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Doctor insights on: Why Cant Cystic Fibrosis Patients Date Each Other

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Why can't cystic fibrosis patient be near each other?

Why can't cystic fibrosis patient be near each other?

Increased infection: I am not a pulmonary or infectious specialist so I would defer the definitive answer to those specialty physicians. My understanding is that cystic fibrosis patients have increased risk of pulmonary infection. Placing two individuals with the same increased risk together would increase their risk even more. ...Read more

Dr. William Walsh
992 Doctors shared insights

Cystic Fibrosis (Definition)

A genetic disorder of the lungs and digestive tract. It causes recurrent lung infections and inhibits growth in patients and average life expectancy of patients with cystic fibrosis ...Read more


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Why can't cystic fibrosis patients be near each other?

Why can't cystic fibrosis patients be near each other?

Sharing: Patients with cystic fibrosis are highly susceptible to lung infections. As a result, if they spend a lot of time together, they can readily swap infections. This is one case where you should shun your parents' otherwise good advice on sharing. ...Read more

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What happens in the body of a cystic fibrosis patient?

What happens in the body of a cystic fibrosis patient?

Cystic Fibrosis: There is not enough space to answer this question thoroughly in this format. Check out the link below, it gives some good information on cystic fibrosis and the various systemic effects:
http://en. Wikipedia. Org/wiki/Cystic_fibrosis ...Read more

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What are the caloric needs of patient with cystic fibrosis?

What are the caloric needs of patient with cystic fibrosis?

CF diet/supplements: The caloric needs of a CF patient can be 20-30% higher or more than someone without cf. The use of calories for example in respiratory effort uses calories that would otherwise not be expended.
Eating a high protein high calorie diet along with CF nutritional supplements will help boost caloric intake.
I hope that this helps. ...Read more

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How does cystic fibrosis affect the patient and their family?

Many ways: This is a chronic disease that can cause a variety of consequences to the patient and their family. This is a very complicated question to be answered briefly here. ...Read more

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What does a typical cystic fibrosis patient look like and feel like?

What does a typical cystic fibrosis patient look like and feel like?

Not clear: Not clear what is being asked. Are you looking for information or looking for a physician for cystic fibrosis? A starting point would be your general physician who can refer you to a specialist, if needed. ...Read more

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What is done to improve the immune system of a cystic fibrosis patient?

Cystic fibrosis: CF is a genetic defect and at this time, it cannot be repaired. Companies such as sangamo pharmaceuticals are working on cures for mono-genetic diseases, and maybe someday a cure could become available. ...Read more

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Is palliative care usually covered by insurance for cystic fibrosis patients?

Is palliative care usually covered by insurance for cystic fibrosis patients?

Should be covered: Palliative care should be covered by insurance, regardless of the underlying diseases a person has. One can call her insurance company to check. Palliative care can be really helpful when a patients diseases can no longer be improved by medical treatments. ...Read more

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Which medications does a cystic fibrosis patient in their mid/late teens take daily?

CF meds: Depends on overall pulmonary and GI status:
if pancreatic insufficient:
-pancreatic enzymes
-cf vitamins
lung disease:
-mucolytics such as pulmozyme
-albuterol-bronchodilator
-chest physiotherapy to clear secretions
-nebulized antibiotics if chronic psuedomonas
-azithromycin if chronic pseudomonas
-anti-inflammatories sometimes
there are also other medications based on disease state. ...Read more

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For what reasons might the pancreas get blocked by mucus in cystic fibrosis patients?

Thick: The secretions in cystic fibrosis are more viscous (thicker) than normal and interfere with normal drainage resulting in blockages of the bronchial tubes of the lung with resultant pneumonia and lung injury. Similar issues involve the pancreas. Newborns with the disease frequently have difficulty passing their bowel movements. ...Read more

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Is it possible to donate a lung to a cystic fibrosis patient if you are a smoker?

Depends: If you are a heavy smoker with significant emphysema you may have reduced your pulmonary reserve to the point that you would have a tough time getting by on one lung, ditto the recipient. You would need to have a full pulmonary function evaluation to find out. ...Read more

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Would it be possible for someone to donate a lung to a cystic fibrosis patient when you are a smoker?

Depends: If your pulmonary function tests show both lungs to have adequate capacity and no significant emphysema then it could be possible. Bear in mind that you both have to be able to live relatively normal lives on the single remaining lung. Both you and the recipient should avoid being in the same room with a cigarette! ...Read more

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Is CBAVD sensitive for Cystic Fibrosis? In other words, if a male patient has both vas deferens, can it be assumed they do not have cystic fibrosis?

Is CBAVD sensitive for Cystic Fibrosis? In other words, if a male patient has both vas deferens, can it be assumed they do not have cystic fibrosis?

Need chromosomal tes: Generally absence of vas deference is associated with cystic fibrosis. However to make a definite diagnosis of caustic fibrosis you need the chromosomal test. ...Read more

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How does gene therapy help a cystic fibrosis patient?

How does gene therapy help a cystic fibrosis patient?

So far not at all: Trying to replace the faulty gene has been a failure so far. The new science of epigenetics tells us that our genes (even "bad" ones) are changed by diet and life style. I havegiven children with CF vitamin supplements. They help greatly but there is no cure. Find a physician who uses nutrient treatment. ...Read more

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Is a high calorie, high fat or high protein diet beneficial to young cystic fibrosis patients?

Is a high calorie, high fat or high protein diet beneficial to young cystic fibrosis patients?

Not high fat: One of the problems folks with CF have is that their pancreatic duct gets blocked. This means that the fat-digesting enzymes from their pancreas can't get to their gut and break down the fat they eat. A high-fat diet would be very bad in this situation. You need to have conversations with your CF doc to optimize your diet. You should have both a pulmonologist and a GI doc on your team. ...Read more

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Does a double lung transplant completely eliminate lung problems for cystic fibrosis patients?

Does a double lung transplant completely eliminate lung problems for cystic fibrosis patients?

It should: Cystic fibrosis is a genetic condition causing significant lung dysfunction. A double lung transplantation replaces the native lungs with supposedly normal lungs, eliminating the problem, but replacing it with problems directly related to transplanted lungs, i.e. Chronic rejection or bronchiolitis obliterans. ...Read more

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Does a successful lung transplant completely get rid of the lung problems for cystic fibrosis patients?

It may: Or you could trade one set of problems for another - even successful lung transplants eventually develop obliterative bronchiolitis after a period of time. Be sure that you meet some post transplant patients who are successful, and compare your quality of life to theirs - if your treatment regimen is oppressive and your lung function is bad enough, you may be better of after a transplant. ...Read more

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How can cystic fibrosis affect p.I.E.S development?

Certainly: Cystic Fibrosis (CF) most common life-limiting genetic disorder of Caucasians, affecting approximately 30K people in the US. A, impacting mainly respiratory function. In recent years patients symptoms better controlled by genetic findings and better medications. Emotional & phys. Development depend on severity, time in hospital, complications. Morb. & mort. Factors afect emotional, cognitive behavior. ...Read more

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Can someone be diagnose with cystic fibrosis in their 40's?

Can someone be diagnose with cystic fibrosis in their 40's?

As a carrier: Genetic carrier testing:
more than 10 million americans are symptomless carriers of the defective CF gene. This blood test can help detect carriers, who could pass CF onto their children. To have cystic fibrosis, a child must inherit one copy of the defective CF gene from each parent. ...Read more

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I have symptoms of cystic fibrosis. Is it possible to start show the symptoms in my 30's?

Yes: Yes it is possible. Presentation of cystic fibrosis varies greatly, and it is possible, depending on your specific mutation (and other factors) to present at a later age. In order to prevent late diagnoses, all states now have a newborn screen in place for cystic fibrosis. ...Read more

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I have family members with cystic fibrosis. Is it possible to start show the symptoms in my 20's?

I have family members with cystic fibrosis. Is it possible to start show the symptoms in my 20's?

Yes: However, usually an adult who is diagnosed so late has usually had chronic problems with cough and "pneumonias". That said I've diagnosed a new case in a 38 year old woman. ...Read more

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What are the chances of a child getting cystic fibrosis among the different racial groups in the u.S.?

What are the chances of a child getting cystic fibrosis among the different racial groups in the u.S.?

Overall 1/3700: Acording to the CF foundation: the overall birth prevalence is 1/3700. It can occur in any race, however the greatest incidence is in caucasians of northern european descent, being 1/2500. The other major groups affected are hispanics 1/13500, african americans 1/15000.
More than 10 million of us carry one part of the defective gene, but to have the disease you must have a copy from both parents. ...Read more

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Can you die of cystic fibrosis?

Yes but: Yes but with early diagnosis and regular care and adherence to prescribed therapy by a pediatric pulmonologist the long term survival has improved greatly in the past two decades. ...Read more

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What is risk of cystic fibrosis?

Depends on genes: The risk of acquiring cystic fibrosis (CF) depends on whether the parents of a child are carriers for the gene. It is estimated that about 1 in 20 americans are carriers of the CF gene. In order for a child to acquire the disease, both parents must be carriers. If both parents are carriers, there is then a 25% chance that the child will acquire the disease. ...Read more

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Can you die from cystic fibrosis?

Yes.: Although the complications of cystic fibrosis are treatable, and although the available treatments are helpful, the disorder shortens the normal life expectancy. ...Read more

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What are symptoms of cystic fibrosis?

Cough, poor growth: Common symptoms of cystic fibrosis include cough, wheeze, recurrent lung infections, poor growth, foul smelling stools, salty sweat, clubbing, and rectal prolapse. The more symptoms the greater the chance of having cystic fibrosis. Most infants today are diagnosed by newborn screening for CF before they develop any symptoms and early therapy can minimize disease symptoms. ...Read more