New Hampshire State House
New Hampshire State House
New Hampshire State Legislators: Don't Repeal the Freedom to Marry
My brother and best friend, Calvin, was tormented all the way through high school because people knew he was gay. There were nights that I worried I may wake up and he wouldn’t be there any longer; crushed by the misery he was forced to endure. When New Hampshire extended marriage to gay and lesbian couples, two years ago, he finally felt accepted. He finally felt like he belonged. Since that day 1,800 loving and committed gay and lesbian couples have married. Today, the right to marriage is under attack in New Hampshire. If HB 437 passes, same-sex couples will no longer be allowed to marry. This mean-spirited attack is nothing more than state sponsored bullying. The bill actually goes on to allow discrimination in employment and housing based on sexuality. When I enlisted in the Marines, I took an oath to defend freedom and liberty. In 2004, I went to Iraq to do just that. As the co-chairman for Standing Up for New Hampshire Families, I am now defending my brother's freedom here at home, and I hope you will help me by telling legislators to vote NO on HB 437. Two recent polls have shown that Granite Staters overwhelming support marriage equality. One poll coming from the University of New Hampshire shows support at 62 percent. It should be obvious that the majority of New Hampshire believes this is a settled issue. When my wife Berta and I were married, Calvin was right there by my side as my best man. I want the opportunity to be his best man when he finds the person he wants to marry. With your help, I know we can ensure that freedom will still be there when he does. Craig Stowell Republican Co-Chair, Standing Up For New Hampshire Families Photo: Craig Stowell on left, Calvin Stowell on right & their twin brothers. For more information on Standing Up for New Hampshire Familiies, check out:http://action.standingupfornhfamilies.org/Craig
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
Congress: Let all children of U.S. military service members unite with their families!
I’m Jenifer Bass, a U.S. Navy veteran, who served for 10 years, one-third in the Asia-Pacific region. It was due to my travel between ports in countries like Japan and Thailand that I first encountered amerasian children, and descendants, of U.S. service members and civilian contractors previously stationed overseas. In the Philippines alone, more than 52,000-plus children were born and left behind after the U.S. Navy withdrew the last of its military personnel in 1992. Right now, the U.S. government won’t legally recognize them as U.S. citizens, despite having been born to an American parent. The Philippine Embassy won't help them either. Today, there are estimated to be more than 250,000-plus children. Many amerasians are caught in a no-man’s land of discrimination and poverty -- most left behind by U.S. service members who are unaware that they’ve fathered children overseas. My friend John Haines is one of these sailors. In 2011, John discovered he was the father of a half-Filipino daughter, Jannette. He attempted to unite with her through the American Homecoming Act -- but was frustrated to learn that the Act did not apply to Filipino children of U.S. service members. Today, all John wants is to be united with his daughter and grandchildren. He, like so many other veterans are living with a “hole in their hearts” as they search for ways to unite with their children. There is hope. The Uniting Families Act of 2017 creates a specialized visa allowing military veterans and eligible civilian contractors to sponsor their children and grandchildren for U.S. citizenship. Blood relationship must be proven by DNA test and the total number of visas granted will be capped at 5,000 each year. The issue takes on more urgency as so many of our veterans from our wars in Southeast Asia are getting older and dying each day -- without the chance to connect, or in some cases, reconnect with their own children. John’s daughter Jannette has already undertaken the DNA testing process, conclusively proving her relationship to her American father. All she’s waiting for is the opportunity to permanently unite with her father. There is a PBS documentary, "Left by the Ship" (2010), documenting a day in the life and the personal struggles as a Filipino amerasian on the never ending search for identity and their struggle to connect to their American military fathers. Please sign this petition to tell Congress that these families cannot wait another day. Pass the Uniting Families Act of 2017 now!
Adverse effect of GOP tax bill on Graduate students in the US
Graduate students in the US are already living at the survival line. They are working hard to push forward the frontiers of science in all directions and trying to make a better tomorrow than today. Their disposable income is barely reaches 20k per year ( stipend for being TA or RA) and this money goes all to their consumption needs with almost nothing left to save. The new GOP tax bill is going to make the tuition waiver taxable which is estimated to cost each graduate student about $2000 a year and this will push most of the graduate students even lower the survival level. As a result, they should cut down their daily expenses to get along with the new budget and this means they will buy and consume less necessary stuff. On the other side, local businesses will suffer as well because students will spend less money in local restaurants, bars, games and etc. In all, this bill is going to put more financial pressure on graduate students and also hurt local businesses across the US. Please sign and share this petition to support all graduate students in the US and also opposing this unfair tax bill.
Make Drug Treatment More Available in New Hampshire
Hello, all. My name is Kerry Anne Garnick. I am a New Hampshire native and a recovering drug addict. In March of 2016, I was on death's door. I couldn't stop getting high despite overdoses, brushes with the law, and multiple attempts to stop using. On March 28, I finally decided that I needed to go to treatment. I told my parents and we started calling different treatment centers all around New England. My first day clean was extremely rough. I was vomiting all day and could not hold down solid food. This was made worse by the fact that I knew that my misery could be temporarily staved off by just getting high "one more time". Because of intense parental supervision, however, I managed to stay clean until I found a treatment center in New Hampshire that had a bed for me. As I was leaving my house, they called me and told me that even with my mother's federal employee insurance, my insurance would not cover the cost. At this point, I was ready to give up. Had it not been for my crying mother, I would probably have left my house that day and gotten high. Eventually, after days of calling and staying on long wait lists, I finally found a treatment center in Pennsylvania that would take me immediately and be covered by my insurance, but the fact that I had to go to Pennsylvania in the first place is extraordinarily dangerous. I think back and see how lucky I am. Had my parents not been able to afford to take time off from work to take me to Pennsylvania, or if they had not been available to supervise me 24 hours a day while I was waiting for a bed, I would have probably died from an overdose. Many of my friends, however, weren't so lucky. During the time that they were waiting to get into treatment, some continued to use and are still using today; others were found dead of an overdose. In 2015, 428 people died in New Hampshire as a result of a drug overdose. This means that per capita, we have one of the worst overdose rates in the country. In a situation this dire, we don't have time to be placed on waiting lists. We don't have the luxury of waiting to find a place that will be covered by the insurance that we have. My plan is simple: Make treatment more available by giving tax incentives for people to open up treatment centers in New Hampshire, allot more revenue to help fund these treatment centers, and make the insurance plans cover more treatment centers around the state. These are necessary, common sense reforms that will save an untold number of lives. Please sign this petition so that we can finally do something about this horrible epidemic. Thank you for your time.
Tell New Hampshire Lawmakers: Helping Animals Is Not A Crime!
My name is Declan. I’m an 11 year old 6th-grader from New Hampshire. I love animals and believe that we have a responsibility to protect them from cruelty and abuse. I need your help to stop the dangerous “Ag Gag” bill that would cause more animals to suffer.New Hampshire’s government is considering a bill that pretends to help animals, but actually protects animal abusers!For years, animal protection charities have been conducting investigations that expose terrible cruelty in the meat, egg and dairy industries. Can you imagine locking chickens in tiny cages where they can’t even spread their wings for their whole lives? Or putting pigs in crates where they can’t turn around or move more than a step forward or backward? I get bored just sitting in my room sometimes when I can't go out and play with friends, so it must be so miserable in these 'factory farm' conditions where they treat animals like commodities instead of living beings.The companies that own the factory farms and slaughterhouses don’t like these videos coming out. You’d think they’d respond by being less cruel to animals so there would be nothing bad to videotape. But instead of doing the right thing, these factory farmers want to just keep us all in the dark about animal abuse and punish those who would expose it!The legislation the meat companies (factory farms) are pushing to try and trick people that they care about the animals, is called House Bill 110. The good news is that we have a chance of stopping this terrible bill. My mom and I are doing this petition because we know our governor, Maggie Hassan, and other lawmakers in New Hampshire care about animals. We need to remind them that animal cruelty is the real crime, not exposing it! I'm just a kid, but I know what's right and what's wrong. And you don't even need to be in school to know that being honest is important. Please join me in standing up for animals by signing my petition – we’re their only voice!
Remove the penalty that prevents people with disabilities from marrying!
When we think of marriage equality, we think about the ongoing fight LGBT couples face, but another minority group must deal with the stark reality that they are better off living in long-term committed relationships, without marriage. Like LGBT couples, these couples are denied the right to over 1,100 rights afforded to married couples. They have been denied access into their loved ones hospital rooms, faced family disputes over wills and have been denied spousal benefits from their partners workplace or the government in the event of their partners death. These are people with disabilities. Many people rely on the government for medical and financial assistance. Without medical insurance they would have no way to live independently. They would be forced into nursing homes (some already are), which would cost the government significantly more than getting Medicare and/or Medicaid does. At the same time, this assistance comes with a price. The government expects married couples to share income and that affects any assistance the couple receives. For many, their spouse makes too much (even if they make meager SSDI payments). This cuts into the healthcare services these couples receive. For some, their able-bodied partners make too much to allow them to qualify for medical assistance, if married, but not enough to pay out of pocket for costly medical equipment, medicine, or any other needs the disabled partner has. Add in the fact that even when a person with a disability can work, the opportunity for quality medical insurance is hard to find, due to their pre-existing condition and you will understand why many couples with disabilities are forced to live in domestic partnerships. Also, if two people with disabilities marry and they are on SSI or SSDI, their payments are CUT significantly, making it hard for them to maintain independence and afford their own food, shelter, clothing or other necessities. The time to stand up is now!! Let your Senators and Representatives know you want to remove the income caps placed on individuals with disabilities, so they can keep the government assistance and still be able to get married. Every loving couple deserves the right to marry. No one should have to choose between their wheelchair and their love, their therapy and their love, their medication and their love, their ability to eat or have a roof over their head and their love!! Those are not choices!! Help make it possible for those with disabilities to share their love without being penalized!Join our fight for marriage equality for people with disabilities:https://www.facebook.com/MarriageEqualityForPeopleWithDisabilities
NH needs a law to have someone committed involuntary to treatment for drugs or alcohol
Please read this story to understand why we need a law In New Hampshire that allows a person to request a court order requiring someone to be civilly committed and treated involuntarily for alcohol or substance abuse. On July 16, 2016 John C. "Bubba" Carter died of a drug overdose. Bubba was first introduced to drugs at the young age of 13. He began drinking alcohol and smoking marijuana. His addiction rapidly progressed into heavier drugs such as, pills, cocaine, and heroin. Through the years, Bubba fought hard to live a life of sobriety, and attended his first rehab at the age of 15. As he continued to struggle, he again entered his second rehab at the age of 16. After leaving his second rehab he attempted to attend AA, and NA meetings weekly. Battling with his anxiety he had a fear of not being accepted by his peers. The stigma of drug addiction surrounded him everywhere he went. While he was dealing with his own demons, he lost friends along the way to this horrible disease. This effected him greatly. During this time his family and friends continued to reach out and offer love and support. On March 17,2016, Bubba with the help of family and friends entered his final detox and rehab before he died. After three weeks there he left the facility and returned home where he continued to spiral out of control. At some point, which we learned later, he maintained 30 days of sobriety on his own between March and April. He was very proud of himself. We then learned he relapsed in May of 2016. Two weeks prior to his death on June 30, 2016, his family and friends attempted an intervention. At this time Bubba was no longer living at his mother's home. Although his family kept in contact with him, they had decided to stop enabling him hoping he would choose recovery again. During this intervention the police were also involved and tried to help him but because Bubba knew all the "right" words to say to the police their hands were tied. We then learned Bubba had been using heroin intravenously. In Massachusetts and other states they have a section 35 which allows a family member, police officer or doctor to have a person civilly commited struggling with addiction commited for treatment for drugs or alcohol. A judge then can have that person committed to a detox for up to 30 days or more. New Hampshire has a civil commitment for mental illness but it does not cover alcohol or drugs. Maybe if we had that option the police or us as family could have had him commited. Things may have been different if we had a law in New Hampshire. We don't know if it would have saved his life but we wish we did have that option as a tool to at least try. Families need more options to help their loved ones who need it! Sign this petition! We need to help save those who are struggling with addiction like Bubba was! Some of us have lost family members and friends to this horrible disease and it needs to stop! Sign this petition to make a NEW HAMPSHIRE law like this available to families!
Stop The Statute of Limitations (SOL) on Sex Crimes - Sexual Assault, Pedophilia, Rape
Lesley Barton’s WWII hero father once said to her, “You should never take advantage of someone that is weak or vulnerable just because you can." Little did he know how much his simple words would one day mean to his beloved daughter as the 1st survivor of 10 (4 in SOL 6 outside of it) known victims to report a 15 yr active and violent serial rapist who continuously got off with slaps on the wrist. The time is NOW to Stop The Statute of Limitations on Sex Crimes for children and adults. Please click the link below to learn more about her and her sisters’ fight against sadistic and emboldened rapist Marc Winner and to really understand the gravity of predators like him who are able to use the statute of limitations against their victims to their advantage. http://www.chicagomag.com/Chicago-Magazine/December-2016/Marc-Winner/__________________________________________Lesley’s story... Over 16 years, she’d hoped and prayed this day would actually never come, because although she knew he couldn’t stop-it was her greatest wish that he would, so no one else would be violently raped by him again. Painfully, that was not the case with 4 in the Statute of Limitations and 10 known total in a 15 year period. The continuous promises made to her when they wanted her to be okay with the plea deal, were not kept. Woman after woman reported him only to be disbelieved and disregarded, because of archaic belief systems even within the justice system and Chicagoland Cook County City and Suburbs being on different computer systems. How senseless is that? This has not been an easy road for her and her sisters. It’s actually been harder than any victim survivor could ever be able to explain. Our msister and brother survivors understand why sexual assault is the most under reported crime, because coming forward in order to protect others from a monster has no upsides due to the revictimization of stigma, harassment, a pretty inept and broken system, and those who want to make rape of all things about politics or shaming and blaming the survivor rather than stopping the perp. It’s been a long 16+ years for Lesley Barton who was the first to report Marc Winner for criminal sexual assault. Even after she came to terms with the unthinkable by finding some joy again she was really thrown for a loop that invasion day almost two years ago now when she found out he was back or actually never left. For he remained active and her reporting him, going to all their trial dates, and his slap on the wrist plea deal didn’t keep him from continuing his proclivity to do irreparable and permanent harm. Lesley no lomger feels any of the unfounded shame or blame any longer. She could really careless what the ignorant callous bullies towards survivors of rape think or say either. She does however feel an immense responsibility to her sisters who survived him, all sister and brother survivors, and the community at large to see this through to the end-to finish this-and to help convict him anyway they lawfully can so he never hurts another living soul again. Many confusingly mock and attack survivor activists who put it all on the line to stop criminals by using the term social justice warrior as a negative connotation on the internet and elsewhere. However, what they don’t seem to understand is that this is NOT a political issue and a violent despicable crime such as rape can never be referred to as “social.” It’s a matter of stopping a violent criminal from seriously hurting others in a way that the survivors receive a life sentence. Rape is actually a CRIMINAL JUSTICE issue-always has been, always will be. As a Criminal Justice issue, one way to end the emboldening of predators like Marc Winner, Brock Turner, Bill Cosby, Harvey Weinstein, James Toback, Kevin Spacey, Brett Ratner, Louis CK, USA Gymnasts Dr. Larry Nassar, Thad Alton, and Denny Hastert (to name only a small few) is to Stop the Statute of Limitations Clock. Predators know very well that they have a time clock they can easily run out during the often decades of time it takes a victim to come forward and be a survivor. The time is NOW to #StopTheStatute of Limitations on Sex Crimes in every state for children and adults, once and for all. There are no statutes in different states on Forgery, types of Fraud, Murder, Manslaughter, Attempted Murder, Arson, types of DUI accidents, and even in a few on Rape, but a few isn’t good enough-Rape is a life sentence, so should be the time period it takes to report it (which remember does not mean the lack of burden of proof) in order to help deter. The system needs to give survivors the time they need to come to terms with the heinous violation to their body and spirit in order to get closure and justice-How can’t everyone have some common sense, reasonably understand, and get behind that? #metoo#Ibelieveyou#stopthestatute
Save Lives: Require Spinal Muscular Atrophy Newborn Screening
August is Spinal Muscular Atrophy (SMA) Awareness Month. Please join our efforts to require SMA newborn screening, and help end the deadly effects of SMA. About SMA: • SMA is the number one genetic killer of babies and children under the age of two.• SMA is a motor neuron disease like ALS.• SMA robs the ability to move, swallow, and eventually breathe. • One in 40 unknowingly carries the gene responsible for SMA.• When two carriers have a baby, there is a 25% chance the baby will have SMA, a 50% chance the baby will be a carrier, and a 25% chance the baby will be unaffected.• One in 10,000 babies is born with SMA. The FDA approved Spinraza as the first treatment for SMA on December 23, 2016. However, newborns continue to go untreated when they would receive the most benefit, as no states are performing SMA newborn screening. Newly diagnosed Type 1 SMA babies treated with Spinraza didn't lose their ability to move, swallow, and breathe, but instead gained strength. Some even crawled and took steps — steps away from the deadly effects of SMA. Newborn babies treated within the first two weeks never lost abilities to SMA, and developed as average babies do. They crawl, eat, stand, and walk. Only newborns with older SMA siblings have been treated this way, as their parents knew to screen for SMA. Every newborn needs to be screened for SMA, so babies born with SMA can develop just as babies without SMA do. For this to happen, SMA needs to be added to the Recommended Uniform Screening Panel (RUSP), states need to require SMA newborn screening, and funding needs to be provided for SMA newborn screening. The Advisory Committee on Heritable Disorders in Newborns and Children (Committee) is scheduled to vote to add SMA to the RUSP at its February, 2018 meeting. Once the Committee votes favorably to add SMA to the RUSP, the Secretary of the Department of Health and Human Services (HHS) will add SMA to the RUSP. This is an important step, as many states look to the RUSP when adding new conditions to screen for. This petition will be delivered to both the Committee, and the Secretary of HHS. States also need to require newborn screening, as the RUSP is only a recommendation, it does not mandate states to test for conditions. We will continue to pursue SMA newborn screening in every state, and this petition will help our efforts. Missouri is the only state to enact newborn screening legislation, and will begin screening for SMA in January of 2019. Federal and state funds are also needed to begin and continue SMA newborn screening. This petition will help us as we advocate for funding with the appropriate federal and state congressional members. Act Now: With an FDA-approved treatment, it is urgent we secure SMA newborn screening. Newborn babies treated within the first two weeks will have the best chance at progressing as they would without SMA. Every baby born with SMA should be afforded this life-saving treatment. Please sign our petition urging Committee to vote to add SMA to the RUSP, urging states to require SMA newborn screening, and urging federal and state congressional members to provide funding for SMA newborn screening.
It is vital that the family court system in New Hampshire experience reform for the interest of justice. Paternity fraud is a serious issue in this state and it is the job of the legislature to enact fair and balanced legislation. It is my goal to see this issue be changed.
It is vital that the family court system in New Hampshire experience reform for the interest of justice. Paternity fraud is a serious issue in this state and it is the job of the legislature to enact fair and balanced legislation. It is my goal to see this issue be changed.