"spinal-muscular-atrophy-uk","status":"publish","type":"organisations","link":"https:\/\/www.familyfund.org.uk\/support\/discover-more\/spinal-muscular-atrophy-uk\/","title":{"rendered":"Spinal Muscular Atrophy UK"},"content":{"rendered":"

Who is Spinal Muscular Atrophy UK?<\/strong> <\/h2>\n\n\n\n

SMA UK supports all who have or are affected by spinal muscular atrophy with information, health advocacy support, and information for staff at neuromuscular centres around the UK.<\/p>\n\n\n\n

How can SMA UK help?<\/strong> <\/h2>\n\n\n\n

SMA UK offer free emotional support, practical advice and guidance to anyone affected by SMA, and can help with decisions around treatment, equipment, education, care and benefits.<\/p>\n\n\n\n

They also provide resources for parents and teachers on daily life with SMA, and can provide free multisensory toypacks that provide visual, tactile and auditory stimulation for infants aged up to 12 months who are living in the UK.<\/p>\n\n\n