Hear directly from a patient advocate about all the strategies she used to recover from Lyme.
Many have asked what I have done in my journey to heal, and I have finally typed it up.
I am the first to say it is a wide combination of things and choices I have made throughout the years that has got me here. Some of which I believe have made a significant impact in moving me forward. Most of the things I believe in exist within the empowering Rise Above Lyme Support Group. I share everything I have tried or still use. We also aim to share things we haven’t tried, as they may work for others. We are a group seeking solutions, first and foremost.
One of the biggest reasons this group was created was to provide hope by providing education, and most of all solutions, to those struggling.
This is just one of the few private pictures I have taken. Ones that I never intended on sharing, but I am learning that vulnerability is okay. It is a small glimpse into just a few moments of years of struggles. I have been to hell and back. But I feel that the things I chose moved me forward. I regret nothing in what I have or have not chosen- I followed my instincts. I am not saying my way is the only way. I am not saying this will heal you. I am not saying other methods are better or worse. I am simply living as an open book, and if sharing what I did helps you then I am certainly not going to be quiet about it.
Am I in perfect health? NO. Do I have bad days? YES. But I have a life now. I am a mother again. I am a wife again. I am a daughter again. I am a sister again. I am a friend to many. I do things in the world again. I laugh a lot. I am drastically better. I choose things that bring joy. And I protect myself.
Have I changed? For sure I have. I am extremely strong and I know it. Hell, I had to be strong enough to treat my child during my own battle. I had to be strong enough to set an example.
Now, I know I am resilient.
I know who I am without a hint of doubt. I have Lyme disease, Rocky Mountain Spotted Fever, Babesia, Bartonella, Erhlichia, TBRF and several more illnesses. I was once bedridden with the worst symptoms a human should ever have to experience.
But now, I wake everyday happy to enjoy my life. I am doing the treadmill consistently and don’t crash afterwards. I no longer live in pain and my brain is fully recovered. I have control over my health and I am grateful for each and every day.
Here is my list of each thing I chose along my healing journey:
(Join the Facebook page for posts on each subject)
💚 I let go of false friendships early on. I held on to the people that stood by me and let the rest go. I let go of anyone who judged me or didn’t believe me.
💚 I do not stay with dismissive doctors. They get fired. I will not let them dismiss me ever again.
💚 I did advocacy work to give me purpose and to fight back.
💚 I do not engage in negativity and avoid it at all costs.
💚 I am always seeking peace and joy wherever I can.
All of these things have contributed to my healing and improving my symptoms. Each thing I did moved me forward in some way. And I regret nothing. 🤜💚🤛
There is hope. You can Rise Above this disease.
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The above material is provided for information purposes only. The material (a) is not nor should be considered, or used as a substitute for, medical advice, diagnosis, or treatment, nor (b) does it necessarily represent endorsement by or an official position of Global Lyme Alliance, Inc. or any of its directors, officers, advisors or volunteers. Advice on the testing, treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient’s medical history.
*Opinions expressed by contributors are their own. Jessica Devine, a lyme disease patient advocate, founded numerous support groups alongside a website, Rise Above Lyme, as a safe space to seek accurate information on any topic related to Lyme and co-infections. Now five years later, that group has expanded into the Rise Above Lyme of today. Her goal is to provide those suffering with hope, comfort, and, most of all, solutions to make each patient’s journey a little easier.
Family Files Federal Lawsuit Against Massachusetts Police and Government for Medically Kidnapping Infant & Toddler at 1 a.m. in Home Invasion
Comments by Brian Shilhavy Editor, Health Impact News
May 10, 2023
A family who took their 3-month-old son to an emergency room in Waltham, Massachusetts last year at the advice of their pediatrician because the infant had a 103 degree fever, is now suing Waltham police and social workers who came to their home unannounced at 1 a.m. in the morning and forced their way into their home to remove both their 3-month-old baby and his 3-year-old brother, with no warrant, simply because an x-ray taken of the baby a couple of days earlier showed a healed fractured rib in the baby.
That was all it took for local authorities to medically kidnap their children, by forcing their way into the family’s home in the middle of the night and terrorizing the young children by kidnapping them and taking them away from their parents.
The parents were eventually cleared of all charges and their children were returned to them, but now the parents are suing to try and stop this from happening to other families.
This story has received national media attention, and The Pacific Legal Foundation has taken up their case and filed a federal lawsuit.
Alarmed by her three-month-old son’s 103-degree temperature and at the family pediatrician’s urging, graduate student Sarah Perkins brought baby Cal to a hospital emergency room just a few miles from their home in Waltham, Massachusetts. Sarah’s husband Josh Sabey, a documentary filmmaker, stayed home with the couple’s toddler, Clarence.
Doctors at the hospital ordered an X-ray to check the ailing baby for pneumonia. To Sarah’s surprise, the scan revealed a roughly two-week-old, healed fracture on one of Cal’s ribs. That’s when a new nightmare began.
Hospital staff notified the Massachusetts Department of Children and Families (DCF), who immediately opened a child abuse investigation. A social worker aggressively interrogated Sarah, who had no idea how her son’s injury happened. After Sarah called home, Josh brought Clarence to the hospital and they too faced DCF’s questions.
Finally, after Sarah and Cal were kept overnight at the hospital, the family was allowed to return home. Although they would be required to check in with DCF in a couple of days, the couple believed the stressful episode was largely behind them.
But the next night around 1 a.m., DCF workers knocked on the family’s door. They were accompanied by Waltham police officers. Although they had no warrant or court order of any kind, DCF had decided to remove the children from the home. Sarah and Josh protested, but when police threatened to break down the door, the couple got their children out of bed. Baby Cal was still nursing, so Sarah got stored breast milk out of the refrigerator for DCF to take. The couple tried to keep three-year-old Clarence calm by telling him he was going on an adventure; but the boy, desperate to stay with his parents, soon began screaming. Undeterred, DCF took both children away into the night and placed them with a foster mother. (Source.)
Here is a video report from CBS Boston with actual video footage from the night the police broke into their home:
Sadly, this is a common story in the U.S. and not rare at all. We have covered dozens of these stories over the past several years.
Another story that received national media attention in 2019 happened in Arizona where a military SWAT-like operation with Arizona police broke down the door of a family at 1 AM because the parents did not take one of their children who had a fever to an emergency room at the request of a doctor.
The child was reportedly sleeping soundly and only had a fever of 100 degrees when the police and social workers arrived in the early morning hours. The family’s security camera captured the break-in which is why the story went viral and received national attention.
As we have reported over the years, taking your child to an emergency room is one of the most dangerous things parents can do these days, as there is a huge industry devoted to “medical child abuse” and “child abuse pediatricians” along with their “child abuse” teams which can only be funded and their salaries justified by finding “child abuse” in pediatric patients brought to the hospital.
Unsuspecting parents bring their child to the emergency room and often end up having x-rays taken of their child, and based solely on an x-ray these “child abuse” pediatric doctors will order a child be seized from their parents, even before an investigation can be conducted.
It is a horrific violation of constitutional rights, as even terrorists, rapists, murderers, etc. are afforded due process of law in the criminal justice system, but parents are not given those same rights in Family Court.
After a medical doctor suggests “child abuse”, the children are often ripped away from the parents without any charges even filed, and then they have to prove their innocence, which can take months or even years, to get their children back.
Here are some previous cases we have covered.
Baby love with Marty Peele. Photo courtesy Peele family.
In 2015 North Carolina mother Marty Peele contacted us after being arrested for “child abuse” because x-rays of her baby showed ribs that were broken and then healed. Local media were publishing stories about her and portraying her as an abusive, criminal mother.
We investigated her story and interviewed friends and family members, and then published her side of the story in December of 2015. The story got a lot of traffic, and about 3 months later producers of the Dr. Phil show contacted us seeking permission to use our article in a show they were preparing on Marty’s story.
These are but a few samples of the hundreds of stories we have published over the years showing how common this problem is. Go to MedicalKidnap.com and search for your own state to see how many stories we might have covered in your state.
There are many reasons why young children can have brittle bones that cause them to break easily, often without their parents even aware of it, and are only found later via x-rays.
We have found that one of the most common factors for brittle bones in children is “vaccine-induced scurvy.”
What a sad state of affairs it is that in the United States today, young, unsuspecting parents are so trusting of medical doctors, and when they trust what they say about childhood vaccines, not only might they have a child that is injured and crippled for the rest of their lives, but often the parents will be blamed for the vaccine-induced injuries and end up having their children medically kidnapped.
To learn more about the medical mafia morally corrupt criminal network of “Child Abuse” doctors and professionals, please get our eBook on this topic, which I am offering to everyone free of charge now in my online store.
A few years ago Wisconsin Watch did a story on how a University of Wisconsin child abuse doctor Dr. Barbara Knox, who was considered a national expert on child abuse, was put on paid leave after colleagues inside and outside of the hospital accused her of intimidation or retaliation, and parents accused her of misdiagnosing abuse. A settlement agreement signed by Knox and UW shielded the reasons behind Knox’s leave from future employers and credentialing boards.
Despite this damning history Knox then took a job as the medical director of Alaska CARES, a child abuse response and evaluation program based at the Children’s Hospital at Providence in Anchorage where further allegations erupted and current and former co-workers complained for months about Knox’s medical judgment and bullying behavior.
“Covidism: Contagious Deception” is the most comprehensive documentary on COVID-19 which thoroughly analyzes both the scientific and political aspects of the COVID-19 mass deception launched in 2020.
The documentary was written and produced by a Health Impact News subscriber, Bonum Vincit (pseudonym), a Bulgarian independent film producer who would like to remain anonymous.
This is an amazing film that features interviews and footage of many of the leading dissenting scientists and doctors who tried to warn the public as this mass deception unfolded. These voices were censored from the corporate media and the major social media sites.
Part 1 carefully examines how authorities worldwide have been gaming the numbers regarding cases, hospitalizations and deaths from the alleged coronavirus. Part 1 also explains how health officials actively suppressed safe and effective treatments for Covid-19, while employing deadly protocols for hospital patients.
Part 2 focuses on the fascinating timeline of events, which led to the global Covid-19 response, and investigates whether or not the science on the lethality and infectivity of Sars-Cov-2 justified countermeasures such as lockdowns and mask-wearing.
Part 3 is a deep dive into the topic of Covid-19 “vaccines,” detailing the plethora of scientific evidence for their unsafe and ineffective nature, while exposing the deceptive tactics of manipulating the statistics.
Part 4 puts all the pieces of the puzzle together, exposing the premeditated sinister political motivations behind the global Covid-19 response, and how it is intricately tied to a much larger agenda – The Great Reset.
The film producer is not accepting any donations for this amazing work, and he wants everyone to freely copy and distribute the film.
If you appreciate his work, please let him know. You can reach him at this email address: covid19_documentary@proton.me
This work was a labor of love, and he began it back in 2020, which means it took him almost 3 years to produce this film.
https://plandemicseries.com/ Mikki Willis and Team Plandemic have made all of their documentaries free to the public.
Watch the 26 minute documentary Plandemic
Watch Plandemic 2: Indoctornation
Download the Plandemic audiobook
Watch The Truth About Ivermectin
Learn about Dr. Zelenko’s lifesaving protocol for COVID
Watch 8 shorts extracted from Plandemic: “The Plan,” “The Real Bill Gates,” “The Birth of Big Pharma,” “The Media,” “Center for Disease Control,” “Who is WHO,” “Fake Checkers,” and “We Are the Ones.”
https://www.realnotrare.com/Read about real stories of those injured by the COVID shots. You can type in symptoms as well as listen to podcasts and get resources.
https://www.stopworldcontrol.com/en Dr. Carrie Madej D.O. discusses the COVID-19 vaccine in this ground-breaking, informative documentary. It is critical you educate yourself and others on this frightening technology that can monitor, track, and potentially control your behavior.
Until three years ago, it wasn’t something to which Jordan Bentz or her mother, Julie, ever gave much thought.
But in September 2020, Jordan, then 10 years old, developed a strange bulls-eye-shaped rash on her leg, after a summer of playing outside and taking camping trips.
“It was just like, oh, you know, I have a rash. It’s not really a big deal,” Jordan said.
Jordan’s mother took her to a walk-in clinic in Calgary.
“I Googled it, and a bulls-eye rash came up, which is the hallmark of Lyme disease. I didn’t know a lot about Lyme, but I knew that wasn’t good. And so we took her to a walk-in clinic,” Julie said.
“Because we didn’t see a tick, (they) said oh, there’s no way that she could have Lyme (disease).”
The doctor prescribed Benadryl and the pair headed home. (See link for article)
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**Comment**
I can hardly read these stories anymore. The continued medical incompetence and/or denial is more than I can handle.
They, like so many others, were kicked from doctor to doctor without obtaining any help or answers.
Tests from Germany and the U.S. showed the presence of Lyme as well as other coinfections.
Treatments have cost them $150,000.
A researcher from the University of Calgary’s Cumming School of Medicine states:
“It changes its coat and constantly puts on new disguises as time goes by so that your immune system is unable to clear it because a new set of variants has popped up. By the time you get antibodies and clear those, yet another set of variants has appeared.” ~ George Chaconas
He also states current tests are flawed as they look for antibodies not bacteria and it takes weeks to develop antibodies, which means many will be seronegative.
CanLyme, The Canadian Lyme Disease Foundation recommends two testing facilities, Armin Labs in Germany and Ingenex Inc. in California.
The article inaccurately states that only 7% go on to develop long-term persistent symptoms caused by an immunological response rather than a continuing infection. This lie has and will continue to be used against patients and will prohibit further treatment.
Don’t underestimate Lyme and if you feel like something’s wrong, keep fighting and looking for answers.
If you discover a tick and want to have it identified you can submit an image of it to https://www.etick.ca/. That site also offers a mobile app for both Android and iOS phones.
I first became aware of Olivia Goodreau about six years ago.
I was at my computer, watching the livestream of the first meeting of the federal Tick-Borne Disease Working Group, which convened in Washington DC in December 2017.
At one point, during the meeting’s public comments, a young blonde girl stepped up to the microphone and confidently said, “My name is Olivia Goodreau, and I am 13 years old…I have had Lyme disease for half of my life, and I do not remember what it feels like not to be sick.”
This poised and well-spoken teenager certainly got my attention. I imagine everybody else watching that day took notice as well.
That was just the beginning of Olivia’s public activism on behalf of Lyme patients. She and her family started an organization called the LivLyme Foundation. It has raised money to help pay for Lyme treatment for children, sponsored conferences, and given research grants to scientists.
Through it all, Olivia has functioned as the public face of the foundation. She speaks to the media, helps plan LivLyme events, and sometimes meets with legislators and prominent researchers—heady stuff for a teenager.
She has also worked with a team of design and development experts to create an app called the TickTracker. It allows people to use their cell phones to report and track the location of ticks.
And now she has written a book.
Mysterious symptoms
In her memoir But She Looks Fine: From Illness to Activism, Olivia tells her story from when she first starts experiencing mysterious health symptoms at age 7.
In second grade, weird things start happening. Her vision goes in and out, and sometimes she finds it hard to move her body. “My back turned into a wooden board,” she writes. “My feet became cement blocks.”
A bizarre episode during a school choir performance brings Olivia to the brink of collapse. She lands in the hospital and endures days of tests, including x-rays, EKGs, and an MRI. None of it reveals anything amiss. One doctor tells her she just needs to drink more water. The family chooses to keep looking for answers.
After she’s been seen by more than 50 doctors, someone thinks to test Olivia for Lyme disease. When her Western blot comes back positive, they give her the CDC-recommended protocol of 30 days of antibiotics. Initially, she feels better with the drugs. But a few days after finishing the pills, her symptoms return with a vengeance.
Eventually, Olivia is seen by renowned Lyme expert Dr. Richard Horowitz. He diagnoses her with chronic Lyme, Postural Orthostatic Tachycardia Syndrome (POTS), various co-infections and a rare blood disorder. Slowly and surely, Olivia writes, his treatments help her feel better. But it doesn’t happen all at once.
Yearning for “normal”
About this time, the LivLyme Foundation is kicking into high gear and Olivia becomes heavily involved in the world of Lyme activism. She clearly takes great satisfaction from this, but she also longs for normal teenage experiences like friends, parties, and school activities.
Regrettably, some unfortunate instances of bullying mar her middle school years. (I’m aware of other young people with Lyme disease who also have been harassed at school. Not only do these kids have to deal with their miserable symptoms, but they must also put up with bad behavior from classmates. It’s the pits.)
A particularly compelling aspect of the book is the advice Olivia gives in the form of six letters. “Dear Parents,” “Dear Doctors,” “Dear Classmates,” “Dear Politicians,” “Dear Scientists and Researchers,” and “Dear Significant Other” speak to what ailing young people need from others in their lives.
Though not mentioned in the book, social media posts tell us Olivia will attend UCLA in the fall. (My alma mater!)
I suspect she will continue as a force to be reckoned with in the world of Lyme advocacy—or anything else she undertakes.