TEAM KATIE!

If you are a regular reader of this blog, you already know a LOT about my sister.

First of all, you know she’s absolutely adorable

Duh.

and married to the best guy in the world

Love the Helds.

You also probably know that she’s…

a wine enthusiast

a lover of fine food

an excellent dancer
a Jenga ninja

a shoe expert
and generally awesome and a total riot to be around.

I think that hits all the high points, no?

What you may NOT know is that she suffers from a chronic auto-immune disorder called Lupus.

The Q+DD on Lupus is this: Lupus is a chronic autoimmune disease that can damage any part of the body (skin, joints and/or organs inside the body). Normally our immune system produces proteins called antibodies that protect the body from foreign substances, like bacteria and viruses. With lupus, your immune system cannot tell the difference between these foreign invaders and your body’s healthy tissues and creates autoantibodies (“auto” means “self”) to attack and destroy healthy tissue. These autoantibodies cause inflammation, pain, and damage in various parts of the body(www.lupusfoundation.org.)

While Katie’s Lupus does affect her everyday life in many ways, Lupus is largely a disease of “flares” and “remission” and Katie is a total fighter and does a good job of showing Lupus who’s boss.

However, for many people, Lupus is quite debilitating and can be fatal.  As of now, the cause of Lupus is unknown and there is no cure.

The Lupus Foundation of America (LFA) is the nation’s leading nonprofit voluntary health organization dedicated to finding the causes of and cure for lupus and providing support and services to all people affected by lupus and next weekend my sister will once again be leading TEAM KATIE in the Birmingham “Walk for Lupus Now”

Last year’s team was incredibly successful in their fundraising goals and in being totally adorable. Witness:

Tiaras for everyone!

Please consider making a donation to TEAM KATIE…every little bit helps…and if you are a Birmingham reader, Katie would LOVE to have you as a part of her team next Saturday, June 5th (and if you wanna come with us from Atlanta, there’s room in the car with La, Brooke, Olive and me!)

Please click here to visit Katie’s personal fundraising page!

See ya in Birmingham!

xx, L

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  1. Katie’s avatar

    I looooove this post- this was so sweet :) Cant wait for the walk :)

  2. Robin Lazarus’s avatar

    Go Team Katie!! Come walk with us on Saturday. I promise it will be tons of fun( we know how to enjoy life) and for a great cause!

  3. Caren Seligman’s avatar

    This was one of the best walks that I participated in last year.
    Katie is one unbelievable girl, she has never given in to lupus and you will never see her use it as an excuse. She is definitely a role model!
    Can’t wait for “Team Katie” to kick butt (oops, Kick Lupus)

  4. Ellen Stern’s avatar

    Yay Team Katie!!!! Wohoooo!

  5. Donna (your Mother)’s avatar

    A beautiful post Lauren!! Can’t wait for the walk with my two beautiful daughters!
    Come join us everyone!

  6. Lindsay’s avatar

    go team katie!!

  7. Lindsay’s avatar

    p.s. lady gaga is “borderline positive” for lupus, too.

  8. Katie’s avatar

    I heard about Gaga, that will raise great awareness (any word is good word I guess) Thanks everyone for the sweet comments, LOVE YOU

  9. Mary B’s avatar

    you’re the best big sis in the whole world. looking forward to tomorrow!

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