Tag Archives: faces of lymphedema

“Faces” Project

Hello, lymphies!

How are you? I hope you’re all doing well and enjoying this beauuutiful weather. It feels like spring is finally here, I love it!

I haven’t heard from anyone regarding my Faces of Lymphedema Project yet, and I was really hoping to get this off the ground. You’ve left me no choice – it’s time for me to beg! Please, please, pleeaseee send in some submissions :) Click on the link to see what the guidelines are, and send your stuff in! My hope is to create an empowering and supportive page with all of your pictures and stories, to show the world (and ourselves!) how we are so much more than our disease.

In addition to the Faces project, I will be writing some big posts soon – including some about clothing, which will include pictures and outfit ideas! – so keep checking back for updates. If you would like to subscribe, you can click on the link on the right side of the page and have updates sent straight to your email. Very convenient!

Much love always,
xxox Alexa

Faces of Lymphedema Project

Hey, everyone! I’ve got super exciting news to share with you, but I’m going to need your help to make it happen. I’ve decided to start a project – The Faces of Lymphedema Project – that will become a new feature on the site. I want to create a page that shows all of us celebrating our lives and not letting our medical condition get in the way of doing the things that we love. The most exciting part is that it will feature the real faces of lymphedema – all of you!!

I need my lovely lymphie readers to help make this happen by sending in some submissions for the page. Here’s what I would like from you:

  • A picture of you – preferably of your face!
  • A small blurb about yourself and the things you enjoy doing – please keep the lymphedema talk to a minimum!
  • Another picture of you doing something you love or something you are proud of – be it a picture of you at dinner with your friends, a painting you did, or a beautiful cake you made… share it with us!

Too often we get so caught up in our lymphedema that we forget that there are so, so many other great things about our lives. We are more than this disease. We are more than our compression garments, and our embarrassment, and our discomfort. We are beautiful people who lead beautiful lives, so why not celebrate?!

Obviously, there is no pressure to share. If you would like to send text but no picture, that’s perfectly fine! Please share as much as you feel comfortable. Once I collect enough, I’ll launch the page – but I will continue to accept more submissions whenever they come in :)

Send your submissions to this email address: facesoflymphedema@gmail.com
I look forward to hearing from you!

xoxo Alexa