Jennifer is 26 years old and was diagnosed in 1999 with Mucolipidosis, (ML) Type III. The road to diagnosis was difficult as Jennifer didn’t present symptoms early on in childhood. Doctors had misdiagnosed Jennifer for 1-1/2 years with another disorder.
Today, Jennifer has had multiple surgeries for her back, lungs, and most recently a left hip replacement. She suffers from osteoporosis and benefits from a quarterly infusion that helps strengthen her bones and provides some pain relief. Mucolipidosis is a progressive disease that has no treatment and has no cure.
Our family has made many friends around the world as we travel on this path of rare diseases. She is only one of approximately 50 patients in the United States with her disease.
Together, our family’s goal is to raise awareness and funds for the National MPS Society. The Society supports research for MPS and related diseases, this includes Mucolipidosis. It is critical we raise funds to develop a treatment for those suffering. There are treatments for some of the MPS diseases that are similar to Jennifer, but no breakthroughs yet for hers.
Jennifer is fortunate that she is attending University and double majoring in biology and psychology at NC State University. She graduates in December. She struggles each day with pain, but has such courage! Her motto, “No, isn’t an option,” resigns with us each day.
Thanks for stopping in and taking a look around the webpage. This page is built in honor of Jennifer.
International MPS Awareness Day is May 15th. We have updated this page in her honor.
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The Klein Family
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The mission of the National MPS Society is to fund research and provide support for families affected by MPS and related diseases.
Please help our family and support the National MPS Society. Every donation will make a difference in the lives of those affected by MPS and related diseases. Please visit www.mpssociety.org for more information.
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