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„Es ist mir und dem Team von HidraMed Solutions sehr wichtig, das Bewusstsein für Hidradenitis Suppurativa zu stärken. Mehr Aufmerksamkeit bedeutet schnellere Diagnosen – und eine schnelle Diagnose ist entscheidend, um die Erkrankung in den Griff zu bekommen.“

Suzanne Moloney
CEO & Gründerin von HidraMed Solutions,
HS-Patientin & -Fürsprecherin

Patienten-Ressourcen

Sehen Sie sich die neuesten Blogartikel von HidraWear und HS Warriors an – mit Einblicken und Tipps für den Alltag mit Hidradenitis Suppurativa.

HidraWear 4 layersLiving with HSGuide To Accessing Hidradenitis Suppurativa Dressings
18 Juli 2025

Guide To Accessing Hidradenitis Suppurativa Dressings

For people with Hidradenitis Suppurativa, one of the biggest challenges can be managing the drainage and odour from their lesions and wounds. It can be messy, embarrassing, time-consuming and make…
Tissue Viability Nurse Specialist Alison Schofield shares expert advice on managing HS lesions—covering hygiene, dressing tips, and skin care to help you stay comfortable and confident.BlogLooking After Your Hidradenitis Suppurativa Lesions
10 Juli 2025

Looking After Your Hidradenitis Suppurativa Lesions

Alison Schofield, Tissue Viability Nurse Specialist, on how to care for your HS lesions and support your skin health. Alison is a registered nurse specialising in tissue viability with over…
HS Week 2025 date and purposeBlogEmpowered Together | Celebrating HS Awareness Week 2025
29 Mai 2025

Empowered Together | Celebrating HS Awareness Week 2025

June 1st – 7th marks Hidradenitis Suppurativa (HS) Awareness Week 2025, a global initiative to raise awareness of one of the most misunderstood chronic skin conditions. At HidraWear, we stand…
HidraWear-Home-Delivery-England-Wales-and-Scotland-with-Bullen-HealthcareNews And MediaHidraWear Delivery Available in England, Wales and Scotland with Bullen Healthcare
27 Mai 2025

HidraWear Delivery Available in England, Wales and Scotland with Bullen Healthcare

We are happy to share that HidraWear is now available for prescription home delivery across England, Wales and Scotland through our healthcare-delivery partner Bullen Healthcare. This collaboration means HS Warriors…
Four girls hiking at sunsetBlogLiving with HS12 Things To Know About Hidradenitis Suppurativa (HS)
8 März 2023

12 Things To Know About Hidradenitis Suppurativa (HS)

Although Hidradenitis Suppurativa (HS) affects at least 1% of the general population it is still mistaken for a rare disease. Here are 12 things that you may not have known…
hidradenitis mindful featuredLiving with HSMental HealthHidradenitis Suppurativa – A Mindful Approach
22 Feb. 2023

Hidradenitis Suppurativa – A Mindful Approach

Living with Hidradenitis Suppurativa Today, I’m going to talk about mindfulness. Now, I’m not a zen Buddhist, or a mindfulness master, far from it! However, I am learning the benefits…
Hair removal and HSBlogLiving with HSHair removal and Hidradenitis Suppurativa
19 Jan. 2023

Hair removal and Hidradenitis Suppurativa

While it is true that hair removal can sometimes irritate your hidradenitis suppurativa, it is always a personal choice. Hair removal should not be obligatory, but it shouldn’t be off-limits…
Tiffany hidradenitis suppurativaLiving with HSOur StoriesTiffany’s HS Story – A Terrible Misdiagnosis
6 Juni 2022

Tiffany’s HS Story – A Terrible Misdiagnosis

Early Signs It all started with a few bumps on my inner thighs, vagina and the occasional butt sore when I was around 17 years old. At first, I really…
Lindsay hidradenitis suppurativaLiving with HSOur StoriesI Felt Alone And That No One Would Take Me Seriously – Lindsay’s HS Story
6 Juni 2022

I Felt Alone And That No One Would Take Me Seriously – Lindsay’s HS Story

My name is Lindsay. I was 15 when I first started getting signs of HS. Of course at that time we had no idea. My doctor just thought that it…
hidradenitis suppurativa wont dim my shineBlogLiving with HSOur StoriesHS Will Not Dim My Shine – Danasha’s HS Story
2 Juni 2022

HS Will Not Dim My Shine – Danasha’s HS Story

Hello, my name is Danasha and I am a Hidradenitis Suppurativa Warrior. I inherited this condition from both sides of my parents' families.  My mom actually has the condition. I…
Candice hidradewnitis suppurativa storyBlogLiving with HSOur StoriesHow I use My Mental Health Experience To Cope With HS – Candice’s HS Story
2 Juni 2022

How I use My Mental Health Experience To Cope With HS – Candice’s HS Story

My name is Candice and I’m 49 years old. As a teen, I started to get lumps on my breasts, armpits, bottom and occasionally my face which coincided with my…
Ashley Hidradenitis Suppurativa StoryLiving with HSOur StoriesRaising HS Awareness Through Film – Ashley’s HS Story
2 Juni 2022

Raising HS Awareness Through Film – Ashley’s HS Story

Let me Introduce Myself! Firstly, Hello! My name is Ashley and I’m a 22-year-old college student and filmmaker from Helena, Alabama. My HS story began when I was around 12…