The little Tyrolean (3) suffers from a life-threatening nut allergy. There is only one special therapy in the USA that can help her – and possibly even put her out of her suffering. But this costs 48,000 euros, so her parents have now launched a fundraising campaign.
The three-year-old from Telfs is exposed to danger every day that could cost her her life. She has suffered from a massive nut allergy – and has done so since she was months old. If she eats even a trace amount of nuts, her airways will swell within seconds and she could suffer organ failure. In an emergency, she is constantly dependent on having trained people around her who can keep her alive with an injection of adrenaline until the emergency doctor arrives. “Unfortunately, in practice it is not easy.” “At first glance it sounds easy, ours Not to give your daughter nuts – but unfortunately that’s not the case in practice. Traces of nuts are now hidden in almost all foods – for example in most packages of normal semolina. We weren’t aware of that,” says Lilly’s dad Dominic Praxmarer. “That’s our greatest wish.” The terrible fear that an accident will happen is the family’s constant companion. That’s why the parents of the 3-year-old looked for a solution – and have now found it. “The Food Allergy Institute in California specializes in the treatment of such allergies and has developed effective immunotherapy. The daughter of a well-known family has already been through this and is now allergy-free. We want that for our Lilly too,” says Praxmarer. All details about the appeal for donations for little Lilly (3) from Telfs in Tyrol can be found at: https://gf.me/v/c/5ft6/lilly-schreib- we-your-story-aboutexpensive special therapy €48,000 are needed for this – money that the family doesn’t have. That’s why she’s asking for donations. Almost half has already been donated. “Donations beyond the target amount are also welcome, as we would like to set up an association for children with a similar diagnosis,” reveals the dad.
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