Hello, this is two years old Jake and he has been diagnosed with a rare autoimmune Desease called Hyper-IgE-Syndrome that affects large areas of his skin on body and Face.

We spent a good amount of time in hospitals getting treatment for neurodermitis with large amounts of cortison but nothing helped until they figured out what the real Problem was.

The treatment is in an early experimental stage and can be done in Switzerland. He also needs stem cell transplant because its hereditary. But its not covered by insurance, because they say they dont see ITS NECCESSARY. As you can see he is in constant pain. Infections everywhere, super thin skin because of the cortison treatment that causes bleedings as soon as he touches his face too harsh. He also had SEVEN ANTIBIOTIC TREATMENTS in 2025.

We are currently on trial against Insurance but it will take a good amount of time. Time we could already put to treatment. We put all our savings in already but its still not enough.

I would highly appreciate every help we can get.