We talk a lot about our research, specifically as it relates to our mouse model, but what is a mouse model? United MSD Foundation Executive Director Amber Olsen explains. buff.ly/3hd5HZ2 #TogetherWeCan #CureMSD #FoundationFriday #MSD #MultipleSulfataseDeficiency

Today we would like to wish a very Happy 9th Birthday to our rare hero Willow 🥳 Willow is living with an ultra rare condition whereby she has a gain on a gene called stat5b located on Chromosome 17. This gain results in a rare immune condition. Some of Willow’s.......

There are many factors that make MSD a good candidate for Gene Therapy - including that we know what gene is affected! Read our blog to learn more: bit.ly/3AoKG6H #TogetherWeCan #CureMSD #MSD #MultipleSulfataseDeficiency #genetherapy

Today on July 7th we remember Prof. Dr. Thomas Dierks, a superb biochemist we were very fond of. He sadly passed away on this day 1 year ago. He made many very important discoveries, one of which identified the responsible gene in MSD which is the Sumf1 gene. 1/3

There's a lot that goes into drug development. We are fortunate in that our drug for gene therapy showed efficacy on the first try. Executive Director Amber Olsen explains. buff.ly/2Tip8b1 #FoundationFriday #TogetherWeCan #CureMSD #MSD #MultipleSulfataseDeficiency

This battle cannot be won alone. It takes all of us working together, helping one another, for us to win. #TogetherWeCan #CureMSD #MotivationalMonday #MSD #MultipleSulfataseDeficiency

In the rare disease world, foundations will provide funding to develop drugs and move through the process towards a treatment in humans. Executive Director Amber Olsen explains. buff.ly/2U75z5t #TogetherWeCan #CureMSD #FoundationFriday #MSD #MultipleSulfataseDeficiency

Today we would like to wish a very Happy 3rd Birthday to our rare hero Aidan 🥳 This little warrior has a rare genetic condition called metachromatic leukodystrophy (MLD) which affects the white matter of the brain and is characterised by accumulation of fats called........

Today, 30th July is the first #MSDWorldDay. The goal is to bring about awareness & support for patients, families affected by MSD, patient organisations representing MSD across the world & researchers that work diligently on vital MSD research #MultipleSulfataseDeficiency more...

Please join us in this crucial awareness. The MSD foundations below selected July 30th in honour of Prof. Thomas Dierks as that date is his birthday! Sadly, Thomas passed away in July 2020, we were very fond of him & are still very sad about the terrible loss. More...

Thomas was a co-founder of the affected gene in MSD which is the SUMF1 gene. The MSD foundations agreed there will be a 'Thomas Dierks Award' for MSD every year, begining this year, it will be given to recognise outstanding contributions to MSD research. More...

Thomas recieved an outstanding contribution to MSD award in 2017 for his critical work. We would like to thank United MSD Foundation (USA- Amber Olsen), Fundacio Cure MSD (Spain- Elisabet Perés Font), Fundacion Cure MSD (Argentina- Sebastian Ballauz), more...

Join us today as we honor our brilliant researchers and brave families on the first-ever MSD World Day. #TogetherWeCan #CureMSD #MultipleSulfataseDeficiency #MSD #raredisease bit.ly/2TMKddW

MSD World Day 2021 youtu.be/wRJ1q8DDmek via YouTube

We are relentless in our pursuit to cure MSD. #TogetherWeCan #CureMSD #MotivationalMonday #MultipleSulfataseDeficiency #MSD #raredisease

Philips Healthcare Yes Sir/Madam, I have filled the form many days back, but I did not get any reply. I hope @philipshealth will help in this regards - Sachin, +919483782071

Wishing Ethan a very happy birthday today! We hope your day is filled with lots of love and lots of fun for you. Take it easy little man! #TogetherWeCan #CureMSD #MultipleSulfataseDeficiency #MSD #raredisease #365campaign

Our BioBank enables our research to move faster and more efficiently and we couldn't have done it without the support and cooperation of our families. #TogetherWeCan #CureMSD #MultipleSulfataseDeficiency #MSD #biobank #raredisease

Over 300 million people worldwide suffer from a #raredisease? Half are children. This month, we'll be sharing information about how you can be a part of raising awareness and advocacy for #rarediseasemonth #TogetherWeCan #CureMSD #MSD #MultipleSulfataseDeficiency