Marcus Ehrhardt
FAQ
Welcome to my FAQ – Answers to the most common questions about Hidradenitis suppurativa (HS)!
Hello and awesome that you’re here! If you’re wondering why I created these FAQ, the answer is simple: Over decades of living with Hidradenitis Suppurativa, I’ve learned and experienced a lot.
I am a group expert in the largest German-speaking self-help group on Facebook, the Akne Inversa Club. One thing has become increasingly clear to me: there are an incredible number of questions, uncertainties, and even heated debates surrounding our disease. That’s exactly why I decided to write these FAQ – to support you with my experience and hopefully provide you with some guidance.
One of the most important lessons from my personal journey is: Please seek professional help early.
If you feel something is wrong with your skin, don’t hesitate to consult a dermatologist. Hidradenitis suppurativa is not “normal acne,” and an early diagnosis can make a huge difference.
And if you notice that the disease is not only affecting your body but also your mental health – which is completely understandable – don’t hesitate to seek support from psychologists. Asking for help is not a sign of weakness but a brave step toward improvement.
In these FAQ, you’ll find answers to questions I get asked repeatedly – both personally and in self-help groups. Some topics spark intense debates, and I try to share my perspective and experiences as clearly and honestly as possible. I’ll update and expand this list from time to time, so feel free to check back often. Perhaps you’ll find the exact answer you’ve been looking for right here.
And if not? No problem! Just send me a message using the email address provided on this page.
If you’re not just looking for my advice but also want to connect with others affected by this condition, there are excellent self-help groups on Facebook that I highly recommend. Just to name a few: Akne Inversa Club (the largest German-speaking self-help group), Akne inversa Hidradenitis suppurativa, and Mullewup. These groups are perfectly organized, highly informative, and full of people who truly understand what it feels like to live with this disease.
The most important thing is: You’re not alone.
There are so many of us who understand this condition and are willing to listen and support. Stay strong and don’t hesitate to ask questions – every question matters!