Are GRIN mutations rare?
March is Grin awareness month. EMG has taken its responsibility in funding research and made support available to GRIN patient and their parents. Why we choose this particular area to

March is Grin awareness month. EMG has taken its responsibility in funding research and made support available to GRIN patient and their parents. Why we choose this particular area to
At EMG, we want to make a difference – not just for clients but also for the community. We have chosen to dedicate time and resources to raise awareness for
Get ready for GRIN Disorder Awareness Month in March. EMG together with CureGRIN, Grin2b, and GRIN parent support groups and associations are partnering in a month-long campaign for all GRIN Disorders.
GRIN Disorders are rare genetic conditions with severe life-limiting consequences. Many GRIN patients are non-verbal, unable to walk, and many cannot feed or toilet themselves. They often suffer severe…
A group of internationals living in the Netherlands have launched a campaign named #alsjeblieftnederland. Urging the Dutch government and the EU to lift coronavirus travel limitations for family members living outside the
March is Grin awareness month. EMG has taken its responsibility in funding research and made support available to GRIN patient and their parents. Why we choose this particular area to
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Looking forward to providing a moving experience,
Nino Nelissen – Founder of EMG