CheckOrphan

19/11/2021

WordPress programming, database skills needed!

www.CheckOrphan.org is dedicated to helping the 100s of millions of people living with rare diseases by empowering them with news and information. And we do it like no other website.

Come help us do it better! We are looking for , and if you are an agency or have you own company we can discuss providing you exposure on so as we grow, so can you!

Well, he did it! THREE marathons in three days to raise money for the Huntington's Disease Association. We can't thank George enough for all that he has done for the charity and those affected by 💚 https://twitter.com/georgerainsford/status/1459938750641983498

07/02/2020

Looking to use your coding prowess for good? Millions of people living with rare diseases depend on CheckOrphan daily and CheckOrphan needs your help to better serve them.

Do you have experience with , , theme development, plugin development, integration, or app planning and development, and , which the current site uses. PHP/Python and other scripting experience is a plus.

If so, come join the CheckOrphan Web Development Team.

Contact (derhamr@checkorphan.org) or learn more here https://lnkd.in/gXad93b

Your source for news & information about rare diseases & orphan products

10/09/2019

Rare but collectively common

Research into rare disease treatment is primarily focussed on Western countries and urban areas. Now the fight is on for equal access globally.

26/08/2019

Interesting talk on finding a solution

Group-B Streptococcus (GBS) remains a leading cause of sepsis and meningitis in babies and a vaccine is required to prevent all types of GBS disease and to p...

26/08/2019

Don't Ever Give up.

Doug Lindsay was starting his senior year in college when he was stricken by a mysterious illness. Doctors were baffled. He eventually realized that if he wanted his life back, he'd have to do it himself.

12/08/2019

Would you like to help make life easier for people with rare diseaes? Come volunteer some of your time with www.checkorphan.org - the leading news and information platform for rare diseases. Contact me at dorota@checkorphan.org for more information

CheckOrphan is a 501(c)(3) nonprofit organization. Contributions to CheckOrphan in the United States and Switzerland are tax-exempt to the extent provided by law.

24/06/2019

Do you love to post, tweet and message for a great cause? CheckOrphan www.checkorphan.org - the leading news and information source for rare disease has plenty of content and we need your help. Contact dorota@checkorphan.org to learn more. It is volunteering opportunity

CheckOrphan is a 501(c)(3) nonprofit organization. Contributions to CheckOrphan in the United States and Switzerland are tax-exempt to the extent provided by law.

24/06/2019

Did you know over 35 M people live with a rare disease in Europe alone? CheckOrphan is dedicated to providing news and information about all rare diseases and we need you to volunteer to be part of our News Team. Contact me at dorota@checkorphan.org to learn more

07/06/2019

Illuminate the possibilities to advance orphan drug development and maximize success by attending . Download the agenda now to learn what to expect >>

06/06/2019

Join us in Boston, June 13-14, for where you will meet a mix of early-stage , leading # pharma companies, , researchers and to engage in a dialogue around . https://bit.ly/30bVkv5

04/06/2019

Bruce L. Levine, PhD, a leading innovator in the cell and gene therapy space discusses his research and outlook on cell and gene therapies, and the importance of partnerships in progressing the field.

Bruce L. Levine is a man you can thank for your future cell therapy