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Cornelia De Lange Syndrome (CDLS) Foundation UK and Ireland
Cornelia De Lange Syndrome (CDLS) Foundation UK and Ireland
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The CdLS Foundation exists to ensure early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome and help people with a diagnosis of CdLS to make informed decisions throughout their lifetime.
In the UK the Foundation is run entirely by volunteers including parents and professionals.
Contact Details
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Organiser
- Jacquie Griffin
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Telephone Number
- 01375 376439
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Email Address
- info@cdls.org.uk
Location
Local Offer
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SEN Provision Type
- Targeted
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Details
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Our service/organisation is part of the Local Offer, please contact us for further information
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Age Bands
- 16-25 years, 11-15 years, 6-10 years, 0-5 years
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Core Response Approved?
- Yes
Service Information
Coverages:
National
Target Audiences:
Adults, Older people (over 65), Adult carers
Support Groups:
Physical impairment
Links for information
Last updated 23rd February 2024