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Research Matters

Research Matters

Dr. Sam Reynolds of Moffitt Cancer Center shares his perspective on the importance of research in advancing understanding and care for Erdheim-Chester Disease. Watch the video and help us ...
Research Funding Opportunity

Research Funding Opportunity

The ECD Global Alliance is accepting Letters of Intent for its 2026 Early Career Investigator Grant. Up to $60,000 USD will be awarded for a two-year research project focused on Erdheim-Chester ...
Our Global ECD Community

我们的全球ECD社区

ECD may be rare, but no one has to face it alone. Across the world, patients, caregivers, physicians, researchers, volunteers, and advocates are working together to build a stronger future ...
Research Brings Hope

研究带来希望

Today's discoveries create tomorrow's possibilities. Research has transformed what we know about ECD and continues to improve diagnosis, expand treatment options, and deepen our understanding ...
Patient and Caregiver Stories

患者与照护者的故事

Every ECD diagnosis has a story. Some stories begin with years of unanswered questions. Others are filled with resilience, courage, and hope. Today we honor every patient, every ...
寻找专业护理

寻找专业护理

罕见病需要罕见的专业知识。 由于ECD极为罕见,许多医疗专业人员在职业生涯中可能从未接触过此类患者。将患者与医生对接…….
尽早发现可节省时间

及早发现可节省时间

For many people with ECD, the road to a diagnosis is measured in years, not weeks. The sooner ECD is recognized, the sooner patients can begin their journey toward answers, expert care, and ...
为什么提高意识很重要

为什么提高意识很重要

One person learning about ECD may not seem like much. But one conversation can lead to an earlier diagnosis. One shared post can reach someone searching for answers. One moment of awareness ...
谣言与真相

谣言与事实

 齐吉知道…… 误区:早期儿童发育障碍(ECD)只影响骨骼。 事实:早期儿童发育障碍(ECD)可能影响全身多个器官,极少数病例不涉及骨骼。每个人的情况都是独特的。 这就是为什么…….
诊断历程

诊断历程

Ziggy Knows... People with ECD spend years searching for answers. Research has shown that after symptoms first appear, it takes an average of 4.2 years to get an ECD diagnosis. Learning ...
常见症状

常见症状

 齐吉知道…… 没有一种症状能单独定义ECD。 有些人会出现骨痛、疲劳、口渴、平衡障碍、皮肤变化、呼吸困难或其他…….
什么是ECD?

什么是ECD?

齐吉知道…… 埃尔德海姆-切斯特病(ECD)是一种极其罕见的血液癌症,可影响身体的许多不同部位,包括骨骼、心脏、大脑、肾脏、肺、皮肤、眼睛以及…….
ECD Awareness, Diane Schriner

ECD Awareness, Diane Schriner

“早期儿童发展(ECD)宣传月”来临了!在这份特别致辞中,ECD全球联盟董事会主席黛安·施莱纳分享了学习、建立联系和提高公众意识如何能带来有意义的改变…….
让我们一起学习

让我们一起学习吧

大家好!我是Ziggy,你们的ECD意识指南。 整个9月,我将分享相关知识、解答常见问题、介绍我们社区中那些鼓舞人心的成员,并帮助…….
Advocacy Creates Change

倡导带来改变

Rare diseases need people willing to speak up. Every conversation about ECD can increase awareness and help patients, families, healthcare professionals, and communities better understand ...
Caring for the Caregivers

关爱护理人员

Caregivers give an extraordinary amount of themselves. They attend appointments, coordinate care, ask questions, provide encouragement, and help navigate difficult days. Their own needs can ...
Families Walk This Journey Too

家庭也在走这段路

ECD affects more than the person who receives the diagnosis. Families become appointment companions, researchers, organizers, advocates, listeners, and sources of strength while navigating ...
Celebrating Our Volunteers

致敬我们的志愿者

Behind so much of what happens in the ECD community are people who simply decided to help. Volunteers contribute their time, talents, experience, and energy to support patients, increase ...
Every Story Matters

每个故事都很重要

No two experiences with ECD are exactly the same. Every patient and caregiver has a story. When those experiences are shared, they can educate others, create connections, and help someone ...
The Power of Connection

联系的力量

There is something powerful about talking with someone who simply gets it. ECDGA chats and webinars give patients and caregivers a place to share experiences, ask questions, exchange ideas, ...
Meet the Patient Navigator

认识患者导航员

Sometimes the most important thing you can hear is, “I can help.” The ECD Patient Navigator helps patients and families find information, understand available resources, connect with the ECD ...
Thank You to Our Research Community

感谢我们的研究界

As we close another week of ECD Awareness Month, we celebrate everyone who makes progress possible. Thank you to the physicians searching for answers, the researchers making discoveries, the ...
Research Is a Team Effort

研究是一项团队合作

Progress happens because people work together. Patients, caregivers, physicians, researchers, volunteers, advocacy organizations, supporters, and ECDGA all play an important role in moving ...
Looking Ahead

展望未来

The future of ECD research is full of possibility. Researchers around the world continue exploring new treatments, better ways to diagnose ECD, and deeper insights into how the disease ...
Celebrating Progress

Celebrating Progress

Not long ago, very little was known about ECD. Today, researchers understand far more about the disease than ever before. Advances in diagnosis, greater collaboration among specialists, and ...
Meet the Experts

Meet the Experts

Behind every discovery are dedicated physicians and researchers working to improve the lives of people with ECD. Their commitment to caring for patients, conducting research, and sharing ...
Clinical Research

临床研究

Every breakthrough starts with a question. Clinical research helps us better understand ECD, improve diagnosis, evaluate treatments, and learn more about how this rare disease affects ...
ECD Care Centers

ECD 保育中心

Hope begins with expert care. ECD Care Centers bring together physicians with experience diagnosing and treating this ultra-rare disease. They also help advance research, educate healthcare ...
How You Can Make a Difference

您如何能带来改变

You don't have to be a scientist or a doctor to make an impact. You can help by: Sharing information about ECD. Supporting ECD Global Alliance. Listening to patient stories. ...
请预留时间!

请预留时间!

2027年,ECD全球联盟(ECDGA)与组织细胞学会(HS)将于8月27日至31日在苏格兰格拉斯哥举办首届联合年会。会议计划安排如下: ...
请预留时间!

请预留时间!

我们很高兴地宣布,第12届年度埃尔德海姆-切斯特病患者及家属聚会将于2027年8月27日至28日在苏格兰格拉斯哥举行! 欢迎患者、护理人员…….
感谢您超越职责范围的付出!

感谢您付出的额外努力!

我们衷心感谢所有为今年ECDGA虚拟趣味跑、健走或轮椅行活动取得如此巨大成功做出贡献的人。 正因为我们这个了不起的社区展现出的慷慨与奉献精神,…….
明天就是最后一天了。

明天是最后一天。.

明天午夜之前,我们的“$10,000配对挑战”即将结束,我们只需再筹集$999.00,即可为ECDGA虚拟趣味跑、健走或轮椅活动解锁全额配对资金。 这不仅仅是一项…….
团队聚焦:落基山之巅队!

队伍聚焦:落基山之巅队!

请向“落基山之巅”队的队长(鲍勃和珍妮特·弗罗切尔)送上热烈的掌声,他们作为ECDGA“虚拟趣味跑、走或骑”活动的一环,完成了令人惊叹的10英里骑行!…….
致社区的一封信

致我们社区的一封信

当有人听到"您患有埃尔德海姆-切斯特病"这句话时,他们往往会有更多疑问,而非答案。 去哪里查找相关信息? 谁能帮助我了解这种疾病? ...
最后一周挑战

最后一周挑战

我们迎来了一个绝佳的机会。 一位慷慨的捐赠者为我们的ECDGA虚拟趣味跑、健走和滑行活动最后几天提供了$10,000的配对资金。 这意味着每捐赠1美元…….
让您的影响力翻倍

让您的影响力翻倍

你知道吗? $50的捐款将变为$100。 $100的捐款将变为$200。 $250的捐款将变为$500。 得益于一位慷慨的配捐者,本周的每一笔捐赠都将以双倍的金额计入…….
快来展示你们的团队吧!

快来展示你们的团队吧!

我们希望在ECDGA第三届年度“跑、走、滑”趣味活动中展示您的风采! 请向我们发送以下照片: 团队成员 步行、跑步或滑行场景 团队聚会 您的照片可能会在我们的社交媒体上展示…….
第二周挑战来啦!

第二周挑战来啦!

第2周挑战来啦! 本周的主题是组建团队! 招募5名或更多新团队成员,你的团队将获得$150的奖励,该奖励将计入你的筹款总额! 邀请…….
快看那个温度计的指针在上升!

快看那个温度计的指针在上升!

在解锁我们的“$30,000”新“影响力挑战”配对目标的道路上,我们已经完成了30%的进度,这全都要感谢像您这样的支持者。 $25 将升级为 $50 $50 将升级为 $100 每一美元都至关重要。…….
斑马齐吉谈保持联系

斑马齐吉谈保持联系

我们很高兴向大家分享一部以ECD社区亲切的吉祥物——斑马齐吉为主角的新动画短片。在这段简短的视频中,齐吉介绍了ECD全球联盟如何每月举办线上…….
“慈善星期二”即将到来

“慈善星期二”即将到来

今天,我们的朋友斑马齐吉挺身而出,致力于提高公众对埃尔德海姆-切斯特病(ECD)患者的关注度并为其争取支持——这是一种罕见且棘手的疾病,亟需更多…….
2月28日:罕见病日

2月28日:罕见病日

在2月28日“#RareDiseaseDay”这一天,ECD全球联盟通过展示条纹图案,呼吁公众关注埃尔德海姆-切斯特病。全球有3亿罕见病患者。由于科学知识的匮乏以及…….
志愿者支持的重要性

志愿者支持的重要性

    ECD全球联盟(ECDGA)是一家致力于为罹患一种名为埃尔德海姆-切斯特病(ECD)的超罕见血液癌症的患者提供支持的非营利组织,现向……致敬…….
2022年ECD年度会议公告

2022年ECD年度会议公告

一个难得的社群将齐聚一堂,相互交流、共同学习。 终于,埃尔德海姆-切斯特病(ECD)患者、家属和医生的社群将再次齐聚一堂!在……期间…….
全球支持率上升

全球支持率上升

今年9月,在2021年“组织细胞增生症宣传月”期间,举办了一场国际组织细胞增生症线上会议。此次网络研讨会由西班牙OR协会组织并主办,…….
罕见病的代价

罕见病的代价

患有罕见病的生活可能很艰难:无论是在精神上、身体上,甚至在经济上都会令人筋疲力尽。2013年的一项名为《罕见病影响报告》的调查(在美国和…….
能源

能源

能源 作者:朱塞佩·德·西蒙内 (2020年3月-4月) 在这段艰难的日子里,我们需要能量来应对新冠病毒。所以,现在我要谈谈能源。 在学校里,我…….
员工聚焦:您的总监

员工聚焦:您的总监

You are likely already a member of the ECD Global Alliance and we hope that you have been able to find help and comfort in the resources that we have available to our members. It is our amazing ...
2020年罕见病日

2020年罕见病日

呼吁所有倡导者行动起来! 2020年2月29日将是由EURORDIS协调举办的第30个国际罕见病日。在这一天及前后,来自各国的数百个患者组织以及…….
疼痛与疲劳

疼痛与疲劳

对于许多患者而言,疼痛和疲劳时刻提醒着他们患有埃尔德海姆-切斯特病。无论是否存在BRAF突变,埃尔德海姆-切斯特病患者都可能出现疼痛和疲劳。…….
给亲人的建议

给亲人的建议

护理人员信息 任何希望与其他关爱ECD患者的护理人员建立联系的护理人员,请联系本组织。 护理工作非常艰辛。对于许多人来说…….
2019年罕见病日

2019年罕见病日

在过去的11年里,“罕见病日”已成为一项标志性活动,旨在向政界人士、临床医生、研究人员和制药公司普及罕见病知识。…….
2019年岁末通讯

2019年年终通讯

又一年即将结束!我们衷心感谢ECD社区一直以来对本组织的支持,感谢大家支持我们履行服务全球家庭的使命。 在……的帮助下…….
十周年挑战

十周年挑战

We are 10 YEARS STRONG!! The ECDGA is raising funds for the future and we need your help!  We ask you to request 10 of your friends or family to donate $10 each for a 10-week ...
未找到结果。.