Helping patients and doctors everywhere get the medicine they need. Before it's available in their country.
Amsterdam, The Netherlands
Joined June 2015
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Everyone.org retweeted
Check out my latest #article: The importance of #thoughtleadership linkedin.com/pulse/importanc… via @LinkedIn
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Yet another family pleading for equal access to life saving treatments. When will we end this disparity? #orkambi #expandaccess globalnews.ca/news/6215408/o…
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Asking pharma companies the same price for a new drug in The Netherlands than in Portugal is unfair, it must be country income based, explain @sjaakvink at the #POLITICOhealth summit 2019
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Check out my latest article: Exponential #medicine, exponential number of #losers linkedin.com/pulse/exponenti… via @LinkedIn
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Thrilled to be speaking at the upcoming Early and Managed Access Programmes conference in a few days. Hope to see you there! #expandaccess #health #medicine
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Check out my latest article: Re-imagining the #statusquo #movement #لبنان_ينتفض linkedin.com/pulse/re-imagin… via @LinkedIn
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Fantastic news that #Orkambi is now available for #cysticfibrosis patients in England! But no one should have to wait 4 years to access the drugs they need. The UK government must fight high drug prices but also the monopolies that allow Big Pharma to hold patients to ransom
Some wonderful news this morning: We’ve agreed a deal to provide Orkambi and other lifesaving Cystic Fibrosis drugs on the NHS. Huge thanks to the many campaigners who have worked so hard, and to Vertex & the NHS. #OrkambiNow
england.nhs.uk/2019/10/nhs-e…
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Here is my latest #article on how to motivate your teams to collaboratively achieve #goals.
linkedin.com/pulse/how-motiv… via @LinkedIn
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New innovations= new hope! #overallsurvival results for @Novartis CDK4/6 inhibitor to treat advanced breast cancer bit.ly/2mF72Ql
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It was a wonderful surprise to receive a visit from the daughter of one of our patients. Fiona came all the way from Taiwan to share her story with @socialmedwork team.
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"Dancing has changed my life completely."
Rebecca (living with MS) found it increasingly difficult to stay active - until she joined a wheelchair dancing group! Read her story: bit.ly/2ZFBCXc #WeAreUndefeatable @undefeatable
Everyone.org retweeted
When I was diagnosed with ALS, I was told I had 6 months to live. That day, our daughters were 1 week and 2 years old.
They are now 2 and 4 years old, and grow more amazing daily.
As for me, well, I just did this—10x up and back. So I’m not only here, I plan to be for a while.
Everyone.org retweeted
HPV vaccination has been extremely successful in girls. Last month a study in @TheLancet found it has significantly cut rates of cancer-causing infections in countries with vaccination programmes newscientist.com/article/220…
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We're looking for some #TuesdayMotivation - are you living with MS and have a story to share?
Whether it's how you dealt with your diagnosis or something you've achieved whilst living with MS - we want to share your stories on our #Instagram bit.ly/2UuNLAJ DM us today!
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. @NICEComms backs skin cancer drug Libtayo for NHS use thepharmaletter.com/article/… #libtayo @NHSEngland #biotech #dermatology #France #oncology @Regeneron @sanofi #UK
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PREMIERE New Invisible Symptoms Animation! Sonia, a woman living with MS, talks through the invisible symptoms people with #multiplesclerosis experience.
Please share to raise awareness & understanding of MS @MSIntFederation @mssociety #MyInvisibleMS @WorldMSDay @MSassociation
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It's #WorldMSDay - and here is a reminder why it's so important to raise awareness.
During MS Week last April, we took to the streets and asked people what they think MS is. Many people have a vague idea what MS is, but lots of them are a bit confused. Let's change that!
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Here is a very special patient story all the way from Manila, Philippines. linkedin.com/pulse/zamier-jr…
