Author: katrin.feichtinger

Parkinson’s disease symptoms
Blogpost
4. July 2022 7 minutes
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Parkinson’s disease: from the first symptoms to diagnosis and therapy

Parkinson’s disease symptoms are very diverse. They begin with trembling of the hands and extend to complete blockage or the complete freezing of body parts. Parkinson’s disease is therefore also known colloquially as shaking paralysis. The neurodegenerative disease progresses very slowly and usually appears after the age of 50. What are the early symptoms? How does the disease progress? And what therapies are available? – You can find out all about this in this blog post.

 

The development of Parkinson’s disease – what happens in the body?

When suffering from idiopathic Parkinson’s (without discernible cause), the dopamine-producing nerve cells in the mesencephalon (substantia nigra) slowly die. The reason for this is still unknown. The falling dopamine level in the brain results in impaired communication between nerve cells and an imbalance of neurotransmitters. The body can compensate for this deficiency sufficiently for quite some time so that it goes unnoticed by the patient. The first typical symptoms occur once approximately 60 % of dopamine-producing nerve cells have died. It is hypothesized that this causes the shaking (tremor) that is so typical for Parkinson’s disease.

Four male figures in drawing showing major symptoms of parkinsons desease

Nonspecific early symptoms of Parkinson’s disease

Even years before apparent symptoms appear, there may be unspecific symptoms indicating Parkinson’s:

Changes in dream phases: Usually, the body is limp while we dream, almost as if paralyzed. It has been shown that years before Parkinson’s was diagnosed, patients would actually perform the actions they dreamt of (talking, laughing, gesturing).

  • Sense of smell might be reduced or disappears completely.
  • Inexplicable joint pain, especially in the arms
  • Interference with color perception
  • Change in handwriting: The longer the patient writes, the smaller and more illegible the writing becomes.
    Depression, fatigue, exhaustion
  • Unspecific digestive issues
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The most common symptoms of Parkinson’s disease

Slowness of movements (bradykinesia):

The patient’s movements become slower and the range of motion decreases (hypokinesia), which may worsen to total loss of motion (akinesia). Both voluntary and autonomic muscle control may be affected. All movements are unnaturally slow. The posture is stooped, steps are small, and/or patients scuttle or shuffle when they walk. Starting or stopping a movement is also difficult. Sudden stopping of a movement, so-called “freezing“, occurs frequently. This increases the risk of falling. Facial expressions and gestures are reduced; laughing and crying seem delayed and look like a grimace. The face seems to become an unmoving mask. The abilities to speak and swallow may also be affected. Fine motor function worsens: manipulating buttons or opening/closing zippers becomes difficult; writing becomes illegible; brushing teeth becomes impossible.

Reactions and accompanying movements are also affected. The patient doesn’t move his or her arms when walking or simply “falls” into a seat due to poor balance. Parkinson’s disease also reduces the speed of thought processes.

 

Stiff muscles:

Parkinson’s disease increases muscle tone, causing the body to become stiffer. Both contracting and stretching muscles may be affected. Deliberate relaxation is not possible. Passively moving parts of the body results in the so-called “cogwheel” phenomenon. The muscles relax in bursts, like a cogwheel. Typical for this stiffness of the muscles is the “floating pillow” sign. When the patient lies down on their back, they cannot put their head down. The muscles are so tense that the head seems to “float” above the pillow.

 

Shaking (tremor):

When relaxed, arms or legs may shake. One half of the body is often more severely affected than the other. Shaking usually occurs in the hands and arms.

 

Insufficient stability of posture (postural control):

Righting and postural reflexes are continuously and unconsciously correcting the position and posture of our body. This balancing process prevents falls. In patients with Parkinson’s disease, the righting and postural reflexes are interrupted. Patients struggle to remain upright. Sudden, unforeseen changes in movement can no longer be countered and corrected in time. Their gait becomes insecure, and they tend to fall more often.

 

Other symptoms:

Patients may also have difficulties swallowing or suffer from incontinence, insomnia, depression, and dementia. Hallucinations, delusions, and paranoia often accompany dementia.

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Does Parkinson’s start in the intestines?

It is becoming more evident that the nervous system in the abdomen is closely linked to the brain. Animal studies were able to show that incorrectly shaped proteins (alpha-synucleins) form in the digestive tract and can spread along the vagus nerve into the brain. Whether Parkinson’s actually starts in the digestive tract and the consequences for treatment options remain open at this time.

 

How is Parkinson’s disease diagnosed?

Parkinson’s disease is often diagnosed based on its typical symptoms. The severity of the disease is assessed based on the Hoehn and Yahr Scale, amongst others. It records the disruption of movements. The Unified Parkinson’s Disease Rating Scale (UPDRS) is another standardized tool for recording clinical symptoms.

Physicians and therapists may perform additional active and passive movement tests to get a clearer picture of the disease presentation and progression:

  • Quick movements like screwing in a lightbulb are no longer possible (dysdiadochokinesis).
  • Passive movement, such as of the elbow joint, results in the cogwheel phenomenon, i.e. the relaxation of muscles in short bursts.
  • Tests to check balance and posture stability are also performed (Berg Balance Scale, Timed Up and Go Test).

Imaging technology such as CT or MRI can be used to exclude other diseases with similar symptoms.

If Parkinson’s is suspected but not confirmed, specific medication can be used to clarify the diagnosis. If the symptoms improve with medication, the patient likely has Parkinson’s. If no change is observed, there may be other causes for the Parkinson’s-like symptoms (secondary or atypical Parkinson’s syndrome).

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Therapy options for Parkinson’s disease

Treatment for Parkinson’s disease must be tailored to the individual patient. Good success can be achieved with medication, physiotherapy, occupational therapy, speech therapy, and psychological support.

 

Medication

The goal of medication is to reduce the lack of dopamine in the brain. The neurotransmitter is either administered directly as medication or the breakdown of existing dopamine is inhibited. The active agents used depends mainly on the age of the patient. The goal of medication is symptom reduction.

 

Deep Brain Stimulation, DBS

If certain conditions are met, deep brain stimulation may be the method of choice for treating the symptoms of Parkinson’s. In a surgical procedure, small electrodes are implanted into certain areas of the brain. The so-called “leads” generate electrical impulses that control abnormal brain activity.

 

Non-medication based treatment

Physiotherapy, occupational therapy, speech therapy, and psychological support are essential parts of treating Parkinson’s. Interdisciplinary cooperation of different therapeutic and medical disciplines can considerably alleviate symptoms.Physiotherapy knows several techniques to improve agility, balance, coordination, strength, and endurance. Technology-based therapy equipment can supplement other treatments.

When living with Parkinson’s disease, independent practice, continued participation in daily life, and support through therapeutic aids can improve the quality of life of patients. The goal is to maintain the independence of the patient in everyday situations for as long as possible.

 

Good to know

Every year on April 11, World Parkinson’s Day takes place.
The aim of World Parkinson’s Day is to create greater awareness of this disease and the living situation of those affected and their relatives.

Aphasia – Lost for words
Blogpost
6. June 2022 5 minutes

Aphasia is a speech disorder. It is caused by damage to the brain or the brain areas which are responsible for speech control, speech comprehension, and non-verbal aspects of speech.

Aphasia mostly occurs following non-progressive cerebral damage, as with a stroke. An acute new speech disorder is one of the main symptoms (FAST principle) for a stroke.

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Types of aphasia

 

Broca aphasia mainly affects the ability to produce speech. Aphasia patients often speak very slowly, seem to take a long time to order their thoughts, or seem unable to find the right words. Any communication takes place in “telegraphic speech”: Affected patients speak in sentences containing only one or two words, often with grammatical errors. Also articulation of words (dysarthria) reading and writing are affected.

Speech comprehension is often not or only partially affected.

Many of those who are affected are impatient with the inability to express themselves or with the long-time communication needs. This can reduce verbal communication even more.

 

Patients with Wernicke aphasia often talk a lot and use words incorrectly. They do not realize that their speech lacks coherence and meaning.

Patients also struggle to understand others, to read, and to write. Sometimes, this means verbal communication is impossible. Non-verbal communication is possible to a certain extent.

Affected patients often respond to their surroundings with severe incomprehension. They cannot understand why the person they are talking to cannot understand them.

 

Amnesic aphasia mainly affects the ability to find the rights words. Speech comprehension, reading, and writing are usually only moderately affected. Communication with the patient is reasonably easy.

 

Severe strokes affecting the middle cerebral artery (Arteria Cerebri Media) can cause both expressive and sensory aphasia, resulting in a complete loss of both the ability to speak and to understand speech. Affected patients use many automatisms, repeat phrases over and over, or speak little to not at all. Reading, writing, and body language are also affected.

This makes communicating with stroke survivors affected by global aphasia extremely difficult and requires patience and empathy from those involved.

Diagnosis of Aphasia

Speech disorders often occur in connection with a stroke. If there is no obvious cause for a speech disorder, it is necessary to exclude other possible reasons (deafness, etc.).

 

Parameters for diagnosing speech disorders

  • Spontaneous speech: How many words are used? How fluent is the speech? Does the patient hesitate?
  • Repetition: Is the patient able to repeat complex grammatical structures?
  • Comprehension: Does the patient identify the named objects? Are they able to follow simple or complex instructions? Is the patient able to answer simple or complex yes-or-no questions?
  • Naming objects: Patients often paraphrase (using phrases such as “the thing you use to tell the time” instead of “clock”).
  • Reading and writing: The abilities to understand written words, to spell correctly, and to write from dictation are assessed.

 

Standardized aphasia tests are carried out to diagnose aphasia.

Two elderly people, a couple, sit and rest

Prognosis and treatment for aphasia following a stroke

The prognosis depends on the degree of cerebral damage and on the severity of the disorder. Other important factors are general health, co-existing symptoms, and motivation.

It is possible that aphasic symptoms disappear by themselves within the first six months of a stroke. Speech therapy supports the reduction of speech disorders and improves the expression and comprehension of speech.

The sooner the patient starts therapy and the more regular the sessions, the better the prognosis. Goal of the therapy is to reactivate verbal communication.

 

Interacting with people suffering from aphasia

Aphasia, such as triggered by a stroke, does not primarily affect mental abilities. It is a speech disorder, not a mental disability. The difference is key when interacting with patients affected by communication problems.

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How to better communicate with aphasia patients

 

SPEAKING

  1. Create a calm environment.
  2. Speak calmly, not too fast, but normally and at a normal volume.
  3. Use short sentences. Small pauses between sentences can help the other person to understand you better.
  4. Use more non-verbal signals. In addition to tone, facial expressions, and body language, writing and images can help affected patients follow to the conversation.
  5. If the other person does not immediately understand you, try rewording.
  6. Where possible, use yes-no questions instead of open questions.
  7. Have one-on-one conversations, as patients with aphasia find personal conversations easier than group discussions.

 

UNDERSTANDING

  1. Listening means waiting: The patient needs more time to say something.
  2. Listen with your heart: Try to understand what the patient is trying to tell you.
  3. Listen beyond the language: Do not interrupt or correct all the time. Just wait, the meaning often becomes clear.
  4. Let the situation speak: Thinking ahead and carefully observing the situation will help you to understand.
  5. Try and decipher the meaning of a statement together with the patient. Be aware of non-verbal communication.
  6. In the case of perseverating repetitions interrupt and distract.
  7. Don’t give up! Use the key phrase: “We’ll figure it out together – start again!”
  8. Hyperfocusing does not work! If needed, use the key phrase: “Maybe you can tell me later.”

 

Antonia – Traumatic Brain Injury

Patient Stories
23. May 2022 4 minutes
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Patient Story: Life and sport after TBI

“We all only have one life, and we should use it.”, says Antonia, 27 years from Munich, starting the conversation. At the age of 18, she suffered a traumatic brain injury (TBI). She spent around 1½ years in the hospital. Read our article, to find out how she is doing today and her recipe for staying positive.

 

Back to life after a TBI

At the end of 2012, Antonia fell out of a window from a height of about 65 feet onto cobblestones. She suffered a traumatic brain injury, numerous internal hemorrhages, a bilateral pneumothorax, multiple upper and lower leg fractures, multiple pelvic fractures, and coccyx, cheekbone, and orbital fractures.

“The prognosis is poor. If she wakes up, it is possible that she will stay in a vegetative state. It may be that she will no longer speak or recognize friends and family and will no longer be able to stand or run. She might not survive the next two months.”, Antonia´s family was told after the accident.

Antonia proved them wrong. Six weeks after the accident she gradually woke up from the coma.

“All over the room, we arranged pictures of Toni with her siblings, family, and friends, to fetch her back to life. When we were picking the pictures, we noticed that there was not a single picture of her where she was not laughing. She is a cheerful soul.”, says Antonia’s mother in the interview.

Ten weeks after the accident she slowly recovered consciousness. “At first I wasn’t sure whether I was still dreaming or already awake.”, says Antonia about the initial period after the coma.

 

Rehabilitation after TBI

Toni, as she is called by her family, surprised doctors and nurses time after time with new progress. For a long time, it was uncertain whether she would be able to see from her left eye, which had been severely damaged. “I had to close my healthy eye and count the number of fingers the doctors and therapists held up, so that they would believe me when I said I could see again.”, laughs Antonia today.

Toni’s social environment was her biggest source of support during her time in the hospital. Every day she was visited by at least one family member. Her friends took turns, making sure that Antonia was regularly with the people most important to her for 1½ years.

Now, around nine years after the accident, Antonia can walk, speak, and follow an almost normal everyday life. She still has a left-side hemiparesis, causing limited movement in her left hand and leg.

 

Gait training after TBI

Antonia’s physical therapy includes regular sessions at the Centre for Hand Therapy and Ergotherapy Laborn in Munich with robotic rehab equipment. She primarily uses Amadeo and Lexo for her rehabilitation.

She is especially delighted by the gait trainer Lexo: “I love being able to feel speed and physical strain again on the Lexo. The flow feels almost like jogging!”

Antonia Issels trains on the gait trainer Lexo

Lexo offers her the advantage of being able to walk faster than what would be possible without support. As a result, the brain receives new stimuli and begins to rebuild the nerve pathways needed for walking at different speeds. This adaptability of the brain is called neuroplasticity.

The guided sequence of movements on the Lexo enables Antonia to move with an even gait. “Lexo is sort of a guide for my brain. This way it relearns a natural walking rhythm. It feels incredibly good,” says Antonia enthusiastically.

Besides her rehab program, Antonia studies social work and runs the Instagram channel sportmithandicap.

Werner David G. – Multiple Sclerosis

Patient Stories
25. April 2022 4 minutes
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Patient Story: How Multiple Sclerosis (MS) gave me new meaning in life

Werner David W. from Graz, Austria is a qualified primary school teacher and children’s book author. And he has Multiple Sclerosis – approximately since he was ten years old.

In an interview, Werner David told us how the disease has changed his life, about the new vocation he has found as a result of his MS diagnosis, and how he integrates robotic technology into long-term rehabilitation.

Werner David W. from Graz, Austria holding a book in his hands

New vocation as a children’s book author

The children’s book “Wilfried, der einsame Stern” (Wilfried, the Lonely Star) was a way for Werner David to give his feelings a meaningful outlet. “Because of the MS disease I often felt very lonely. I then asked myself what is the loneliest thing in the universe. A star is so far away from everything, that must be the loneliest thing.“, Werner David said in an interview about the origin of his book.

The children’s book is a touching story about friendship and loneliness which aims to show children that loneliness doesn’t always have to be a bad thing.

Werner David W. from the back sitting in front of a group of children reading from a book

The disease with a thousand faces

Talking to Werner David, it becomes clear that has been through a lot. He was diagnosed with MS at the age of 18, but he had likely already been suffering from the chronic inflammatory autoimmune disease for several years.

Like other autoimmune diseases, MS causes the body to turn against itself. The immune system attacks the body’s own structures and destroys them as if they were harmful pathogens. As a result, the brain can no longer transmit movement impulses to the body, or they cannot be transmitted correctly.

People with MS experience paralysis, loss of coordination, or painful muscle cramps, among other things. MS typically takes a relapsing remitting form. The degree of disease activity is different for each patient. It is for this reason that MS is also referred to as the disease with a thousand faces.

 

Robotic equipment in long-term treatment of MS

In Werner David’s case, the disease mainly affects his lower limbs. He has been in a wheelchair for ten years.

Robotic equipment like the OMEGO Plus helps him with his rehabilitation. During inpatient as well as outpatient therapy, he often uses the bicycle function: “Even though I can no longer move my legs myself, the assistive therapy on the Omego Plus allows me to ride a bike again.”

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Therapy for foot drop

Werner David also uses the foot lift function on the Omego Plus in his therapy to address foot drop. Even though he is in a wheelchair, the training provides health benefits for him.

By mobilizing his legs and ankles with Omego Plus, he is able to:

  • train his endurance
  • prevent muscle atrophy
  • stimulate cardiovascular system and metabolism
  • preserve mobility
  • build muscle strenght
  • improve joint care
  • reduce risk of thrombosis

In addition, the areas of the brain that are responsible for controlling the movement are specifically stimulated.

A red round graphic with a angry face

Don’t let negative thoughts get the upper hand

During difficult periods, it helps Werner David to focus on what’s going on in his thoughts when they’re going round and round: “It’s not about always thinking positively. That’s simply not possible. Negative thoughts come up from time to time. It’s important to accept negative thoughts and not allow them to take over. That way, I always find my way back to a positive attitude to life.”

 

We wish Werner David continued success with his rehabilitation and look forward to many more great children’s books!

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Author: Michaela Partel

 

Sources:

Website Werner David Wiechenthaler

Images: Werner David Wiechenthaler

Multiple Sclerosis
Blogpost
11. April 2022 6 minutes
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Multiple Sclerosis – How the autoimmune disease turns life upside down

Repeatedly twisting an ankle, tingling or numbness in one arm or leg, great fatigue throughout the day or blurred vision can be symptoms of multiple sclerosis (MS).

Multiple sclerosis (Encephalomyelitis disseminata) is one of the most common neurological disorders. The typical age of onset is between 20 and 40 years old. An MS diagnosis raises many questions for patients as well as for their relatives. This article tries to provide some answers.

 

Causes of MS

MS is a chronic inflammatory autoimmune disease. The immune system attacks the body’s own cells in the patient’s brain and spinal cord.

Despite worldwide research, the causes of MS are not yet clear. Classical MS theory assumes that three factors cause the condition to manifest:

  • Genetic predisposition: Approximately 15% of MS patients have immediate or extended family members who were also diagnosed with MS
  • Environmental influences in childhood: Viral infections (e.g. Epstein-Barr virus) or vitamin D deficiency
  • Trigger event in adulthood: It is not yet absolutely clear what such a trigger event might be. In most cases, emotional stress precedes the first acute episode of the disease.

There is a consensus in the scientific community that complex interactions of environmental, genetic, and epigenetic factors are the probable cause for onset of the disease.

What are the symptoms of MS?

The symptoms are varied and manifest differently in each patient. This is why MS is also called the “disease of a thousand faces”.

There are different types of MS. In most cases (85–90%), the disease is intermittent-relapsing.

Neurological symptoms appear relatively suddenly, subside over several weeks, and often regress completely.

MS is not always diagnosed immediately. A diagnosis may take years.

As the disease progresses, symptoms may not regress completely after an acute episode, leaving residual impairments. The condition can become chronic, and symptoms may gradually worsen over time.

In rare cases (10–15%), the disease progresses from onset. This form has no distinct acute episodes.

The symptoms vary depending on the areas of the brain and/or spinal cord affected by inflammatory lesions. Some possible symptoms include:

  • Optic neuritis (inflammation of the optic nerve) – Common first symptom; deterioration of vision, usually in one eye; foggy or hazy vision; pain may occur.
  • Paresthesia Common first symptom; sensory impairments such as tingling, tightness around joints, numbness; often described as a sock-like or glove-like sensation; difficulty sensing temperature.
  • Ocular motility disorder – e.g. double vision; nystagmus (uncontrolled horizontal or vertical eye movements).
  • Paresis (weakness) / plegia (paralysis) – Initial mild weakness, such as “tiredness” in an arm or leg; frequent ankle twisting or joint stiffness; paralysis is rare in early stages.
  • Coordination Problems– Often develop during the disease course; e.g. vertigo, loss of balance, tremors.
  • Vegetative dysfunction – Changes in bladder function, frequent urinary tract infections, sexual dysfunction, altered sweating.
  • Psychophysical symptoms – Fatigue (abnormal fatigability), marked exhaustion that improves with rest.
  • Psychological changes – Cognitive impairment, such as reduced attention or cognitive performance; depression.

MS has many faces:

  • Appoximately1/3 of patients with MS experience no significant impairment throughout their life.
  • Approximately 1/3 of patients with MS experience limitations that interfere with everyday activities. Living a normal life is mostly possible (e.g.: professional occupation, family planning).
  • Approximately 1/3 of patients with MS experience significant impairments (e.g.: inability to work, loss of ability to walk).
Picture of a group of people while training on a mat

How is MS diagnosed?

Preparing a detailed medical history and good patient documentation are critical for diagnosing MS.

If MS is suspected, the suspicion can be verified by taking a sample of cerebrospinal fluid from the spinal canal or with the help of an MRI.

 

Drug therapy for MS

During an acute episode, cortisone therapy can help to shorten the episode and reduce its consequences.

Options for long-term therapy depend on the form of MS. Various medications are used to influence the immune system. The immune system is either suppressed (immunosuppression) or influenced (immunomodulation). An effective immunotherapy can have a significant positive impact on the progression of the disease or the impairment caused by it.

 

Rehabilitation and conservative MS therapy

Rehabilitation for MS patients is designed to help preserve physical, social, and/or occupational skills. The treatment options are as varied as the symptoms of the condition itself. Physical and occupational therapy, speech therapy and psychotherapy can help patients to cope with everyday activities.

Rehabilitation goals:

  • Preserving or improving functional capabilities
  • Promoting independence and mobility
  • Promoting and maintaining involvement in family life, social environment, and work
  • Preventing and/or treating possible deficits caused by MS
  • Alleviating psychological changes
  • Reducing the amount of care required

An essential part of outpatient therapy is an active lifestyle – whenever possible. Studies show that physiotherapy increases patient mobility and muscle strength, reduces fatigue, and improves the quality of life.

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Young artist sitting in a wheelchair and painting a picture

Living with MS

Accepting the diagnosis and learning to develop strategies for new daily routines will help patients keep control and maximize independence.

Deliberate “disease-free” time spent with friends, outdoors, or engaging in a hobby can help individuals to see themselves as persons rather than patients. However, this may be easier said than done. Conversations with other patients (e.g. in self-help groups) or psychotherapy may be helpful.

Physical activity, in particular, is important for maintaining skills and physical awareness. Nevertheless, it is also important to accept one’s own limits. Too little, but also too much activity can have an adverse effect on the progression of the disease. Try to find enjoyable activities that are within your physical capabilities.

It is important that family and other people in the patient’s environment are open regarding MS. Relatives too are often overwhelmed by the diagnosis. Talking to each other about the uncertainties and the challenges can prevent misunderstandings.

Every patient develops his or her own strategies when living with MS.

Neuroplasticity – How learning and rehabilitation work
Blogpost
28. March 2022 4 minutes
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Neuroplasticity – How learning and rehabilitation work

The human nervous system consists of the central nervous system and the peripheral nervous system. The brain and spinal cord form the central nervous system. As “conductors,” the nervous system orchestrates everything happening in the human body.

 

How our brain, spinal cord, and body communicate

The peripheral nervous system extends throughout our bodies like a network. It acts as a “scout” and reports external information to the spinal cord and on to the brain. Simultaneously, it forwards instructions from the brain through the spinal cord to the arms, legs, and other parts of the body. The nervous system and the body are in constant communication, using electrical signals.

The following are examples of how the central and the peripheral nervous systems work together:

  • Our skin contains cells that are part of the peripheral nervous system. They send information via the spinal cord to the brain, such as the ambient temperature. When the brain receives the information “it’s hot,” it activates the sweat glands to cool the body down. When it gets the information “it’s cold”, it triggers muscle contractions to heat the body through shivering.
  • Our nose is also part of the peripheral nervous system, detecting smells. The brain identifies the smell and reacts accordingly. Based on previous experiences, the smell of fresh cake stimulates our appetite.

 

Brain plasticity or how we learn

Imagine our brain and spinal cord like a network of roads – some are used all the time, and some are hardly used at all. Motorways form the busiest roads. Routes seldom used fall into disrepair and become narrow paths with a cracked surface.

After a neurological injury, we need to start using the narrow paths more often to turn these into motorways. Slowly but steadily, the human brain and spinal cord start to improve these paths and create new motorways.

In neuroscience, the term “plasticity” refers to the brain’s and spinal cord’s ability to modify its cells’ architecture, structure, and function. The brain and spinal cord are adaptable like plastic. Hence the term “neuroplasticity”.

Do you remember what it was like to drive a car for the very first time? Placing the clutch, selecting a gear, looking over your shoulder to keep an eye on traffic – all of that can be very overwhelming. After gaining experience over time, driving happens virtually automatically. This is neuroplasticity at work!

 

How the brain and spinal cord change

Neurogenesis – continuous formation of new nerve cells (no matter the age!)

New synapses – new experiences create new nerve cell connections

Enhanced synapses – frequent repetition and practice strengthen nerve cell connections

Weakened synapses – unused connections become weaker or even inactive

Picture of a male child playing with plasticine

Using the neuroplasticity principle in the rehabilitation process

A stroke, a traumatic brain injury (TBI), or a spinal cord injury (SCI) cause damage to some brain regions or to the spinal cord. To return to the metaphor: the neurological damage causes road closures. Depending on which brain or spinal cord areas are affected, either the roads from the brain to the body (efferent nerve fibres) or from the body to the brain (afferent nerve fibres) become hard to navigate. The results are paralysis, spasticity, and/or perceptual disorders.

Learning and training change the brain and spinal cord. The nervous system looks automatically for new routes if one road is closed. The more frequently we use these new roads, the broader they get, and the more navigable they become.

After a stroke, movement of the fingers may be limited. Targeted training during rehabilitation may stimulate new and/or improved connections to form. Improved neuropathways may make it possible to move the fingers once more.

This phenomenon is well known by musicians. Research has shown that in players of bowed instruments, the areas in the cerebral cortex controlling finger movements are larger than in individuals who have never learned to play an instrument. Practice makes perfect! This training principle applies to rehabilitation as well.

Neurological damage can feel final. But they may not be. Depending on the severity of the injury or disease, the nervous system can change and adapt.

Talk with your physician about the possibility of improved function via neuroplasticity after neurological damage or disease.

Author: Michaela Partel

 

Sources:

Annunciato, N. (2021). Training: Plastizität des Nervensystems. Vienna: Physiozentrum für Weiterbildung

De Gruyter, W. (2017). Pschyrembel. Klinisches Wörterbuch. 267th edition Berlin / Boston

Nowak, D. (2011). Handfunktionsstörungen in der Neurologie. Würzburg: Springer Verlag

Principles of Experience-Dependent Neural Plasticity: Implications for Rehabilitation After Brain Damage, 2008

De Marées, H. (2003). Sportphysiologie. Köln: Sportverlag Strauss

Increased Cortical Representation of the Fingers of the Left Hand in String Players, 1995

Patient Motivation: The role of health data
Blogpost
14. March 2022 4 minutes
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Patient Motivation: The role of health data in physical and occupational therapy

Patients often experience multiple side effects as a result of a stroke or traumatic brain injury (TBI). In addition to the physical limitations, the health event can alter a patient´s life forever.

That realization can be hard to accept. Not surprisingly, many post-stroke patients struggle emotionally with problems like low self-esteem and lack of hope. They can also feel lethargic and unmotivated. A very high percentage of stroke survivors faces mental health crises, like depression and anxiety.

With these barriers in mind, how can physical and occupational therapists motivate their patients to keep moving forward in their recovery?

 

Health Data is the answer

Data is increasingly becoming the heart of everything we do — and healthcare is no different. Objective data from rehabilitation technology can help doctors and therapists to adapt the therapies according to the patients progress.

Numbers foster motivation and can generate hope in patients. By seeing daily or weekly improvements, patients tend to perform more exercise repetitions and exert more effort.

All Tyromotion devices include TyroS, a sophisticated therapeutic software developed by and together with therapists. TyroS uses gamification and data to help patients in the following ways:

 

1. Make Therapy Fun and Engaging

Games like Pac-Man and Asteroids have remained popular for a reason. Gaming harnesses our intrinsic desire to perform and reach higher goals. Competition, even with oneself, can be a critical motivator, and it fits perfectly into the rehabilitation environment.

Gamification of therapy takes otherwise dull and mundane tasks and makes them fun and engaging. For instance, patients are encouraged when they receive positive feedback or when they beat their own high score.

In addition to the instant feedback of gaming, therapists can share a more global picture of progress. Daily, weekly or monthly analytic reports help patients further visualize their achievements.

Since advanced rehabilitation technology is software-based, grading treatment plans is simple. Therapists can start with easier exercises and develop personalized programs based on patient ability and progress.

These devices also allow patients to move through therapy at their own speed. When a patient is ready, the therapist can increase the difficulty of each task to fit the client’s individual needs. Grading can also help the therapists to ‘push’ patients on by increasing the difficulty.

Graphic of a male doctor from the back standing in front of a data sheet

2. Visualize Progress

Re-learning to walk or performing certain daily tasks is often a slow and frustrating process. That’s why physical and occupational therapists need every tool possible to keep patients engaged. In addition to the gamification of therapy, sensor-based devices can provide helpful feedback that can inspire patients.

Sensor technology acquires patient information that is not necessarily visible to the naked eye. Therapists can draw from this data to plan and evaluate the therapy process.

By sharing numbers and infographics, practitioners can better communicate with patients. These snapshots of incremental progress help patients recognize what they can’t see in real-time. This can give hope when hope feels lost and inspires patients to persevere.

Whether through a graph, a bar chart or numbers alone, helping people visualize their progress can be a powerful motivator. According to a study, “a patient’s perception of therapy, in terms of its relevance to daily needs, the perceived potential to reduce disability and improve quality of life play a role in motivation.”

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3. Relearn Activities of Daily Live (ADLs)

Sensor-based technology is helping patients of varying impairments relearn the so-called activities of daily living like dressing or feeding. Tyromotion’s sensor-enabled devices, including Pablo , Pablo Lower Extremity and Tymo, provide meaningful data that measures:

  • Overall movement
  • Limb flexion and extension
  • Exerted force
  • Gait parameters
  • Asymmetries in gait patterns
  • Stability and coordination

Neurological events such as stroke or traumatic brain injury can take away a great deal from the affected person. Data and gamification can help to increase motivation and redirect focus in a positive way.

Progress, whether slow and steady or rapid, is a step forward in recovery. Data offers objective markers that can provide hope and inspiration to patients as well as ultimately lead to better outcomes.

 

Sources:

Emotional & Behavioral Effects of Stroke

Design strategies to improve patient motivation during robot-aided rehabilitation (2007)

Advanced Rehabilitation Technology: Hope to pediatric Patients
Blogpost
28. February 2022 6 minutes
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Advanced Rehabilitation Technology offers Hope to pediatric Patients

Over the past decade, the rehabilitation sector has made great strides in incorporating advanced technologies into the pediatric rehab environment. This includes designing adjustable devices to offer the benefits of advanced rehabilitation technology to even the smallest of patients.

Pediatric pricture of a patient using a Tyromotion device and playing a game with tyroS

Benefits of advanced rehabilitation technology include:

  • High dose repetitions: Rewiring brain to create new neural connections is possible, thanks to neuroplasticity. By circumventing the damaged areas, patients can develop alternative neuropathways that can make correct movement easier. Therapy using advanced rehabilitation technology provides the high dose repetitions pediatric patients need to strengthen those pathways.
  • Makes therapy fun: With interactive games and virtual reality, advanced rehabilitation therapy devices can hold a child’s attention. Instead of repeating monotonous movements, children have fun during therapy. Patients race a car, shoot balloons or harvest apples and still make progress in therapy. The movement may be the same, but the child will consider it a time of play.
  • Real-time feedback: Advanced rehabilitation therapy devices provide real-time feedback. This can help therapists to determine when to increase the difficulty of their exercises and challenge the child to do more. Additionally, children are eager to beat themselves from session to session.

Advances and benefits of technology-based therapeutic devices allow pediatric patients with cerebral palsy, stroke, or spinal cord injury, to make great progress during rehabilitation.

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A female therapist and a young male patient in a therpy room. The child has a happy face and wearing a face mask

Helping Cerebral Palsy Patients with ADLs

One of the most common pediatric motor disabilities, cerebral palsy (CP), causes patients to struggle with activities of daily living (ADL). Walking, eating, or dressing can be problematic.

Whether from prematurity, low birth weight, or in-utero stroke, CP almost always requires a child to undergo years of neurological rehabilitation.

The goal of therapy is to allow children to participate in family, community, and educational environment as much as possible.

Cerebral palsy can limit upper extremity control and cause Ataxia (lack of muscle control or coordination). The limitations that come with the inability to control arms, hands, or fingers can complicate ADLs. Some children with CP also struggle to synchronize small muscles and perform tasks such as holding a key or grasping a handle.

The more a child practices, the better he or she will get. This is also true for fine motor skills. Advanced rehabilitation devices make it for children easier to stick to monotonous tasks.

Myro includes real-life objects and offers the possibility to train press-, pull- and rotation-movements as well as cognitive abilities. While playing, children expand their range of motion (ROM), motor function, and strength. These movements also help stimulate the brain and reinforce new neuropathways.

Children with CP may also have trouble maintaining balance, posture, and coordination. Many require gait therapy to improve postural control, loading symmetry, and weight shifting while limiting compensation. Sensory devices like Tymo and robotic gait trainer like Lexo provide children support during gait therapy.

Especially in the therapy with children, motivation is crucial. The playful approach, fostered by advanced rehabilitation devices, help to keep motivation level high during therapy.

A male child in a therapy room using the interactive rehabilitation device Myro and a therapist standing by his side

Benefits to pediatric Stroke Patients

Pediatric stroke is relatively rare – affecting approximately 25 out of every 100,000 newborns and 12 out of every 100,000 children under 18 years of age. Pediatric stroke survivors face many challenges, including hemiplegia or hemiparesis, epilepsy, or cognitive difficulties.

As these children develop and grow, physical and occupational therapies play a crucial role in expanding the limits of what the child will be able to do.

For patients with hemiplegia or hemiparesis, robotic therapy has proven effective for hand rehabilitation. A study that measured the success of robotic therapy in children with hemiparesis found “significant improvements in bimanual hand use, as well as impairment-based scales.” The participants were able to transition these skills into real-life play. This type of finding can provide hope to children with a more severe form of hemiplegia.

 

Providing Hope to pediatric Spinal Cord Injury Patients

Spinal cord injuries affect approximately 2 out of every 100,000 children. Diving into a shallow pool, sustaining a sports injury, or being involved in a car accident are the top three causes of pediatric spinal cord injury.

Unfortunately, these accidents cause potentially permanent impairments. A spinal cord injury leaves a patient needing to relearn the actions and movements that once seemed so natural. For a child or teen, this new disability can be devastating.

 

Advanced rehabilitation therapy can help. It can stop further atrophy or stiffening of muscles, depending on the location and severity of the injury. In addition, children can adapt to do things differently. Compensation strategies or re-learning of specific motor skills through neuroplastic change can help.

Interactive devices address visual, cognitive, and motor ability weakness through gaming. While children have fun, they are simultaneously participating in active rehabilitation and increasing the chance to make improvements.

The Role of Fun in pediatric Rehabilitation

Modern therapy devices allow children to train in a playful way. Therapy programs look and feel a lot like computer or console games. All of a sudden, therapy isn´t that frightening anymore. These devices prove that fun and monotonous therapy tasks can be combined.

Modern rehabilitation devices encourage a children’s natural play instincts. They practice necessary movements and have fun in therapy. Motivation increases. The children want to get better and better. Beating their own high score becomes the goal. The improvements children may see after physical or occupational therapy can instill a sense of self-confidence and foster independence.

The next few years will bring further progress in the rehabilitation of children and adolescents. This gives hope to young patients and parents.

Shoulder and hand pain after a stroke
Blogpost
31. January 2022 6 minutes
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Shoulder and hand pain after a stroke: Prevention of pain syndromes

Paralysis is a common symptom after a stroke, especially of the upper limb. In addition, sensory disorders and depression can lead to inattention to the affected arm or hand.

It is not uncommon for stroke survivors to lie on their paralyzed arm or for the affected fingers to get caught in the spokes of the wheelchair. The resulting injuries can lead to severe pain and significantly delay the rehabilitation process.

 

Pain syndromes in the hand or shoulder after a stroke

When pain symptoms begin, for example in the shoulder, the pain is usually localized to one area of the shoulder joint. If not addressed in a timely manner, it can become a severe, generalized pain.

The paralyzed hand is particularly at risk of developing permanent limitations in mobility due to pain symptoms. Here, the typical signs of inflammation such as swelling, redness and heat are initially evident. To prevent pain, the hand is moved even less and the limitation in mobility increases. A vicious cycle begins.

If pain is already occurring in the wrist or shoulder, affected patients should consult medical advice. Medications can help to disrupt the pain process.

 

How to prevent pain in the hand and shoulder after stroke

To prevent pain symptoms, correct positioning of the arm or hand affected by paralysis should be started as early as possible.

The correct positioning in the wheelchair:

  • Even for short distances, use a wheelchair table or arm support upon which the affected arm or hand can be rested.
  • Provide a soft support surface (e.g. a towel).
  • Place the affected hand palm down on the table.
  • Some individuals find that a rolled-up towel or soft stuffed animal in the affected hand to be comfortable. If the fist involuntarily closes tightly around the fabric, it might be better to choose another object or talk to your therapist about suitable support materials, like splints.
  • Make sure to sit up straight. This ensures a physiological joint position in the shoulder joint.
  • The affected hand should be positioned in the patient’s field of vision.

If you are a wheelchair user, avoid long periods of poor sitting posture as best as possible. Be cognizant of positions that put your shoulder at risk of becoming painful.

The correct positioning while lying:

Even when lying down, care must be taken to ensure that neither the hand nor arm is trapped.

  • Stretch the arm at a 90-degree angle at the side of the body.
  • The wrist should be elevated to approximately the same level as the heart to prevent blockages in the arm and ensure lymphatic return.
  • A pad under the arm can be helpful.
Graphic of a female person sitting in a wheelchair

Splints and orthoses after stroke

Splints are particularly important in the early stages after a stroke. On the one hand, they enable safe positioning of the affected hand, and on the other, they can protect the wrist during active movements. Occupational therapists and orthopaedic technicians can make splints which are individually tailored to the patient’s needs.

Orthopedic specialty markets also offer ready-made splints in various sizes.

Picture of massaging a painful hand

Exercises to prevent pain after stroke

Active or passive movement is an important factor in preventing pain in the upper limbs after a stroke. In occupational therapy or physical therapy, therapists assist patients with specific movements. In addition, the affected arm or hand should be moved carefully outside of therapy time.

Patients can try to move the affected hand themselves with their healthy hand:

  • Move the fingers of your healthy hand and observe what movements the fingers can make.
  • Hold the affected fingers in the healthy hand and try to guide them through the observed movements carefully and slowly.
  • Move the fingers individually and then several together.
  • Movements must only ever be made in the pain-free range of motion.

As soon as you can move the fingers of your affected hand yourself, try to actively perform movements in the pain-free range several times a day.

Even if the paralyzed hand is still weak and can’t grasp yet, regular active movements help to strengthen the muscle, improve coordination, and increase sensitivity. This prevents pain syndromes.

If a patient is unable to develop strength in his/her own fingers, therapists can train the caregiver to move his/her hand passively.

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Particular care in the event of neglect

Preventive measures are more difficult when patients suffer from “neglect” as a result of a stroke. Patients with neglect ignore the affected half of the body or one half of the room. This increases the risk of injury.

If, for example, the patient sits on the neglected handtrapping it, the patient may perceive pain, but may not localize it or react to it. The hand can remain trapped for hours. This can lead to inflammation with severe swelling.

These patients in particular are dependent on support from relatives, caregivers, and therapists. Care must be taken to ensure that the positioning is closely monitored.

 

Neuropathic pain

Neuropathic pain is a nerve pain that occurs even without visible reason. The cause of this pain is associated with damage to the nerve tissue in certain parts of the brain or spinal cord. This pain is often described by patients as burning, stabbing, and shooting, but can also present as dull and pressing. It is usually excruciating pain.

If a diagnosis of neuropathic pain is made, medication is started early. Successful treatment requires interdisciplinary cooperation between doctors, therapists, and psychologists.

Injury-related pain in the upper limb after a stroke is not inevitable. Stroke patients, caregivers, and therapists should be particularly careful with the affected arm or hand in the initial period following the stroke.

Author: Hannes Aftenberger

 

Sources:

Diagnostik und Therapie komplexer regionaler Schmerzsyndrome (CRPS) (2018)

Kumar, P. (2019). Hemiplegic shoulder pain in people with stroke: Present and the future. Pain Management, 9(2), 107–110. https://doi.org/10.2217/pmt-2018-0075

How Advanced Rehabilitation Technology helps Spinal Cord and Brain Injury Patients
Blogpost
17. January 2022 4 minutes
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How Advanced Rehabilitation Technology helps Spinal Cord and Brain Injury Patients

After a Spinal Cord Injury (SCI) or Traumatic Brain Injury (TBI) devasting long-term dysfunctions may occur. Physical, emotional and financial hardships may follow. Patients are often overwhelmed by the new life situation.

Advanced Rehabilitation Technology-based devices provide patients new hope during recovery. High intensity, large numbers of repetition and a game-based approach change occupational and physical therapy settings as we know it today rapidly.

Robotics, sensors, virtual reality, and gamification allow a patient’s attention to divert away from the stress and anxiety of their health problems.

Adjustable devices offer real-time feedback to the therapist and the patient. Data from each device can be analyzed to determine when to increase the difficulty of the exercises and to challenge patients to reach higher goals.

Read on to learn more about how advanced rehabilitation devices can help SCI or TBI patients.

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Benefits to Patients with Spinal Cord Injury

Spinal cord injury is the second leading cause of paralysis in the United States. Spinal cord damage can cause a sudden loss of motor function, range of motion, sensation, and strength. Depending on the location and the severity of the damage, the patient can experience mild to moderate limitations in the legs, arms or the whole body. The damage can occur due to an accident or an illness.

While researchers hope to fully repair damaged spinal cords in the future, they haven’t yet developed that ability. In the meantime, physical and occupational therapy can help improve the lives of people affected.

There is evidence showing that activity-based-therapy can improve independence and functional ability for people with SCI. The patient may be able to relearn specific movements and regain skills to help them with activities of daily living (ADLs), such as eating and dressing.

Advanced rehabilitation devices use motor-learning-principles which can help patients to re-establish daily activities. By leveraging the brain and spinal cord’s neuroplasticity, patients can establish new neuropathways and acquire new motor skills.

 

Benefits to Patients with Traumatic Brain Injury

According to the Center for Disease Control and Prevention (CDC), traumatic brain injury (TBI) is a leading cause of disability. Each year an estimated 1.5 million Americans sustain a TBI.

TBIs can occur in many ways, including car crashes, accidental falls, violence, or assault. Regardless of how the injury occurs, patients who experience a TBI often struggle with motor, cognitive and emotional problems. Some of them last months, some years or some may last a lifetime. Statistic shows that approximately five millions TBI survivors sustain long-term neurological deficits.

Advanced rehabilitation technology can support patients in many ways during their recovery. Virtual Reality provides promising results, offering patients an highly emotionally engaging experience.

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Assessing and Building Life Skills after Spinal Cord Injury or TBI

Technology-based therapeutic devices can be used to assess and help reduce:

  • Deficits in vestibular function and balance
  • Impairments of executive dysfunction and memory
  • Abnormalities in cognition and attention issues
  • Difficulties with motor skills needed to live independently

Advanced rehabilitation technology can inspire patients with spinal cord and traumatic brain injury to persevere. From gait and balance therapy to upper and lower extremity exercises, technology-based devices push the limits of what is possible.