Cystic Fibrosis

Cystic fibrosis is a condition that creates sticky mucus in the lungs and digestive system. This can lead to lung infections and digestive problems.

Cystic fibrosis is caused by a defect in a gene called the cystic fibrosis transmembrane conductance regulator. This defective gene causes a production of mucus that is thicker and more sticky than normal.

Symptoms of cystic fibrosis include recurring chest infections, yellowing of the skin and whites of the eyes (jaundice), irritable bowel symptoms, a persistent cough, wheezing, exercise intolerance and inflamed nasal passage or stuffy nose.

Signs of cystic fibrosis are a persistent cough with thick phlegm, wheezing, repeated lung infections, a constant stuffy nose or sinusitis, foul-smelling greasy stools, constipation and poor weight gain and growth.

Cystic fibrosis facts – One in every 25 people (2 million) in the UK carry the faulty cystic fibrosis gene and don’t even know it. Facts about genes are that they can change and alter pending our environment and our beliefs.

By 2025 the number of people with cystic fibrosis living into adulthood is expected to increase by 75%. 1000 new cases of cystic fibrosis are diagnosed each year. More than 75% of people with cystic fibrosis are diagnosed by age 2. More than 50% of the cystic fibrosis population are aged 18 plus.

Cystic fibrosis is tested for at birth, with the majority diagnosed by aged 2. Some people however, aren’t diagnosed until they are adults.

Cystic fibrosis is diagnosed by screening at birth, this is diagnosed via a sweat test to measure the amount of salt, if this comes back abnormally high they will receive a positive diagnosis.

People with cystic fibrosis can be expected to live to around the age of 44 years old, but new studies are showing that this age is increasing.

Cystic fibrosis genetic testing involves looking at a persons DNA to see if they are carrying the CFTR gene.

Treatments for cystic fibrosis vary from pharmacuetical drugs, lung transplantation, a healthy diet and psychophysiological approaches.

Hypnotherapy can be used for cystic fibrosis as the lungs, breathing and digestive track are all controlled via the autonomic nervous system (ANS). The ANS works subconsciously outside of our awareness to maintain our health and wellbeing. Hypnotherapy targets subconscious processes to affect a change, therefore it may be highly beneficial for cystic fibrosis treatment.

Cystic fibrosis could be argued as a state of hypnosis, the condition is maintained subconsciously by the autonomic nervous system (ANS). Therefore, hypnosis may be used to change the informational flow within the body. This is theoretically possible, as genes have been shown to change pending our beliefs and environment.

Cystic fibrosis is a genetically inherited disease that affects the content of water and salt found in the body’s cells. People born with cystic fibrosis carry this condition with them for their whole lives, and it can severely affect their digestive system, lungs, and other major organs of the body, making simple, everyday tasks more difficult. However, there is much that can be done to reduce the often debilitating effects of this disease. 

This audio production is designed to help the listener with managing the symptoms of cystic fibrosis. By clearing negatively charged Emotional Memory Images from your external screen, your mind and body are able to adapt to the present moment, helping you to better cope with the symptoms of cystic fibrosis. This audio is your own personal 1 to 1 session with Matt, always available at your convenience.

Matt’s calming, assuring voice gently guides both your conscious mind and unconscious mind towards transformation through the left and right ear respectively. By tapping into the body’s psychoneuroimmunilogical mechanisms – the link between the mind, nervous system and physical wellbeing – this audio helps your mind to relax and control your reactions to the symptoms of cystic fibrosis.

For best results, listen to this audio download first thing in the morning or during the day, every day for 4 weeks. Ensure you’re free from interruptions and distractions when listening. Download now to start managing cystic fibrosis today.

This audio is a .MP3 file, compatible with smartphones, tablets, PC’s and other electronic devices.

Audio length: 30 minutes.