First we understand. Then we help.
Patients’ wellbeing as benchmark
To live up to our vision and bring better outcomes to more patients, we focus on the needs of patients in everything we do. In order to define what is really needed, we actively collaborate with patient organizations, healthcare providers and business partners. Our clinical development programs mirror the real-world challenges that patients, carers and clinicians face every day. We investigate innovative and flexible treatment options that meet the individual therapeutic needs of every affected person and offer real added value to their quality of life.
Closer to every patient
We are well aware of the challenges our patients face every day. Knowing that with our therapeutic solutions we provide life-changing assistance and improve their quality of life, motivates us to continue to do our best.
Get to know their stories.
Calum is affected by cerebral palsy. He talks about how important it is to accept ourselves.
Lynne, who suffers from dystonia (blepharospasms), and her partner talk about their long road to diagnosis and what treatment was able to achieve in a very short time.
What matters to us.
Our motivation arises from the experience of our patients. When we see that their medical conditions are improved by our efforts and that we can improve their quality of life, that’s what drives us further. Get to know our patients and their stories to understand our mission.
Insights into their experiences:
In an accident, my thigh was burnt by a motorbike exhaust. I would like to thank Contractubex for making my scar look so much better after five months of treatment.
My family doctor recommended that I try Pantogar, which contains specific active ingredients that the hair needs. So my dream of long, healthy hair came true after all.
I am 40 years old, I had a stroke 10 years ago. Since then, the whole right side of my body is spastic. My goal is to make further progress and maintain my independence as long as possible.
Having cerebral palsy, I struggle with any activity that you would use two hands for normally. I wasn’t able to tie my shoe laces until I was about 15. But I found a way, so I now I can do it with one hand, which is really good.
If you have Parkinson’s people stare anyway but if the saliva runs … you can’t really be among people anymore, you're marginalized. But two days after the injection all the symptoms are gone and if it starts again, I'll go back.
I have dystonia. For five years, my husband, my children and my mother had to accompany me everywhere. Two days after the first injections, I could move around again independently and even drive a car.
Information that helps.
To fall ill initially means loss of control. Those who acquire knowledge about the disease, but also about therapy options and how to deal with it in everyday life, can regain control over their own situation bit by bit. That is why we have developed various platforms with comprehensibly prepared information for patients and their relatives.
We work closely with different patient organizations. As such, we can better understand and serve the needs of patients and healthcare providers. It also allows us to share valuable knowledge, resources and networks with each other because we also share the same goal – to improve the situation of people suffering from severe diseases such as dystonia or cerebral palsy.