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  The Reality of Living with Polycythemia Vera: Patti’s Story

  After being diagnosed with polycythemia vera (PV), Patti continues to live with purpose, passion and heart. She embraces

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  Hereditary Angioedema; Living with the unpredictable

  Hereditary Angioedema (HAE) is a rare genetic condition that causes painful, recurrent swelling in various parts of the

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  2026 Takeda Innovators in Science Award Highlights

  This highlight reel from the 2026 Innovators in Science Award with Nature celebrates exceptional early‑career scientists

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  Brooklyn Park, MN, USA, is part of Takedas manufacturing network

  Celebrating 10 years as part of Takeda, Brooklyn Park is a purpose-driven manufacturing site with meaningful impact. Gui

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  Campbell and Christina’s Story: Living Fully with Secondary Immunodeficiency

  After Campbell is diagnosed with multiple myeloma, he and his wife Christina are faced with an unexpected additional cha

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  Allegonda’s Story: Living with CIDP

  Allegonda is a busy and energetic flight attendant. She never would have imagined that she would be impacted by a rare,

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  Learning to embrace life: A PID Patient Ambassador shares his story of living with CVID

  In this moving testimonial, Gary reflects on how the immune deficiency, hypogammaglobulinemia, has impacted his life.H

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  Kevin’s Story: Living with CIDP

  Kevin discusses his journey to being diagnosed with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and the new

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  My PID journey: Creating balance as a parent and caregiver

  Making time for yourself and taking opportunities for activities and socialising can help parents create more balance in

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  My PID journey: Parenthood and immunodeficiency

  Parents living with immunodeficiency can feel worried about how much to tell their children and when. They may feel conc