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    Added on April 09, 2009
"Lena Wyraz"

Lena Wyraz
From the parents of: Lena Wyraz
Lena Wyraz was born on December 16th, 2008 in Zakopane, Poland.
Her birth gave us new hope and great joy. Sadly about one month after she was born, Lena was taken to a hospital with serious underweight, anemia and symptoms of pneumonia. Doctors not being able to cure all of the symptoms and facing worsening Lena's general conditions decided for a blood transfusion which helped to solve the situation in a short run. Unfortunately the test result show increase of chlorine in sweat and with other clinical symptoms the diagnosis was very clear: Cystic Fibrosis (CF). Currently there is no known cure for CF. We are living in hope looking for the day when the term "incurable" will no longer be valid for CF. We would like to give Lena a chance to reach that day. Unfortunately state support in Poland is nothing you could compare with other countries. We are struggling to provide Lena with available treatment methods, medicines, supplements and rehabilitation equipment.

Now when we know what we are fighting with we are searching and hoping to meet on our way people of goodwill who could support us in this uneven battle.

Thank you all - Magdalena and Piotr

Web site: none
Parents e-mail: Magdalena Czerwinska-Wyraz and Piotr Wyraz
Lena Wyraz   Lena Wyraz   Lena Wyraz  




**Important Information From Lone Star PL**
Lena Wyraz is a registered patient at the foundation "Polish Society Against Cystic Fibrosis". Lone Star PL will send all (100%) donations received to Lena Wyraz sub account, which is controlled by the PSACF foundation. Then the funds will be used as needed to pay for Lena medicine, medical equipment and medical treatment only!

When making a donation to help Lena Wyraz, please write on your check or credit card transaction "LenaW"
For more information please go to: How to Donate Page. ** All donations to Lone Star PL are tax deductible.

For more information how to help polish children who are suffering from Cystic Fibrosis
please visit: Polish Society Against Cystic Fibrosis website.





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