Paul Pietrowski Foundation Web
Site
Duchenne Muscular Dystrophy
Anyone can say that they want
to make a difference in life.
Here is your opportunity to
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This is Paul today
he is 16 years old Click the Image and
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| Paul Pietrowski, a 16-year-old past Des Plaines resident,
has Duchenne muscular dystrophy, a disease that is rapidly destroying his
muscle tissue. His family is desperately struggling to save their only
son. The only hope for Paul is a myoblast transfer treatment.
March 2008 URGENT UPDATE Due to his health, Paul needs to go back to the Ukraine
immediately for another stem cell treatment. The cost of the trip will
be approximately $5,500.00. Sadly, the Paul Pietrowski Foundation has been
completely depleted of funds.
2002-2006 Paul’s Journey Before Paul’s first treatment in 2002, he was strictly confined to his wheelchair. He couldn’t even lift his arms. He was underweight and very weak. Unlike his outgoing personality now, he was very shy and quiet. After his first treatment in 2002, he started gaining a little bit of weight and he started to talk a little more. Each year since then he has gone to the Ukraine at least once a year for more treatments. After each treatment he gains more strength and ability to do things for himself. He has gained more weight, he’s getting taller, and he can keep his head up by himself. He can now lift his arms all the way up in order to do exercises. This is also due to the fact that Paul and his mom have been going to the pool since 2005 so he could get physical therapy in the water. This ongoing treatment is quite expensive, but it is necessary to keep Paul strong and healthy. Paul also has regular visits at the doctors at Yacktman Pavilion Lutheran General Hospital. Every six months Paul sees a cardiologist and neurologist, and every 12 months he has a visit with an orthopedic doctor. Once a week he has physical therapy at home. Thanks to all the people and organizations, Paul has the following installed at home: “Stair Lift,” “Ceiling Lifts” in every room, and an “Adjustable Hospital bed” in his room. In the last few years, Paul has come out of his shell as he has gained strength and confidence. He enjoys the outdoors and isn’t afraid to make friends at school. He is very outspoken and outgoing. He is attending classes with his peers and he receives good grades. When he does his homework he can now write with a pen or pencil and he can type on the computer very quickly. Diana, his older sister, says “I’ve never seen Paul so happy!” Please continue to support Paul in his battle to live. Your support equals more time that Paul can spend with his sisters and mother and father. Not only does the treatment add time to Paul’s life, it radically improves it. Things like eating by himself, holding a book up to read it, and reaching out for a hug are things that we might take for granted, but Paul depends on you and I for the luxury of enjoying them. June 15, 2007 – Paul Undergoes Heart
Surgery
2007 Update Return to top of Page Paul is now 16 years old. At this time Paul is getting
bigger and taller and he needs more stem cells. The next visit at “EMCELL”
clinic is scheduled for next year, but there are currently no funds available
to him. Paul also has regular visits at the doctors at Yacktman Pavilion
Lutheran General Hospital. Every six months Paul sees a cardiologist and
neurologist, and every 12 months he has a visit with an orthopedic doctor.
Once a week he has physical therapy at home. Thanks to all the people and
organizations, Paul has the following installed at home: “Stair Lift,”
“Ceiling Lifts” in every room, and an “Adjustable Hospital bed” in his
room.
Paul goes to H.D. Jacobs High School in Algonquin, and will be entering his junior year in the fall. He has regular classes and understands the material he is taught at school. He receives good grades, learns very well, he is able to read, write and do all his work like a regular student. When Paul is at school he has friends, talks to people, and asks for help when he needs it. Because of his stem cell treatments, he can lift his arms to eat his food and drink by himself at lunch time. He is a very smart boy and has dreams and goals like everyone else. He loves to read books and go to the movies with his two sisters, ages 19 and 13. His sister Diana said that he loves to go shopping with his parents (just like most teenagers). When asked to describe her little brother, Diana said that Paul is very funny and sensitive. She also said that he never gives up, even when other kids put him down because of his condition. Please continue to support Paul in his battle to live. Your support equals more time that Paul can spend with his sisters and mother and father. Not only does the treatment add time to Paul’s life, it radically improves it. Things like eating by himself, holding a book up to read it, and reaching out for a hug are things that we might take for granted, but Paul depends on you and I for the luxury of enjoying them. |
Be sure to check back often for fundraising events!
Would you like to sponsor or hold an event for Paul? Contact
us today!
You can check out the Doctor's website at www.emcell.com.
More Good News. Paul
is back home. Read his Story!
Read about
Fund Raising Success Stories
Read about
Myoblast Transfer Treatment Success Stories
For donations or information please call 847-297-0101
Paul Pietrowski Foundation
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1000 Executive Way, Ste 202 Des Plaines, IL 60018 |
Paul thanks you for your consideration.
Check our Progress and see our Contributors and Sponsors
Comments or Questions E-Mail
us
Attention Guests: If you are looking for medical advice on this
or any
other medical topic there are some links on our Links
Page
and more all over the Web. Ask your doctor and/or get options and
opinions from other Medical Professionals.
Thank You and Good Luck
Home | Goal | Contributors | Links
We would also Like to Thank The Following People for their Help
Thank You
(Listed Alphabetically)
Joe Circolone of Aetna Bearing Co. and Aetna Bearing Co.
Father Cysterian Church in Willow Springs
Karen Dane
Jeff Franzen
Karen Henrikson
Emily Johnston
Wendy Johnston
Roman Karp
Amy Maatta
Kathy Maatta
Jim Mader-selling dinner/dance tickets
Marty and Leslie Malone-selling dinner/dance tickets
MaryEllen McKenna
Ryan McKenna
Dennis Mlynski (Maine West Athletic Boosters)
Holly Napravnik
John Noonan (Rosemont Cavaliers)
North School, Des Plaines
Jarek Nowik
Jim and Elizabeth O'Malley-selling dinner/dance tickets
Dariusz Pietrowski
Diana Pietrowski
Edyta Pietrowski
Marzenna Pietrowski
Paul Pietrowski
Mike & Rhonda Ramsey-selling dinner/dance tickets
Oscar Rodriguez
Special Interest Answering Service
Diane Thorne
Lenny Thorne
Melissa Thorne Cruz
Robert Thorne
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