Lyme Disease Patient Advocacy

Lyme-Patient-Advocacy

Advocacy plays an important role in any illness, but for illnesses that are controversial or not well understood in the medical community, advocates are crucial.

Advocates are responsible for lobbying representatives to help increase research funding. They sponsor conferences, which allow researchers to share their findings and provide an avenue for physicians to stay up to date on the latest developments.

Advocates organize fund-raising campaigns for research, and increase public awareness of the illness and how it affects patients. They initiate petition drives, start support groups, and post commentary on their blogs about events that directly affect the welfare of patients.

On a personal level, advocates are responsible for making sure ill children and their families are protected, and their civil rights upheld.

Many people are too ill to do advocacy work, but anyone can participate by signing a petition, or sending an email, or a posting a tweet when events that affect our community arise.

The cumulative effect of advocacy efforts, from organizing major fund-raising drives to simply signing a petition, is that all of our lives are made easier.

Advocacy Sites for Lyme Disease

Lyme Disease Association, Inc. (LDA)

LymeDisease.org (formerly CALDA)

Lyme Disease Network

Lyme Disease United Coalition

LymeInfo.net

Lyme Disease Association of Australia

Last Updated: 5/5/15


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