Hi Friends and Family,
Bobby and I are partnering with Lymphatic Education & Research Network and raising money for 2019 CA Run/Walk to Fight LE & LD and we will be walking in the fight this Sunday in Santa Monica .
As many of you know I have a rare disease; Dercums Disease with secondary Lymphedema and Secondary Lipedema which all severely disable and greatly impair my lymphatic functioning and my other diseases and co morbities .
We sincerely appreciate your support . Every bit of support and awareness makes a difference in the lives of those living with these diseases. Most of us with lymphatic disease who even have insurance- it does not cover any of our needs. This non profit is advancing greatly in pushing Ca legislation to pass laws in getting us medical care, treatment , supplies and equipment , as well as educating doctors and patients with compassionate understanding of these diseases and care. Please won’t you join in our efforts this weekend by firstly praying for us , and click on our team to donate any amount. It only takes a mere 30 seconds.
All proceeds go directly to the lymphatic network (.org)
Hit “learn more “ icon on the top of this campaign page to find out more about this Event.
Thank you , We appreciate it so very much ! And we welcome any encouraging comments for our “walk about “ below.
You can join our team and come walk with us live or do a virtual walk through the campaign as well !
( We also need your prayer support so I’m able to go a few yards ! )
Blessings , The De Casas’s