View allAll Photos Tagged MultipleSclerosis
Swedish's MS Center actively participates in research studies and clinical trials. In March 2012, the Center's team was involved with more than 24 clinical research projects.
Paralyzed Veterans of America hosts its third annual Summit + EXPO, bringing together top researchers and health professionals to share best practices and learn about the latest research, treatments and therapies in spinal cord injury/disease and multiple sclerosis (MS) health care. To learn more about Summit 2013, please visit www.pva.org/summit2013.
Paralyzed Veterans of America hosts its third annual Summit + EXPO, bringing together top researchers and health professionals to share best practices and learn about the latest research, treatments and therapies in spinal cord injury/disease and multiple sclerosis (MS) health care. To learn more about Summit 2013, please visit www.pva.org/summit2013.
احتفال رابطة تصلب الأعصاب المتعدد القطرية - مسك - باليوم العالمي لمرض تصلب الأعصاب المتعدد
26.May.2010
رابطة تصلب الأعصاب المتعدد القطرية
I'm reading "New Hope and Pratical Advice for People with MS and Their Families: Multiple Sclerosis" by Louis J. Rosner and Shelley Ross.
I highly recommend this book for those who have MS and their families, no matter how long you've had the disease and how much you know. It's enlightening and easy to understand.
I also recommend it to health care professionals. It's so scary how little health care professionals know about MS - and we learned this the hard way when my Mom went into the hospital for her recent MS episode.
November 19, 2010.
احتفال رابطة تصلب الأعصاب المتعدد القطرية - مسك - باليوم العالمي لمرض تصلب الأعصاب المتعدد
26.May.2010
رابطة تصلب الأعصاب المتعدد القطرية
The loss of the body, documentary on multiple sclerosis directed by Marc Nadal, made in Tyumen (Russia).
'ПОТЕРЯ ТЕЛА (The loss of the body)'.
Made with the support of the BIOCAD company.
Director: Marc Nadal.
Duration: 90 min.
Country: Russia
Genre: Documentary.
A flock of sheep in West Lothian have turned orange to celebrate MS Week 2012 (30 April – 6 May). They have been given the coat of animal-friendly paint by farmer Andrew Jack to help raise awareness of multiple sclerosis in Scotland.
©DN Anderson
Kent Andersson (Swedish Association for Persons with Neurological Disabilities) discusses the workshop with Reni de Boer (Dutch MS Research Foundation).
On April 18, 2010, it really happened. I walked the entire 3.2-mile WalkMS in a dress and high heels. To be honest, I wasn’t sure I could walk the whole way with the shoes, and seriously considered taking them off a couple of times. But I knew that at the end of the Walk, I can take the shoes off and the discomfort would eventually go away. My wife, and everyone else with multiple sclerosis, doesn’t have that luxury. So I just kept walking. One step at a time.
Thank you so much for everyone who sponsored me – your donation is helping to make the National MS Society an even better resource for people with multiple sclerosis. Thank you very much for everyone who walked with me on our team – I’m glad you didn’t mind going so slow. Thank you to everyone who has enthusiastically responded to this whole thing – every message I received really inspired and touched me. Thank you to Lan Yin “Eiko” Tsai for inspiring the look of my ensemble. And most of all, thank you to my wife for encouraging me and understanding the very serious ‘why’ behind this silliness.
Photo by Nahleen Blake
On our way to Namche Bazaar - one of the many suspension bridges we crossed.
Taken by Aaron McCourtie
An MS staffer goes through paper work before the start of the Express Scripts MS Bike Ride (MS 150) in Columbia in Boone County Missouri.
Please check out my photos at: notleyhawkins.imagekind.com/
©Notley Hawkins