From Shock to Hope: How I transformed my Parkinson’s Journey

In this powerful conversation, one of Lilians clients share a deeply inspiring story of transformation. Lilian is illuminating for the world how stress manifests not just mentally but physically—here, in the form of shock.

In this powerful conversation, Lilian sits down with one of her clients 58 year old, to share a deeply inspiring story of transformation. Through her work, she is illuminating for the world how stress manifests not just mentally but physically—here, in the form of shock following a serious accident, which contributed to debilitating symptoms years later.

Together, they delved into therapy to uncover the root causes of these symptoms, rooted in stressful traumas. By processing and releasing these traumas, he has experienced significant relief from the physical effects of accumulated stress, as well as the associated embarrassment.

Remarkably, he has not yet completed the full 12 sessions he originally purchased, because now more important tasks has taken center stage in his life. This shift in priorities is itself a profoundly positive sign of the progress he has made.

Join us as Lilian and her client explore this journey, highlighting the profound mind-body connection and the hope that knowledge about stress reduction and tailored trauma therapy can bring to those living with the physical echoes of chronic stress .

You can listen to the video/audio interview, or you can read a shorter version of the interview below.
It is people from Lilians HOPEshortcut Community who have requested most of the questions.



Lilian: People are really interested in your timeline, and since we’re exploring this connection between stress, trauma, and Parkinson’s, I’d love to hear the bigger picture too. How would you describe your childhood?

Interviewee: I’d say it was happy, loved, and secure. My mom and dad split up when I was about seven, but looking back now, 50 years later, I don’t feel like I had a difficult childhood at all.

Lilian: And school? How was that time for you?

Interviewee: Relatively happy. I still keep in touch with some friends from my primary school, the under-11s one. Then I went to a school in central London for bright boys. It was fairly strict, but again, looking back, I felt happy. By 16, I’d kind of outgrown it a bit and became a slight rebel, so I went off to sixth-form college, which was unusual back then.

Lilian: It sounds like you were a pretty confident teenager.

Interviewee: Teenagers always have their insecurities, but yeah, relatively confident.

Lilian: What about further education and your early career? Any major stress there?

Interviewee: I did a degree and a master’s. Exam time always brings some stress, but compared to others, I took it in my stride. People used to call me quite relaxed when everyone else was panicking.

Lilian: And your jobs afterward? You’ve had a few roles. any high-pressure ones?

Interviewee: Right after university, I worked as a biomedical engineer designing medical equipment until I was about 30. Then I left to start my own business supplying equipment to hospitals. There were stresses, running a business, building it up, managing staff, but I wouldn’t say I was significantly adversely affected by stress. As the person in charge, there’s always a certain level of ongoing stress, though.

Lilian: Then there was a switch – an accident. How old were you, and what happened?

Interviewee: I’d just turned 50. I was married, father of three school-aged kids. We were having a family barbecue in the garden. I went back to the barbecue after heating it up, but the gas had gone out. I reignited it without realizing a big cloud of gas had built up. There was an explosion, and I got quite badly burnt.

Lilian: Did you feel the shock in the moment?

Interviewee: It was like in the movies – everything went into slow motion. Then the physical bang of the explosion, and afterward this huge sense of shock. At the hospital, my body went into a kind of shock state, whole-body trembling. They gave me something like morphine to settle me down.

Lilian: How bad did the doctors say it was?

Interviewee: They didn’t really spell it out at first, but you could see on their faces it was serious. I was taken to a specialist burns unit, but compared to what they usually see, they said, “This isn’t too bad.” My legs were the worst—skin burnt off from the knees down, all bandaged up. There were lesser burns elsewhere, mainly from the waist down because gas is heavier than air and sits lower. It took a month or two for full physical recovery.

I came home bandaged up like the Michelin Man, legs wrapped, lying in bed on the top floor, kind of in isolation, waiting for the skin to regrow. They used ointments and mesh to help. I was amazed how the body heals itself. Within four or five weeks, I had fresh skin on my legs.

Lilian: Did the accident force you to close the company, or did you just take a break?

Interviewee: No, by then the company had a good management team. I was minimally involved during recovery, and things ran nicely.

Lilian: Let’s talk about the timeline after the accident. When did you notice your first symptoms?

Interviewee: Looking back, on a family holiday in France the summer after the explosion, I noticed I couldn’t smell anything. I didn’t think much of it then. About two to three years later, during the COVID lockdown, my left foot started dragging and catching on the floor sometimes. Everything felt weird back then, so I kind of ignored it, didn’t want to go to a doctor or hospital and risk picking up something worse. I was officially diagnosed in 2022, but the symptoms probably started 12–18 months before that.

Lilian: What made you finally seek help?

Interviewee: Symptoms built up. I had what was diagnosed as frozen shoulder—stiffness and restricted movement in my left shoulder, plus the earlier foot issues on the left side. Eventually I saw a neurologist, and within minutes he said it was Parkinson’s disease.

Lilian: How did that diagnosis hit you?

Interviewee: Complete shock. I thought it was some nerve entrapment. The shock affected me for about six months. I imagined a much worse future, incurable, degenerative, progressively getting worse. I felt like I had only a handful of years left moving normally, hoping for a cure around the corner.

Lilian: What changed your perspective?

Interviewee: I started researching things that could help symptoms. Exercise made a huge difference, my mood and outlook shifted to optimism and hope. There was a real turning point: we had building work done, and the builders put metal girders in the garden for foundations. I thought, “I can’t walk along that beam—my balance is gone.” But each day I tried, and suddenly I felt almost all my symptoms ease from the balance work. I’d run back to the house feeling things weren’t only going to get worse—there was something I could do.

Lilian: And medication—when did that start?

Interviewee: At diagnosis four years ago, the neurologist started me on low-dose Rasagiline (1 mg). He said we’d probably review it in six to seven months and that in seven to ten years I’d likely be on a cocktail of three or four drugs. But with exercise, sleep, and later stress work, my medication hasn’t increased. I’m still basically on that starter level after three years. I haven’t been on L-Dopa, but I’ve been on low-dose ropinirole (a dopamine agonist) for about a year—just one tablet a day. We decided not to increase it after starting our work together.

Lilian: When were your symptoms at their worst?

Interviewee: Usually tied to stress or anxiety, tremor in my left hand, curling up of the hand, anxiety, trouble multitasking, feeling overwhelmed. Never extreme, but dragging my leg, facial rigidity, reduced smell, reduced arm movement.

I felt embarrassed going out because of the gait issues. I’d worry beforehand about social events, and that anxiety made symptoms worse—almost self-fulfilling.

Lilian: You mentioned a trip to Spain with old friends—how did that change?

Interviewee: The year before working with you, I spent half the weekend in the hotel, anxious about my walking, stressed, and I left early.

This year, after we talked through the fears and resolved some underlying stuff, it was completely different. A bit of anxiety at the airport, but then I was fully engaged for three days—fantastic time. My brother even said, “Are you on some new medication? You look so much better.” Huge difference.

Lilian: And trips into central city—did that anxiety ease too?

Interviewee: Yes. I’d get anxious the day before about department stores or traveling in.

Now, after working through the stress triggers, I have a more positive mindset, if I’m not walking great, who cares? Lots of people aren’t. I notice it when I look around, and then I walk with more ease. Very quickly after one session, I tested it and had a much better experience.

Lilian: So now symptoms don’t restrict your activities as much?

Interviewee: Not at all. I don’t let them hold me back, and life is more enjoyable. It’s a virtuous spiral.

Lilian: Most people believe nothing can be done about Parkinson’s. What made you look in another direction?

Interviewee: Seeing positive effects from exercise, noticing symptom-free mornings after good sleep, and knowing stress intensified everything for me. I considered general counseling, but then I found you, and it fit perfectly—what I was looking for.

Lilian: If we make the bold claim that the barbecue accident—the shock, the freeze response—tipped you into Parkinson’s, what do you think now?

Interviewee: I agree. I fleetingly wondered if the accident caused it right after diagnosis but dismissed it because it didn’t fit conventional theories. Now, after our work, I’m fairly confident it was the most significant trigger. Lying on the hospital table, whole body vibrating in shock—that was worse than any Parkinson’s tremor I’ve had, but similar in concept.

Lilian: Do you have fears about the future now?

Interviewee: No more than the average person. I’m generally positive—more so now—and feel symptoms are much more under my control with exercise, meditation, yoga, stress reduction. Some even say getting the diagnosis was lucky, it forced lifestyle changes that help prevent other issues. What I thought was the end of normal life might have been the start of something better.

Lilian: How has this changed you beyond the symptoms?

Interviewee: I’ve become more accepting, if walking isn’t great one day, I don’t worry. I have lost some of that need to be “perfect.” It’s helped the family too, I’m more outgoing again, less withdrawn. My wife notices; she laughs at me doing my dancing exercises. Life feels lighter.

Lilian: Any diet changes that helped?

Interviewee: About a year after diagnosis, we shifted—with my wife’s help—to a more Mediterranean-style diet. Healthy anyway, but hard to pinpoint its exact effect compared to exercise, sleep, and stress reduction, which I notice immediately.

Lilian: You didn’t go heavy on supplements or experimental stuff?

Interviewee: As a biomedical engineer, I tried things like red LED light therapy, but nothing helped dramatic. I avoided the supplement rabbit hole you see in patient groups—people stacking dopamine boosters in untested combinations. For me, stress reduction, exercise, yoga, and meditation have had the biggest, most noticeable impact.

Lilian: Anything else you’d like to say to the world?

Interviewee: Just that I’d encourage people to try stress reduction work with you, Lillian—because it works.

Surviving Early Medical Trauma and Relieving Parkinson’s Symptoms

I underwent surgery as a baby (approx. 1950) around six months old without any anesthesia. I was essentially operated on while fully conscious and in pain, likely strapped down and immobilized.

The interviewer is Lilian Sjøberg, a practitioner focused on trauma healing and stress reduction for Parkinson’s symptoms (via the HOPE Shortcut method). The Interviewee is a man in his 70th sharing his personal story and how it ended up in a diagnosis of Parkinson.

Lilian: I’d like to start by hearing a bit about your life story. You have a particularly compelling background that’s relevant to anyone born before 1984. That year medical science recognized that infants also younger than six months have a fully developed nervous system capable of experiencing pain like adults. How did this discovery relate to your early experiences?

Interviewee: It’s hard to overstate the impact. I underwent surgery as a baby (approx. 1953) around six months old without any anesthesia. I was essentially operated on while fully conscious and in pain, likely strapped down and immobilized. That was my very first experience of the world: born into torture. It set a foundational message that life begins with betrayal and suffering.

I didn’t trust anyone after that—not even my mother. It wasn’t a great way to start.

Lilian: In my work helping people with Parkinson’s, we focus on reducing accumulated trauma and stress, because the earlier the trauma, the deeper its lifelong effects. On a scale of 0 to 10, where 10 is the worst, how would you rate the impact of that infant surgery on your life?

Interviewee: Easily a 10. Overwhelming.

Lilian: When did you first connect this to your life challenges?

Interviewee: Only about two years ago. My parents had mentioned the scar from the operation, but I didn’t think much of it until I started exploring after some breath work sessions. I researched infant surgeries online and learned they were routinely done without anesthesia back then, often with babies tied down. That realization hit hard.

Lilian: How do you think it affected you physically over the years?

Interviewee: I’ve always found it easier to have out-of-body experiences than to feel fully in my body. Coming back into my body feels difficult. I was never fully dissociated in a dramatic way, but there was always a sense of detachment. Pain that intense, especially as an infant, triggers survival mechanisms, like leaving the body to cope.

Lilian: That’s a classic freeze response: when pain is overwhelming, the body numbs out or dissociates. In later sessions, you’ve described moments of feeling truly “at home” in your body for the first time, like returning after being away. That infant surgery was likely one of your core, foundational traumas, perhaps the biggest.

Interviewee: I agree.

Lilian: You’ve also faced other health challenges, like neck cancer. How did you handle the diagnosis and treatment?

Interviewee: Surprisingly easily. I had a compassionate doctor, and when I agreed to surgery, there was this powerful exchange of energy across the desk, it felt supportive. I paid privately for the best care. But my distrust of authority figures runs deep, likely tracing back to that early surgery.

Lilian: That distrust showed up again with your Parkinson’s diagnosis. Tell us about when symptoms began.

Interviewee: About two years ago. It started in my right arm. I couldn’t sign my name properly anymore. Then jerkiness in the arm, progressing to more pronounced tremors. A friend noticed my walking was off; I wasn’t heel-striking correctly with my right foot. I felt slowed overall. The specialist diagnosed Parkinson’s after I described the symptoms.

Lilian: How did the diagnosis feel?

Interviewee: On one hand, expected; on the other, horrible. They didn’t discuss the future much, which was actually a relief. I’ve avoided dwelling on progression because focusing on worsening seems to make it happen faster. I’ve chosen not to know every detail, life’s surprises are better than constant fear.

Lilian: The doctor suggested medication?

Interviewee: Yes, but I refused. I tried it for a week. It caused constipation and made me feel out of control of my body. My early experiences taught me not to trust doctors or pills.

Lilian: You’ve noticed stress accelerates symptoms.

Interviewee: Definitely. Major shocks slow me down even more. Like after a friend’s death, when things worsened noticeably and I had to stopped driving.

Lilian: So you sought alternative paths: Any standouts?

Interviewee: Yes, Saunas, rebounding, medical Qi Gong, Brandy Gilmore’s work, and many more. Nothing dramatically reversed the core slowness, though many other symptoms improved or slowed. Slowness has been the persistent issue, possibly age-related too, but the trauma work we’ve done has helped the most.

Lilian: In our sessions, we’ve released trauma after trauma. You’re unusually skilled at sensing body memories and letting them surface. How do you do it?

Interviewee: I quiet my mind, focus on the symptom or topic, and let impressions float up without forcing or over-analyzing. It’s natural for me just allowing what’s there to emerge.

Lilian: That ability lets us process multiple body-stored traumas per session. For example, we linked specific stiffness in your thighs and calves to teenage sports competitions and the intense stress of racing starts. Even athletic pressure from youth tied into proving you weren’t “weak” after early vulnerability.

Interviewee: It felt nonsensical at first, but it made sense upon reflection. Untangling that stressful history has been incredibly helpful.

Lilian: Your career was also competitive, climbing the corporate ladder while staying driven. A common thread: always striving to be the best, perhaps to counter early feelings of helplessness.

Interviewee: Yes, without realizing how competitive I was.

Lilian: We’ve worked on the early traumas with your operation. Doctors saved your life, but the trauma lingered. You’ve shifted from anger to a neutral feeling. Any final thoughts for others with Parkinson’s or chronic conditions?

Interviewee: The trauma-healing process gives real hope. Symptoms improve during sessions, though sustaining hope between them is challenging. Releasing these old layers, especially the infant surgery, has made me more forgiving and present. It’s not a quick fix, but addressing root traumas and stress offers a path forward that conventional approaches didn’t.

Lilian: Thank you for sharing so openly. Your story highlights how early, unrecognized trauma can shape a lifetime, and how revisiting and releasing it can bring profound relief.

Saras testimonial

Sara had experienced symptoms for two years. Having to quit my job and slow down due to tremors, stiffness, pain and bradykinesia.

Sara’s story and her emerging proof
of what stress reduction can do

People have asked for “proof” that what I am doing is helping. We can get proof when doctors find a way to measure improvement and start to help us.
Until this, we can offer testimonials in text and video. Here is a video with Sara, and below is a text from her hand.
Enjoy
Lilian

I have asked Lilian to allow me to share my experience with HOPEshortcut.com so far. My name is Sara Sutton, and I am from Utah, USA. Diagnosed 7 years ago with Parkinson’s, I had experienced symptoms for two years before that time. Having to quit my job and slow down due to tremors, stiffness, pain and bradykinesia gave me time to contemplate my situation.

How did this happen to me? How did I come to this uncontrollably deteriorating physical condition, which my neurologist assured me would continue to get worse for the remainder of my life?

That is when I tried to discover the origins or causes of my symptoms.

My neurologist’s diagnosis was very short on answers. He explained to me that basically, if a person with symptoms responded to Carbidopa/Levodopa then it was a good probability that they had Parkinson’s. What???

Millions of people around the world have an incredibly wide range of onset and placement of body symptoms but they are all grouped into one box by a medication which could affect even a wider range of body symptoms, Parkinson’s or otherwise?

My first response to C/L was projectile vomiting! But as symptoms progressed, I gradually tolerated Sinemet. By that time, I needed help with dressing and showering etc.

Eventually, the neurologist suggested DBS surgery, and feeling I had no better alternatives, I went for it in January of 2023. The change was dramatic. I was able to dress, shower, and drive a car again. But DBS is not a healing therapy, and symptoms have and are expected to continue to develop and worsen. 

I realized that my symptoms were always worse under stressful situations, but I didn’t think there was anything I could do about this until I found the book by Lilian Sjøberg “Interviews with People with Parkinson’s: Clients in inspirational conversations 

The information in this book and on Lilian’s website, HOPEshortcut.com, opened me up to the understanding that with guidance, I can make improvements in my health and symptoms by managing them directly.

Drawing on Lilian’s knowledge and aid, I have completely dropped my medication from 5-6, 25/100 carbidopa/levodopa per day to zero.  I learned from Lilian’s research how dopamine chemically breaks down into adrenaline, which answered my questions about how to avoid over-medication and dyskinesia in the future.

Since cutting out my meds, I am calmer and have been able to overcome insomnia for the first time in 5 years, with the luxury of sleeping 8 hours at night.

With Lillian’s coaching, I have become less anxious, my pain is greatly lessened, my balance and gait have improved, and I have more endurance each day.  I am even dialing down my DBS amplitude so I can directly treat more of my symptoms.

Roberts and Lilian’s new book is an inspiring attestation to the validity of her empowering theories. 

I have found her community meetings to be highly motivating, and have met inspired, like-minded people who share this journey.   

I am joining Lilian’s course, which begins in January 2026, to continue my healing. 

Sara Sutton

Lillian’s Journey: Uncovering the Stress-Chronic Illness Connection

Ten years ago, Lillian embarked on a life-changing quest to unravel the mysteries of chronic illness. Her journey began in the wake of personal challenges

A decade of insight into cutting the Gordian knot of chronic illness

Ten years ago, Lillian embarked on a life-changing quest to unravel the mysteries of chronic illness. Her journey began in the wake of personal challenges: her then-husband’s battle with Hodgkin’s lymphoma, a diagnosis that struck while he was pursuing a PhD in physics and raising their two-year-old son. The doctors’ revelation that this type of cancer often affected highly educated young men sparked a question that defied her biology master’s training: could factors like education—something within our control—play a role in disease?

This question lingered, fueled by stories that challenged conventional medical wisdom. Lillian heard of a man with multiple sclerosis who defied expectations by regaining mobility, a feat that seemed impossible based on her academic knowledge. Driven by curiosity and armed with her new training as a coach and therapist, Lillian set out to explore what was really at play. After a personal loss left her with time to reflect, she dove into a self-described “nerdy” quest to uncover the truth behind chronic illness.

In 2015, Lillian conducted an experiment that would shape her path. She worked with four individuals—a woman with burning mouth syndrome, a man with multiple sclerosis, a man with Parkinson’s, and a war veteran with severe PTSD—offering each five intensive coaching sessions. 

The results were astonishing. While she couldn’t cure their conditions, Lillian significantly alleviated specific symptoms. The veteran’s mood improved noticeably, the woman’s burning mouth symptoms subsided, the man with multiple sclerosis regained temporary use of his arm, and the Parkinson’s patient’s tremors consistently calmed during sessions. These outcomes pointed to a common thread: stress.

Lillian’s work with the Parkinson’s patient, who lived in her city, deepened her insights. She observed that his tremors often flared when he thought about work, reinforcing her hypothesis that stress was a critical factor. 

When she lost her corporate job to outsourcing, Lillian seized the opportunity to dedicate five to eight hours a day for three years to research. She uncovered studies linking stress to symptoms across various diagnoses, from war veterans mirroring Parkinson’s symptoms to animals exhibiting instinctual stress responses. 

Her “aha” moments crystallized: chronic illness symptoms were deeply tied to stress, instinctual responses, and dopamine’s role in the body’s mammalian fight-or-flight mechanisms.

In 2019, Lillian founded a company to share her findings, later partnering with Parkinson’s advocate Gary Sharp to reach more people. She authored books in Danish and English, interviewing clients to provide living proof of her discoveries. By 2024, she launched her “Overcome” courses, initially for Parkinson’s patients and later for other chronic illnesses. These courses empower participants to build their own evidence of the stress-illness connection, understand their body’s responses, and take actionable steps to manage symptoms.

Lillian’s mission is clear: to break the myths surrounding chronic illness diagnoses and highlight stress’s profound impact on long-term health. Her clients have even begun educating their doctors, sparking a grassroots shift in understanding. As Lillian looks to the next decade, she’s optimistic about reshaping how we view and treat chronic conditions.

Ready to explore the stress-chronic illness connection for yourself? Join Lillian’s Overcome courses to uncover the science, build your own proof, and take control of your health. Visit the page where she invites you to a free workshop and start your journey today!

Tiny houses

Velkommen til vores Tiny House Netværk!

Inspirerende møder i dette netværk, hvor vi samler folk med en fælles drøm om at bo i tiny houses. Her møder du andre, der deler dine ideer om bæredygtige og enkle boformer.

Tinyhouse netværk?

Vær med til et netværk hvor vi samler informationer, og personer der vil det samme. Tilsammen ved vi alt hvad der er værd at vide.

Vi mødes i Zoom.

We don’t spam! Sjældne emails, mulighed for at skrive dig fra.

Velkommen til vores Tiny House Netværk!

Vi har allerede afholdt et par inspirerende møder i dette netværk, hvor vi samler folk med en fælles drøm om at bo i tiny houses. Her møder du andre, der deler dine ideer om bæredygtige og enkle boformer.

Vores mål er at mødes én gang om måneden for at udveksle viden, erfaringer og kontakter. Sammen ved vi en hel masse, og jeg har allerede lært utrolig meget om de mange spændende byggeprojekter, der er i gang rundt omkring.

Hvorfor gør jeg dette?
Jeg brænder for at skabe et tiny house-bofællesskab og har energien til at kickstarte dette netværk.

Ved at bruge de platforme, jeg allerede arbejder med i mit firma, kan jeg organisere og forbinde os.  Du hjælper med din deltagelse, viden og med at dele opslaget så vi kan bleve rigtig mange. (Og beklager at du ender på min hjemmeside når du bekræfter din email. )

Jeg tror på, at vejen til vores drømme om tiny houses går gennem netværk – sammen kan vi finde de rette personer, der vil tage initiativ til at starte ét eller måske flere bofællesskaber.

Lad os tage det næste skridt sammen!

Lilian Sjøberg
Iværksætter og ildsjæl

Links til inspiration

Kurser

Avnø bofællesskabs uddannelse

Sociokratikursus: En måde at “lede” bofællesskaber på

Projekter i gang

    Sjælland

    Fyn 

    Jylland

     

    Lilian Sjøberg-book

    Interviews of people with a Parkinson’s diagnosis from around the world reveal that it does not have to be this way. Instead, hope and self-reflection can be part of the solution to a better life.

    Interviews with People with Parkinson's: The Shortcut to Hope and Healing.

    About the book:

    “Parkinson’s is traditionally diagnosed as a disease that only gets worse over time. This book challenges that view.

    Interviews of people with a Parkinson’s diagnosis from around the world reveal that it does not have to be this way. Instead, hope and self-reflection can be part of the solution to a better life. People can recover or improve, not via quick fixes or miracles, but with supporting psychotherapy and an understanding of why the body, due to chronic stress or trauma, has ended up reacting the way it does.

    People from many different countries talk about their lives and experiences before and after diagnosis, whether or not they decided to take medication, and how conversations with Danish online therapist and biologist Lilian Sjøberg have given them not only hope but also noticeable improvements in quality of life and reduction in symptoms for a disease that is otherwise considered chronic and incurable. The commonality is that all cases seem to have arisen from a form of chronic stress or early trauma, and when this is addressed, hope and improvements are found.

    The interview format allows the reader to draw their own conclusions along the way as the interviewees describe their journey of getting better, and also inspires readers without chronic illness to think about the relationship between mind and body. Finally, it gently prompts Western medicine to look at the human being with a broader, more holistic perspective than in the past.”

    And help us share if you want to break the myths about Parkinson´s.

    It is available as an “e-book” via the courses part of our website 
    [this is also a supportive way to buy it, as Lilian (and danish tax) gets all proceeds].

    Different Amazon adresses around the world - take care

    Here amazon book version. remember to change to your country

    Comment on facebook and video
    Lillian’s new book is a game changer for chronic illness as it shows we can get better from what is thought to be fatal neurologic ailments. Run, don’t walk and get a copy. Your life will improve dramatically.
    Suzanne Congdon
    PWP

    A 4 minutes long feedback about my book

    Amazon Customer

    Reviewed in the United Kingdom on 28 September 2024

     
    Written in a friendly and easy-to-understand manner, this book addresses PD-related issues and it’s symptoms and gives an insight into how if affects the lives of those with PD through their own personal stories and the steps they are taking to enhance their well-being and quality of life without the constant use of medication! Well done to Lilian Sjøberg for writing the book and the continued support you give to people through your research and therapy and to Gary Sharpe who is a great inspiration to those around him. I would highly recommend this book.

    Reviewed in the United States on August 26, 2024

    Such a wonderful guide book for anyone living with Parkinson’s disease. A fresh and unique approach to dealing with this condition. Bravo!

    Hopeful

    Reviewed in the United States on August 25, 2024

    I loved this book it confirmed many of my symptom observations as a newly diagnosed PWP there’s definitely a strong relationship between adrenaline and dopamine. I hope this leads to more studies and treatments in this area. Meanwhile I’m trying all I can to reduce the fight or flight response. Thank you.
     

    Bringing back hope for folks with a Parkinson’s diagnosis

    Reviewed in the United Kingdom on 17 August 2024

    I may be biased, since, as a person with a Parkinson’s diagnosis myself, Lilian Sjoeberg has been my therapy coach for a couple of years, in which time she has helped me to significantly reduce my symptoms, keep my drug burden to a minimum, and improve my quality of life… but I really do feel this book is essential reading for anyone who has a Parkinson’s diagnosis. It is also essential for anyone who cares for, works with, or provides services to, folks with PD. In fact, the findings of the book translate well to many other chronic conditions, and should even be of interest to healthy people who want to avoid chronic illness in the first place.

    Recently* UCLA Health movement disorders neurologist Dr. Indu Subramanian “… drew upon patient voices and lived experiences to identify the common pitfalls of Parkinson’s diagnoses.” She says “how a diagnosis is delivered and the words that are used can impact a patient for years, with some patients falling into long periods of demoralization and hopelessness… in fact, I think it’s a very treatable disorder… giving hope, giving the patient agency is a critical part of the [diagnosis] message.”

    This book aims to provide a significant part of that proposed solution, and to bring back hope for those who are already under a curse of doom due to a medical authority figure giving them diagnosis of hopelessness.

    Lilian Sjoeberg lets the people with Parkinson’s diagnoses who are bucking the “it’s all hopeless” message, and are reducing symptoms and/or the amount of drugs they are taking, speak for themselves, by pulling together transcripts from a series of life history interviews she has done with them, and essays they have written.

    The main finding of these shared life histories is that Parkinson’s is the result of life long accumulated stress and trauma, a life lived in fight or flight, and eventually getting stuck in the freeze stress response. This is a much more hopeful story than that of irreversible cell death in the brain of unknown origin, as it allows us to actually make sense of what happened to us, and see that Parkinson’s is the body doing what it was designed to – to help keep us alive.

    The solutions then reveal themselves as stress reduction, trauma healing, becoming a calmer, more relaxed person, and becoming more stress resilient. The interviews and essays provide real world examples of the types of strategies that these folks with a Parkinson’s diagnosis have found helpful, and tell of the successes that they are having. Their lived experiences hence provide templates for others to follow on their own healing journeys.

    *”Delivering the diagnosis of Parkinson’s disease- setting the stage with hope and compassion”.

    You can get better!

    Reviewed in the United States on August 12, 2024

    If you’r trying to maintain a positive attitude after a PD diagnosis, this book is for you. Lilian Sjøberg spent years collecting stories from Pwp who have learned to live better with PD symptoms. These aren’t superficial stories. These are in depth in

    the Movement Monk and Lilian Sjøberg

    Prepare to dive deep into Lilian Sjøbergs groundbreaking findings that have the potential to revolutionize how we approach and heal conditions like PTSD, Parkinson’s, trauma, chronic tension, and pain. Get ready for a mind-blowing journey that could change your life.

    Enlightening interview with the brilliant researcher and
    mind-body connection expert, Lilian Sjøberg

    Benny Fergusson from the MovementMonk.xyz​

    I had the pleasure of sharing an enlightening interview with the brilliant researcher and mind-body connection expert, Lilian Sjøberg. Prepare to dive deep into her groundbreaking findings that have the potential to revolutionize how we approach and heal conditions like PTSD, Parkinson’s, trauma, chronic tension, and pain. Get ready for a mind-blowing journey that could change your life.

    About Lilian and Mind-Body Therapy

    Lilian Sjøberg is an expert in mind-body connection therapy, has dedicated her career to exploring the intricate relationship between the mind and body. Through her extensive research and practice, she has discovered that by nurturing this connection, individuals can achieve remarkable healing outcomes. Lilian’s insights have the potential to revolutionize how we approach and treat conditions that have long been considered difficult to address..

    Lessons Learned

    During our conversation, Lilian shares a treasure trove of lessons that will leave you pondering the true potential of mind-body connection therapy.

    Here’s a sneak peek at some of the mind-bending insights you can expect:

    1. Observing Healing in the Present Moment: Discover how cultivating awareness and mindfulness can tap into your body’s innate ability to heal itself.
    2. Bridging the Mind-Body Gap to Heal Chronic Disease:
      Lilian exposes the hidden emotional and psychological factors that
      underpin chronic conditions, revealing the keys to lasting healing and
      well-being.
    3. Links between Stress, PTSD, and Parkinson’s Disease:
      Prepare to have your assumptions shattered as Lilian unveils the
      surprising connections between stress, trauma, and the development of
      Parkinson’s disease. It’s time to rewrite the rules.
    4. Defragging Stress to Regulate the Nervous System:
      Master techniques for defragmenting stress and taking control of your
      nervous system, a crucial step towards unlocking peak performance and
      vitality.
    5. Body Memories and Trauma’s Links to Physical & Mental Disease:
      Brace yourself for a mind-blowing exploration of how trauma can
      manifest as both physical and mental ailments. Lilian shows us how
      mind-body connection therapy holds the key to unlocking profound healing
      potential.

    Conclusion

    That wraps up this mind-blowing conversation with the remarkable Lilian Sjøberg. We’ve ventured into uncharted territory, redefining our understanding of mind-body connection therapy and its potential to heal conditions that were once deemed untreatable. It’s time to unleash your own healing power and rewrite the rules of what’s possible.

    (Below you see a list of content in this hour long video)

    Body memmories

    4 minutets from the above long video.
    What are traumatic body-memories? Can childhood trauma be affecting your body today? And how can we get back into a parasympathetic nervous system state, so the body can heal? In this interview with Lilian Sjøberg we explore her research and findings of improving conditions like PTSD, Parkinsons, Trauma, Chronic tension and pain through mind-body connection therapy.

    Fight flight freeze

    4 minutets from the above long video.
    What happens when the nervous system is stuck and triggered into a state of fight, flight and freeze? And how can we get back into a parasympathetic nervous system state, so the body can heal? In this interview with Lilian Sjøberg we explore her research and findings of improving conditions like PTSD, Parkinsons, Trauma, Chronic tension and pain through mind-body connection therapy.

    Time to break the myths -
    Ofcause you can become better

    17 Lessons On Healing Trauma & Chronic Stress With Mind-body Connection Therapy

    In this interview with Lilian Sjøberg we explore her research and findings of improving conditions like PTSD, Parkinsons, Trauma, Chronic tension and pain through mind-body connection therapy. 00:00:00 Introduction to the power of mind-body therapy
    00:00:35 About Lilian and mind-body therapy
    00:05:02 Lesson 1: Observing healing in the present moment
    00:07:08 Lesson 2: Bridging the mind body gap to heal chronic disease
    00:10:08 Lesson 3: Links between stress, PTSD and Parkinsons disease
    00:13:41 Lesson 4: Defragging stress to regulate the nervous system
    00:15:57 Lesson 5: Body memories, trauma links to physical & mental disease
    00:20:40 Lesson 6: Intellectualising trauma as a self protective mechanism
    00:23:27 Lesson 7: How to start healing trauma and the nervous system
    00:27:40 Lesson 8: Working with different types of trauma
    00:29:39 Lesson 9: Stress vs stressors: How trauma can form
    00:35:41 Lesson 10: What is trauma really?
    00:40:00 Lesson 11: The effects of trauma and stress build up on the body
    00:42:01 Lesson 12: Triggers, trauma and body memories as a survival mechanism
    00:44:20 Lesson 13: How to mindfully navigate self protective mechanisms
    00:48:51 Lesson 14: Somatic Therapy: How I healed my body
    00:51:58 Lesson 15: The embodiment path to healing the nervous system
    00:54:47 Lesson 16: Moving forward in the face of fear
    00:58:18 Lesson 17: Self expression & societal conditioning
    00:59:40 Outro

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    Client after 3. sessions

    How overthinking is not going to help a person who has a disease

    Becoming Aware of my Overthinking Mind
    and Making Friends with my Inner Four-Year-Old

    HOPE shortcut

    The method where people with chronic diseases such as Parkinson’s can reduce their stress-related symptoms and, with persistent work, break free of their diagnosis

    One week after third session with Lilian and the Hope Shortcut

    My Overthinking Mind
    During my third session, Lilian and I talk about the inner dialogue, thoughts, the voice or voices in my head.

    My mind has several voices running constantly. It is like having a TV on in the background that is constantly narrating, planning, ruminating, rehearsing, arguing, suggesting, doubting. It changes the channel frequently. It practices future conversations, or rehashes past ones. It plans for things that never happen. An overthinking mind can be dangerous – triggering the fight flight or freeze response continually.

    One of its most interesting habits of my over-thinking mind is that it intricately plans escape routes. How would I get my infant son and the dog out of the window if the house caught on fire? Where would I hide if a gunman came to the house? It goes over the sequence of events in detail. I don’t sit down and plan these things. My mind just does it on its own.

    Lilian tells me that not everyone’s mind is like that. Upon Lilian’s suggestion, I ask my friend what her mind is like. I assume, her mind is like mine constantly ruminating, worrying and planning. She has kids. I am sure she has a lot on her mind. She laughs and says her mind is usually pretty blank; it might have a dancing clown in it like Homer Simpsons’. That sounds peaceful.

    “My mind has several voices running constantly.

    It is like having a TV on in the background that is constantly narrating, planning, ruminating, rehearsing, arguing, suggesting, doubting”

    We think we have a similar way of thinking - but we have not

    We ask each other, “what do you think?” and get a story.


    Next time ask in detail about HOW your friends are thinking.


    Are they thinking in pictures, written text, a speaking voice, or with feelings?
    How many voices do they use to think? 0, 1, 2, or more? Everything is ok, but having only 0 or 1 voice makes life easier and healthier.


    Around 1/3 of the population are hardly thinking and doing well. The rest are thinking about yesterday’s regrets and the worries for tomorrow, or thoughts that drag your attention away from your body and the constant feedback you get from here.

    My inner Four-Year Old
    I notice that my freeze ups are often precipitated by internal pressure. There is the internal pressure I put on myself to do the things that I “should” do. I know I don’t want to do it, but I push myself anyways. Or I put pressure on myself to do something at 1000% effort. Somewhere inside, there is an inner protest or maybe an inner wisdom.

    Lilian coaches me to have compassion for myself if I freeze up. To say to my body:
    Its ok. This is what is right now, you are safe.

    I have a profound experience when I have the opportunity to practice this. I sit through a freeze up and just let it be ok the way it is. This experience is profoundly different for me and I feel a shift.

    There is the internal pressure I put on myself to do the things that I “should” do.

     

    I know I don’t want to do it, but I push myself anyways..

    Somewhere inside, there is an inner protest or maybe an inner wisdom.

    I realize that I have been practicing relaxation and calming techniques for years. But I didn’t listen. I was just trying to get my body and mind to shut up and do what I wanted it to do.

    This is one of the great things that my four-year old son has taught me. He is what people describe as “spirited”. I cannot just shush him. He demands to be heard and understood. Even if his concerns seem inconsequential to me, I have to listen, I have to acknowledge and empathize and then he will calm down. I can’t just tell him: “That’s silly. Don’t be upset about that.”

    But I have not been listening to my body, to myself. My inner spirited four-year-old has concerns and is refusing to budge I have just been telling her: “That’s silly, don’t be upset about that” calm down, and do as you are told.

    The good thing about spirited children, is that they bust up old patterns. They refuse to just comply with expectations and the “shoulds” that we try to force upon them. Therefore, they force us to evolve, to grow, to learn, to examine the shoulds that we have applied to ourselves and to rethink them.

    Lilian is a bit like a spirited four-year-old. She is here to bust up old patterns and assumptions and evolve our way of thinking about stress and chronic illness.

    Nicole St. Arnaud
    23. march 2021, Alberta Canada

    This is the third of a series of blog posts on the progress in Lilian Sjoeberg’s Hope Shortcut program for chronic illness.

    You can learn more about her program here

    The inner child

    The inner child is a metaphor for you having a practical side.
    You are maybe still hurt if someone is making comments as the bullies made in your school.


    When you get an extraordinary feeling that is somewhat out of proportion with what happened, the “inner child” can still remember the past episode.


    It is never too late to get a happy ending to this episode. Never too late to get a “happy” childhood. We cannot change what happened, but we can release the feelings connected to the devastating events