CheckOrphan

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!

CheckOrphan 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

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 ([email protected]) or learn more here https://lnkd.in/gXad93b

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

Rare but collectively common

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

Interesting talk on finding a solution

Imperial researchers are working to tackle Group-B Streptococcal infections 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...

Don't Ever Give up.

This college dropout was bedridden for 11 years. Then he invented a surgery and cured himself 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.

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 [email protected] for more information

CheckOrphan 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.

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 [email protected] to learn more. It is volunteering opportunity

CheckOrphan 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.

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 [email protected] to learn more

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

RareDiseaseAgenda

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

Home | Rare Disease Summit

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