The Ultra Rare Disease, Disorders, & Disabilities Foundation

Wednesday, 23 March 2016

aHUS Canada applauds approval of first treatment for fatal, ultra-rare disease affecting children

aHUS Canada applauds approval of first treatment for fatal, ultra-rare disease affecting children
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 09:13 2 comments:
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Ultra-rare disease Hereditary Tyrosinemia Type 1 highlighted on The Balancing Act® airing on Lifetime Television

Ultra-rare disease Hereditary Tyrosinemia Type 1 highlighted on The Balancing Act® airing on Lifetime Television
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:46 1 comment:
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New drug helps young Ottawa girl fight ‘ultra rare’ disease | aHUS Canada | SHUa Canada

New drug helps young Ottawa girl fight ‘ultra rare’ disease | aHUS Canada | SHUa Canada
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:21 No comments:
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Tuesday, 22 March 2016

Government confirms it is abandoning cuts to Personal Independence Payment | Contact a Family

Government confirms it is abandoning cuts to Personal Independence Payment | Contact a Family
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:59 No comments:
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Friday, 18 March 2016

Rare Girl | Ehlers-Danlos Syndrome - Short Documentary

Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 10:38 No comments:
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Sunday, 13 March 2016

urddad-foundation on eBay

urddad-foundation on eBay
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 17:07 No comments:
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About | Ultra rare disease foundation

About | Ultra rare disease foundation
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 05:37 No comments:
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Saturday, 12 March 2016

What are Rare Disease Diagnostic Obstacles?

What are Rare Disease Diagnostic Obstacles?
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 10:15 No comments:
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Wednesday, 9 March 2016

Home | Ultra rare disease foundation

Home | Ultra rare disease foundation
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 03:59 No comments:
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Tuesday, 8 March 2016

Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Family Alliance (HLRCC)

Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Family Alliance (HLRCC)
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:43 No comments:
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Thursday, 3 March 2016

U.K. Aims at $15B Gene Therapy Industry | GEN Magazine Articles | GEN

U.K. Aims at $15B Gene Therapy Industry | GEN Magazine Articles | GEN
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:32 No comments:
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Blog | Ultra rare disease foundation

Blog | Ultra rare disease foundation
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 04:38 No comments:
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Wednesday, 2 March 2016

Duchenne A&E Pack – Just another WordPress site

Duchenne A&E Pack – Just another WordPress site
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 08:24 No comments:
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Ultra-Rare Diseases in Patients | Alexion Official Website

Ultra-Rare Diseases in Patients | Alexion Official Website: Many rare & ultra-rare diseases are severe, chronic & progressive, with high mortality rates & no effective treatment options.
Posted by The Ultra Rare Disease Disorders And Disabilities Foundation at 07:12 No comments:
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Blog Archive

  • ▼  2016 (29)
    • ▼  March (14)
      • aHUS Canada applauds approval of first treatment f...
      • Ultra-rare disease Hereditary Tyrosinemia Type 1 h...
      • New drug helps young Ottawa girl fight ‘ultra rare...
      • Government confirms it is abandoning cuts to Perso...
      • Rare Girl | Ehlers-Danlos Syndrome - Short Documen...
      • urddad-foundation on eBay
      • About | Ultra rare disease foundation
      • What are Rare Disease Diagnostic Obstacles?
      • Home | Ultra rare disease foundation
      • Hereditary Leiomyomatosis and Renal Cell Cancer (H...
      • U.K. Aims at $15B Gene Therapy Industry | GEN Maga...
      • Blog | Ultra rare disease foundation
      • Duchenne A&E Pack – Just another WordPress site
      • Ultra-Rare Diseases in Patients | Alexion Official...
    • ►  February (12)
    • ►  January (3)
  • ►  2015 (36)
    • ►  December (5)
    • ►  November (5)
    • ►  July (1)
    • ►  June (9)
    • ►  May (4)
    • ►  April (4)
    • ►  March (1)
    • ►  February (5)
    • ►  January (2)
  • ►  2014 (6)
    • ►  December (6)
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