***ACTION ALERT*** Lymphedema Treatment Act Re-introduced

Sarahlicious
on 3/27/15 4:38 am - Portsmouth, OH

It's time to act! HR 1608 - The‪ Lymphedema‬ Treatment Act has been re-introduced to Congress!

So please use the easy system to contact your representative and ask that they co-sponsor the bill. Please share with your family and friends, you don't have to be a patient, anyone can write in on our behalf.

http://www.capwiz.com/lymphedematreatmentact/issues/alert/?alertid=63098021&PROCESS=Take+Action

I have Lipedema and Lymphedema. I also have a passion for Obesity and Health Insurance Advocacy

Blog: born2lbfat.com Facebook: Born2lbFat Twitter: @born2lbfat

Batwingsman
on 7/12/15 8:45 pm - Garland, TX

  Any update on this yet, Sarah?   

  I'm so tired of feeling like I have the "stepchild" of diseases, and one that is so "un-invisible" no less ..  

Frank talk about the DS / "All I ever wanted to be was thin, like that Rolling Stones dude ... "

HW/461 LW/251 GW/189 CW/274 (yep, a DS semi-failure - it happens :-( )

Sarahlicious
on 12/9/15 8:18 am - Portsmouth, OH

Dealing with the government is a long process, but at least in the end it will be fixed. Update now is we have 170 cosponsors in the House of Reps and the bill has been introduced into the Senate. So it's time to write your Senators.

https://goo.gl/6DwqQx

I have Lipedema and Lymphedema. I also have a passion for Obesity and Health Insurance Advocacy

Blog: born2lbfat.com Facebook: Born2lbFat Twitter: @born2lbfat

(deactivated member)
on 2/23/18 1:08 pm

You GO Sarah!! I'm really proud of you for leading this ( necessary) charge ...

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