Bringing HS (Hidradenitis Suppurativa) Out Of The Dark | Jackson Gillies

In TEDxTalks by Christopher Foley8 Comments

"Have you ever woken up one morning to discover an abscess that would grow to the size of a baseball in your armpit? I have. I have HS or Hidradenitis Suppurativa, and so does up to 4% of the population. That's 230 million people, and yet no one is talking about it. Well, I will."

"Let food be thy medicine, and medicine be thy food"Hippocrates

Jackson Gillies is an 18-year-old student at Santa Barbara City College whose life took a major turn when he won Santa Barbara’s Teen Star USA crown in 2016. Since then he has performed at the Concert to End Gun Violence Across America with Kenny Loggins and opened for Jim Messina at the William Sansum Diabetes Center fundraiser, among many other noteworthy appearances.

Jackson is a spokesperson for the Juvenile Diabetes Research Foundation for whom he has made national TV public service ads with Mary Tyler Moore and a DVD titled “Almost Bionic” about the Artificial Pancreas Project. Jackson, a Type 1 diabetic since age 3, has come full circle, this year becoming one of 250 Type 1 diabetics who took part in the international Closed Loop Artificial Pancreas Trial.

Four years ago Jackson developed the first sign of another disease. After more than a few misdiagnoses, his condition was finally pegged as Hidradenitis Suppurativa, an autoinflammatory disease that causes painful skin abscesses. HS afflicts as many as four percent of the population (potentially 30 million people), yet is rarely discussed or studied. HS can be physically, psychologically, and socially debilitating, the lesions affecting the most sensitive parts of the body, places where there is skin to skin contact. The painful abscesses can take months or years to heal.

Despite all this, and after five surgeries, Jackson conceived, produced, and starred in the “Something That Matters Concert” to raise awareness about Hidradenitis Suppurativa. He was the first performer to step into the light about the disease. His TEDx talk, “Bringing HS (Hidradenitis Suppurativa) Out of the Dark”, will continue this quest, to spread the word about HS, to help other sufferers understand their disease, and hopefully to encourage researchers to work on a cure


  1. Amazing story. I remember Jackson as a little boy. He’s a true warrior and will overcome. I’m
    Following his story and pray for him. Connie you are an amazing mom. So proud of what he’s become. TED talks will be amazing. Can’t wait to hear it. Xo Eileen

  2. Jax, you know this but I’ll say it again…you are my hero!!!

  3. Jackson stinks. I hear his big brother is so much cooler. 😛

    Way to go bro, wish I could be there.

  4. Jackson, so happy that you share your knowledge, talents and experiences. Congratulations!

  5. Jackson, it takes a special kind of bravery to be so vulnerable. Thank you for opening my eyes to your beauty. Paula

  6. I was recently diagnosed. I started realizing something wasn’t right 4 years ago. Now, I’m scarred in my groin area. It’s terrible. My friend set up an appointment 6 months ago due to it, her appointment is this Wednesday. That’s how bad it is, my friend has also been suffering and I didn’t know and 6 MONTHS before her 1st appointment. I just got my refferal sent in.

    My husband suffers but not from HS directly. My flares get so bad I can’t walk, sit, or stand; it feels like fire pokers are being dug into my inner thighs and groin.

    Please. We need to talk about this.

  7. I remember Jackson as a little boy, enjoy to go to work with his father and come to the bank I used used to work. Jackson always humble and always with smile… I sad that he has to live though this. Jackson you are in my prayers, I have always appreciated you because must of kids used to like ice cream or cake, you had to say no to things because it was not good for your HS… We love you little Jackson and keep going, keep looking for your dreams.

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