View allAll Photos Tagged joinhands

American Bible School for rarediseaseday 2015

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS #joinHANDS

facepainting, hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

The Committee for Orphan Medicinal Products (COMP) is the committee at the European Medicines Agency that is responsible for reviewing applications from people or companies seeking 'orphan-medicinal-product designation'.

 

Learn more: www.ema.europa.eu/ema/index.jsp?curl=pages/about_us/gener...

Members of #SPEC and #SPJ team up to raise awareness for Rare Disease Day 2015

Aiden is a survivor of a Rare Lung Disease.

Congenital pulmonary airway malformation (CPAM) is a rare congenital birth defect that includes a cystic mass of abnormal lung tissue. A cystic mass is a noncancerous tumor that is filled with fluid or other material. This condition used to be referred to as congenital cystic adenomatoid malformation, or CCAM. In CPAM, the cystic mass cannot function as normal lung tissue. Males have this condition slightly more often than females.

In the picture an MD child in the Ceder forest in Lebanon enjoying a summer day with his family

Alnylam Pharmaceuticals employees raised and joined hands in support of Rare Disease Day at one of our Cambridge, MA office.

RD-Connect is an international, EU-funded project facilitating research on rare genetic diseases to improve diagnosis and develop new treatments. RD-Connect colleagues are proud to participate in the Rare Disease Day and here you can see us raising hands to show solidarity with rare disease patients around the world!

CSL Behring: Employees from the CSL Behring Commercial team in Japan (Hokuriku) show their support of Rare Disease Day! CSL Behring is a biotherapies company committed to saving lives and improving the quality of life for people with rare and serious diseases worldwide.

un après midi où je faisais une sieste caline avec mon petit garçon de 5 ans .

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

Alexis Lato has Neurofibromatosis and her mommy,Elise works with us as Adecco. We love the Lato family and support them in whatever they need!

Participants at our #RareEU2015 event raising and joining hands for Rare Disease Day!

Samuel has Immune Thrombocytopenic Purpura and is raising hands in support! Thanks for all you do!

I was diagnosed with stiffperson syndrome in 2009. I am one in a million. I shared my story with my son's 5th grade class. Together we made poster to spread awareness for those who suffer from a rare disease and give HOPE!

Florence stadium for rarediseaseday and trisomy 9 mosaic babies

5 years ago we started to celebrate our Rare Disease Day, this year we have increased the number of participants up to 600 people and more than 15 patients associations united.

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS #joinHANDS

Cette année nous avons tenté de reproduire le logo du rare Disease Day en peinture!

A wonderful friend of mine made this picture for me, because I'm a computer dummy and just couldn't successfully get it right.

So this picture means a lot to me.

Family and friends of 6 Histio Warriors gather together to help raise awareness for Rare Disease Day.

the wilderness society's 'hands across the sand' event for 2015, highlighting public concern for the potentially disastrous consequences if a spill similar to the deepwater horizon oil-spill in the gulf of mexico was to happen in our waters, given that the company responsible - BP - is currently applying to drill in the great australian bight

 

glenelg beach, south australia, australia

 

#joinHANDS

#oilfreeseas

#oilspillsR4eva

Our son, Joe is diagnosed with a very rare genetic mutation. Today his school, Ridge Ruxton School, along with his family and friends show their support for this great cause.

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

the wilderness society's 'hands across the sand' event for 2015, highlighting public concern for the potentially disastrous consequences if a spill similar to the deepwater horizon oil-spill in the gulf of mexico was to happen in our waters, given that the company responsible - BP - is currently applying to drill in the great australian bight

 

glenelg beach, south australia, australia

 

#joinHands

#oilfreeseas

#oilspillsR4eva

A compilation of supporters of MichaelAnn who has a rare disease, BPAN.

This is part of the administration staff at New York State Parks, Long Island Region. Photographed in front of the Administration building in Belmont Lake State Park, Babylon, New York on February 28, 2017.

hands across the sand, an event organised by the wilderness society, south australia

 

the rally calls on the community to 'join hands in support of a clean energy future and to oppose BP's plans to begin deepsea drilling in the Great Australian Bight whale nursery and siesmic testing in the sensitive waters off Kangaroo Island by Bight Petroleum, which are planned to begin in 2015'

 

semaphore foreshore reserve and beach, adelaide, south australia

 

hands across the sand

 

#BP_BIGRISKS

#joinHANDS

the wilderness society's 'hands across the sand' event for 2015, highlighting public concern for the potentially disastrous consequences if a spill similar to the deepwater horizon oil-spill in the gulf of mexico was to happen in our waters, given that the company responsible - BP - is currently applying to drill in the great australian bight

 

glenelg beach, south australia, australia

 

#joinHANDS

#oilfreeseas

#oilspillsR4eva

U12 Florentia Rugby per trisomia 9 a mosaico

I am 25 years old barreling SLE and fibromyalgia .. It's hard being at a crucial age on my life. SLE has been debilitating to me and although I have many things on hold in life. I still push on and appreciate everyday for what it is!

Raising my hands here in Gloucester for Juvenile Dermatomyositis which is a rare inflammatory muscle disease affects 3 in a million children each year in the UK.

Klippel-Feil syndrome patients of all ages, from across the globe, submitted recent photos for Rare Disease Days Raise and Join Hands For Rare Disease 2017, to patient organization Klippel-Feil Syndrome Freedom! We put together this image, of 150 KFS patients who need research, care, and understanding. Klippel-Feil syndrome is a rare skeletal disease that affects 1 in 42.000. Our symbol of hope is the skeleton key. Research is key! We are #KFStrong!

Thank you!

 

Visit us

Facebook: www.facebook.com/KlippelFeilSyndromeFreedom/

Instagram: @kfs_freedom

Twitter: @KFS_Freedom

I suffer from Ehlers Danlos Syndrome, A genetic illness with notes you're that please me very disabled. My cheeky kitten Gandalf keeps me company during the day when everyone is at work.

Hi my name is Stephanie. I have a rare disease called Cystinosis.

We walked a 2 mile trail to raise awareness for Rare Disease Day. Martin Mueller IV, the founder of the Martin Mueller IV Achalasia Awareness Foundation, Inc. has Achalasia, a rare disease that occurs in 1 out of 100,000 people.

the wilderness society's 'hands across the sand' event for 2015, highlighting public concern for the potentially disastrous consequences if a spill similar to the deepwater horizon oil-spill in the gulf of mexico was to happen in our waters, given that the company responsible - BP - is currently applying to drill in the great australian bight

 

glenelg beach, south australia, australia

 

#joinHands

#oilfreeseas

#oilspillsR4eva

the wilderness society's 'hands across the sand' event for 2015, highlighting public concern for the potentially disastrous consequences if a spill similar to the deepwater horizon oil-spill in the gulf of mexico was to happen in our waters, given that the company responsible - BP - is currently applying to drill in the great australian bight

 

glenelg beach, south australia, australia

 

#joinHANDS

#oilfreeseas

#oilspillsR4eva

1 2 ••• 25 26 28 30 31 ••• 66 67