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Patients and caregivers are having more discussions about the impact and diagnosis of HS, suggesting they come online mostly to share their struggles of the diagnosis and the larger impact of the disease in their lives.

Patients and caregivers are having more discussions about the impact and diagnosis of HS, suggesting they come online mostly to share their struggles of the diagnosis and the larger impact of the disease in their lives.

The distribution of topic discussions among HS patients and caregivers is less focused on symptoms, but most focused on the impact and diagnosis of the disease.

HIDRADENITIS SUPPURATIVA 
PATIENTS & CAREGIVERS

n:232k

 

What does it mean for us?

Life Impact

People come online first and foremost to discuss the impact of HS on their life. 

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Life Impact

People come online first and foremost to discuss the impact of HS on their life. 

Picture8.png

Life Impact

People come online first and foremost to discuss the impact of HS on their life. 

Picture8.png

Life Impact

People come online first and foremost to discuss the impact of HS on their life. 

Picture8.png

Life Impact

People come online first and foremost to discuss the impact of HS on their life. 

Picture8.png
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