Orphan Reach

Orphan Reach: Emmes' global Rare Disease Center. We partner with innovative biotech companies to bring new therapies for rare diseases to the market.

[Rare Diseases Clinical Research Network @rarediseasesnet]

Virtual #RareDiseaseDay at @NIH 2022 is next Monday, Feb. 28! Register here: https://t.co/u8u3HWTspM #RDDNIH

Check out this thread for information on sessions w/@rarediseasesnet speakers ⬇️
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[RARE Revolution Magazine® @RareRevolutionM]

#LightUpForRare! Will you help make a global chain of lights for #RareDiseaseDay2022 to show your support for the rare disease community and unite across the world?
#RareDiseaseDay2022 #TuesdayTakeover @GeneticAll_UK @rarediseaseuk

[Rare Disease Day @rarediseaseday]

Rare Disease Day is just around the corner... are you ready to get involved?

Watch our recorded webinar and learn how to prepare your social media communication ahead of Rare Disease Day 2022.

➡️Watch now: https://t.co/paVqkelYOE

#RareDiseaseDay

[Orphan Reach @Orphan_Reach]

Spend few minutes to sign up to the #RareDiseaseDay new webinar about ways to introduce rare diseases to young children, taking place on the 17th February 2022

https://t.co/Q2HNuVEugY
#RareDiseasDay2022 #RareDiseaseMonth

[Rare Disease Day @rarediseaseday]

Spend few minutes to sign up to the #RareDiseaseDay new webinar about ways to introduce rare diseases to young children
📅 17 February 2022
🕑 14:00 CET
https://t.co/est8ZF3iQM

[Orphan Reach @Orphan_Reach]

Nada is determined to spread awareness about Epidermolysis Bullosa and fight against social discrimination.

Read Nada's story and share your own: https://t.co/iqa01ROPk0
#RareDiseaseDay2022

[Rare Disease Day @rarediseaseday]

22-year-old Nada from Egypt is living with epidermolysis bullosa, a rare disease that affects the skin.

Nada is determined to spread awareness about Epidermolysis Bullosa and fight against social discrimination.

➡️Read Nada's story and share your own: https://t.co/HpSS51G0Cu

[Orphan Reach @Orphan_Reach]

#RAREfact #RareDiseaseDay2022

[Rare Disease Day @rarediseaseday]

Around the world there are 300 million people living with a rare disease. 🌎

Are you one of them?

Share your story today and help raise awareness: https://t.co/LbKfyChrOU

#RareDiseaseDay

[Orphan Reach @Orphan_Reach]

Inside the rare disease centre which aims to accelerate biotech growth...

DDW’s Megan Thomas spoke with Thomas Ogorka our Managing Director about the potential of our rare disease centre.

You can read the interview here: https://t.co/UC3uGKJ6On

#raredisease #rarediseasecentre

[RARE Revolution Magazine® @RareRevolutionM]

Come and visit our stand at #WODC Barcelona and pick up a copy of our latest #FutureofRare in print.

[Emmes @EmmesCRO]

For #WorldPneumoniaDay, we're sharing a study with Emmes authors of #pneumococcal #vaccines published in 2018 #StopPneumonia #EveryBreathCounts https://t.co/P6OoSa2PMI

[Orphan Reach @Orphan_Reach]

@EmmesCRO's strategic partnership with MedGenome is aimed at accelerating breakthrough treatments, powered by human genomics, for #raredisease patients.

Click here to read more: https://t.co/NIV8TPZOcP

[Emmes @EmmesCRO]

We have launched a strategic partnership with @MEDGENOME to focus on advancing #raredisease research! This collaboration will support patient recruitment, and create standard control arms for advanced statistical models of treatment effect. #wodc2021 https://t.co/148vngVvib

[Orphan Reach @Orphan_Reach]

We are delighted to be exhibiting at World Orphan Drug Congress in Barcelona next week! You can visit us at booth #19 to meet with our experts, and to learn all about our exciting launch as @EmmesCRO's Rare Disease Center.

#WODC #WODCEurope #RareDisease

[Emmes @EmmesCRO]

We are excited to announce Orphan Reach: Emmes' Rare Disease Center! This global specialty center is dedicated to the advancement of #raredisease research by providing specialized clinical trial design & execution capabilities @orphan_reach
Learn more: https://t.co/pq1dlecDOU

[Orphan Reach @Orphan_Reach]

#BREAKING: We are excited to announce the launch of Orphan Reach as @EmmesCRO's Rare Disease Center! The center will incorporate Emmes’ world class reputation in public health research, with the expertise of Orphan Reach.

Learn more: https://t.co/R4aEEF5Ltw

[Beacon for Rare Diseases @RareBeacon]

Do you have the ability to build strong relationships with a variety of people?

Yes?

Apply to join the team as our new Fundraising Officer!

Read the job description now and apply before 9am on 1st December

Good luck & we look forward to meeting you!

👉https://t.co/19OY4aj2Hy

[Orphan Reach @Orphan_Reach]

As part of #mitoawarenessweek Please view this short animation which gives a simple overview of #mitochondrialdisease

[The Lily Foundation @4Lilyfoundation]

During World Mitochondrial Disease Week we'd love every single one of our followers to take a few seconds to RT this short animation which gives a simple overview of #mitochondrialdisease

It's time to talk about #mito

Thank You! ❤

[The Lily Foundation @4Lilyfoundation]

Please RT and help raise awareness during World #MitochondrialDisease Week. Thank you.
#lilyfoundation #mitoaware

[The Lily Foundation @4Lilyfoundation]

We are starting World #MitochondrialDisease Week with this simple statistic. Some might say it's only one, but for families that one is their everything. There are few effective treatments & NO CURE for #mito Please RT to raise awareness. Find out more: https://t.co/MQpNRa7KOJ

[Orphan Reach @Orphan_Reach]

🎈Today is World #Duchenne Awareness Day 🎈 #WDAD2021

[Share4Rare_eng @Share4Rare_eng]

🎈 Today is World #Duchenne Awareness Day 🎈 #WDAD2021

Join the awareness campaign by sharing the materials created by @worldduchenne ❤️ https://t.co/7oQgMTx3h4
#rarediseases #neuromusculardisease #research

[Joining Jack @alljoinjack]

Today is @DuchenneDay help us #SpreadTheWord to raise awareness for Duchenne Muscular Dystrophy #WDAD2021
https://t.co/f4UdxuVbtd

[World Duchenne Awareness Day 🎈 @DuchenneDay]

🗓 Join the online educational event on Adult Life & Duchenne!
→ Experts share their experience and knowledge on adult life and #Duchenne
→ Duchenne adults from different parts of the world share their experience of living with Duchenne
https://t.co/XjFMCro0Xs #WDAD2021