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Dermatologists that Specialize in HS 

If you are looking for a dermatologist who specializes in HS, check out the lists on the HS Foundation website and the HS Connect website

HS Flare, Lifestyle, and Food Journal


Enjoy this free download! I wish you the best of luck on your HS & healing journey. 

Journaling: A Powerful Tool to Finding Triggers 

Food & Supplements for HS

Food Sensitivities and HS 

If you would prefer to read this information in article form, head over to to read my article on Food Sensitives and HS.


School Lunch Letter

Support Groups and Resources 

HS Connect is your one stop shop for TRUSTED HS information! We have 80+ articles about all things HS, product suggestions, mental health resources, open surveys, clinical trials, and studies specifically for our community and so much more!

•Connecting those who suffer from Hidradenitis Suppurativa and the medical community who treat us with support, solutions and resources.




•Articles and blogs


•Product suggestions



•Wound care


Facebook support group

Hope for HS is a 100% volunteer, grass-roots, patient and caregiver directed non-profit organization, supporting and advocating for Hidradenitis Suppurativa patients since 2013.

•We first came together at a local support group and realized that there is so much work to be done! Who better to do it, and be sure that it is done right, than the people that live with this disease every day?


•Since 2013 we have successfully launched several new chapters for virtual and in-person support groups, creating a bridge between HS doctors and patients in their area. Our perennial efforts to raise awareness through events, speaking engagements, and national proclamation campaigns empower members of the HS community to get involved and create change for patients everywhere.

Hi everyone! My name is Selina Ferragamo and I try to use memes and humor to provide comic relief, support, and advice on living with Hidradenitis Suppurativa. If you need a laugh and distraction from the pain, check out my social media account, @hidradenitis.selina.


International Association of Hidradenitis Suppurativa Network provides the help you need to best manage your Hidradenitis Suppurativa, while promoting advocacy, awareness, education, legislation, support, and wellness of HS.

•International Association of Hidradenitis Suppurativa Network (IAHSN) was established in June 2012 to help HS patients and their caregivers bridge a gap in medical treatment with their primary care physicians and/or dermatologists.

•Since IAHSN's inception our mission has been to provide advocacy, awareness, education, support, legislation and wellness to patients, and to provide resources to caregivers. IAHSN's strives to help HS patients better manage hidradenitis suppurativa, and to have a better quality of life.

•Hidradenitis and Me Support Group facilities monthly Zoom meeting that focuses on self-care. 

•Hidradenitis and Me Support Group is a non-profit organization that provides a safe space for those who are living with Hidradenitis Suppurativa (HS). Our organization facilitates monthly support groups that focus on mental health and self-care with an objective to encourage others to live and enjoy life the best way they can, despite HS challenges.




We empower people living with HS and inflammatory diseases to better understand their disease state and take courageous action toward receiving treatment, engaging with community, and improving their overall quality of life.


Mental Health Resources/Referrals


  • Erin Martinez (located in Michigan)


    • 313-203-2077

    • Mention of HS or Jillian Ondreyka/Embrace Health Nutrition directly will be helpful to direct the referral


  • Search engine


    • You can filter by insurance, issue/reason for seeking therapy, type of therapeutic intervention, etc.

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