Block ID: #section–hero-page-block_6284e6cbbf5e5

Wolfgang Rosenthal Gesellschaft – Making a difference together

Block ID: #section–text-block_6284e710bf5e6

A youthful 40 years

With fresh, appealing initiatives such as “Show your face!” and “Speak up”, the Wolfgang Rosenthal Gesellschaft (WRG), a self-help association for lip and palate malformations, is keeping up with the times, despite its proud age of now over 40 years. Founded in 1981 by parents of cleft children, the association is dedicated to providing advice, information and education on cleft lip and palate. In this way, the WRG spreads awareness of and sensitivity for cleft-related issues and makes a valuable contribution to society – and to our work!

The parents’ self-help association was named after the German oral surgeon and concert singer Wolfgang Rosenthal, a pioneer in the field of interdisciplinary treatment of cleft lip and palate. Throughout his life, the Berlin-born surgeon developed innovative surgical and treatment techniques to provide his patients with ever better care and long term outcomes. Even though Wolfgang Rosenthal unfortunately did not live to see the founding of the WRG, he would certainly have been thrilled to see the wide range of services that the association now offers for those affected and their families.

Our two organizations share a common goal and outlook, and we would like to further build on this in the future. Many of our donors are affected by cleft, either personally or indirectly through one of their loved ones, and some are members of the WRG as well. This exchange is very valuable for us.


Seminars and anniversary celebrations

The WRG regularly offers workshops and seminars on cleft lip and palate related topics. Persons personally affected by cleft, their friends and relatives, or simply the interested public – all are welcome. This July, a weekend seminar was held on the topic “Expertise of affected persons is in demand!”. At the sports and educational facility in Wetzlar, the WRG offered a series of workshops and a colorful social program for all ages. To conclude the weekend, the association’s 40th anniversary was celebrated. We were happy to be there and take part.

The WRG is never at a loss for words and never afraid to stand up and “show its face”. A heartfelt thank you for that!

New genetic study sheds light on how cleft lip and palate forms
There is still no reliable method to prevent the development of a cleft lip and palate. This is in no small part due to the fact that there is not one clear cause: Cleft has a multifactorial origin. One important factor is genetic. Here too, however, the situation is not clear-cut - there is no such thing as "the cleft gene". A group of researchers at the University of Bonn has now added to our knowledge about cleft by investigating the 98% of genes that do not themselves directly contain blueprints for proteins.
Daimler Symphony Orchestra: Charity concert for Deutsche Cleft Kinderhilfe
On Saturday, Nov. 26, 2022, the Daimler Symphony Orchestra Stuttgart, with pianist Marcel Mok and under its longtime musical director Matthias Baur, played a benefit concert for the Deutsche Cleft Kinderhilfe. The orchestra, a project of music enthusiasts from the Daimler Group, has been in existence since 1978. Former Stuttgart mayor Dr. Wolfgang Schuster gave a welcoming address.
24 Gute Taten Advent calendar – featuring Deutsche Cleft Kinderhilfe!
For many, the pre-Christmas season would not be complete without an Advent calendar. Small treats or loving gifts sweeten every December day. But another thing can also be hidden behind the doors: good deeds! The 24 Gute Taten ("24 Good Deeds") charity Advent calendar makes sure of that: every day, a charitable project from the fields of health, environment, education and many more is presented and supported with the proceeds from the sale of the calendars. This year, one of the projects presented once again is one by Deutsche Cleft Kinderhilfe!
From our projects
The story of Maui, cleft child from Colombia
Our new project to help children with cleft lip and palate in Colombia begins with a very unusual case. Maui was born with a cleft lip and palate. His parents belong to an indigenous people and do not know how to get him the help he needs. By a happy coincidence, Julia, a Swiss woman living in Colombia, is a neighbor of the family and offers to help. In search of treatment options, she comes across Deutsche Cleft Kinderhilfe.
Video: Impressions from Bolivia
The parents of our cleft children are always full of gratitude. When their child is born with cleft, they often do not know what to make of the malformation, much less that it can be treated. And even if they do - most of our little patients come from the poorest of backgrounds. Their parents could never afford the operation. It is an unimaginable happiness for them to learn that their children can receive qualified treatment, and free of charge even. This wonderful, touching film from our Bolivian aid project captures these special moments of happiness.
Video: Impressions from Pakistan
This film, made for our Pakistani partner organization, the Al-Mustafa Welfare Societey, by the father of one of our patients, shows scenes from our work in Karachi. From here, our senior surgeon Prof. Ashraf Ganatra treats cleft children from poorest families. He operates the children from Karachi at the Al Mustafa Medical Center. In order to reach the many needy families living outside the city, he also regularly heads out to local provincial hospitals to treat cleft patients there.