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Learn everything you need to know about Hidradenitis Suppurativa from the below blogs. If you would like to feature on our blog, please email info@hidrawear..com.

Hope for HS

Hope for HS

Hope for HS is a USA based organisation providing essential information and support services for people with hidradenitis suppurativa. We firstly met Sandra and Angie from Hope for HS at the North American HS Symposium in Toronto in 2018. We were certainly blown away...

Hidradenitis Suppurativa and Heat

Hidradenitis Suppurativa and Heat

Summer is here! It’s the start of the summer and time for a bit of reflection. According to the BBC weather, it was the hottest and driest May on record in the UK. I love the sun, and I love being in the garden. However, what I don’t love is the way my HS reacts to...

Lets Talk about Hidradenitis Suppurativa

Lets Talk about Hidradenitis Suppurativa

We all know that living with HS can knock you down. It can make life a bit difficult sometimes and it can be hard to stay motivated. But life can be good, despite HS. We contacted some fellow HS warriors to talk about hidradenitis suppurativa and share some advice...

Hidradenitis Suppurativa and Caffeine

Hidradenitis Suppurativa and Caffeine

Last year, after my diagnosis, I read dairy, brewer’s yeast and sugar were the primary dietary triggers of HS. Other triggers included nightshades (potatoes, peppers, spices, etc.) and there might be a lnk between hidradenitis suppurativa and caffeine. This was a...

My Child Has HS – How Do I Help Them?

My Child Has HS – How Do I Help Them?

Firstly, being diagnosed with Hidradenitis Suppurativa can be a very scary thing. Secondly, there isn’t a whole lot known about HS. Therefore the important questions you have about the skin condition can remain unanswered. Certainly the only thing scarier than being...