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Running for Rare Diseases | "Alone we are rare, together we are strong"

"Alone we are rare, together we are strong"

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Running for Rare Diseases | "Alone we are rare, together we are strong" | running4rare.org Reviews
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&quot;Alone we are rare, together we are strong&quot;
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1 donate
2 events
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5 runners and patients
6 phil’s friend
7 posted on
8 justin hopkin
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Running for Rare Diseases | "Alone we are rare, together we are strong" | running4rare.org Reviews

https://running4rare.org

&quot;Alone we are rare, together we are strong&quot;

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1

Online Silent Auction | Running for Rare Diseases

http://running4rare.org/silent-auction-2

Darr; Skip to Main Content. Runners and RARE Community Partners. 2016 Runners and RARE community partners. 2015 Runners and RARE Community Partners. 2014 Runners and RARE Community Partners. 2013 Runners and RARE Community Partners. The online silent auction is NOW LIVE and will close at 12:59:59 on Thursday, April 28, 2016. Access the auction here: http:/ auction.runningforrarediseases.org/. New items will be added every day, so check back (and bid) frequently! Join 118 other subscribers.

2

patient partner | Running for Rare Diseases

http://running4rare.org/tag/patient-partner

Darr; Skip to Main Content. Runners and RARE Community Partners. 2016 Runners and RARE community partners. 2015 Runners and RARE Community Partners. 2014 Runners and RARE Community Partners. 2013 Runners and RARE Community Partners. Posts tagged patient partner. Never Thought I’d Become a Marathoner, But Here I Am. July 31, 2016. 2 Comments ↓. Read more ›. Posted in Running Stories. WeRunTogether from Boston to Paris. April 30, 2015. No Comments ↓. Read more ›. Posted in Running Stories. April 27, 2015.

3

weruntogether | Running for Rare Diseases

http://running4rare.org/tag/weruntogether

Darr; Skip to Main Content. Runners and RARE Community Partners. 2016 Runners and RARE community partners. 2015 Runners and RARE Community Partners. 2014 Runners and RARE Community Partners. 2013 Runners and RARE Community Partners. WeRunTogether from Boston to Paris. April 30, 2015. No Comments ↓. Read more ›. Posted in Running Stories. Tagged with: Paris Marathon. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 118 other subscribers.

4

Justin Hopkin | Running for Rare Diseases

http://running4rare.org/author/justinh

Darr; Skip to Main Content. Runners and RARE Community Partners. 2016 Runners and RARE community partners. 2015 Runners and RARE Community Partners. 2014 Runners and RARE Community Partners. 2013 Runners and RARE Community Partners. View all posts by Justin Hopkin. April 30, 2015. 12 Comments ↓. Read more ›. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Join 118 other subscribers. New York City Marathon. Welcome to Running for Rare Diseases.

5

providencehalfmarathon | Running for Rare Diseases

http://running4rare.org/tag/providencehalfmarathon

Darr; Skip to Main Content. Runners and RARE Community Partners. 2016 Runners and RARE community partners. 2015 Runners and RARE Community Partners. 2014 Runners and RARE Community Partners. 2013 Runners and RARE Community Partners. WeRunTogether from Boston to Paris. April 30, 2015. No Comments ↓. Read more ›. Posted in Running Stories. Tagged with: Paris Marathon. Trying on the Jersey (aka Singlet). January 14, 2015. 3 Comments ↓. Read more ›. Posted in Running Stories. Join 118 other subscribers.

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rareundiagnosed.org rareundiagnosed.org

RUN Story -

https://rareundiagnosed.org/run-story

Recent Posts & St. RUN’s NBA Initiative: NBA Teams to Host Rare and Undiagnosed Families! March 3, 2017. Rachel Nielsen: Harmons Cooking School Experience from Make-A-Wish. March 3, 2017. UNDIAGNOSED IS A DIAGNOSIS:. Living in a Diagnostic Odyssey x 4. I have three children that are officially diagnosed as. They have an Undiagnosed genetic dysfunction. I am Undiagnosed as well. We live in the world of the unknown. We live in a diagnostic odyssey, times four. As well as the. Or Chairing Utah Rare. And, I ...

blog.addgene.org blog.addgene.org

Addgene Blog: A Better Way to Share Science | Inside Addgene

http://blog.addgene.org/topic/inside-addgene

Technology Transfer / Licensing. Technology Transfer / Licensing. Tips for Technical Support Calls. Posted by Eric J. Perkins. On Sep 20, 2016 10:39:02 AM. Running for Rare Disease, Running for FOP, Running for AJ. Posted by Guest Blogger. On Sep 15, 2016 10:30:00 AM. This post was contributed by Kurt Swanson a structural biologist and protein engineer currently working at Sanofi Pharmaceuticals in Cambridge, MA. That runs on behalf of the National Organization for Rare Disorders (NORD). On Jul 7, 2016 1...

ngly1.org ngly1.org

News | NGLY1

http://www.ngly1.org/news

Curing, treating and connecting. President Obama congratulates the NGLY1 community. NGLY1 parent and University of Utah Professor Matt Might. Was invited to White House for the announcement on the President’s Precision Medicine Initiative on Friday, January 30th:. By The White House. Before the announcement, the NGLY1 father and a handful others were invited to meet privately with the President to share their stories of success in precision medicine. Professor Might thanks the President. Dr Collins thank...

afternoonnapsociety.blogspot.com afternoonnapsociety.blogspot.com

the afternoon nap society: disclaimer

http://afternoonnapsociety.blogspot.com/p/disclaimer.html

The afternoon nap society. Fostering the patient voice in medicine — advocating for health. 8226; The information provided on this blog site is not intended nor recommended as a substitute for professional medical advice, is for general information only, and is designed to support, not replace, the relationship that exists between you and your physician. Always talk with your doctor if you have questions about your symptoms, diagnosis and treatment. 8226; Following, contacting, or ‘friending’...8226; Fee...

amysamerica.com amysamerica.com

cancer | Amy's America

https://amysamerica.com/tag/cancer-2

One girl, infinite adventures…. Posts Tagged ‘cancer’. On April 11, 2015 1 Comment. I know I don’t really blog about my cancer experience anymore, but it doesn’t mean that I don’t think about it every day. Once you have had cancer, it will never. Be part of your every day life. Today was a prime example. As most of you know because you’ve been following this blog for most of my journey (thank you! That wasn’t too bad – it was really a cute cut and I knew the hair went to something good. And then came che...

amysamerica.com amysamerica.com

chemotherapy | Amy's America

https://amysamerica.com/category/chemotherapy

One girl, infinite adventures…. Archive for the ‘chemotherapy’ Category. On April 11, 2015 1 Comment. I know I don’t really blog about my cancer experience anymore, but it doesn’t mean that I don’t think about it every day. Once you have had cancer, it will never. Be part of your every day life. Today was a prime example. As most of you know because you’ve been following this blog for most of my journey (thank you! And then came chemo. The morning I woke up to hair all over my pillow, I knew it was t...

amysamerica.com amysamerica.com

recovery | Amy's America

https://amysamerica.com/category/recovery

One girl, infinite adventures…. Archive for the ‘recovery’ Category. On April 11, 2015 1 Comment. I know I don’t really blog about my cancer experience anymore, but it doesn’t mean that I don’t think about it every day. Once you have had cancer, it will never. Be part of your every day life. Today was a prime example. As most of you know because you’ve been following this blog for most of my journey (thank you! And then came chemo. The morning I woke up to hair all over my pillow, I knew it was time&...

afternoonnapsociety.blogspot.com afternoonnapsociety.blogspot.com

the afternoon nap society: Hurt Society: Planes, Trains & Automobiles — ePatient Travel Edition

http://afternoonnapsociety.blogspot.com/2014/12/hurt-society-planes-trains-automobiles.html

The afternoon nap society. Fostering the patient voice in medicine — advocating for health. Hurt Society: Planes, Trains and Automobiles — ePatient Travel Edition. My relationship with planes has changed over the years. I remember being little enough to curl up like a cat in my single seat and eventually having to stretch out to put my head in my mother's lap. Regardless of the method, it's always held that so long as I have a window and music, I can travel for hours. The downside to ear plugs is that ot...

afternoonnapsociety.blogspot.com afternoonnapsociety.blogspot.com

the afternoon nap society: I Am More Than My Disease: A Project of Identity for World Rare Disease Day

http://afternoonnapsociety.blogspot.com/2012/02/i-am-more-than-my-disease-project-of.html

The afternoon nap society. Fostering the patient voice in medicine — advocating for health. I Am More Than My Disease: A Project of Identity for World Rare Disease Day. On Feb. 29 patients affected by rare disease will celebrate the 5th Annual World Rare Disease Day. In support of World Rare Disease Day and the people who are the patients, The Afternoon Nap Society. Or simply click on " Create your Own. In the large text box, fill in the name of your disease (such as Marfan syndrome. Continue filling in ...

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Running for Rare Diseases | "Alone we are rare, together we are strong"

Darr; Skip to Main Content. 2015 Runners and Patient Partners. 2014 Runners and Patients. 2013 Runners and Patients. April 30, 2015. 11 Comments ↓. Greetings from your RFRD team member in the Mountain Time Zone. I am Justin but better known as Garrett’s dad in many circles, including the RFRD crew. Garrett has the honor of being Phil Maderia’s patient partner this year. When …. Read more ›. WeRunTogether from Boston to Paris. April 30, 2015. No Comments ↓. Read more ›. Posted in Running Stories. How can ...

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Running for a Reason: to END LUPUS NOW

We love to run. We love to give back. And we love to look great running and giving back. Running 4 a Reason. Celebrates our active lifestyle with attractive, well-crafted apparel, accessories and running chotchkies. Our goal is to help you look and feel good, with a portion of profits going to local and national charities. Click here to learn more about our charities. A FEW REASONS WHY WE RUN. Beer, Wine and Chocolate. Raise Money and Awareness for Special Causes. We Run for Many Reasons . . .

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Running for a Reason: to END LUPUS NOW

TeamLUPUS is running in the Chicago Marathon. To raise awareness of LUPUS. And to help in the FIGHT. To find a CURE. We hope you'll join us in our journey as we train, run in local races in Seattle and Chicago, share running tips we learn along the way, and of course share LUPUS facts and awareness with as many people as we can reach. Follow our Walking for a Reason team on their Walking4Reason Facebook. To help meet our goal, we're creating various L UPUS. P lease check out our items on our donation page.

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Running4Recovery | Running 4 Recovery

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Raising money and awareness for victims of Domestic Abuse. TeamInferno – Best Wishes. January 29, 2014. With only two days to go before the big #TeamInferno event at police Headquarters in Cambridgeshire it is time for me to extend a very warm note of thanks to everyone who has made it possible, and everyone who is taking part. So far online donations and offline sponsorship has topped 1400. This does not include the profits that we anticipate will be made on the night itself. December 19, 2013. At Runni...