Some updates: “Faces” Project & Donations

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Hey, lymphies! I hope you’re enjoying this chilly October weekend. I have a couple updates to share with y’all: “Faces” Project The Faces of Lymphedema Project is something I started in January to celebrate Lymphies beyond their lymphedema, and to help the community get to know each other better. I finally received a submission to the…

Hey, lymphies! I hope you’re enjoying this chilly October weekend. I have a couple updates to share with y’all:

“Faces” Project

The Faces of Lymphedema Project is something I started in January to celebrate Lymphies beyond their lymphedema, and to help the community get to know each other better. I finally received a submission to the Faces project, from the lovely Laura Sfiroudis. I encourage you to check out her story, and learn about this wonderful, ambitious young woman who studies health, loves to travel, and is a budding chef.

I would love for the rest of you to submit your stories to me to share on the site! If you’re interested, you can send a short biography and a photo (optional) to facesoflymphedema@gmail.com. For more information, click here.

Donations

I am still collecting donations for the Lymphatic Research Foundation. So far we’re 20% of the way to the $2,500 goal. Please donate if you haven’t already; even a donation as small as $5 can help! Pass the link on to your family and friends, post it to your Facebook or Twitter – get the word out! All the donations go straight to the Lymphatic Research Foundation, to help further research of lymphedema and other lymphatic diseases.

The link is https://lymphatic.ejoinme.org/thelymphielife. Thank you – your help is much appreciated!!

Comments

2 responses to “Some updates: “Faces” Project & Donations”

  1. Yay! Alexa, you’re an inspiration to us fellow lymphies! It’s really great to see the “faces” of us and hear our stories. I will send mine in soon! Nothwithstanding, it’s admirable that you’re raising funds for lymphatic research!

    1. Thanks, Rosie! I’m glad to do it :) and yes – please please please send one in!! I think it’s great to see what all the other lymphies are like beyond our condition. Lymphedema is a big part of our lives, but it’s not by any means our WHOLE life.

      (Except me, I guess, because I run a blog about it. hehe)

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