PERMANENT CURE TO IDIOPATHIC PULMONARY FIBROSIS USING HERBAL MEDICATION

BY DR. REIGN FRANK

Freedom from Idiopathic Pulmonary Fibrosis (IPF)

Myriad of demands of users of VITEEN Anti-Fibrosis Herbal Medication to share their testimonies and encourage others was what led to the creation of this blog. As we all know, Idiopathic Pulmonary Fibrosis (IPF) has been one of the most diseases that leads to the increase in mortality rate world-wide. In life, there is nothing like a hopeless situation when one is willing to try. This is an information guide to patients suffering from Idiopathic Pulmonary Fibrosis (IPF) and aimed to know some essential information and help them to know how herbal medicine is most appropriate to cure it. I have combined the wisdom of ancient traditions, clinical experience, and dedicated years to understand the power of healing the body through nature. Think about this, before most Western medicines are sold to humans, it undergoes all manner of testing using animals to know their reactions. This is a natural fact. When we talk about Herbal Medicine, we refer to a treatment modality using the inherent healing properties of plants as medicine.  Our search for light begins when we get fed up with gross darkness. Most of these pharmaceutical drugs do not carry the desired properties that would give a satisfactory flow from the hopper to the die cavity of tablet presses.

The parts of the plant used include roots, seeds, leaves, flowers, stems and indeed the whole plant depending on the herb. Active ingredients found in herbs are supported by synergistic actions of all its other chemical constituents. This synergy allows the herb to exert its therapeutic affects and at the same time remove the potential for unwanted side effects. Herbs are medicines with many actions available in a single plant. Increasing incidence of Adverse Drug Reactions (ADRs) is the key growth driver. ADR imposes a substantial burden on healthcare systems and is one of the prominent causes of morbidity in developed countries. It's well known that as days turn into weeks, weeks into months and months into years, the western medications have been associated with myriad of side effects than good. Instead of looking for ways to get rid of these, they end up increasing the amount of the dose that reaches the brain thereby making the brain less effective. 

However, some people still buy into the belief that modern treatments are more effective, because these are what had been inculcated into their minds by Our western doctors and of which they have numerous side effects and are incompatible with patients' current conditions which destroys their system the more. So many people out there have been discouraged from ''natural medicine'' These doctors have raised fear and apprehension to enslave humans in the chains of chemical known drugs. Most Idiopathic Pulmonary Fibrosis patients have lived in there fears for decades. It has denied them the true love of mother nature through HERBS that comes with no side effects.

In a statement of one famous Doctor by name: Dr. Alan Greenberg, MD who is a retired physician said that: unless you are in a serious accident your best chance of living to ripe old age is to avoid doctors and hospitals and learn nutrition, herbal medicine and other forms of natural medicine. Almost all drugs are toxic and are designed only to treat symptoms and not to cure anyone. Most surgery is an accessory the sooner you learn this the better off you will be. 

I must let you know that western healthcare system is completely dysfunctional by its design and function. The system is built with human sickness or diseases in mind not actually you. This has been the sole reason they resort to medications and surgery not considering the side affects it causes to your health. If this makes you feel sad, it is actually a statement of reality. 

There is No to keep swallowing pills when natural medicine can help. Liberate yourself from the shackles of pharmaceutical medications. And use natural herbal medicine like VITEEN ant-fibrosis get totally free from idiopathic pulmonary fibrosis (IPF). I know a lot of you might be thinking I am saying this to convince you. Very far from it but you must know that natural medicine and treatment over centuries have proven to be very effective to cure ailments. 

Most people who doubts natural cure through herbs failed to look inward and ask objective questions. They willingly become blinded to the power within and refused to push the bottom of courage which life breakthrough decisions are anchored on. The fields to ask: If Western doctors can provide treatment for decades with chemical drugs, what stops them from providing a cure? When should I keep buying drugs for control, Instead of cure? The answer is quite a simple one. "A patient cured is profit lost". We all know this fact but fear has kept most patients as medical experimental puppet who's precious life is used to test western pharmaceutical drugs that does not offer a cure. 

Today we are doing everything to let people know about the power of mother nature. We want people to break free from IDIOPATHIC PULMONARY FIBROSIS (IPF) through VITEEN anti-fibrosis Herbal medicine. All life came from nature and nature never forsakes its own. Over the years we have done this without relenting. My herbal medicine is very effective as it is made based on the present symptoms Herbs used in making VITEEN ant-fibrosis are tonics to body systems; they support generalized well being and create resilience in times of stress. Our medicine is designed to alleviate symptoms and strengthen body systems. Herbs used in making VITEEN ant-fibrosis are individualized, they are chosen to simultaneously treat based on the medical history of the individual which eventually produce a cure by restoring balance and increasing vitality which brings about increased energy, improved health and a greater sense of well being.

This is quite different from pharmaceutical formulations that commonly have one action and combined chemicals that react negatively to its users. We would like to state here that idiopathic pulmonary fibrosis (IPF) as a medical topic is broad. So we cannot claim to cover every topic on the subject on our blog. We therefore encourage those interested to visit other medical blogs and websites for more knowledge. Research over the years has shown that Conventional Medications has been unsuccessful in curing neurological IDIOPATHIC PULMONARY FIBROSIS (IPF) which is part why this blog is put up to enlighten and also provide a platform for users of VITEEN ant-fibrosis HERBAL MEDICATION to share their testimonies and others experience breakthrough from IDIOPATHIC PULMONARY FIBROSIS (IPF)

What Is Idiopathic?

The word idiopathic means an unknown source of something. Just as an idiopathic disease is any disease with an unknown cause or mechanism of apparent spontaneous origin. Idiopathic diseases are those that have come of themselves, that is, without ascertainable cause.

What Is Idiopathic Pulmonary Fibrosis (IPF)?

Idiopathic pulmonary fibrosis (IPF) is the most common type of pulmonary fibrosis. Pulmonary fibrosis is a group of serious lung diseases that affect the respiratory system. "Pulmonary fibrosis" is a general term that can apply to scarring or stiffening of the lung tissue from a number of different reasons. Adding the term "idiopathic" means none of the known causes of PF have been found and that the patient's symptoms, physical exam and high-resolution CT (HRCT) scan finding are consistent with IPF. The other distinction is treatment. IPF has two FDA-approved medications to slow the progression of the disease. These drugs aren’t approved to treat other types of PF. Pulmonary fibrosis scars and thickens lung tissue. It impacts the connecting tissue in the lung and the alveoli (air sacs inside the lungs). Idiopathic pulmonary fibrosis (IPF) is a serious lung disease. When you breathe in, oxygen moves through tiny air sacs in your lungs and into your bloodstream. From there, it travels to your organs. IPF causes scar tissue to grow inside your lungs and makes it hard to breathe. It gets worse over time. Idiopathic pulmonary fibrosis (IPF) is a serious lung disease. When you breathe in, oxygen moves through tiny air sacs in your lungs and into your bloodstream. From there, it travels to your organs. IPF causes scar tissue to grow inside your lungs and makes it hard to breathe. It gets worse over time. According to the western doctors, there’s no cure for IPF. For most people, symptoms don’t get better, but treatments can slow the damage to your lungs. Everyone’s outlook is different (Their belief) Some people will get worse quickly, while others can live 10 years or more after diagnosis. There are treatments to help you breathe easier and manage your symptoms. Lung damage from IPF is irreversible and progressive with conventional medication, In some cases, it can be slowed by certain medications. Occasionally, people with IPF will be recommended for lung transplant which is totally wrong. This is one of the reason you should come give Mother nature a chance and see how you would be a living testimony because it's  not over yet until it's over. 

IPF is a type of interstitial lung disease, which is sometimes called pulmonary fibrosis. All interstitial lung diseases cause fibrosis (lung damage and scarring). There are many types of pulmonary fibrosis, but IPF is the most common. IPF is a rare disease. In the US, a rare disease affects fewer than 200,000 people; in the EU, it affects fewer than one in 2,000 people. Worldwide, a rare disease affects about 13 to 20 out of every 100,000 people. Around 100,000 people in the US have IPF right now, and doctors diagnose 30,000 to 40,000 new cases of IPF each year.  Medical experts have a hard time pinpointing exactly how many people have pulmonary fibrosis. According to one study, idiopathic pulmonary fibrosis affects at least 200,000 people in the U.S. The four known approaches allows physicians to monitor disease progression and advise patients and their families. However, it is not known if the stages of this model reflect distinct biological or clinical phenotypes and the therapeutic and prognostic value of this system is limited.  

Novel methods of IPF staging have recently been developed. The GAP model includes four baseline variables that were found to be predictive of outcome, as identified by logistic regression. These factors are: gender (G), age (A) and two lung physiology variables (P) (forced vital capacity and diffusing capacity of the lung for carbon monoxide). The clinical utility and accuracy of staging models may be further improved in the future by the integration of dynamic parameters that can be measured over time, as well as biological data from biomarkers which may be able to directly measure disease activity. The development of an evidence-based, multidimensional IPF staging model that builds on the current staging approaches to IPF is an important objective for improving the management of IPF.

What are alveoli?

Alveoli are tiny, delicate air sacs in your lungs. They help get oxygen into the bloodstream when you inhale.

In pulmonary fibrosis, the thin walls of these air sacs start to scar and thicken. When that happens, it’s harder for the air sacs to do their job and get oxygen to the rest of the body.

Is pulmonary fibrosis a terminal illness?

Yes, healthcare providers typically consider pulmonary fibrosis a terminal illness. Pulmonary fibrosis is a progressive disease (gets worse over time). There is no cure, and it eventually leads to death.

Many things factor into how long and well people can live with pulmonary fibrosis. The disease may get worse quickly (over months) or very slowly (over years). Newer medications may help slow the disease progression. Research continues to focus on improving therapies.

How does pulmonary fibrosis progress?

Pulmonary fibrosis symptoms typically develop slowly. You may notice vague signs
(or no symptoms at all) in the early stages. How long it takes for symptoms to get worse is different for everyone. Healthcare providers can’t easily predict how pulmonary fibrosis progresses. Your symptoms may get worse very slowly, over years. In some cases, the disease may lead to severe symptoms rather quickly (over months).

What is the life expectancy for people who have pulmonary fibrosis?

Some people live only months after a pulmonary fibrosis diagnosis. Others live several years. Many factors affect your prognosis. Even your provider can’t predict some of these factors. If you’ve been diagnosed with pulmonary fibrosis, you can take steps to help your body stay in its best possible shape: Be proactive to avoid getting sick: Pay close attention to hand washing, and avoid direct contact with anyone you know is sick. Having pulmonary fibrosis means your body can’t recover as easily from infections that other people may fight off with little effort.

Keep up-to-date with vaccines: Lung scarring makes it harder for the body to fight against infections. Get vaccinated for pneumonia and influenza (flu) to minimize your risk. Practice healthy habits: Stay active and make smart food choices. Get plenty of rest, and quit smoking.

How is pulmonary fibrosis diagnosed?

Your healthcare provider will ask you about your medical history. You’ll also have a physical exam to carefully evaluate your symptoms. They may use a stethoscope to listen to you breathe, listening for abnormal sounds (like crackling). Pulmonary fibrosis can look a lot like other, more common lung diseases, which can make diagnosis challenging. Your provider may also order one or more tests to diagnose pulmonary fibrosis:

Blood tests: Your provider may order blood tests to rule out other illnesses or reasons for your symptoms. Lab tests can also help providers track disease progression (how it affects your body over time) after diagnosis.

Imaging tests: A chest X-ray or a CT scan may help rule out other lung-related illnesses. These pictures can clearly show lung scarring and may confirm a pulmonary fibrosis diagnosis.

Breathing tests: These tests are also called pulmonary function tests. Different devices measure lung function and capacity (how well your lungs work).

Oxygen desaturation study: This test measures oxygen levels in your blood. You walk for six minutes with a probe attached to your finger or forehead.

Biopsy: A surgeon removes a small lung tissue sample through a small incision in the ribs. Providers sometimes perform a lung biopsy to confirm a pulmonary fibrosis diagnosis.

Other risk factors of pulmonary fibrosis include:

Older age: Most people who get pulmonary fibrosis develop it in the second half of life, between ages 50 and 70. Male biological sex: Pulmonary fibrosis affects more men than women. However, cases in women have risen in recent years.

Smoking: Cigarette smoking increases your risk of getting pulmonary fibrosis.

Working around dust or fumes: Regularly breathing in chemicals or hazardous substances can damage the lungs. Farmers, ranchers, hairdressers, stone cutters/polishers and metal workers may be at increased risk.

Other medical conditions: In some cases, another medical condition (such as the autoimmune disease rheumatoid arthritis or a viral infection) leads to pulmonary fibrosis .

Other factors: Radiation exposure, such as radiation therapy to treat cancer, can damage lung tissue. So can some medications, including chemotherapy and certain heart medications.

CAUSES OF IDIOPATHIC PULMONARY FIBROSIS

exposure to certain types of dust, such as metal or wood dust.

viral infections.

a family history of IPF – around 1 in 20 people with IPF has another family member with the condition.

gastro-oesophageal reflux disease (GORD)

smoking.

SYMPTOMS OF IPF

Pulmonary fibrosis symptoms include:

Discussing symptoms with your doctor is key to determining the severity of your
PF. You might be asked about how frequently you become breathless or how often you cough. Worsening breathlessness and cough don't always mean the disease has progressed. But knowing your symptoms helps your doctor better understand your particular disease. Few of which are

Rounded and swollen fingertips (clubbed fingers): Clubbed fingers occur when soft tissues at the fingertips become swollen and spongy. This straightens the natural curvature of the nail bed, causing a clubbed appearance. Proliferation and edema of connective tissue result in loss of the normal angle between the skin and nail plate and excessive sponginess of the nail base. Acropachy is an alternative term for clubbing. Acquired clubbing is often reversible when the associated condition is treated successfully. 

loss of appetite (anorexia) and weight loss:

 

Decreased appetite is when your desire to eat is reduced which could in turn lead to weight loss. It may occur with conditions affecting the digestive system or along with more generalized conditions, such as infection, dehydration, or chronic disease. Weight loss is one of a series of reported symptoms in Pulmonary Fibrosis (PF). According to a range of health resources, weight loss in PF is described as being gradual, unintended, and inexplicable in patients with the disease. In the early stages of the disease, patients usually don’t have problems maintaining their normal weight. As pulmonary fibrosis progresses, however, patients tend to start losing weight. Several factors contribute to this, such as loss of or decreased appetite related to medications that cause nausea; persistent cough and cough medications that cause dry mouth, nausea or drowsiness; and depression, which is common among patients with chronic diseases.

Fatigue (extreme tiredness, no matter how much you sleep): Fatigue is a term used to describe an overall feeling of tiredness or lack of energy. It isn't the same as simply feeling drowsy or sleepy. When you're fatigued, you have no motivation and no energy. Being sleepy may be a symptom of fatigue, but it's not the same thing.

Shallow spurts (shallow breathing): Shallow breathing, thoracic breathing, or chest breathing is the drawing of minimal breath into the lungs, usually by drawing air into the chest area using the intercostal muscles rather than throughout the lungs via the diaphragm

SHORTNESS OF BREATH: Shortness of breath — known medically as dyspnea — is often described as an intense tightening in the chest, air hunger, difficulty breathing, breathlessness or a feeling of suffocation.it's an uncomfortable condition that makes it difficult to get air into your lungs. especially during or soon after you exercise.

Dry Cough: The cough associated with PF is usually a dry, hacking cough. It can be triggered by talking, eating, laughing or exercising. It is important to distinguish between PF-related cough and other well-known causes of cough (such as GERD, post-nasal drip and asthma).

Depression: Yes. It is not unusual for patients with PF and their families to feel depressed or anxious. You may experience feelings you wouldn’t necessarily label as depression but coping with these feelings is still difficult.

Different categories of PF.

Idiopathic Pulmonary Fibrosis (IPF)

The most common type of PF is IPF, which stands for idiopathic pulmonary fibrosis. This means this type of PF has no known cause. Approximately 50,000 new cases of IPF are diagnosed each year. Most IPF patients first start noticing symptoms between the ages of 50 and 70 years old. It is more common in men, but the number of cases of IPF in women is on the rise.

PF from Diseases

Some cases of PF are caused by autoimmune diseases like rheumatoid arthritis, scleroderma or Sjogren's syndrome. Certain viral infections and gastroesophageal reflux disease (GERD) are also risk factors for PF. GERD is a condition in which acid from your stomach backs up into your throat. Some people who have GERD may breathe in tiny drops of acid from their stomachs, which may injure the lungs.

Familial PF

Familial PF is very rare. PF is considered familial when two or more members within the same family have idiopathic pulmonary fibrosis (IPF) or any other form of idiopathic interstitial pneumonia (IIP). There are genes that have been linked to PF but much is still unknown about this field. If someone in your family has had any type of interstitial lung disease, be sure to speak with your doctor and a genetic counselor about your risk.

PF from Exposures

PF can be caused by exposure to hazardous materials. Examples include occupational exposures such as asbestos or silica. Some cases of PF are caused by breathing in bird or animal droppings. Radiation treatments and certain types of medications can cause PF. Cigarette smoking also increases a person's risk of developing PF.

THE FOUR STAGES OF IDIOPATHIC PULMONARY FIBROSIS

When someone is diagnosed with pulmonary fibrosis, it is normal to wonder: how advanced is the disease? There is no formal staging system for pulmonary fibrosis. Physicians use different factors, like the ones listed below, to describe the disease as mild, moderate, severe or very severe:

Stage 1(Early): Recently diagnosed

Stage 2(Mild): Needing oxygen with activity, but not at rest

Stage 3(severe): Needing oxygen 24 hours a day, with activity, at rest and during sleep

Stage 4(very severe): Advanced oxygen needs (needing high-flow oxygen or when a lightweight, portable delivery system is unable to meet a patient’s needs).

Stage 1: Recently diagnosed

Early symptoms of IPF can include fatigue, shortness of breath with activity, and a dry IPF cough. Some people with stage 1 IPF may not show symptoms at all, or only experience them with extreme exertion, such as climbing several flights of stairs. 

When you're first diagnosed with IPF, doctors may also conduct a series of tests to understand disease progression and decide on treatment options. They may ask questions about symptoms, particularly shortness of breath and cough. Pulmonary Function Tests (PFTs) or Lung Function Tests show doctors how much air the lungs can hold, and how forcefully someone can push air out. They may also conduct a six-minute walk test to measure how much you can exercise and your shortness of breath during activity. 

Treatments at this stage include the two FDA-approved treatments for IPF, Esbriet and OFEV, and lifestyle changes such as quitting smoking and continuing to exercise.

Stage 2: Some oxygen needed with activity, but not at rest. As IPF progresses, shortness of breath with activity becomes more common. Coughing is typically more common at this stage as well. 

Doctors prescribe patients oxygen to use with activity at this stage, based on oxygen saturations with rest and activity. Patients can monitor their oxygen saturation with a pulse oximeter to make sure the flow is correct, maintaining a saturation equal to or greater than 89%. While it may feel more difficult, it's important to continue exercising at this stage. Oxygen with activity should help you feel better. 

Stage 3: Needing oxygen 24 hours a day 

At this stage, patients feel shortness of breath with activity. Their oxygen levels are low enough to require oxygen at rest, but they will not feel short of breath while at rest. Cough and fatigue can continue to be bothersome.  Exercise can continue to help those with IPF improve energy levels and symptoms, even with 24-hour oxygen. 

Stage 4: Advanced oxygen needs (high-flow oxygen when a portable, lightweight oxygen machine no longer meets patient needs) When a portable, lightweight oxygen delivery system no longer meets a patient's needs, doctors will recommend a high-flow oxygen in a non-portable delivery system.  High-dose oxygen can't be delivered by portable oxygen containers, so those at this stage may feel isolated socially. It's important for family and friends to continue to offer support, and for those living with IPF to talk to their doctors if they're feeling depressed.

IDIOPATHIC PULMONARY FIBROSIS LIFESTYLE

What is the role of diet in living with pulmonary fibrosis?

The main role of your diet is to help you maintain an ideal weight. Being over or underweight can impact your ability to breathe. There are no specific supplements or vitamins that have been shown to make a difference for patients with PF.

Living with Pulmonary Fibrosis

When you are diagnosed with pulmonary fibrosis, it is normal to have many questions about what life is like living with this disease. Below are expert answers to some common questions from patients about living with PF. Be sure to learn about the basics of PF, how it is treated, how to live well and where to get support. 

How important is pulmonary rehabilitation in treating pulmonary fibrosis? 

Pulmonary rehab will help you stay in good physical shape which will improve your quality of life. It also offers psychosocial support, which is so important to quality of life. Learn more.

Can I travel with pulmonary fibrosis?

Yes. Flying might require the use of oxygen during the flight, and you will need to check with the airline about arrangements. Driving should pose no issues. If you use oxygen, make sure you’ve done your homework so you know where you are getting oxygen during each leg of your trip. There are more logistics involved, but many people with pulmonary fibrosis travel well with no problems. 

Should I move somewhere so I can breathe better if I have pulmonary fibrosis?

It is more difficult to breathe at higher altitudes. It is recommended that pulmonary fibrosis patients live at a lower altitude. Try and avoid areas where air quality is poor. Talk with your doctor about your concerns and consider the potential pros and cons of moving before making a decision.

Will I need to stop working if I have pulmonary fibrosis?

You should be able to continue working until your symptoms make it too difficult. If your job is very physical, you may need to stop working sooner.

Is pulmonary fibrosis hereditary? Should siblings and children be evaluated?

PF can run in families. There are several genes associated with familial pulmonary fibrosis, but those genes aren’t present in everyone with a family history of the disease. There is currently no genetic test that can show who is a carrier of the disease or who is at risk of developing the disease if there is a known family history. Genetic testing is not recommended in most cases because it doesn’t change the recommended treatment or prognosis. If there is a family history of PF, everyone in the family should tell their doctor about it and keep an eye out for PF symptoms.

Are pulmonary fibrosis and COPD the same?

No, pulmonary fibrosis and chronic obstructive pulmonary disease (COPD) are not the same. However, they are similar in some ways. Pulmonary fibrosis and COPD are both lung diseases that get worse over time. Both conditions can make breathing difficult.

But these conditions affect your lungs differently:

Pulmonary fibrosis: Providers classify pulmonary fibrosis as an interstitial lung disease. The interstitial tissues are cells that make up the space between blood vessels and other structures inside the lungs. Pulmonary fibrosis damages these cells. It is a rare disease.

COPD: COPD is a more common type of lung disease. Diseases like emphysema and chronic bronchitis are types of COPD. In COPD, lung tissue is damaged, alveoli are destroyed and airways can get irritated and inflamed (swollen). 

What’s the difference between IPF and COPD, and why do people get confused?

It can be easy to confuse IPF and COPD. Both diseases affect the lungs, are progressive, and share many symptoms. These common symptoms include shortness of breath that gets worse with time, chronic cough, and fatigue. However, the way they damage the lungs is different. In IPF, your lungs become scarred, stiff, and thick, and this damage isn’t reversible. In COPD, the airways and air sacs in your lungs become blocked, but you can control the symptoms, even in later stages of the disease. Both illnesses benefit from early treatment, but IPF tends to have a worse outcome; the average survival time is only two to three years after diagnosis. IPF usually affects people over the age of 65, but COPD affects people who are a little younger – usually over the age of 40. The two conditions can differ in noticeable ways. Coughs. COPD usually gives you wheezing coughs with mucus in your throat. With IPF, you’ll likely have a dry, hacking cough.

FDA-APPROVED MEDICATION FOR IDIOPATHIC PULMONARY FIBROSIS (IPF)

Currently, two drugs are FDA-approved for treatment of idiopathic pulmonary
fibrosis (IPF), which is the most common form of PF. These include nintedanib (Ofev®) and pirfenidone (Esbriet®). These medications are called anti-fibrotic agents, meaning that they have shown in clinical trials to slow down the rate of fibrosis or scarring in the lungs. These drugs are approved for patients with mild, moderate and severe IPF. While neither medication is recommended over the other, one may work better for you. Your doctor will work with you to prescribe treatment tailored to your needs. While taking these medications, you will be monitored closely for any serious side effects because of the debilitating side effects . Monitoring will include routine blood work to make sure your liver remains healthy. Ask your doctor for a referral to a palliative care specialist who can help you manage any side effects from the drugs. Some other medications are: 

Drugs to Reduce Inflammation

There are certain types of PF (excluding IPF) that respond to treatment with steroids. Steroids, also known as glucocorticoids, are a class of medication that reduces inflammation (swelling). Corticosteroids can have harmful side effects, especially when used long term. You will need to be carefully monitored if you are on long-term steroids. Other groups of medications prescribed to reduce inflammation include azathioprine, cyclophosphamide and mycophenolate mofetil (Cellcept®, Myfortic®), which work by suppressing the immune system.

Drugs to Treat Acid Reflux

Doctors may recommend anti-acid medications to treat gastroesophageal reflux disease (GERD), a digestive condition that commonly occurs in people with idiopathic pulmonary fibrosis. There are different types of anti-acid medications (e.g., Proton pump inhibitors including Prilosec OTC® and  Nexium® as well as H2-Blockers including Zantac® and Pepcid®) that are prescribed to help block the formation of or minimize the amount of acid in the stomach. By doing so, it helps to reduce the amount of acid from the stomach that enters the lungs.

Drugs to Treat Cough

A dry, hacking cough is a common symptom of PF. Treating cough is mostly trial and error. What works for one patient may not work for another. Some treatment options for cough include: Over the counter cough medicine like Robitusson® and cough drops. Prescription cough medicine like hydrocodone (Tussionex PennKenetic®) and benzonatate (Tessalon Perles®) Thalidomide (Thalomid® ) may be used for serious cases of cough in some patients. There are ongoing clinical trials for PF drugs, including ones to help relieve cough. Visit clinicaltrials.gov to see if any are available near you or ask your doctor.

COMMON SIDE EFFECTS OF PHARMACEUTICAL MEDICATION MAY INCLUDE BUT NOT LIMITED TO:

nausea, vomiting, loss of appetite; stomach pain, heartburn, upset stomach;

diarrhea; headache, dizziness, tired feeling; weight loss; cold symptoms such as stuffy nose, sneezing, sore throat; joint pain; or sleep problems (insomnia). Liver Enzyme Elevations and Drug-Induced Liver Injury. Photo sensitivity Reaction or Rash Gastrointestinal Disorders. feeling sick, tiredness, diarrhoea, indigestion. yellowing of the eyes or skin, loss of appetite, itchy skin, your pee turns a darker colour, feeling tired, pain in the upper right side of your stomach.

WHY WESTERN MEDICINE DOES NOT TREAT ILLNESS EFFECTIVELY? 

Herb is a plant or plant part used in its entirety, while a drug is a synthesized copy of one chemical Pharmaceutical component, companies often make the mistake of isolating an active from an herb, or extracting that active out of the herb without the herb's other naturally occurring ingredients; or even worse, of making and producing a synthetic copy of the active. What they end up with is a drug that is far from what nature produces-without the benefits of the synergistic interactions of the herb's original ingredients-often resulting in negative actions or undesirable side-effects. Most of the tools currently used by modern medicine, including most of the drugs that are in use today, have only been around for a few decades or less while herbs has been for millennium. Apart from that, a painful truth is that English medications are made based on the profit they will continue to generate for their makers. Knowing fully well, that when a patient is cured, they will certain to lose profits. So they will ensure continuous chain to these drugs.

VITEEN anti-fibrosis Herbal Medication

The bright side (wonderful news) is that there is hope for healing and permanent CURE for Idiopathic pulmonary fibrosis (IPF) via VITEEN. By cure I mean the cessation of lifelong lung disease, lung scarring (tissues scar and thicken over time), making it harder to breathe.upper respiratory infection, Clubbing, fingertips or toes that look different,Cyanosis, bluish skin (in fair-skinned people) or gray or white skin around the mouth or eyes (in dark-skinned people) from too little oxygen in the blood. as they are explored, and a gradual titration off of medication, with the cure lasting- without continuing any medication. VITEEN is made on an order, based on extensive medical history, it is not like prescription or over-the-counter medication where the same kind of drug is given to every patient, each patient receives specialized treatments. It is all "natural", no chemical added or preservative. VITEEN herbs are grown by us and in most cases we import quality herbs to complement our production which is done to ensure result and quality. It is always subjected to comprehensive & practical approach of testing equipped with high-performance to ensure its quality free of pesticides, contaminants, heavy metals and solvents and by doing, we ensure efficacy, purity and proper dissolution. VITEEN herb extracts are non-alcohol base which is why it is far effective. While most commercially available extracts are made with an alcohol base, we make use of other type of solvents- vinegar - to absorb the flavors of our herbs. These, solvents and the extracts made from them are safe to consume for those who want to avoid alcohol in their diets. It stimulate the liver to maintain and improves the brain capabilities. It alleviates brain fog. It is naturally safe even to those that may not have used Herbal medicine. . It is liquid,  and it has no bitter taste or irritating odor. It can be shipped anywhere in the world! A certified and tested herbal products you can trust for good health and general well-beings. We have use this medicine on more than a thousand patients from different countries, who are permanently free of Idiopathic pulmonary fibrosis (IPF) and now living a better and fulfilled life. VITEEN open up the path to a true and successful/lasting recovery and enable you to be able to eventually put all of your distressing experiences behind you. Instruction on how to gradually switch to VITEEN comes along with the medicine, so there wouldn't be any relapses.

MONEY BACK GUARANTEED

Money Back Guarantee Our products have been manufactured under strict Risk

Free Quality Guid elines and they undergo testing at every stage of production to ensure full compliance with our specifications. They further undergo independent testing to ensure efficacy, purity and proper dissolution. We have worked hard to select the finest supplements in the world, but in the end, we are not happy unless you are satisfied. So for this reason we offer you a 100% Money Back Guarantee. The gallons/bottles may be returned if you are unhappy with the improvement of the patient after the first month, I will provide you with a full refund. We conduct business with integrity. That is why we offer our superior products straight at the most affordable price. 

Order for VITEEN anti-fibrosis

Once you place order, your Door-2-Door Courier Service to the World and Door-
to-Door Delivery order will be available for shipping within 8- 9 working days using convenient, reliable and on-time courier services USPS, FedEx and Dhl Worldwide. Most orders are delivered in about 3-5 business days. We use an industry standard encryption technology to guarantee the secure data transmission during transaction. We also absolutely guarantee the privacy information of our customer. IPF affects IPF is a rare disease. In the US, a rare disease affects fewer than 13 to 20 out of every 100,000 people, and doctors diagnose 30,000 to 40,000 new cases of IPF each year. By sharing your experiences, together we can end the stigma. We all came from nature. We live with nature. Nobody can survive without nature. No diseases are resistant, No one needs to die untimely from IPF. No one should live on drugs forever. It is possible to break free from the pattern controlled by one's thoughts and actions, and to become truly liberated and capable of living life to the fullest. 

Contact: 

To schedule a consultation to review your symptoms and to determine the most effective among the available options: Send all details and get a reply to: dr.reignfrank@gmail.com

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                        last updated on 1, January 2020

STORIES/TESTIFIERS OF THE GOOD WORKS OF VITEEN anti-fibrosis 

                                                (Testimonies)

Live video testimonials

These are some of the live videos testimonies of the uses of VITEEN anti-fibrosis Herbal medication.  The freedom has restored happiness back into their various homes. They didn't want to do this but I had to convince them that if they don't do it, how will the people going through some same know that they are not alone and they could also be free from the chains of chemical based treatment.  Lots of testimonies keeps coming in on a daily. You too can be free.

   

Mr. Anderson's Live video Testimony

There are so many Testimonies gotten from the use of VITEEN anti-fibrosis. We can't keep uploading all for the sake of privacy. We usually seek permission from our Customers before posting their testimonies. Here is another: 

   

          

 I WON MY BATTLE WITH IPF THROUGH VITEEN anti-fibrosis. 

My name is Jon Raymond. I live Wiltshire, UK. This is my battle of life's health with Idiopathic Pulmonary Fibrosis (IPF) and how I became permanently cured by Dr. Reign's Herbal medicine called VITEEN anti-fibrosis. In the New Year of 2006 I noticed that it was harder for me to run for trains, walk uphill and climb stairs. This had been happening quite frequently for a couple of months. I'd noticed it was getting harder to breathe doing fairly simple things.  I visited my GP and was sent for a chest x ray, but the results got lost so I decided to visit a specialist privately.  This was when I was diagnosed with IPF but wasn't sure until I went for a Biopsy and it was confirmed that it's truly IPF. 

After the shock I decided that life should go on as near normal as possible and continued working full-time in a high pressure and stressful professional job travelling and pitching for contracts until I had to accept I couldn't carry on in Spring 2007. I was admitted to hospital where I spent almost 17 days struggling to get the best administration of treatment. I was discharged on the 18th day but returned back for my diagnosis to be reconsidered and changed to a different type of ILD, non-specific interstitial pneumonitis (NSIP) with a slower progression but still a terminal condition. It was now a life of struggle because I was almost completely dependent to carry out tasks that I used to perform very easily. idiopathic as we know means not a lot is known about this disease. Before this, I had been a healthy, happy non-smoker. I had a lust for life and an appreciation of every moment that comes by. IPF is a devastating disease and I find it hard to understand how there is still no cure because it's not AIDS. Despite the over 5,000 that dies each year here in the UK, I wonder why it's still called a rare disease. It's funny but I guess I had to accept my fate because even the doctor created much fear already that I could only live 6 months to 2 years more. 

So I was doing nothing else but counting days to the day of my demise. My Pulmonologist could hear 'crackles' on my lungs and wanted a third opinion from a another specialist, which he referred me for marked 'urgent'. By this stage I'd started to deteriorate quite quickly and a double lung transplant was considered to be my only medical hope. I had assessments to see if I was a suitable candidate, and put on the transplant waiting list at Wythenshawe hospital. I was going online to see the number of patients who have successfully done the transplant and the ones that survived it. Going from facebook to YouTube, then Twitter, to almost all the social networks you could think of , reading comments of people. The scaring part of it was the comments and the stories of those parents, siblings or friends of those who gave up the ghost during the transplant. As a result, I wanted to decline going for it because I just don't wanna go into the theater and not come out alive because despite how my condition was, life was still very precious. 

I tried to check further to see why there wasn't cure or any other way the transplant could be avoided when I saw a live video of one Mrs. Helen Daniel and the comments beneath. I noticed some of the comments were attesting to what she was saying. For good 3 days I was on it. Researching more about the Herbal medicine (VITEEN anti-fibrosis) until contacted the Doctor via his email that was provided. He asked me a lot of questions which I rightfully give answers to. My herbal medicine was delivered in just 4 business days. March 22, 2022 would make it 5 years since I was cured permanently from this disease which doctor told me I had just 6 months to 2 years to live. If you see me and I didn't tell you I once had IPF, you won't know because every part of my body was restored 100%. The other part of it is that there is no single side effects like those that comes with Pharmaceutical drugs. Herbal medicine is truly the best anyone would think of. Dr. Frank, you may not remember me but I want to encourage you to keep up this good work while on my part I will keep spreading your name to those that needs to hear this.  

Jon Raymond .... 

 My Success story from IPF

 My name is Jamie Tierney.  I lived in Ohio for over 23 years with
my loving husband and our 3 grown children. We recently relocated to Georgia after retirement. It was not up to about 5 months after we relocated I started to feel some symptoms but I couldn't understand my body system anymore because at first, I thought it was as a result of change of environment until about 10 months later, it was now unbearable but wasn't free to go for test because of the Covid that was ravaging everywhere. I was sincerely scared of being separated from my family.  life was being somewhat of a roller coaster. My first diagnose was communicated through a phone call from my doctor on a Friday afternoon around 5p.m.  This was when I started to notice difficulty in breathing or even doing things I used to enjoy doing. 

The second appointment was with my personal doctor after 3 weeks who then referred me to a pulmonologist. It's the pulmonologist that confirmed to me I have been infected with IPF. Imagine being told that you have a disease you have never heard of, a disease with no known cause for which there is no effective medical treatment and no cure. It has advanced also. I started reading books on how to deal with it.  There came a day I went to visit my oldest sister Sharon. We were discussing when I took a break for my daily walk and found myself gasping for air. I called for help. I ended up in the hospital. I was 59 years old, I thought after retirement  I will be having more time to spend with my children and grandchildren. Many of the things I loved to do suddenly looked out of reach. Why me? Why now? What caused this? 

What do I do now? The doctor told me that I had no more than 3–5 years to live. That’s it. That was the message. So I went online, seeing if I would get a book to keep my hope alive. So I started believing the course of treatment for my advanced stage lung cancer was set: I would endure chemotherapy and radiation, but I wasn't optimistic about my health. My whole world turned upside down. Thanks to the Internet, I saw a video testimony of  Dr. Reign Frank who has cured thousands of people with his herbal medicine called VITEEN anti-fibrosis. I read written testimonies also, so I was convinced and placed my order of his product (VITEEN anti-fibrosis). Just 2 Months of use gave my health a dramatic improvement which rebuild my life. I started making progress in breathing, my dry cough started to give way. I could now sit a day with just about 2-3 times coughing. I wrote to Dr. Reign if I should stop the medication since I was almost getting myself back completely but he refused. He said I must complete the dosage or else there might be a chance for it to resurface. Over a period of 5 months, MY LIFE WAS COMPLETELY BACK. The long struggles was worth it. I am now loving life again because I could sit play and watch my gran-kids jump around. What a joy of given a chance to live again with my family. I want you all out there to know that recovery involves knowing your limits. It took me long time to figure that out. VITEEN anti-fibrosis herbal medication preserved my life. I am grateful.  

Jamie Tierney...

posted: March 13, 2020

6 YEARS  IDIOPATHIC PULMONARY FIBROSIS CURED

with VITEEN anti-fibrosis

By Marvis Bush

Marvis Bush

I was diagnosed in November 2016 and have been taking Esbriet since January 20017. Of course no one can say for sure or speak to our life span with any sort of certainty, but I agree: positive thinking and optimism can go along way in navigating life with a chronic illness for sure . My pulmonologist was having two IPF patients who were diagnosed 10 years ago.  The longest patient case he has ever had is 17 years. I became friends with them because I just feel that they are the first of my kinds I have come in contact with. I was still very much okay although not at the same rate as before, but happy to have some forum to turn to for information and support. Just to make sure I don't leave the surface of the earth before the stipulated time that the deadly ailment would give.  I was very discouraged with my outlook, only compounded by suddenly facing family issues  and upheaval in my job. The stress was incredible. I could not take more than a few steps without being breathless. Depression started rising. I could not shower as the warm, moist air made it impossible to breathe.  I coughed so much my throat was raw. I was prescribed a steroid. 

The pulmonologist gave me 6 months to a year to live; said my lungs were “filling up fibrosis.” but my PCP suggested I get a consult from a pulmonologist to establish a new baseline on my ILD.  Consequently, I was prescribed OFEV, although I do not present common symptoms of the disease.  He said the medicine  can slow the disease, but he did not/ could not  provide an estimated time of my demise.  I still feel fine just can’t do the things I could do a year ago. I have a cough and I’m on oxygen 24/7. This was excruciating because I never knew my life would ever be truncated at any point. My mind was that once Covid is over,  I plan to get out and get active again. Until my daughter who was schooling in Baylor College of Medicine returned home to check up on me. When she asked how I was doing I responded like all was okay with a smile on my face but she knew something wasn't right. When she came closer and be like dad is it getting any better, I just said it's not taking the meds that is the main problem, but side effects from them. The rate at which I was emaciating was questionable. Tears began to roll down her cheeks.  She went inside. A day before she was going back to college she said to me "Dad, you have to stop these medications you're on" I said what? That would mean a death sentence to me. She said I know but I have a better option.

 A week later she brought two gallon of brown liquid with some in form of blended herbs. She told the doctor (Dr. Reign Frank) my age and the drugs I have been taking and how long I have been on them. So he sent along how to gradually switched to the herbal medicine. I guess those information was what he used in giving me the prescription of the VITEEN anti-fibrosis herbal medicine.  I am here to say I'm not yet done with my dosage of it but from the improvement so far, it's a 100% guarantee that I can recommend it to anyone who is being tied in the fears of the warnings given to us that we can only manage IPF but can't be cured. It's a big lie from the pit of hell. I am a living testimony. And the 2 friends from my former Pulmonologist who had it for good 10 years are fast getting better just like me. When you are at the end of your rope, tie a knot and hold on. It doesn't matter how many times you get knocked down. Money won't be enough to appreciate you from breaking me free from this bondage Dr. Reign but until death I will keep spreading the good news of VITEEN anti-fibrosis.

 MY STORY OF IDIOPATHIC PULMONARY FIBROSIS (IPF)

I was diagnosed IPF ( they believe familial) 2017. Have been taking OFEV. My PFT is every 6 months with an X-ray every year. My X-ray shows no advancement of the scarring and my #’s on the PFT have not decreased I was just like a walking corpse. I didn't know how explain this to people because the machine shows it's not causing as much as the pain I was feeling. I was not on oxygen but the effects of this Disease was always present. Of course, when you consider almost any disease, think about the ongoing progress in treatments, that is likely the case almost every time but my mind was not always at peace because I was just living on each day waiting for the death would finally. But there was this determination that whatever they say the expectancy may be… they will still be wrong.  All hope was lost to be sincere.  I was so glad to hear some of the dialogue and the responses I saw on different forum and they were so helpful! Of course no one can say for sure or speak to our life span with any sort of certainty, but I agree: positive thinking and optimism can go along way in navigating life with a chronic illness for sure. I knew one of my other cousin who passed while waiting for a lung transplant at 3 years of this disease.  It just goes to show that it certainly does mean that we all are individual and subject to the fate of not really knowing.

On one faithful Sunday morning, I stumbled on a youtube video that was anchored on the effectiveness of herbs to the human body. I was listening and watching the video and I began to read so many comments under it about how so many ailments that prove abortive to Western medication and how so many of them have been eradicated with herbal medicine. Immediately I began to feel something strange to start searching for herbal medicine for idiopathic pulmonary fibrosis. I was searching and searching for over 3 hours. I was reading different blogs about herbal medication. Until I stumbled on this blog: curetoidiopathicfibrosis.blogspot.com. I listened to some of the testimony videos and once, I saw the need to give it a try. Besides, I was only living, hoping that someday death would just come and put an end to everything. So I scheduled a consultation with Dr. Reign Frank. After about 5 days of placing an order with a small amount compared to what I have spent ever since I was diagnosed, I was delivered my VITEEN anti-fibrosis Herbal medicine. It was just 3 weeks of use that I started to notice drastic improvement. I didn't believe it because even the pulmonologist told me it could only be managed but there is no cure. How come I was experiencing a different thing? I asked myself. I continued with the medication. After exactly 3 months, I slept for about 14 hours after eating excessively. Which was shocking to me. Well to surmount it all, today I'm 100% back on my health. Now I'm experiencing the true meaning of good health with no single side effects from VITEEN anti-fibrosis. Thanks to you Dr. Reign. I don't think you will ever be forgotten. My family sends their regards. 

Linda Kurz...... 

THERE IS STILL LIFE

Evans Holt's Story 

In honor of VITEEN anti-fibrosis Awareness, I’d like to tell you, in my little way, what it’s been like
living with a terminal lung disease. “Everybody is different, and I know very well from social media that some people can be diagnosed and die very quickly, and others go on for years. As one of my doctors explained: “You are standing at the top of a very steep cliff — there is no doubt about that — and one day you are going to fall off. How and when it happens, nobody knows. You might fall straight to the bottom in a whoosh, or you might tumble gently down, no one knows which. But it will happen.” Until then, I was busy working to maintain my lung function and health. I still gets plenty of air into my lungs, but extensive scarring, confirmed by a relatively low DLco reading, indicates that only a small amount of the oxygen I inhale reaches my bloodstream.  If the oxygen isn’t getting into my body, it doesn’t really matter how much is reaching my lungs.” And I refused to accept that nothing could be done. 

Despite the limitations imposed by idiopathic pulmonary fibrosis (IPF), and the knowledge that nothing will halt its relentless progression, I remain pragmatically optimistic about the future. “I don’t have things on my ‘bucket list’, mainly because to do anything involving two people on oxygen is a military manoeuvre, but Doris (my wife) and I still have so much to look forward to.“Our goals are to see each important stage of life with our grandchildren. I could no longer manage the heavier jobs around my garden which I used to help my wife with. “I had to stop mowing the grass about 18 months ago because it’s all uphill and even with a light electric mower it was too much of an effort.  In the past two months I’ve had to give in and accept that I can no longer do the vacuuming, I get too breathless getting down to do the edges. 

My wife Doris would have helped me with some of all these but she was seriously battling with stroke. It was hell I must confess. I try to keep active, positive and talk about my IPF with wife and friends, this helped to a great deal. Doris and I decided to test how I could manage at elevation. In August 2011, we drove to Hurricane Ridge in the Olympic Mountains at about 5,000 ft (1,520 m) elevation. I could not walk across the parking lot without stopping to catch my breath. It was horrible. By April 2012, my deterioration began to accelerate. Without oxygen, a slight grade became difficult and stairs were a killer. I put together a backpack of oxygen and continued to exercise almost daily at a cardiac rehab program. With 2 L of oxygen I was able to walk a few miles. I felt good physically. I even took a fishing trip in May with my brother-in-law. We took 42 tanks of oxygen and I used them all. cough was becoming an issue.  I remember being yelled at by one at a shopping mall. 

I felt like committing suicide. It was more a constant clearing of my throat, just plain irritating to me and to those around me. I always cough when speaking or out of breath. I explained all of my frustration to Michael my college mate. Exactly 2 weeks and 3 days later, he drove to my house to tell me he has found a cure to my ailment (IPF). At first I didn't believe him, he noticed it and came closer, showed me the email from the Doctor (Dr.Reign Frank), it then I started to show interest.I still was finding it difficult to believe so because of that has had to order for it with his money that I will pay double if it eventually works for me, I agreed. After about 6 business days after explaining and sending my diagnose results to him, the herbal medicine was delivered to my doorstep. I didn't go ahead to start taking it immediately. I wrote to him that I have gotten my anti-fibrosis herbal medicine. So he wrote the prescription on how I should be taking it. Low and behold, with no side effect, things began to change for good. After about 4 months, I paid my friend (Michael) triple the amount he ordered the Herbal medicine with. I appreciate Dr. Reign Frank so much through my friend Michael because if not for him, I wouldn't have the Knowledge to give herbal medicine a try that would result to my freedom from this bondage I was in for years. VITEEN anti-fibrosis is the final solution to you out there who is struggling with Idiopathic Pulmonary Fibrosis (IPF).