
More perspective for Laurin and his family
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About this project

Laurin, born on 4.10.2007, has been struggling with health problems since birth. He had difficulty sucking and suffered from muscle tension problems. Although his developmental delay was medically clarified, the cause remained unclear. Laurin received early intervention and attended the SPC. At almost 3 years old, he began to walk, but his development was slow. Doctors determined that he was physically and mentally disabled and would be dependent on assistance for the rest of his life. Laurin does not have Angelman syndrome, but his developmental delay remains.
Laurin requires constant care and has a severe disability card. He has a reduced developmental level and cannot speak. His behavior is often misunderstood as he expresses himself by crying. He has a reduced sense of pain and needs to be diapered. Laurin loves cars and animals, but he requires around the clock supervision.
Laurin has had two seizures and suffers from generalized tonic-clonic seizures. He is dependent on emergency medication. Despite his challenges, he is a happy child who loves the water, the ocean and animals. Donations for therapies and assistive devices are needed for him.
Laurin's mother, Katrin, also struggles with her health. She has suffered from multiple sclerosis (MS) since 2009 and Crohn's disease since 2015. The diseases have serious consequences such as paralysis, optic neuritis and extreme fatigue. She is unable to work due to her illnesses, but continues to fight for her children.
Oliver, Laurin's father, lovingly cares for his son even though he has health problems of his own. Sisters Leonie and Lilly are also severely affected and fight for a normal life.
The Frank family faces great challenges, but they remain strong and hopeful.
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