Lymphedema - my friends know how much I hate this nasty affliction. It has been made even more frustrating by the fact that our medical insurance community has chosen to ignore that it is a chronic and debilitating medical condition requiring continuing daily care. Insurance has not paid for any help since the year after I was first diagnosed.
Two years ago, the Susan B Komen Foundation funded a replacement sleeve for me, but they were not able to help out. My expensive compression sleeves are almost threadbare.
Today I received an email from dear friend Lizzie who ran across a website that helps women like me. Please feel free to pass it around!!
http://toddlerplanet.wordpress.com/2011/01/05/cant-afford-lymphedema-sleeves/
Can’t Afford Lymphedema Sleeves?
Are you or do you know a breast cancer survivor? Please read today’s post and pass it on.
If you can’t afford to purchase a lymphedema sleeve, gauntlet, and/or
glove, and you can’t manage your post-mastectomy swelling, Crickett’s
Answer and LympheDIVAs want to help.
Today, I am pleased to announce a NEW opportunity for
breast cancer survivors who have had a
mastectomy and/or
axillary dissection of the lymph nodes due to breast cancer and have
swelling of one or both arms but
cannot afford the $200-$500+ cost for two sets of the compression
sleeves and gauntlets that survivors with lymphedema must wear every day
to keep the swelling in check.
Although lymphedema sleeves are medically necessary, they are not covered by Medicare OR most insurance plans
under current law,
and thousands of survivors go without the sleeves, needlessly suffering
congestion, swelling, and pain that interferes with their normal
activities.
Crickett’s Answer, a 501(c)3 nonprofit organization founded in memory of Crickett Julius, has just joined forces with
LympheDIVAs to help other breast cancer survivors who fight not
just the beast that is breast cancer but
also
the fallout of side effects that includes lymphedema, which may limit
survivors’ activities. By working together, they are now able to
provide needed lymphedema sleeves and gauntlets to women who need them
but cannot afford them out-of-pocket or convince their insurance
companies to pay for them. They do this in honor and memory of their
loved ones.
Crickett
Julius survived breast cancer only four months, but her mother and
cousin are dedicated to helping other women enjoy their life
post-diagnosis through Crickett’s Answer, a 501(c)3 organization that
provides wigs, mastectomy products, oncology/mastectomy/ lymphedema
massage, facials, and other pampering services as a way to help women
feel feminine and beautiful after losing their hair and/or breasts.
LympheDIVAs was founded by
Rachel Troxell and
Robin Miller, friends and breast cancer survivors who wanted to create a
more elegant and comfortable compression sleeve. Rachel continued to
build the company during her later recurrence. Even though she died two
years ago, at the age of 37, her father, mother, and brother continue
to grow the company in her honor and in the hope that LympheDIVAs’
compression apparel will continue to inspire breast cancer survivors
everywhere to feel as beautiful, strong, and confident as Rachel was.
To ask for help, please download and complete the forms at
Crickett’s Answer, writing in “lymphedema sleeve and gauntlet” on page 2 of the application.
To help someone else, please copy and paste this post on your blog or email it to a friend (or your local cancer center!).
To donate, go
here.
To help change the law so that this medical garment is covered by cancer survivors’ insurance, stay tuned for more about the
Lymphedema Treatment Act when it is reintroduced in the 2011 Congress.
Because of these women, these three thirty-something women who didn’t
ask to
get breast cancer, and the men and women who love them, there is now
help for women who can’t afford lymphedema sleeves, a medically
necessary garment not typically covered by insurance. Their legacy
lives on.