Chromosome 18 Registry and Research Society (Europe)
Registered Charity: SC040399
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Benefits of becoming a Member
- Family conferences in Europe
- Access to the family and adult listserves, which are daily email posts where families discuss challenges and successes.
- There are listserves for 18q-, 18p-, ring 18, Tetrasomy 18p and a new one for young adults.
- Latest research into Chromosome 18 abnormalities, from UTHSCSA (America).
- Contact with families around the world facing similar challenges.
- Making friends
- Links to other European organisations.
Research
- Encourage the participation of European families and clinicians in the ongoing research into all Chromosome 18 disorders.
- Setting up links with peadiatric clinics in the UK and Europe.
- Our hope is that all children affected by the disorders will be able to access a whole range of successful treatments and therapies which have resulted from research carried out by The Chromosome 18 Registry and Research Society.
In English(PDF 351Kb)
En Français(PDF 515Kb)
Im Deutsch(PDF 471Kb)
In Italiano(PDF 378Kb)
W języku polskim(PDF 386Kb)
En español(PDF 341kB)
Στα ελληνικά(PDF 422Kb)
To pay by Credit Card
- Go to Virgin Money Giving.
- Type in Chromosome 18. We should be at the top of the short list.
- Click on Donation.
- Go through the relevant steps telling us what the donation is for.