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.

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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
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