It supports LMBBS sufferers and their families, through our helpline and information leaflets about the syndrome. It has a twice yearly newsletter, plus an Annual family conference which allows sufferers, families and professionals to learn more about LMBBS. This is then followed up with a Conference report, which is sent to all its members.
Raise money
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- Email it to friends and family
- They can donate online easily and safely with a credit/debit card
- The money goes straight to
Laurence-Moon-Bardet-Biedl Society
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