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CONTACTS AT UMDF.ORG

The United Mitochondrial Disease Foundation

Tania Hanscom

8085 S●●●●●●g Road

Pit●●●rgh , Pennsylvania, 15239

US

1.41●●●●8077
ta●●●●@umdf.org

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The United Mitochondrial Disease Foundation

Tania Hanscom

8085 S●●●●●●g Road

Pit●●●rgh , Pennsylvania, 15239

US

1.41●●●●8077
ta●●●●@umdf.org

View this contact

The United Mitochondrial Disease Foundation

Tania Hanscom

8085 S●●●●●●g Road

Pit●●●rgh , Pennsylvania, 15239

US

1.41●●●●8077
ta●●●●@umdf.org

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Home-The United Mitochondrial Disease Foundation | umdf.org Reviews
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The United Mitochondrial Disease Foundation
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1 Mitochondrial Disease
2 MitoAction
3 Shoffner
4 CureMito
5 UMDF mitochondria
6 mitochondrial disease
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8 coupons
9 reviews
10 scam
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Home-The United Mitochondrial Disease Foundation | umdf.org Reviews

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The United Mitochondrial Disease Foundation

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New Website Redirector-The United Mitochondrial Disease Foundation - OLD

http://www.umdf.org/site/c.dnJEKLNqFoG/b.3558759/k.8256/Frequently_Asked_Questions.htm

You have been redirected here because you attempted to reach a page on our old website. We apologize for any inconvenience. Click here to go to our new homepage!

2

-The United Mitochondrial Disease Foundation - OLD

http://www.umdf.org/site/c.otJVJ7MMIqE/b.5719933/k.BE8C/UMDF_Advocacy_Week.htm

Sorry, the page you requested was not found. To go to the home page. The United Mitochondrial Disease Foundation - OLD.

3

Home-The United Mitochondrial Disease Foundation - OLD

http://www.umdf.org/site/c.otJVJ7MMIqE/b.5472191/k.BDB0/Home.htm

Our mission is to promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and to provide support to affected individuals and families. Washington, D.C. June 15-16, 2012. I nformation and registration - click here. June 13-16, 2012. Information and registration - Click here. Day on the Hill. June 14, 2012. Register to advocate here. Here are the top ten most visited pages on the UMDF website this month. What is Mitochondrial Disease? Types of Mitochondrial Disease.

4

-The United Mitochondrial Disease Foundation - OLD

http://www.umdf.org/site/c.otJVJ7MMIqE/b.5709419/k.D891/fontfont.htm

To Donate to Isabella's Fund. Isabella “Ella” Magee was born in Tulsa, Ok on August 21, 2008. She was beautiful and healthy and everything that we prayed for. She had colic for a few months, but grew out of it and was smiley, happy and incredibly chatty most of the time. We celebrated the holidays with her in tow and she did wonderful, loving the attention with every stop. Through research, the medical world one day will have the resources to help parents and their children like Ella win the battle again...

5

Home-The United Mitochondrial Disease Foundation

http://www.umdf.org/site/c.otJVJ7MMIqE/b.5692879/k.3851/What_is_Mitochondrial

Attention Patients, Family Members and Caregivers! Enroll now in the Mitochondrial Disease Community Registry to advance the development of treatments and cures. What is Mitochondrial Disease. Types of Mitochondrial Disease. Other Diseases Linked to Mitochondrial Disease. Adult Advisory Council Team. Ask The Mito Doc. Energy for Life Walks. Participate in an Event. Patient Evaluation for Professionals. Deciding When to Refer. Mitochondrial Disease in Adults. UMDF's Path to a Cure. Donate to an Event.

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Life at the White House: November 2008

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Life at the White House. Saturday, November 22, 2008. Logan and his cast. Okay so I don't post here very often. It's not easy to keep 1 blog going let alone 2. I do like this one because I can post many more pictures here but most people know our caringbridge address better. I would first like to start off by saying I love my son very, very much. There is nothing I would not do for him. He is normally quite fun to be with and I enjoy spending time with him. Posted by The White Family. Logan and his cast.

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Lone Star Handicap Vans. Governments / Schools / Non-Profits. About Us . Here is our story. I was shocked at the prices…$40,000 - $60,000 for a van, and a used one at that? Who can afford to pay that? A wheelchair accessible van is a necessity, not a luxury! I was determined to find a more reasonably priced vehicle for my family. I found FR Conversions, Inc. after an exhaustive online search. I couldn’t believe the prices! Vanguard Mobility Solutions is proud to be the Western States Representative for ...

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Route 5: November 2009

http://routefive.blogspot.com/2009_11_01_archive.html

Join our family on the Way. Time Article on Mitochondrial Disorder. Regan's Brace by Spinaltech. Lincoln Christian College and Seminary. United Mitochondrial Disease Foundation. Because You Told Me. We're a family of five who began in Dallas, TX. Even though we have small town roots, we love the city and never thought we'd leave! View my complete profile. Sunday, November 15, 2009. Because You Told Me. Subscribe to: Posts (Atom).

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Courtagen Gives Back | Courtagen

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Courtagen ENABLING PRECISION MEDICINE. Scientific and Strategic Advisors. What are Developmental Delay, Intellectual Disability and Autism Spectrum Disorders? What are Lysosomal Storage Disorders? What are Mitochondrial Disorders? What is Cyclic Vomiting Syndrome? What are Developmental Delay, Intellectual Disability and Autism Spectrum Disorders? What are Lysosomal Storage Disorders? What are Mitochondrial Disorders? What is Cyclic Vomiting Syndrome? Talk About Curing Autism. Genetic Testing for Epilepsy.

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Our lives Nina and Darin and mitochondrial Leigh disease story: January 2013

http://ourlivesninaanddarinandourstory.blogspot.com/2013_01_01_archive.html

Our lives Nina and Darin and mitochondrial Leigh disease story. Sunday, January 13, 2013. We didn't post from last year, the year that we would like to forget most parts, it has been something that it’s hard to describe, something that the people are not usually used to, however, it is behind us and our motto is really to stick to today, to live today as our whole life, to embrace all the good moments and to forget the bad as soon as possible. Nina drives with Mickey Maus. Hello Kitty in our. So, to get ...

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Medical Humanities: Patients & Physicians — Elisabeth Tova BaileyElisabeth Tova Bailey

http://www.elisabethtovabailey.net/patients-and-physicians

Patients & Physicians. Medical Humanities Patients and Physicians. Wild Snail book has glided into the medical world where it is being read by physicians, medical researchers, patients and their caregivers and families. For a desk copy to consider for medical humanities curricula or hospital reading groups, please contact amazes@workman.com. See sidebar for national patient support group links. To read. Chapter 6, “Time and Territory,”. From The Sound of a Wild Snail Eating. If using in the classroom.

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Love Karina: July 2009

http://love-karina.blogspot.com/2009_07_01_archive.html

Saturday, July 4, 2009. June 26, 2009 was a very special night for the Colon Family. Arianna was in a vocal performance and sang a duet with family friend, Karly Mani. As a surprise to us, they sang a tribute to little Karina, their butterfly. It was a very emotional performance for everyone, especially for those of us who love Karina. There was not a dry eye in the theater! Here is a link to the video:. Http:/ www.youtube.com/watch? Subscribe to: Posts (Atom). Subscribe To Love Karina's Blog. Watermark ...

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Home-The United Mitochondrial Disease Foundation

Attention Patients, Family Members and Caregivers! Enroll now in the Mitochondrial Disease Community Registry to advance the development of treatments and cures. What is Mitochondrial Disease. Types of Mitochondrial Disease. Other Diseases Linked to Mitochondrial Disease. Adult Advisory Council Team. Ask The Mito Doc. Energy for Life Walks. Participate in an Event. Patient Evaluation for Professionals. Deciding When to Refer. Mitochondrial Disease in Adults. UMDF's Path to a Cure. Donate to an Event.

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