*This is our Landing Page. We had to go online earlier than planned. We are working hard to go online soon.*
This is the global umbrella for all those who suffer from Urticaria. In order to be able to represent and enforce our interests worldwide, we have founded this independent organisation.
Due to current developments, we see the need to spread informations as quickly and widely as possible. Please help us all! Share the information so that we can reach as many people as possible all over the world.
We, a very experienced team in the field of urticaria, have spent the last 4 years building an independent and authoritative patient organisation for people and their relatives in Europe.
Those who fight can lose. Those who don't fight have already lost.
I want to encourage and spread confidence.
As soon as you give up hope, all is lost.
Health is the first duty in life.
Let us stick to the bitter truth. Here you will find only beautiful photos of us. Some of you can see in the mirror what some of us look like when things aren't going so well. Oh yes, not all of us want to be on the page with a photo.
Do you want to join us?
Would you like to support?
We have a lot of work to do and can use any help in all areas. Get in touch. Tell us in which area you would prefer to contribute and ideally your professional skills. We are looking forward to read from you!
Since the beginning of last year, people who had never been sick before have been reporting to us that they reacted with urticaria to one of the vaccinations. Some cases are very severe and made us very concerned.
It has also hit some of our ranks particularly hard. A few of them are over months unable to work.
Since people continue to contact us daily, we decided last autumn to conduct an independent investigation. Get involved. Share the link to the form. As many people as possible need to participate!
Our independent organisation. We have been in existence for 4 years and have worked independently since the beginning. Our investigation is also carried out independently. We attach the greatest importance to this for the sake of all those affected.
Please fill out the form below. We ask as many people as possible who are affected to enter their data in our lists. The more people participate, the more meaningful it becomes.
We use the data for internal evaluations and research. All participants can register on our website and view the results as well as the exact numbers. We publish a summary, which we use to advocate for people with urticaria, depending on the results. Registration right afterwards.
There will be a members' area that will allow us to quickly and easily share information with you and keep you up to date in a protected area. It will also help all those who want to network with each other. Those who are involved in this project can easily organise their projects together, even across countries.
We keep your data strictly confidential and adhere to the International Data Protection Guidelines. For more on the data protection regulation, see the imprint.
Promise. We won't spam you with newsletters!
You will only receive an email from us if it is really important.
Or have a question?
We’re here and happy to help.
© Global Urticaria Association