Thank you for visiting our Langa Family Big WOW page!! To our new supporters, hello (!!) and please read our story (further below) about how Wilson's Disease (WD) has greatly impacted our lives over the last 10 years. To our supporters and attendees of previous years’ Big WOWs (hello to you, too!!), unfortunately, due to COVID-19 we are not holding an event that includes food, beverages, speakers and activities as we have in prior years. The national committee has gone fully virtual for the event this year.

Please click the donate button (to the right) to donate and support the fight against Wilson's Disease. All funding will go towards the WD Patient Registry. "The Patient Registry creates a framework for advances in diagnosis, treatment and potential cures for the disease. Not only will the current generation of Wilson's Disease patients benefit , but this registry will serve as a roadmap for future generations to come." Please visit www.wilsonsdisease.org for more information. Please note that we will be accepting donations throughout the month of October. The donations link will be deactivated at 11:59p.m. on 10/31/2020.

OUR STORY:

For the past 10 years, Constantin Langa (now 37 years old) has been struggling with Wilson Disease (WD). Constantin's symptoms started when his son Traian was only 3 months old, and his wife, Nichole, and him were just learning how to be new parents.

Some of Constantin's first symptoms included excess saliva, toe and hand cramps, tongue and body tremors, dystonia, slurred speech, and balance loss (most all of which, he still struggles with today). It took him and his family 6 months from the start of his serious symptoms to get a diagnosis. By many measures though, they consider themselves very fortunate to have gotten a diagnosis within that timeframe, especially when others in the WD community were wrongly diagnosed or it took even longer for them to get a diagnosis. It was a very traumatic period for his family, as Constantin, a healthy and successful man, was falling apart, and his wife was taking care of a new baby. That “baby” (Traian) is now 10 years old, and Constantin and his wife were blessed with the birth of their second child (eight years later), a beautiful healthy girl named Adina, who is now 2 years old.

Part of the reason Constantin is a survivor is because he was diagnosed “early” enough to catch the fatal onset of the disease (although genetic testing at birth would have been the most ideal solution). However, getting a diagnosis was no easy matter. His family ran from doctor to doctor, and every time the doctors were either baffled, told them what Constantin didn’t have, or they were provided a wrong diagnosis. The first diagnosis they received was anxiety and depression, but they never gave up searching for answers because that just didn’t seem correct. His family knew that there was something more going on. It wasn't until he took an MRI, and the neurologist saw the "panda face" that Constantin was finally on the path toward a diagnosis. The MRI, plus lab and genetic testing, and the discovery of Kayser-Fleischer Rings in his eyes solidified the diagnosis. Thanks to a doctor at Johns Hopkins and assistance from a WD Center of Excellence doctor at Yale, they had an answer.

Over this period of about 6 to 8 months, the neurological manifestations of WD took Constantin suddenly from a very healthy, active lifestyle and holding a full-time job in Washington, D.C. to completely debilitating neurological effects of not being able to perform any basic function without assistance. Constantin's symptoms greatly worsened 3 weeks following the start of the chelation therapy medication. The doctors tried to save his liver by getting as much copper out of his body as quickly as possible. As a result, his neurological system was compromised.

Ten years into this WD journey, daily life is still a struggle and Constantin still requires 24-hour assistance from caregivers and family. However, his determination to get better means that even though he can't attend the regular therapies (aquatic, modified yoga, neurofeedback, acupuncture, acupressure, speech, etc.) he used to prior to COVID-19 (which has resulted in additional neurological challenges for him) he continues to push and try to overcome. Even these many years later, they are defying the odds and continue to see improvements.

Our hope is to raise awareness for WD, so that we can prevent future generations from the same devastating situation. Early diagnosis and treatment is the key! Thank you for supporting us and the WD community as we work together to better the lives of our fellow human beings!! Stay safe out there.

With Love, The Langa Family

All donations are used to fund the Patient Registry Research Project for Wilson Disease.  The Wilson Disease Association is a 501 c (c) organization in the United States.