February 21, 2019
If you or a loved one was recently diagnosed with C3 glomerulopathy (C3G), you may be feeling scared or overwhelmed. And as you’ve probably already discovered, due to the rarity of this condition, relevant tools and information are often limited and difficult to find.
Luckily, you’ve come to the right place. The WeC3G community was created to give patients and caregivers the support and resources necessary to manage C3G disease while continuing to live their best lives. With the addition of the blog, you will now have access to timely, relevant information that can help you do just that.
In an effort to raise awareness of this rare disease and bring learnings and insights to the community space, the blog will feature posts dedicated to 3 main topics: Understanding C3G, Living With C3G, and News About C3G.
These posts will help you get a better understanding of this complex illness. They will break down scientific and medical subject matter into simpler, easier-to-understand topics. While helping you better understand C3G, these posts will also focus on things like how to explain the condition to friends, family, and colleagues.
Living With C3G
Being diagnosed with a chronic illness is not easy. But it’s important to remember that your diagnosis is only a part of your life, not the whole thing. From eating right to joining support groups, there are many things you can do to ease the burden of this disease. These posts will provide tips and tricks for maintaining a healthy lifestyle after a diagnosis.
News About C3G
As more research is done and doctors develop a better understanding of this condition, more progress continues to be made. WeC3G is committed to keeping you informed on the latest updates and events pertaining to C3G. From clinical trials to patient meet-ups, you can find timely, relevant news here.
Let this blog be a trusted resource for understanding, managing, and living with C3G. Check back often for updates or register for WeC3G emails so you never miss a post.
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