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Two women embracing

STORIES AND
SUPPORT

PATIENT STORIES

HEAR FROM OTHERS

GPP affects everyone differently. Learn from other people’s experiences with GPP and build your support network.

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hear from others

LIVING WITH GPP

GPP may make you feel isolated, but remember that you’re not alone. Learn about others' experiences with GPP.
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Christine Sat In A Room

WHEN A FLARE HAPPENS

Hear from Christine and others who share their personal flare experiences and how they cope.
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A Male GPP Patient Describes Their Experiences

WHAT IS GPP?

GPP can affect your life in many different ways. Learn what it's like for others going through a similar journey.
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GET SUPPORT 

BUILD YOUR SUPPORT NETWORK

dermatologist

DERMATOLOGIST

  • Let your dermatologist or primary care doctor know if you have feelings of anxiety or depression so they can direct you on how to get help

  • Ask whether your dermatologist can recommend a mental health specialist or support group for people with skin conditions to help you manage your emotions as you deal with GPP

loved ones

LOVED ONES

  • It may be hard to open up to loved ones, but letting them know how GPP is affecting you (socially, physically, and emotionally) may help them better understand your needs and help them provide you with better support

gpp community & resource

GPP COMMUNITY & RESOURCES

Find out what other people with GPP are doing to cope with the disease. You might find other GPP patients or communities through local psoriasis or rare skin disease organisations.

  • Join a patient support group

  • Join a patient advocacy group

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International Federation of Psoriasis Associations Logo

IFPA

The International Federation of Psoriasis Associations (IFPA) is the global leader in fighting psoriatic disease, calling for access to early, correct diagnosis. The IFPA believes in affordable, high-quality, essential treatment for those living with psoriatic disease.
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