Dear WDA supporters,
On July 3, a young man in his early 20’s and also a Wilson Disease patient, lost all hope. Using an assisted suicide program, he took his own life because he believed he would never overcome what happened to his body as a result of Wilson’s Disease.
I wish my words could be more eloquent about this loss to our community. We have Wilson Disease patients within the organization, that at one time considered or failed at suicide, and they attempted to change his mind. Leadership of the WDA asked him to have hope and wait. They were not successful. As painful as this is for you to read and for the people that tried to save him, there are important reasons to share this sad news.
We don’t know who is on the very edge of despair. You might be reading this right now. We want you to take heart. This is a very critical time in medicine where scientists are developing gene therapies that were only a dream a short while ago. New drugs are in clinical trials. The rate of medical advances is accelerating.
There was a time when premature babies could not survive and now they can. There was a time, when there were no antibiotics. There are surgeries and procedures and therapies that were only ideas a decade ago. There are cures for hepatitis C , and promising results for HIV. We agree that there has been a slow start to even recognizing Wilson Disease much less treat it, but we are pushing ahead because there now exists a global community of researchers and physicians all looking at Wilson Disease. We have started a comprehensive Patient Registry.
We will not quit and we will not lose hope.
In the meantime, what makes a person lose all hope is something I cannot answer. Stopping your medications is not the answer. If you are having difficulties getting your medications, contact us.
What can we do as a community? Let us get Wilson Disease showing on the medical community radar. Let’s raise awareness by wearing our Big wow shirts or caps or telling someone about Wilson disease. How about sharing your stories about the struggles and challenges of this terrible disease with us online at "We are Wilsons," so other patients don’t feel alone and isolated. Let us be kind to each other, even when we are having a bad day. Choose Wilson Disease to be your charity and ask others to be supportive too. Let’s celebrate every step of progress so that those on the edge of despair will not lose hope. When we are quiet, we are invisible. The old adage, "out of sight, out of mind." is true.
For tangible ways you can help we have a page on our website listing many things you might do. Here is the link to that page. Ways you can help page I would like to highlight having a Big wow walk because they create excitement and awareness and also because it is coming up quickly and we need more volunteers. I also mentioned the “We are Wilson’s” page where all you do is send in your story and photo. Donations can be made on our website main page or through the Ways you can help page. Corporate sponsors reading this, we need your help too.
Please contact me if you have any questions about ways you can help now or in the future. Remember, many of you have been fortunate enough to have been diagnosed early but others of our community are suffering both physically and emotionally. This disease affects generations.
(414) 961-0533 extension 3000
Wilson Disease (WD) is an autosomal recessive disorder of impaired copper (CU) transport caused by mutations in the ATP7B gene. WTX101 (bis-choline tetrathiomolybdate) is a first-in-class copper-protein-binding agent with a unique mechanism of action, under investigation as a novel therapy for WD. It is formulated as an enteric coated tablet (15 mg strength) for oral administration. The purpose of this study is to evaluate the efficacy of WTX101 administered for 48 weeks compared to standard of care (SOC) in WD subjects aged 18 and older.
This website is not intended to provide advice on personal medical matters or to substitute for consultation with a physician. The WDA does not accept advertising for this website.
1732 First Avenue #20043. New York, NY. 10128 | 866-961-0533 or 414-961-0533