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      • There are support groups around the world for people and families affected by FTD. We are part of an international consortium bringing those groups together called World FTD United. In the UK, we help to run support groups for people and families affected by FTD through Rare Dementia Support:
      www.ftdtalk.org/support/
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  2. People living with FTD and their friends and family are welcome to join our London support group meetings or to see what regional support groups might be available. Please visit our Meetings page for details of upcoming meetings.

  3. In the UK, we help to run support groups for people and families affected by FTD through Rare Dementia Support: FTD Support Group: focused on carers of people with any form of FTD. PPA Support Group: focused on people with PPA and their carers and family members.

  4. Families affected by fFTD are welcome to join our fFTD Support Group meetings. There is also a separate FTD support group for people with symptoms. More information on upcoming meetings can be found on our Meetings pages .

  5. AFTD Support Group for People with FTD. A mutual support group that is facilitated by AFTD staff and meets monthly via Zoom. Contact info@theaftd.org or 866-507-7222 for more information.

  6. Support groups can offer useful advice and emotional support to people living with FTD and those who care for them. There are specialist support groups for younger people with dementia or FTD and for people affected by familial FTD (see our page for details).

  7. Rare Dementia Support runs national groups providing support and information for people with FTD, their families and carers. Contact details can be found online at raredementiasupport.org. The Rare Dementia Support Network were vital in supporting me following my mum's diagnosis of FTD. - Shaheen.

  8. Families affected by fFTD may find coming along to our fFTD Support Group meeting helpful, which is held annually. We also invite carers to join our separate FTD Support Group meetings.

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