Volunteer Opportunities

Call or email for more information 414-961-0533 or info@wilsonsdisease.org

Social media

If there are any volunteers that are proficient in multiple social media that can help promote what the WDA is doing using the WDA accounts We’d like to hear from you.

Marketing

The WDA believes it could benefit from a person that works currently or recently in a professional capacity in marketing. If we have such a person in our audience we are looking for some project-related advice.

Twitter users that tweet.

This is a priority now.  The Wilson Disease Association has a twitter handle @wilsondisease.  We’ve developed a good following on Facebook and started a YouTube channel but have not developed our Twitter feed or following.  Your help is critical now. We could use an army of twitter retweeters.  Call or email for more information 414-961-0533 or info@wilsonsdisease.org

Editing help

Sometimes we just need a good editor to proof read and correct Copper Connection articles.  Needed are a command of English and great grammar.

Legal

We would like to enlist attorneys for occasional legal assistance. Please contact Judi Keller info@wilsonsdisease.org if interested

Donations

Your support allows the WDA to maintain this website, produce educational materials, support research, and hold meetings for people living with WD, their families, and the healthcare community.

Membership

Your support allows the WDA to maintain this website, produce educational materials, support research, and hold meetings for people living with WD, their families, and the healthcare community.

Peer to Peer Fundraiser

Starting a fundraiser is easy to do, and it’s fun. We’ll even give you all the tools you’ll need to make a difference. With your help we can ensure critical steps of our 5 year plan get completed. This fundraiser requires no parties, walks or selling anything. You just send it out to people that you know. Contact Judi Keller at judi.keller@wilsonsdisease.org if you require further assistance with setting this up.

We Are Wilsons

Share Your Story
We will be collecting patient stories and photographs to post on our website, Facebook and soon, Instagram. The Wilson Warrior stories have proven to be inspirational and we think we need a way to collect any story.

Final Gift Plan

Consider WDA in a “Will” or Final Gift Plan
The Wilson Disease Association is 35 years old and is represented by board members from across the country and Canada. We have volunteers and partners globally and spearhead research that impacts our patients directly but affects a broader population beyond our patients. The long term importance of what the Wilson Disease Association does is limited only to the imagination because it affects generations of families around the world. Please consider the Wilson Disease Association in your will. Giving in this way is not restricted to the wealthy or a gender.

Corporate Matches

Let us help you find employers and corporate donors to match your donation.
As a benefit to employees, many companies increase the impact of their employees’ gifts to WDA by providing matching contributions. Most corporations provide a 1:1 match; while some companies will double or even triple the matching amount to further encourage and leverage their employees’ philanthropy.

Facebook Picture Post

Share a picture of yourself on Facebook
Help us spread the word by sharing a picture of yourself holding a sign with a message that we can post on Facebook and Instagram.

Facebook Fundraiser

Start your own fundraiser on Facebook
We’ll help you get started and give you tips to reach your goal.

WILSON DISEASE ASSOCIATION

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