Dr. Robert Bransfield’s Speech to Harrisburg Bill Rally


Read below or Click here for Dr. Robert Bransfield’s Speech  – Pennsylvania HB629 Rally



Table of State Lyme Bills

Lyme Bills, Laws, Policies, Memos, Resolutions, Hearings by state & year with status listed.

The LDA has compiled the data in this table on bills, laws, resolutions, hearings over time in various states across the US. The status of each item indicates what action was taken by the governing body, for example, the bill was passed, it died, it was made into a resolution, memo, policy statement, etc.  

The table is provided for informational purposes only.  The LDA does not have staff to provide any further information on these bills.


 Click here for pdf of excel spreadsheet

LDA State Legislation & Action Table Updated

phoca thumb l 2002 145The Lyme Disease Association Inc. (LDA) has been working for 28 years to stop the spread of Lyme and TBD and to find a cure for chronic Lyme disease. LDA has educated multi-state officials from legislators to governors to health departments and continues to work with county and local officials who often are looking for ways to control tick-borne diseases in their specific areas, which may be more heavily endemic than the state at large.
LDA has also worked with other Lyme groups across the US in many states to develop, pass, and implement state legislation when other actions have not succeeded. In this table, you can view some legislative efforts across the US and perhaps find ideas to use in your state. Some actions have been successful, some not. Situations vary among states and legislation can be a long and dangerous road to take so embarking on it should be carefully considered.
Link to table
Link to LDA testimonies
Link to Legislative Advocacy

Legislative Advocacy Tips

Reprinted with permission from the Lyme Times ( Spring 2005, Number 41)

By: Pat Smith, President, Lyme Disease Association, Inc.
Lorraine Johnson, Executive Director, California Lyme Disease Association

Passing legislation to combat problems associated with Lyme disease can help correct some of the problems Lyme patients face, or it can exacerbate the very problems that it is intended to address. This article will provide you with a framework to think about legislative issues and will discuss some of the pitfalls you should avoid.

Educate Before You Legislate

Before you begin this whole process, it may be beneficial to ask for hearings on Lyme disease in your state. You can (and should) also have hearings in connection with an introduced bill, but often they are necessary before the birth of legislation itself to make lawmakers understand the need for legislation. These hearings are valuable tools which can educate legislators about Lyme disease itself and also the problems facing patients. If done in an organized fashion, they can have a positive influence on the legislative and policy-making process.

Have facts prepared to support your case, and have reliable, intelligent witnesses prepared to testify. Be selective about witnesses, who can turn legislators against the cause if they are unduly strident or antagonistic. It is good to include a mix of both patients, physicians, and possibly other experts. If you have access to favorable testimony from vector control districts or department of health officials, this should be included. Witnesses should have prepared testimony. It is important to coordinate witness testimony so that all important points are covered without unnecessary duplication given the time constraints.

To date, significant hearings have been held in New York, Rhode Island, Texas, Michigan, Connecticut, and California. Some of these hearings were legislative; others were public entities such as advisory committees, the attorney general’s office, and the state department of health.

Beyond legislative hearings, patients can meet individually with their representatives at their local offices or participate in state lobby days. To prepare for these activities, patients should educate themselves about Lyme disease and be prepared to be factual and not emotional. Lobby days are a great way to bring focus on an issue and rally the troops. Lyme advocates can arrange a day to meet at the capital and visit legislative offices in small groups. Patients can also arrange a meeting with a legislator they or a friend personally know, or one who has Lyme disease in his/her family, or who has been sympathetic to health issues. These one-on-one meetings add a personal touch that helps turn individual legislators to your cause.

Strength in Numbers and Coalitions

Maximize your numbers by coordinating with other Lyme groups including national ones and other groups outside of Lyme with a similar agenda. In New York, for example, the Lyme community was able to work with the Foundation for the Advancement of Innovative Medicine (FAIM). Its agenda coincided with that of Lyme patients: namely, the need to reform the Office of Professional Medical Conduct (OPMC). LDA has worked with many state groups and individuals and helped provide an orderly process for grassroots support in their states.
LDA has also been invited by many state legislators to educate and to provide input into legislation. Remember also that 501(c)(3) organizations are limited in the amount of lobbying they can do, so check with your accountant or attorney on this issue.

Initial Considerations for Legislation

Legislation should never be developed in a vacuum; it is complicated. No one has all the answers because the variables are many, and they change constantly. Legislators often are election rather than issue-oriented. That may be an advantage if you can muster up the numbers to persuade them, or it may be a disadvantage if your numbers are small. Be proactive. Take time to understand the politics in your state before you begin. Who is introducing your bill? Do they really support it or are they giving you “lip service” on the issue and introducing it knowing it will never move? Selecting a legislator to sponsor your bill may determine whether your bill will be successful or not. Do they have the support of their party? Do they need bipartisan (2 party) support, and do they have it? Is the support only in one house or both houses of the legislature? Generally speaking, it is easier to get a bill introduced and passed in the house/assembly than in the senate.

Decide what points you want in the bill. Look to other states that have successfully passed legislation, since legislators do usually not like to be “first.” If you borrow a bill from another state, make sure that you check how its provisions apply in your state. It may be different. You may be asking for doctors to be notified of a complaint in 30 days when you state regulations already say 10 days. If your bill is to be part of or replace chapter 10, find out what chapter 10 is and how your bill fits there.

Advocates in different states have used a number of legislative approaches, including those listed below:
the reformation of medical board practices to provide increased levels of due process to physicians,

doctor protection against actions by medical boards,

mandatory insurance coverage for long-term Lyme disease treatment,

informed consent for those who are using treatments considered non-standard,

Lyme in public education reforms (state-adopted Lyme curriculum, mandatory teacher in-service for educators with students with Lyme disease in NJ),

establishment of Lyme advisory councils, commissions (to advise governors, health departments, legislators: CA, DE, NJ, MA),

Lyme awareness resolutions, and

support of federal Lyme research initiatives.
What is contained in your bill usually determines in which legislative committee(s) it must be heard. Check with the sponsor to determine if there is a way to keep it out of a committee if you know that committee chair or a member is vehemently opposed or if the committee poses a particular problem because of budgetary constraints on your state. For example, sometimes insurance or budget committees are obstacles to success. Check out legislator credentials online for clues to position, or ask the legislator who is helping you.

Deadly Combinations

Controversial areas where powerful lobbies will play a major role, such as mandatory insurance, are best handled as a separate bill. If you combine it with doctor protection, for example, it is likely that both issues will be derailed, and it will usually be harder next time. For example, in Pennsylvania a house bill was introduced combining doctor protection for those who treat long-term and mandatory insurance coverage for patients. Insurance companies fought against it, although it passed the house. The bill was never considered in the senate. The physician protection portion of the bill probably would have had a better chance had the mandatory insurance coverage been handled in a separate bill. Insurance companies will be prepared to fight, and they often contribute to legislative campaigns, especially senate campaigns. Campaign financing records are public in most states, and some are even on the internet. Find out who your obstacles may be and be prepared to educate them more vigorously. Have constituents from districts of suspected opposition legislators prepared to meet with and lobby those people.

In Rhode Island, the LDA RIC was successful in having two separate bills passed, although there were behind the scenes machinations which almost derailed the legislation. Fortunately, they had very committed legislators who withstood a lot of pressure and stuck with the bill. The Rhode Island Lyme Commission, created to study the problem in the state, heard two nights of testimony. The LDA contacted each of the testifying doctors to ensure that all the issues were thoroughly covered by professionals and that testimony was not unnecessarily repetitious. Patients testified at one of the hearings. Patients were cautioned not to reveal treating doctor names either in written or spoken communications for protection of the physicians.

First, the doctor protection bill was passed, which provides that doctors cannot be brought up on charges by the medical board strictly for providing long-term treatment. Next, the governor’s office was able to reach an agreement with Blue Cross/BlueShield requiring medical treatment for Lyme patients. The insurance company began to undermine that agreement almost immediately. A bill was then introduced and passed requiring treatment. To placate the insurance lobby, the bill had a sunset provision so that it expired at year’s end. The rationale was to try it for a year. The next year, after extensive debate and lobbying against it by the insurance company, the sunset provision was removed. To date, patients have been able to get coverage under the law.

Bills that Hurt

“Any bill is better than no bill at all” is not a good philosophy with legislation. Passing legislation is difficult. Repealing a law after you have discovered it has hurt you may be impossible. Be prepared to kill your bill through grass roots efforts or through the sponsor (some states give this power to the sponsor, others do not) if something goes wrong. For example, New Jersey had a mandatory insurance bill introduced in 1993. Unfortunately, the sponsor “turned” after his election was over, and amended the bill to favor the insurance industry. Instead of providing mandatory coverage for physician prescribed treatment, the bill was amended to provide that after 56 days of antibiotic treatment, further insurance coverage was subject to a second opinion by a panel of doctors, regulated by the department of health. The proposed second opinion panels probably would have routinely ruled against extended treatment unless they were populated with Lyme literate physicians, and Lyme literate physicians were not comfortable applying for panel membership, because the environment in New Jersey had been hostile to Lyme treatment for years. The medical board of New Jersey was the first to press charges against doctors for Lyme disease treatment, and insurance companies had been harassing doctors for providing treatment. Moreover, the doctor panel would be under the Department of Health, which was not known to be Lyme friendly.

In essence, the 56 day period would have become de facto treatment guidelines and would have worked against patients who were denied further treatment and whose only recourse was court. The courts would have viewed the 56 days as the treatment guidelines. Ultimately, the bill had to be sacrificed because of the sponsor’s after-election alterations, although it had passed in both houses, albeit in different form. The next year, the sponsor said his bill or no bill at all, and sadly, we had to choose no bill, since other legislators were not willing to buck his influence.

A similar situation occurred in Connecticut. There, a bill was passed that provides for 30 days of IV and 60 days of oral medication and then requires a second opinion from a neurologist, rheumatologist, or infectious disease specialist. Doctors in those specialties who are willing to concur with long-term treatment are few, and pediatric ones are almost non-existent. Thus, this bill, which was intended to help Lyme patients, has made it more difficult to obtain extended treatment. It was introduced without those provisions, but was amended in response to pressure by the insurance industry. Those supporting the bill were probably unaware of the negative impact these changes would have upon patients, but the insurance lobby was not. Attorney General Blumenthal is using this new law to ensure patients rights to extended treatment instead of allowing insurance companies to use it as a restrictive guideline, which is how the insurance companies have attempted to interpret this law. The ongoing concern is the difficulty in finding the authorized second opinion.

The Governor Holds the Ultimate Power

You must try to educate the governor to the need for the legislation also. In New York, the OPMC reform bill was vetoed by the governor due to outside group opposition, although the bill was not a Lyme bill per se. You may be able to get what you want tacked onto another bill, or the most important provisions put into another related popular bill less likely to be opposed.


Be proactive, not reactive, and remember that legislation may solve some of your problems or it may add to them. Be cautious, move slowly, and choose your allies carefully. Legislation frequently depends on relationships developed over time. Even when you do not have a legislative agenda for the year, taking the time to educate with one-on-one meetings and state lobbying days help set the groundwork for the future. Legislation is one of the most powerful advocacy tools available to the Lyme community. The educational learning curve in Lyme disease is steep. Only legislation and judicial action afford patients the opportunity of a full airing of the issues. However, legislation is cheaper, less time consuming, more likely to be effective, and offers greater maneuverability if the tide turns against you. Make sure you and your sponsor have a contingency plan to abandon or actively lobby against the bill if it becomes patient unfriendly, and be prepared to use it.

Note: History of political activity in different states and at the federal level can be found in the Lyme Disease Association’s Lyme Disease Update: Science, Policy, & Law which can be ordered on www.LymeDiseaseAssociation.org.


How To Help

People often look for ways to help educate about Lyme disease but do not know how to begin. If you are working on your own, you can check for support groups in your state or region and contact them to ask how you can help with their efforts.  Or you can work on your own by reaching out to your local officials first, who may often be your neighbors or parents of your children’s friends. Talk to them about Lyme and tick-borne diseases. Share simple information with them first, how Lyme has affected your family, provide pamphlets and information about how widespread it is in your community.  

Go to your town council/committee meetings and share your concerns publicly. Talk to them about how children are at the highest risk. Perhaps they might host a Lyme seminar, or use environmental measures to control ticks on public property, or post public property with signs warning about ticks. Do the same at your local board of education meetings, and county government meetings. Explain how debilitating the disease is and that it also has a high financial cost to the patient/family and to society.

You may also try to educate state officials but that may be harder to do on your own. Enlist your friends and family, the local PTA, Rotary, or Elks and ask them to support your efforts.

LDA has developed a list of low cost recommendations to use at the state level. Agency titles may differ from state to state.

Who Implements
What is Implemented
Why it Is Recommended
Public Lands Agency

Post parks alerting people to presence of ticks, tick avoidance, proper removal procedures.


DOE (Dept. of Education)/DOH (Dept. of Health)

Encourage schools to keep properties maintained, post tick warnings where necessary, and develop trip policies reflecting high risk areas

DOE (Dept. of Education)

Encourage schools in endemic areas to provide educational forums on Lyme disease for staff and students.

Prevention and funding considerations
Environmental Protection

This agency may oversee hunting & fishing licenses and it could issue advisories to sportsmen with its material, especially in the areas of prevention and tick removal. Courses for hunters should include prevention materials.

High risk groups
Police, Fire, Emergency Personnel

Add prevention materials to their training requirements

High risk groups

May 2018 Declared Lyme Disease Awareness Month

LDA Proclamation 2018States and counties throughout the US have proclaimed May Lyme Disease Awareness Month.

Many states and counties have taken steps to raise awareness regarding Lyme and tick-borne diseases.  Declaring “May Lyme Awareness Month” is one move to help remind people spring is here, ticks are out, prevention & proper education are your best tools to staying healthy.

Proclamations are issued by governors and resulutions are adopted by the legislature.  The LDA salutes and thanks all the governors, legislators, Lyme groups, and advocates who have helped raise awareness throughout the year.  Your efforts make a difference!

See if your state has joined in May Lyme Awareness & Read the state proclamations.

States and counties throughout the US have proclaimed May Lyme Disease Awareness Month.

Many states and counties have taken steps to raise awareness regarding Lyme and tick-borne diseases.  Declaring “May Lyme Awareness Month” is one move to help remind people spring is here, ticks are out, prevention & proper education are your best tools to staying healthy.

Proclamations are issued by governors and resulutions are adopted by the legislature.  The LDA salutes and thanks all the governors, legislators, Lyme groups, and advocates who have helped raise awareness throughout the year.  Your efforts make a difference!

We thank our neighbors to the North for joining in the efforts to prevent the spread of Lyme.

Please click on your state to see what has been done.

Arkansas New York Minnesota
Colorado Oregon  
Maine Virginia  
North Carolina Vermont  
New Hampshire Nova Scotia – Halifax  
New Jersey Nova Scotia – Pictou  

Lyme Disease Association, Inc. Proclamation

LDA Proclamation 2018(Click picture for pdf)









House Resolution Introduced by US Rep. Faso

House Faso Lyme Resolution(Click picture for pdf)









Arkansas Proclamation

AR Lyme Proclamation 2018(Click picture for pdf)












CO Lyme Proclamation 2018(Click picture for pdf)











Maine Proclamation

ME Lyme Proclamation 2018(Click picture for pdf)











Minnesota Proclamation

(Click picture for pdf)











North Carolina Proclamation

NC Lyme Proclamation 2018(Click picture for pdf)











New Hampshire Proclamation

NH Lyme Proclamation 2018(Click picture for pdf)











New Jersey

State of NJ Joint Resolution Occurring Each Year

NJ Joint Resolution Each Year(Click picture for pdf)

Manchester County Proclamation

NJ Manchester Cnty Lyme Proclamation 2018b(Click picture for pdf)










New York

NY State Legislative Resolution

NY Lyme Resolution 2018(Click picture for pdf)


NY Erie County Resolution

NY Erie Cnty Lyme Resolution 2018(Click picture for pdf)


Oregon Proclamation

OR Lyme Proclamation 2018(Click picture for pdf)










Virginia Loudoun County Resolution

NH Lyme Proclamation 2018(Click picture for pdf)










Vermont Proclamation

VT Lyme Proclamation 2018(Click picture for pdf)









Nova Scotia – Canada

Halifax Proclamation

NovaScotia Halifax Proclamation 2018(Click picture for PDF)









Pictou Proclamation

NovaScotia Pictou Lyme Proclamation 2018(Click picture for PDF)

NYS Senator Seward Calls for Study of Link Between Lyme & Mental Health


2018 NYS Sen James SewardNew York State Senator James SewardThe following excerpts are from New York State Senator James Seward’s Press Release:

ALBANY, 03/29/18 — State Senator James L. Seward (R/C/I/Ref-Oneonta) joined this week with his senate colleagues to call on the state to investigate the impact Lyme and tick-borne diseases (TBD) may have on mental health. The senate unanimously passed legislation (S.7171) co-sponsored by Senator Seward that would require the state to study the link between infectious diseases, blood-borne pathogens and mental illnesses. The bill is the first step in a process that could lead to a better understanding of the incredible impact these diseases can have on the overall health of New Yorkers.

In August of 2017, Senator Sue Serino, chairman of the Senate’s Task Force on Lyme and TBDs (of which Senator Seward is a member) and Senator Kemp Hannon, chairman of the Senate Health Committee, held a comprehensive public hearing to look critically at the state’s response to the Lyme and TBD epidemic. It was there that testimony was given by patients, public health experts and mental health professionals that indicated that psychiatric symptoms related to Lyme and TBDs could directly impact quality of life and long-term health of patients if not properly addressed. Patients described battles with mood disorders, anxiety, depression and other mental health related issues. However, witnesses also testified that because health care providers and advocates may not immediately connect mental health issues with the emergence of these diseases, too often these symptoms go unchecked or are ultimately attributed to other causes leading to ineffective treatment and stigmatization.

“The Senate Task Force on Lyme and Tick-Borne Diseases has performed groundbreaking work and helped focus the spotlight on tick-borne illnesses,” said Senator Seward. “We know more today than ever before about these debilitating ailments and are making strides in prevention and treatment. Studying Lyme in relation to mental health is a logical step forward that can lead to improved diagnosis and treatment plans that can improve patient outcomes in the short- and long-term.”

Click here for the full press release

Click here to Download Bill Text and for more info

May Declared Lyme Disease Awareness Month

LDA Proclamation

See if your state has joined in May Lyme Awareness & Read the state proclamations.

States and counties throughout the US have proclaimed May Lyme Disease Awareness Month. Many states and counties have taken steps to raise awareness regarding Lyme and tick-borne diseases. Declaring “May Lyme Awareness Month” is one move to help remind people spring is here, ticks are out, prevention & proper education are your best tools to staying healthy.

Proclamations are issued by governors and resolutions are adopted by the legislature. The LDA salutes and thanks all the governors, legislators, Lyme groups, and advocates who have helped raise awareness throughout the year. Your efforts make a difference!

We thank our neighbors to the North for joining in the efforts to prevent the spread of Lyme.

Please click on your state to see what has been done.

Alabama        Georgia  Michigan      Oregon   Canada – Halifax Cnty
Arkansas  Maine Minnesota Pennsylvania      Canada – Wolfville Cnty
Colorado  Maryland           New Jersey    Wisconsin        
Delaware  Massachusetts     New York           


Lyme Disease Association

LDA May Lyme Disease Awareness Proclamation 2017(Click picture for pdf)










Alabama May Lyme Disease Awareness Proclamation 2017(click picture for pdf)













AR Proclamation(click picture for pdf)












Colorado May Lyme Disease Awareness Proclamation 2017(click picture for pdf

Governor John Hickenlooper grants COTBDAA’s request for proclamation….

Buena Vista Colorado Board of Trustee Meeting
Proclamation for May Lyme Awareness Month (First item on agenda)
May 11, 2017









House Concurrent Resolution

Viewable online Or click here for pdf of certificate

 Delaware May Awareness House Resolution Certificate

Article: May is Lyme Disease Awareness Month (Town of Henolopen Acres)

Delaware May Awareness ResolutionDelaware Speaker of House Pete Schwartzkopf, Marian Eastman and other Lyme disease advocates









Georgia May Lyme Disease Awareness Proclamation 2017(click picture for pdf)












Maine May Lyme Disease Awareness Proclamation 2017(click picture for pdf)












MD Proclamation(click picture for pdf)










Massachusetts May Lyme Disease Awareness Proclamation 2017(click picture for pdf)












Michigan May Lyme Disease Awareness Proclamation 2017(click picture for pdf)http://www.michigan.gov/snyder/0,4668,7-277-57577_59874-410773–,00.html








New Jersey

New Jersey May Lyme Disease Awareness Proclamation 2017(click picture for pdf)

 Proclamation on the left is from the Governor









NJ JointResolution(click picture for pdf)


Joint resolution from the General Assembly 2017, Also saluting the work on the Lyme Disease Association 








May 30, 2008: Joint Resolution designating the month of May as “Lyme Disease Awareness Month.”

 Link above is from the NJ state legislature declaring every May Lyme Disease Awareness Month.

2017 NJ Proclamation Assemblymen Dave Rible, Sean Kean and Patricia Smith(L to R) Assemblyman Sean Kean, LDA Pres. Pat Smith, Assemblyman Dave Rible








New York

NYS Senate and Assembly Pass Resolutions Declaring May ‘Lyme Disease Awareness Month’

Erie County                                       Dutchess County

New York Erie County May Lyme Disease Awareness ProclamationNew York Dutchess County May Lyme Disease Awareness Proclamation 2017









(click pictures for pdf’s) 

Erie County Legislature declares May as Lyme Disease Awareness Month


 Oregon May Lyme Disease Awareness Proclamation 2017(click picture for pdf)










(Click pictures for pdf’s)

Governors Proclamation                      Chester County Proclamation

PA Governors Proclamation PA Chester County Proclamation



PA Senate Resolution (Pg 1 and 2)
Click here for online version

PA Senate Resolution Pg1PA Senate Resolution Pg2


Lyme Disease Association of Southeastern Pennsylvania(L to R) Bob Serino; Pat Smith, President, LDA ;Doug Fearn, President, LDA of Southeastern PA












Wisconsin May Lyme Disease Awareness Proclamation 2014(click picture for pdf)


2017 Senate Joint Resolution 45 / 2017 Assembly Joint Resolution 41

Madison Area Lyme Support Group:
May is Lyme Awareness Month in Wisonsin since 2004






 Canada, Nova Scotia – Halifax County

Canada Nova Scotia Halifax May Lyme Disease Awareness Proclamation 2017(click picture for pdf)









Canada, Nova Scotia – Wolfville County

Canada Nova Scotia Wolfville May Lyme Disease Awareness Proclamation 2017(click picture for pdf)




CO Governor: May Lyme & Tick-Borne Disease Awareness Month

Governor Hickenlooper Proc May 2017 loMonica White, Co-Founder/President of the Colorado Tick-Borne Disease Awareness Association, a Lyme Disease Association Affiliate, has announced that Colorado Governor Hickenlooper granted their request for proclamation: May 2017, Lyme and Tick-Borne Disease Awareness Month in Colorado!

“Many of our residents and visitors are at greater risk for exposure to ticks through both work and their pursuit of outdoor adventure within Colorado and beyond. Common belief is that Lyme does not occur in Colorado. However, Lyme has been documented in both competent reservoir hosts, including the Mexican Pack rat and other small mammals, as well as in competent tick vectors,” Monica White wrote in her letter to the LDA announcing the news. White notes “a shortage of physicians within Colorado and adjacent western states with the experience necessary to recognize, diagnose and adequately treat Lyme and other tick-borne diseases.” She thanks Governor Hickenlooper for recognizing and supporting the growing need to elevate awareness of Lyme and Tick-Borne Diseases within Colorado. Click here to read letter

Says LDA President Pat Smith, “The LDA congratuates  the Colorado Tick-Borne Disease Awareness Association for their efforts to educate about tick-borne diseases in the region, an area that lacks understanding about how many diseases are now a problem, not only there, but also across the country.”  She added, “we are a mobile society, taking our families and pets all over the US. Everyone needs to understand how to protect their families and what to look for while traveling and after returning home. This proclamation will help raise that awareness. ”

Governor Hickenlooper’s proclamation acknowledges that serious health complications, sometimes fatal, can arise from Lyme and tick-borne diseases; that the rate of infection in Colorado may be underreported for all tick-borne diseases due to the difficulty of diagnosis; and that support group membership for those battling Lyme and other tick-borne Diseases is growing annually within Colorado. For all issues recognized by the Governor, read the full proclamation here.

Lyme Disease Association ColoradoMonica White, Co-Founder/President of the Colorado Tick-Borne Disease Awareness AssociationThe LDA sponsored Lyme & Other Tick-borne Diseases: 1st Rocky Mountain Forum in Colorado, “Elevating Tick-Borne Disease Awareness in Colorado” May 7, 2016, a free event which was hosted by a Biting Back: Elevating Tick Awareness in Colorado, a group led by Monica White, which evolved into the Colorado Tick-Borne Disease Awareness Association.  Speakers on a variety of topics were brought in for the  program on ticks in the region and across the country and the diseases they carry. Lyme disease symptoms and Lyme disease treatment were discussed by two physicians, Dr. Daniel Cameron, NY, and Dr. David Martz, CO, and the State of Tick-Borne Diseases 2016 was presented by LDA President, Pat Smith.  Monica White and Nancy Wrigley were moderators.

This event made CBS Denver News: Channel 4 did in depth interviews of Dr. Dan Cameron, Immediate Past President of the International Lyme & Associated Diseases Society, and Pat Smith, President, Lyme Disease Association, Inc. CBS also aired two new video clips on Lyme in the region in July 2016, featuring a video with patients in Colorado with Lyme, and then one with LDA President Pat Smith and the Bird Banders who are collecting ticks for a study on ticks in Colorado—a study spearheaded by Biting Back and supported by the LDA.  Click here to learn more about the forum and to see news clips.



LDA Recent Lyme Legislation Testimony

NH, ME, OR, CT: A number of states have recently introduced various Lyme legislation and LDA has submitted testimony to legislative Committees in New Hampshire, Maine, Oregon, and Connecticut in the past 2 months.

In New Hampshire, the bill HB0363 which authorizes legislature to declare May Lyme Disease Awareness Month and requires link on state website to ILADS was passed by the House with an amendment and is now in the Senate.  Link to LDA Testimony     Link to Bill

In Maine, An Act To Improve Access to Treatments for Lyme Disease, (LD 422 HP 289) was referred to Committee in both Houses for concurrence.  Link to LDA Testimony     Link to Bill

In Oregon, Senate Bill 916 was introduced into Senate Committee which allows professionals treating and diagnosing Lyme to do so consistent with ILADS guidelines and other provisos. 

Link to LDA Testimony  Link to Bill

In Connecticut, Senate Bill 207 would provide funding for Lyme disease prevention programs in Connecticut and funding to develop and implement a regional community prevention program for Lyme disease and other tick-borne illnesses utilizing the BLAST Lyme disease prevention program model. $170,000 would be for DPH to develop social marketing campaign on prevention and S280,000 to develop/implement prevention using the BLAST model. It is now # 76 on the Senate calendar.  Link to LDA Testimony     Link to Bill