Tag: lymphedema
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“I always end up still feeling good about my body”: How one woman with Parkes Weber Syndrome stays positive
Isa-Bella shares her story of positivity and hope in her own words.
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Memorial Day Weekend’s #StompOutLE Walk
Meeting other people with lymphedema is always exciting — it’s kind of like discovering friends you never knew you had!
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Help support the National Lymphedema Network!
Throughout the month of May, the National Lymphedema Network is running their second annual virtual walk to raise money for lymphedema education and awareness!
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That’s a wrap!
I went into my wrapping treatment thinking my leg would magically shrink and look “normal,” but that’s not what happened — the progress, although real, was not linear.
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Lymphedema Awareness Day
Today is a day for us to join together and use our voices not only to spread awareness about lymphedema, but to celebrate our amazing community.
