Research4ml is a patient organization made up of parents whose children suffer from mucolipidosis (types II, II/III and III alpha/beta). There is currently no cure or treatment for ML and research is scarce.
Driven by the lack of research about this ultra rare and quite complex disease, we came together and decided to join our voices in order to attract interest and secure funding for research that could benefit our children by curing or slowing the disease progression. In our effort to achieve this, we are supported by the Gesellschaft für Mukopolysaccharidosen e.V., a German self-help organisation which focusses on MPS (Mucopolysaccharide) and related lysosomal diseases.
The MPS e.V. has agreed to designate donations specifically for research targeted to treat Mucolipidosis. We look forward to your valuable support in our effort to help our children and future children diagnosed with the disease. Please use the “donate” button in the top mainu to donate.
Feel free to contact us should you have any queries or comments: info@research4ml.org