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How Do I Get The Latest Updates On HSDisease.com?

Last updated: August 2021

The internet is ripe with information on hidradenitis suppurativa and other conditions that affect the skin. Unfortunately, sometimes it can get to be a little too much. Perhaps it leaves you feeling like you are trapped in an internet browser with too many tabs open. Meanwhile, you have questions:

HSDisease.com is home to articles, videos, and recipes written by:

We also offer a place to vent your concerns in our forums section and much more. But maybe you are tired of browsing all day? If only there were a way to get weekly highlights on all of our daily published articles. The good news is that you do not need to do any strenuous research. We have done it for you by curating content that matters to you.

How to sign up for newsletters

We make it super easy! Promise. Just click on the button below, enter an email address, and hit "subscribe."

What is in the HSDisease.com newsletter?

Stories

At the bottom of each newsletter, we offer a chance to read stories submitted by community members. Community members are people like you who come to our site and interact with other members!

We are always accepting stories from you! If you are interested, tell us your diagnosis journey, how you found a routine that works for you, or anything HS-related. And if you are not ready, that is ok. You can catch up on others’ stories on our website at any time.

Recipes

I spy something delicious! Occasionally, below our articles and stories section of the newsletter, you will find a featured recipe. We understand that some ingredients listed in our recipes may be a trigger food for some people. Please be sure to omit or substitute any ingredients that do not work for you. Each recipe includes this disclaimer, as well as a photo, prep time, ingredients, directions, and nutritional facts.

Interested in sharing your favorite "safe" recipe with us?

Polls

We try to keep things interesting by engaging you with a poll in each newsletter. It usually relates to diagnosis, symptoms, treatment, or related conditions. You do not have to participate, but we love it when you do! It lets us know a little bit more about your experience living with HS so we can create more content that fits your needs.

Community Poll

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Beyond newsletters

We know newsletters are not for everyone, and that is ok. We just want you to know all of the options available to you as our valued community member. You can also find us on Facebook, Instagram, and Twitter. Give us a follow and connect with others.

We are here for you, wherever you are in your HS journey. 💜

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This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The HSDisease.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

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