Topic

Health and Safety

1,258 petitions

Update posted 13 hours ago

Petition to Maryland Lawmakers

Better Sex Offender Laws to Protect our Children

Did you know that currently in the State of Maryland, it is not against the law for a Tier III Registered Sex Offender to be alone with a minor?  It is considered child neglect or endangerment to leave a young child home alone or in a car, but you can tuck a child into bed next to a convicted pedophile and walk away for the night having committed no crime.  In 2017 my family fell apart when I discovered that my husband had abused one of my daughters.  He was later indicted on felony child sex abuse charges, held in jail without bond, and eventually accepted a plea deal for a 10-year suspended sentence and a lifetime registration as a Tier III Registered Sex Offender.  Several months ago, one of my daughters revealed that on her "supervised" visits with Daddy, the family member that was entrusted with providing the supervision was allowing her and her sister to sleep alone with Daddy.  Child Protective Services and Law Enforcement got involved, eventually determining that no actual laws were broken, because it is currently not against the law for a registered sex offender to sleep alone with a child.  Therefore, it is solely up to me to continue fighting as to why I refuse to allow my children to return to that previous visitation situation.  It is hard enough to become a single mother of three daughters without warning, to lose 75% of your household income in one day, to try to carry your children through the most traumatic event of their lives, let alone having the additional burden of exhausting all of your energy and resources in constant battles to protect your children.  The legal fees have already topped $23,000, and who knows how much higher they will get. According to Darkness to Light, a non-profit organization dedicated to preventing child sexual abuse, about one in ten children will be sexually abused before their 18th birthday.  There are an estimated 42 million child sexual abuse survivors currently living in the United States, and as much as we would like to think that the predators are far removed from our families, 90% of child sexual abuse victims knew their abuser. This year, there will be approximately 400,000 babies born in the U.S. that will eventually become victims of child sexual abuse unless we do something to stop it.  The problem is much more wide spread than many of us would like to believe, as the statistics are drastically under reported.  According to the National Sexual Violence Resource Center, only 12% of child sexual abuse is ever reported to the authorities. The Maryland Coalition Against Sexual Assault reports that 73% of child victims don’t report the abuse for at least one year, with 45% not disclosing for at least five years.  Nearly 70% of all reported sexual assaults, including assaults on adults, occur to children ages 17 and under. We would like to think that we can identify someone who isn't safe, and protect our children from them, but it's not always that easy.  Sometimes unsafe people look just like safe people.  Sometimes the unsafe people are coaching your kid's soccer team, or at a birthday party at Chuck E Cheese, or sitting next to you in church.  Once someone has been identified as unsafe, there should be laws in place to ensure they cannot have the opportunity to offend again.  Currently the only restriction in the State of Maryland is that a registered sex offender cannot step foot on school property.  But there needs to be more when the conviction involved a child.  Abusers should not be allowed at any event designated for children, regardless of whether or not it's on school property, and they most certainly should not be legally allowed to be alone with children.  Help me keep my children safe.  Help me keep YOUR children safe and create boundaries to minimize the opportunity for someone convicted of abusing a child to gain access to your children.  Child safety is greater than abuser rights. Please sign this petition and share so it can reach more supporters.  If this reaches other states, research the laws where you live, and if they are inadequate, message me and I will help you fight in your state, too.  If you have any feedback on other avenues to pursue these laws, or even suggestions on resources for my personal family situation, please contact me at keepthebabiessafe@gmail.com.  Thank you so much for your support. 

Momma Bear
24,755 supporters
Update posted 17 hours ago

Petition to Scott DesJarlais

Name VA mental health building in honor of vet who was turned away- Sgt. John Toombs

Sgt. John Toombs served for 6 years in the Army National Guard and deployed to Afghanistan in 2011-12.  He came home with PTSD and struggled with substance abuse.  He entered the 90-day treatment program at the Murfreesboro, Tennessee V.A. On November 22, 2016, he was kicked out of the inpatient treatment program.  He had been sober for 70 days when he was abruptly discharged for being late to get his medications. When he was also turned away at the V.A. E.R., he uploaded a video to Facebook saying he had been kicked out "like a stray dog in the rain."  Then, in the future mental health building across from the E.R. that turned him away, he hung himself. On May 24, 2017, Tenn. Rep. Scott DesJarlais introduced bill H.R. 2634 that would name the building where John took his life the "Sgt. John Toombs Residential Rehabilitation Treatment Facility".  While the bill passed the House unanimously on Sept. 25, 2018, it unfortunately died in the Senate and needs to be reintroduced in the new congress. By signing this petition, we respectfully ask Rep. Scott DesJarlais to reintroduce the bill, and we also ask each and every member of the House and Senate to vote in favor of renaming the Murfreesboro building in memory of Sgt. John Toombs, the veteran who was turned away when he needed help the most.  May it stand as a promise to our veterans that we are listening and we will do better to prevent veteran suicide.

J. Montgomery
24,264 supporters
Update posted 17 hours ago

Petition to Donald J. Trump, Donald J. Trump, Jeff Flake, John McCain, Donald Trump, Tulsi Gabbard, Raúl M. Grijalva, Beto O'Rourke, Mike Coffman, Earl Blumenauer, Walter B. Jones, Lindsey Graham, Dave Joyce, Carlos Curbelo, Ryan Costello, John H. Rutherford, Ruben Gallego, Tom O'Halleran, Kyrsten Sinema, Andy Biggs, Paul A. Gosar

Fight For Those Who Fought For You

A Call to Reason As Veterans of the United States Armed Forces we call on the Veterans Health Administration (V.H.A.) to fully recognize cannabis as a viable treatment option, which is a far less toxic alternative to commonly prescribed pharmaceuticals. Leaders are increasingly aware of the devastation to former military members (and their families) caused by inappropriate prescription of opiates, SSRIs, Benzodiazepines, and other pharmaceuticals. In 2011 the V.H.A. established internal policy officially outlining their position on cannabis, allowing physicians in “legal” states to discuss its use with their patients, at their own discretion. Multiple attempts have been made to resolve the inability of veterans to incorporate cannabis into their official treatment plans. Each and every one of these attempts have been sabotaged. The V.H.A. needs to take action on this issue. Federal leadership in the Executive and Legislative branches of our government need to understand the enormity of this pharmaceutical impact and available remedy. The fact is, veterans are self-medicating with cannabis. Most turn to cannabis after pharmaceutical options, some of which include warnings of suicidal ideation, fail. This situation is untenable. Because the V.H.A. is a federal program, operating in all fifty states, veterans are federal patients and require equal medical treatment/access to cannabis, regardless of state laws. Accordingly, an expansion of existing V.H.A. policy which would meet our needs is in order. The status quo is medically unethical. We request and require: Unobstructed ability to engage in open and honest dialogue with our V.H.A. Primary Care Teams about our use of cannabis, where we can then develop proper treatment plans, documenting our experiences. The ability to participate in research programs conducted by V.H.A., which would further assist us in our understanding of medical cannabis, and how to best introduce it into our treatment regimen. The ability to receive recommendations for cannabis from our V.H.A. Doctors, should that be the agreed upon treatment plan. Prescriptions from the V.H.A. filled at local dispensaries, or where dispensaries are not located/permitted, getting those scripts filled at the V.H.A. Pharmacy. A cannabis farm at every major V.H.A. healthcare facility designed to teach veterans about their medication, how to grow it, and to supply the hospital Pharmacy. This discussion, this reform, is long overdue. Join us.      

1620 Legion
147,909 supporters
Update posted 18 hours ago

Petition to U.S. House of Representatives, U.S. Senate, New Hampshire State House, New Hampshire State Senate, New Hampshire Governor, The US Senate, Beth Bell, MD, Sylvia Burwell, Dr. Tom Frieden, Rima Khabbaz, Chris smith, Collin Peterson, Alex Azar, II

Calling for a Congressional investigation of the CDC, IDSA and ALDF

We are experiencing a health crisis here in New Hampshire and across the country with the growing epidemic of Lyme disease. A number of legislators have personally been affected and have introduced legislation to address this problem. Here are just a few recent examples. Massachusetts Representative David Linsky: “The occurrence of Lyme disease has reached near epidemic proportions in Massachusetts. Virtually every family in Massachusetts has been affected by Lyme disease in some way. Lyme disease is a public health crisis in the Commonwealth.” Read more… Connecticut, Rhode Island, New York Senator Richard Blumenthal: "Today for me culminates more than a decade of work and probably a decade more, because I've seen firsthand the devastating, absolutely unacceptable damage done by Lyme disease to individual human beings, Connecticut children and residents whose lives have been changed forever as a result of Lyme disease” Read more…. New Jersey, Pennsylvania Congressman Chris Smith: "It seems everywhere I go, someone comes up to me to talk about how Lyme disease has severely impacted their lives or someone they know," Read more… Virginia Virginia Governor’s Task Force Chair Michael P Farris, Esq: "Doctors here in Virginia are committing malpractice by saying the ELISA test is sufficient." Read more… Texas Sen. Harris says he was severely affected by the disease, but “got a lucky break.” His doctor, constrained by a disciplinary board that limited antibiotic use for tick-borne illness to 1 month or less, arranged for 17 physicians to take turns writing prescriptions for Sen. Harris’s treatment. Read more… Two HoustonTexas physicians tested their chronically ill patients for Lyme disease via CDC Western blot criteria finding all patients positive for the infection in a state where the prevalence of Lyme infected ticks is only about 1-2%. “No history of bull’s-eye rash or illness following tick bite was reported by these patients.” The CDC defines “Lyme disease” exclusively as a zoonotic illness. Congenital and gestational transfer cases have been disregarded for reasons not evident to us”. Read more… Congenital Transmission of Lyme: 28 Peer-Reviewed Studies After spending four years on this subject the following statement from a physician on the front lines treating the late stage Lyme epidemic for a quarter century rings true: “In the fullness of time, the mainstream handling of chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.” We have studies proving persistent infection after antibiotic treatment for mice, dogs, ponies, monkeys, cows, iris biopsy, and ligamentous tissue but if you perform a simple Yahoo search for the following statement, “There is no convincing scientific evidence that chronic Lyme exists” you will find the top search results are connected to “elements of academic medicine” involved in the denial of the late stage Lyme epidemic. Persistent Lyme infection: 273 Peer-Reviewed Studies Circular reasoning: "Suppress all evidence and then proclaim there is no evidence" “One way to stop an epidemic is to redefine it by narrowing the disease's diagnostic criteria so tightly that it's hard for any chronically ill Lyme patient to fit the profile and obtain insurance reimbursement.” Read more… The following CDC letter (Dec 1996) addressed to former Senator Alfonse D’Amato promising to inform the medical community that the CDC’s Lyme case definition was created for reporting purposes only and not intended for clinical diagnosis is yet another failure on the part of the CDC to follow up on their responsibilities. Countless numbers of Lyme patients have been denied treatment and insurance reimbursement as a result of the restrictive case definition.  Read more… Jan 2004 testimony from Paul Mead, M.D., M.P.H. Medical Epidemiologist from the CDC’s Division of Vector-Borne Infectious Diseases: “No surveillance case definition is 100% accurate. There will always be some patients with Lyme disease whose illness does not meet the national surveillance case definition.”  Read more… Seronegativity in Lyme borreliosis: 103 Peer-Reviewed Studies There has been a combined effort on the part of the CDC, IDSA and ALDF to use the media for propagating the Lyme disease disinformation campaign following Chomsky's propaganda model. They have used Medscape, Family Practice News, The New England Journal of Medicine, The Lancet Infectious Diseases and now The American Heart Association to spread the disinformation. This deliberate campaign is aimed at purposely confusing our medical community to keep case numbers artificially low by omitting the late stage of the disease entirely as there is absolutely no medical training whatsoever for the later stages of this disease (Willful Ignorance) so patients are often ping ponged though the medical community for years or decades before obtaining a late stage Lyme diagnosis. Nine Steps to Deny an Epidemic on a National Level 101 Letter to the editor of Clinical Infectious Diseases questioning the validity of Dr Alan Steere’s research. Read more…. Letter to the editor of Clinical Infectious Diseases questioning the validity of Dr Gary Wormser’s research. Read more…. Dr Alan MacDonald’s letter to the editor of Clinical Infectious Diseases questioning the reality of the abstract by Lantos, Auwaerter, and Wormser: Read more….. Agenda-driven bias:  “People with these types of agendas may be more likely to abuse meta-analysis due to personal bias” NEJM editor: “No longer possible to believe much of clinical research published” When “evidence based medicine” has been spun to fit bias agendas and the patient voice has been intentionally ignored who investigates the dishonest science? Email message sent to the editors of the publications listed above announcing this petition. Read more… It’s all about the VACCINE It has become blatantly obvious that the CDC will go to great lengths to insure that Lyme disease remains within its narrow definition in order to fit the vaccine model. Chronic Lyme does not fit any vaccine model.  The CDC has long known about the virulence and persistence of this spirochete focusing on a vaccine as the cure-all to this world wide epidemic. The late stage/chronic Lyme community has become collateral damage for a vaccine market in the course of a government sponsored initiative as Baxter’s phase III clinical trials are underway. The CDC has aligned itself with institutions/researchers with a bias against persistent infection and has misused its authority by inappropriately allotting government funds to Mass General Hospital (Dr Alan Steere) and New York Medical College (Dr Gary Wormser) as identified in the following communications. Read more…. The Principle Investigators of the two previous Lyme vaccines: Allen C. Steere for SmithKlineBeecham's LymeRix and Gary Wormser for Connaught's vaccine (which never made it to market) have conceptualized a disease that would enable vaccine development. The one-size-fits-all Lyme treatment guideline (lead author: Gary Wormser) matches the conceptualized disease. A preventive vaccine for Lyme disease would not satisfy the FDA if a chronic persistent infection and seronegative disease exist. Post-treatment Lyme disease syndrome is simply a fabricated medical condition disguising treatment failure. Seronegativity in Lyme borreliosis: 103 Peer-Reviewed Studies It remains questionable that a Lyme disease vaccine is practical for an infection that produces a lack of immunological memory (unlike Measles, Mumps etc.) so the Wormser study fabricating a six year strain-specific immunity makes perfect sense for the marketing/acceptance of such vaccine as identified in a letter to Editor in Chief, Ferric C. Fang, M.D. Infection and Immunity.  Read more… The producers of the documentary, “Under Our Skin,” submitted a Freedom of Information Act (FOIA) request to investigate possible conflicts-of-interest of three Centers for Disease Control (CDC) employees who control public health policy for Lyme disease. (Barbara Johnson, Paul Mead and David Dennis) That request was finally fulfilled (May 2012) from the Department of Health and Human Services (five years later!). The information received is highly redacted with approximately half the information cut. What does the CDC know about Lyme disease that requires hiding from the public? The Centers for Disease Control has betrayed the public trust. For more on the FOIA see Poughkeepsie Journal article # 1    article # 2 By Mary Beth Pfeiffer Mary Beth Pfeiffer of the Poughkeepsie Journal highlighted the worst conflicts of interests between federal officials and a core group of researchers receiving government grants in the “ties that bind” page. Read more… Who is responsible for the “highly pathogenic” clone of the Lyme disease bacteria, (Borrelia burgdorferi) found in Europe and North America as reported by the journal Emerging Infectious Diseases? Read more… The following list establishes who knew what and when identifying their contribution to the disinformation campaign aimed at denying persistent Borrelia infection. When subpoenas are issued CDC officials cannot claim conflicts of scheduling issues and must attend to testify under oath regarding the mishandling of Lyme disease. Congressional Investigation Subpoena List 1. CDC Officials DAVID DENNIS (1) (2) (3), C. Ben Beard, Barbara Johnson (1), Paul Mead (1), Joseph Breen     Former NIH Lyme Program Officers Phillip Baker, Edward McSweegan (1)(2) 2. IDSA Lyme Treatment Guideline Authors  (1) (2) (3) (4) Gary P Wormser (1), Raymond J. Dattwyler (1), Eugene D. Shapiro,          John J Halperin (1), Allen C. Steere (1), Mark S Klempner (1),   Peter J. Krause, Johan S. Bakken, Franc Strle, Gerold Stanek,                  Linda Bockenstedt (1), Durland Fish (1) (2), J. Stephen Dumler, Robert B. Nadelman     Academic Medicine Paul Auwaerter, Arthur Weinstein (1) 3. The American Lyme Disease Foundation Phillip Baker, (1) (2) Executive Director Please call your legislator and respectfully urge immediate action from the U.S. Senate and U.S. House of Representatives to fully investigate the facts surrounding the failures of leadership and management deficiencies by requesting a Congressional investigation of the CDC, IDSA and ALDF (Find your Senator) (Find your Representative) Yolanda Foster on Lyme disease, one of the "Real Housewives of Beverly Hills” Dr Alan MacDonald on Alzheimer's and Lyme disease, “The Biology of Lyme Disease: An Expert's Perspective” Remarks: World Wide Lyme Rally & Protest Kenneth B. Liegner, M.D. Lyme disease testing flaws and conflicts of interests The Barry Marshall affect on chronic disease Inconvenient truths Bullying of Lyme patients List of abbreviations CDC: Centers for Disease ControlIDSA: Infectious Disease Society of AmericaALDF: American Lyme Disease Foundation Carl TuttleHudson, NH03051 Website: New Hampshire Lyme Misdiagnosis  Letter to the Editor, The Lancet Infectious Diseases Published May 2012 The Tuttle family was featured on New Hampshire Chronicle’s “Living with Lyme” with the program archived on their site in six small segments for viewing on the computer Part 1, Part 2, Part 3, Part 4, Part 5, Part 6

Carl Tuttle
73,441 supporters