![NISHA SHARMA(@NISH124) 's Twitter Profile Photo NISHA SHARMA(@NISH124) 's Twitter Profile Photo](https://abs.twimg.com/sticky/default_profile_images/default_profile_200x200.png)
The Cause of Chronic Diseases.
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#Sadhguru InLA #Sadhguru #InnerEngineering
#RareDiseaseDay , #showyourrare #ThursdayMotivation #TBT #ThankfulThursday #IshaFoundation #Guide2Joy #Meditation , #Mindfulness #Wellbeing
![NISHA SHARMA (@NISH124) on Twitter photo 2019-03-01 01:14:37 The Cause of Chronic Diseases.
bit.ly/2EEr4jU
#SadhguruInLA #Sadhguru #InnerEngineering
#RareDiseaseDay, #showyourrare #ThursdayMotivation #TBT #ThankfulThursday #IshaFoundation #Guide2Joy #Meditation, #Mindfulness #Wellbeing The Cause of Chronic Diseases.
bit.ly/2EEr4jU
#SadhguruInLA #Sadhguru #InnerEngineering
#RareDiseaseDay, #showyourrare #ThursdayMotivation #TBT #ThankfulThursday #IshaFoundation #Guide2Joy #Meditation, #Mindfulness #Wellbeing](https://pbs.twimg.com/media/D0iRDIQVYAAW3Mt.jpg)
![makenna houston(@makennahouston1) 's Twitter Profile Photo makenna houston(@makennahouston1) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1421953895912271875/ZYKMlTUe_200x200.jpg)
![Spina Bifida Hydrocephalus Ireland (SBHI)(@SBHIreland) 's Twitter Profile Photo Spina Bifida Hydrocephalus Ireland (SBHI)(@SBHIreland) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1169271359341518848/ChDphgpT_200x200.jpg)
Today is #RareDiseaseDay – a day which celebrates the lives of the 300 million people worldwide living with a rare disease. Join us as we advocate for equity in social opportunity, healthcare & access to diagnosis & therapies for people living with a rare disease.
#ShowYourRare
![Spina Bifida Hydrocephalus Ireland (SBHI) (@SBHIreland) on Twitter photo 2022-02-28 14:19:00 Today is #RareDiseaseDay – a day which celebrates the lives of the 300 million people worldwide living with a rare disease. Join us as we advocate for equity in social opportunity, healthcare & access to diagnosis & therapies for people living with a rare disease.
#ShowYourRare Today is #RareDiseaseDay – a day which celebrates the lives of the 300 million people worldwide living with a rare disease. Join us as we advocate for equity in social opportunity, healthcare & access to diagnosis & therapies for people living with a rare disease.
#ShowYourRare](https://pbs.twimg.com/media/FMsJA1dXEAQpYbw.jpg)
![🎭Laura🎭 and 🦄Angelina🦄(@Angelin52659191) 's Twitter Profile Photo 🎭Laura🎭 and 🦄Angelina🦄(@Angelin52659191) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1785637360450871296/xM5plcjd_200x200.jpg)
Rare Disease Day 2024
Angelina, our 8p Wonder!
Chromosome8p23.1 Deletion
I ❤ someone who's rare....and AWESOME!!!
#ShowYourRare
![🎭Laura🎭 and 🦄Angelina🦄 (@Angelin52659191) on Twitter photo 2024-02-29 17:24:24 Rare Disease Day 2024
Angelina, our 8p Wonder!
Chromosome8p23.1 Deletion
I ❤ someone who's rare....and AWESOME!!!
#ShowYourRare Rare Disease Day 2024
Angelina, our 8p Wonder!
Chromosome8p23.1 Deletion
I ❤ someone who's rare....and AWESOME!!!
#ShowYourRare](https://pbs.twimg.com/media/GHhWFBbWoAA8KFb.jpg)
![Ehsan Ullah, Ph.D.(@ehsanullahx) 's Twitter Profile Photo Ehsan Ullah, Ph.D.(@ehsanullahx) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1602866192972136449/P3V1LVsE_200x200.jpg)
I’m proud to be part of the effort to better understand and treat #RareDiseases !
Let’s raise awareness and support for those who need it the most!
#ShowYourRare #RareDiseaseDay 2023 #RareDiseaseDay Rare Disease Day #MedTwitter #GeneChat #Genomics #Bioinformatics
![Ehsan Ullah, Ph.D. (@ehsanullahx) on Twitter photo 2023-02-28 06:01:29 I’m proud to be part of the effort to better understand and treat #RareDiseases!
Let’s raise awareness and support for those who need it the most!
#ShowYourRare #RareDiseaseDay2023 #RareDiseaseDay @rarediseaseday #MedTwitter #GeneChat #Genomics #Bioinformatics I’m proud to be part of the effort to better understand and treat #RareDiseases!
Let’s raise awareness and support for those who need it the most!
#ShowYourRare #RareDiseaseDay2023 #RareDiseaseDay @rarediseaseday #MedTwitter #GeneChat #Genomics #Bioinformatics](https://pbs.twimg.com/media/FqCD4xSWwAEZ-49.jpg)
![Eray Çoşan(@erayco) 's Twitter Profile Photo Eray Çoşan(@erayco) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1119463173470523394/5SZt3pu__200x200.jpg)
'Show your rare, show you care', Nadir tarafınızı gösterin ve değişim başlasın. #aifdrare ; #nadiryüzünügöster ; #showyourrare , rarediseaseday.org/events/world
![Eray Çoşan (@erayco) on Twitter photo 2019-02-28 17:43:51 'Show your rare, show you care', Nadir tarafınızı gösterin ve değişim başlasın. #aifdrare; #nadiryüzünügöster; #showyourrare, rarediseaseday.org/events/world 'Show your rare, show you care', Nadir tarafınızı gösterin ve değişim başlasın. #aifdrare; #nadiryüzünügöster; #showyourrare, rarediseaseday.org/events/world](https://pbs.twimg.com/media/D0gpEeDX4AALXMx.png)
![Pairend - NGS Cloud(@pairendNGS) 's Twitter Profile Photo Pairend - NGS Cloud(@pairendNGS) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1365931764812759041/acI0D1Z6_200x200.jpg)
S61 cevabı aşağıda, yarın yeni sorumuz ile görüşmek üzere. #ShowYourRare #Nadirizveİçinizdeyiz #RareDisease
![Pairend - NGS Cloud (@pairendNGS) on Twitter photo 2020-11-19 08:52:40 S61 cevabı aşağıda, yarın yeni sorumuz ile görüşmek üzere. #ShowYourRare #Nadirizveİçinizdeyiz #RareDisease S61 cevabı aşağıda, yarın yeni sorumuz ile görüşmek üzere. #ShowYourRare #Nadirizveİçinizdeyiz #RareDisease](https://pbs.twimg.com/media/EnLJ5ahXUAAQS53.jpg)
![Aspen(Difficult Time🪶🍁🕊)©AspenBrave®™(@Write2Fite) 's Twitter Profile Photo Aspen(Difficult Time🪶🍁🕊)©AspenBrave®™(@Write2Fite) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1497664850389995521/o-w4jiKn_200x200.jpg)
👆PLEASE READ ABOVE🫶
#Anemoia is a survival mechanism for millions due to the #inequity of #OrphanDrugPrices for millions suffering on this #RareDiseaseDay2024 😞
On #LeapDay & EVERYDAY:
#BeBrave & #ShowYourRare 🧬
#YouMatter 🫂
With hope,
Aspen🕊️
👇
youtu.be/t9fMNNsdPjU?si…
![Aspen(Difficult Time🪶🍁🕊)©AspenBrave®™ (@Write2Fite) on Twitter photo 2024-02-29 18:36:11 👆PLEASE READ ABOVE🫶
#Anemoia is a survival mechanism for millions due to the #inequity of #OrphanDrugPrices for millions suffering on this #RareDiseaseDay2024 😞
On #LeapDay & EVERYDAY:
#BeBrave & #ShowYourRare 🧬
#YouMatter🫂
With hope,
Aspen🕊️
👇
youtu.be/t9fMNNsdPjU?si… 👆PLEASE READ ABOVE🫶
#Anemoia is a survival mechanism for millions due to the #inequity of #OrphanDrugPrices for millions suffering on this #RareDiseaseDay2024 😞
On #LeapDay & EVERYDAY:
#BeBrave & #ShowYourRare 🧬
#YouMatter🫂
With hope,
Aspen🕊️
👇
youtu.be/t9fMNNsdPjU?si…](https://pbs.twimg.com/media/GHhmgdDbkAILBYl.jpg)
![Santos FC(@SantosFC) 's Twitter Profile Photo Santos FC(@SantosFC) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1732185787859390464/0LyqfyYr_200x200.jpg)
Cerca de 13 milhões de brasileiros convivem com uma doença rara, 75% deles podem ser crianças. As doenças podem ser raras, mas o cuidado não! #ShowYourRare Rare Disease Day
![Santos FC (@SantosFC) on Twitter photo 2019-02-28 23:00:00 Cerca de 13 milhões de brasileiros convivem com uma doença rara, 75% deles podem ser crianças. As doenças podem ser raras, mas o cuidado não! #ShowYourRare @rarediseaseday Cerca de 13 milhões de brasileiros convivem com uma doença rara, 75% deles podem ser crianças. As doenças podem ser raras, mas o cuidado não! #ShowYourRare @rarediseaseday](https://pbs.twimg.com/media/D0hpXAWXQAAmSaf.jpg)
![Order of Asclepius(@asclepians) 's Twitter Profile Photo Order of Asclepius(@asclepians) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1686561091202285568/tCbnPCIq_200x200.jpg)
Resident Members of the Order of Asclepius raise their hands for RARE!
Learn about rare diseases at rarediseaseday.org.
We are many.
We are strong.
We are proud.
... and we are stronger together! 💪
#CareForRarePH #NRDW2021 #RareDiseaseDay #ShowYourRare #OAServia
![Order of Asclepius (@asclepians) on Twitter photo 2021-02-25 03:42:30 Resident Members of the Order of Asclepius raise their hands for RARE!
Learn about rare diseases at rarediseaseday.org.
We are many.
We are strong.
We are proud.
... and we are stronger together! 💪
#CareForRarePH #NRDW2021 #RareDiseaseDay #ShowYourRare #OAServia Resident Members of the Order of Asclepius raise their hands for RARE!
Learn about rare diseases at rarediseaseday.org.
We are many.
We are strong.
We are proud.
... and we are stronger together! 💪
#CareForRarePH #NRDW2021 #RareDiseaseDay #ShowYourRare #OAServia](https://pbs.twimg.com/media/EvCus0aVgAEX6us.jpg)
![Pensemos en Cebras México(@PCebras) 's Twitter Profile Photo Pensemos en Cebras México(@PCebras) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1318044725065224193/Ovq9RyRa_200x200.jpg)
📢Ya estamos a 20 días de conmemorar el Día Mundial y Nacional de las Enfermedades Raras dónde la prioridad son siempre los pacientes, por ello el visibilizar y alzar la voz es tarea diaria.
#conmemorandoytrabajando #rarediseaseday2023 #rarediseasday #cebrasmexico #ShowYourRare
![Pensemos en Cebras México (@PCebras) on Twitter photo 2023-02-09 02:39:03 📢Ya estamos a 20 días de conmemorar el Día Mundial y Nacional de las Enfermedades Raras dónde la prioridad son siempre los pacientes, por ello el visibilizar y alzar la voz es tarea diaria.
#conmemorandoytrabajando #rarediseaseday2023 #rarediseasday #cebrasmexico #ShowYourRare 📢Ya estamos a 20 días de conmemorar el Día Mundial y Nacional de las Enfermedades Raras dónde la prioridad son siempre los pacientes, por ello el visibilizar y alzar la voz es tarea diaria.
#conmemorandoytrabajando #rarediseaseday2023 #rarediseasday #cebrasmexico #ShowYourRare](https://pbs.twimg.com/media/Fofe3BoXgAEa30Y.jpg)
![Roberto Martín(@PsicoMarRod) 's Twitter Profile Photo Roberto Martín(@PsicoMarRod) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1144546726864465920/WHgWp6pf_200x200.jpg)
Este 2020 va a ser especial por tener un “día raro”. El 29 de Febrero, como cada último día de febrero, se celebra el Día Mundial de las #EnfermedadesRaras para seguir dando visibilidad a la necesidad de investigación y al cuidado de los pacientes.
#ShowYourRare #ShowYouCare
![Roberto Martín (@PsicoMarRod) on Twitter photo 2020-01-14 09:41:56 Este 2020 va a ser especial por tener un “día raro”. El 29 de Febrero, como cada último día de febrero, se celebra el Día Mundial de las #EnfermedadesRaras para seguir dando visibilidad a la necesidad de investigación y al cuidado de los pacientes.
#ShowYourRare #ShowYouCare Este 2020 va a ser especial por tener un “día raro”. El 29 de Febrero, como cada último día de febrero, se celebra el Día Mundial de las #EnfermedadesRaras para seguir dando visibilidad a la necesidad de investigación y al cuidado de los pacientes.
#ShowYourRare #ShowYouCare](https://pbs.twimg.com/media/EOO4U4WXkAEJc0J.jpg)
![Expo City Dubai(@expocitydubai) 's Twitter Profile Photo Expo City Dubai(@expocitydubai) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1640286642630950912/d7zKEwAJ_200x200.jpg)
Today, we are very happy to welcome the UAE Rare Disease Society and friends to open Expo’s Portals and to Al Wasl Plaza as we celebrate Rare Disease Day, coming together in solidarity with all heroes and families living with rare diseases.
#Expo2020 #Dubai #ShowYourRare UAE Rare Disease Society
![Ass. Catalana Neurofibromatosis(@acnefi_org) 's Twitter Profile Photo Ass. Catalana Neurofibromatosis(@acnefi_org) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1361876345/acnefi_200x200.jpg)
![Denise Strohsahl(@SSC_Marketing) 's Twitter Profile Photo Denise Strohsahl(@SSC_Marketing) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1578494122511503365/XgEiQwda_200x200.jpg)
Hi, I’m Denise. I was born with Ehler-Danlos Syndrome (EDS), a rare genetic disorder: My connective tissue is damaged, which affects ligaments, tendons, cartilage, skin, blood vessels & organs. It’s an invisible illness. #RareDiseaseDay #ShowYourRare (1/2)
![Denise Strohsahl (@SSC_Marketing) on Twitter photo 2019-03-01 16:14:41 Hi, I’m Denise. I was born with Ehler-Danlos Syndrome (EDS), a rare genetic disorder: My connective tissue is damaged, which affects ligaments, tendons, cartilage, skin, blood vessels & organs. It’s an invisible illness. #RareDiseaseDay #ShowYourRare (1/2) Hi, I’m Denise. I was born with Ehler-Danlos Syndrome (EDS), a rare genetic disorder: My connective tissue is damaged, which affects ligaments, tendons, cartilage, skin, blood vessels & organs. It’s an invisible illness. #RareDiseaseDay #ShowYourRare (1/2)](https://pbs.twimg.com/media/D0lfDolWoAEKk1u.jpg)
![Pharmacy Students Association KE(@kephsa) 's Twitter Profile Photo Pharmacy Students Association KE(@kephsa) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1322986703032930305/w0M2VGvW_200x200.jpg)
'Empathy knows no boundaries. On #RareDiseaseDay , let's raise awareness, support, and hope for those facing uncommon health challenges. Together, we can make a difference. 💙 #ShowYourRare '
![Pharmacy Students Association KE (@kephsa) on Twitter photo 2024-02-29 04:48:17 'Empathy knows no boundaries. On #RareDiseaseDay, let's raise awareness, support, and hope for those facing uncommon health challenges. Together, we can make a difference. 💙 #ShowYourRare' 'Empathy knows no boundaries. On #RareDiseaseDay, let's raise awareness, support, and hope for those facing uncommon health challenges. Together, we can make a difference. 💙 #ShowYourRare'](https://pbs.twimg.com/media/GHepBFWXwAEeUuX.jpg)
![Autoinflammatory UK -Making the Invisible Visible(@PeriodicFeverUK) 's Twitter Profile Photo Autoinflammatory UK -Making the Invisible Visible(@PeriodicFeverUK) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1031985002010079233/HzYkLu8l_200x200.jpg)
Just arriving for #ISSAID2019 ! Looking forward to an incredibly productive time, discussing key issues re #autoinflammatory conditions and rare disease, meeting wonderful people and learning! #raredisease #showyourrare
![Autoinflammatory UK -Making the Invisible Visible (@PeriodicFeverUK) on Twitter photo 2019-03-30 17:54:07 Just arriving for #ISSAID2019! Looking forward to an incredibly productive time, discussing key issues re #autoinflammatory conditions and rare disease, meeting wonderful people and learning! #raredisease #showyourrare Just arriving for #ISSAID2019! Looking forward to an incredibly productive time, discussing key issues re #autoinflammatory conditions and rare disease, meeting wonderful people and learning! #raredisease #showyourrare](https://pbs.twimg.com/media/D27LiewW0AAng0-.jpg)
![Order of Asclepius(@asclepians) 's Twitter Profile Photo Order of Asclepius(@asclepians) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1686561091202285568/tCbnPCIq_200x200.jpg)
The Order, the WVSU MSC, and AMSA-WVSU support the Filipino rare disease community in their call to increase public awareness and support for Filipinos living with a rare disease – Rare is many, strong, and proud!
#CareForRarePH #NRDW2021 #ShowYourRare #OAServia
![Order of Asclepius (@asclepians) on Twitter photo 2021-02-25 05:27:03 The Order, the WVSU MSC, and AMSA-WVSU support the Filipino rare disease community in their call to increase public awareness and support for Filipinos living with a rare disease – Rare is many, strong, and proud!
#CareForRarePH #NRDW2021 #ShowYourRare #OAServia The Order, the WVSU MSC, and AMSA-WVSU support the Filipino rare disease community in their call to increase public awareness and support for Filipinos living with a rare disease – Rare is many, strong, and proud!
#CareForRarePH #NRDW2021 #ShowYourRare #OAServia](https://pbs.twimg.com/media/EvDGpZsUcAo_QIL.jpg)
![Sarepta Therapeutics(@Sarepta) 's Twitter Profile Photo Sarepta Therapeutics(@Sarepta) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1675206386437828609/TjHdAvtT_200x200.jpg)
Watch Louise Rodino-Klapac, SRPT’s SVP, Gene Therapy, take the #DMDIceCupChallenge , recognizing and raising awareness with our Ohio #GeneTherapy team on #RareDiseaseDay . Learn more about the significance of the day here: rarediseaseday.org and #ShowYourRare
![Karaiskakio(@Karaiskakio) 's Twitter Profile Photo Karaiskakio(@Karaiskakio) 's Twitter Profile Photo](https://pbs.twimg.com/profile_images/1732705861519151104/eq0ylqmd_200x200.jpg)
Παγκόσμια Ημέρα Σπάνιων Νοσημάτων και στο Karaiskakio διενεργούνται πρωτοποριακές έρευνες για τη μελέτη και εξεύρεση νέων θεραπευτικών προσεγγίσεων για την αντιμετώπιση σπάνιων νοσημάτων.
#showyourrare #showyoycare #RareDiseaseDay2021
![Karaiskakio (@Karaiskakio) on Twitter photo 2021-02-28 08:06:29 Παγκόσμια Ημέρα Σπάνιων Νοσημάτων και στο @Karaiskakio διενεργούνται πρωτοποριακές έρευνες για τη μελέτη και εξεύρεση νέων θεραπευτικών προσεγγίσεων για την αντιμετώπιση σπάνιων νοσημάτων.
#showyourrare #showyoycare #RareDiseaseDay2021 Παγκόσμια Ημέρα Σπάνιων Νοσημάτων και στο @Karaiskakio διενεργούνται πρωτοποριακές έρευνες για τη μελέτη και εξεύρεση νέων θεραπευτικών προσεγγίσεων για την αντιμετώπιση σπάνιων νοσημάτων.
#showyourrare #showyoycare #RareDiseaseDay2021](https://pbs.twimg.com/media/EvTH6aQWYAc145-.jpg)