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Založeno 11. 11. 2020

We Dream Big for HAE Juniors!

Jennifer Preston
Holy Cow!! We've met our goal early! But, let's not stop here. Let's raise as much money as we can to help these kids and this organization trying to give them as much support as they need.

Will you help me support the organization that supports children and teenagers suffering from the disease HAE?

Everyone who donates will get a chance to win a 45-minute online private chat with me! Winners will be announced on Nov. 26 on my Instagram and YouTube  pages on Thanksgiving, 26 Nov 2020.
HAE Junior is a non-profit patient organization with the aim of participating in improving the quality of life of children and adolescents diagnosed with hereditary angioedema (HAE) and their families. The association was established in December 2019 in Prague on the initiative of its parents. HAE is a rare lifelong disease that manifests itself in frequent painful swellings in various parts of the body. Living with HAE means repeated temporary health problems, frequent acute examinations and injections, long-term mental strain, and other limitations.

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HAE Junior z.s.