The PDA Contact Group was founded in 1997 by Jan Seaborne, who is the mother of a child diagnosed with PDA. Jan now runs the group with the support of other parents who also have children diagnosed with the same condition. The group is affiliated to Contact a Family. The aim of the group is to offer support, advice and information to anyone involved with an individual diagnosed with PDA, whether child or adult. Where possible, as a group, we are able to put parents with a newly diagnosed child in touch with other
| New | PDA Contact Group Forum Board |
New |
Membership of the PDA Contact Group is free, however we require anyone wishing to access the private forums on the PDA Contact Group Forum Board to register their details.
Details for contacting the group can be found on the contacts page