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Hey Slimmies


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your are a rack of bones, it's a wonder that your not healthy. my god Eat.

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you better be up to 125 by time Vegas comes around

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Once again I have trolled into a thread seeking trannies, only to be disappointed.

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you weigh 114 pounds?!?!?!?!? I am never letting you flame me again.... omg!

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Now Matt honeyyou need to understand lolI'm anurse and ', I know exactly what imtalking about!
loooooooooooooooooooooooollooooooooooooooooooooooolloooooooooooooooooooooollooooooooooooooooooooolloooooooooooooooooooollooooooooooooooooooolloooooooooooooooooollooooooooooooooooolloooooooooooooooollooooooooooooooollooooooooooooolloooooooooooollooooooooooollooooooooolloooooooollooooooollooooolloooollooolloollol
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He has CF....... you are a nurse and still make statements like this?God help the patients you see.
you might actually be retarded
Yes he has CF, so a little weight is not going to harm him if he puts it on slowly and builts it as muscle. It will strenghten his lungs actually. So here is data backing my statementsnow I will accept apologies you morons, you think you know it all.125 is realistic and I am not saying to do it in 1 day but over months. Minocycline in the Antibiotic Regimen of Cystic Fibrosis Patients: Weight Gain and Clinical ImprovementIncreased weight gain and some clinical improvement was seen during treatment with minocyclineThose patients with severe disease gained more weight than those with mild or moderate disease, and males gained more than females. When minocycline hydro chloride was not the drug in use, patients lost weight and their health declined. Nutrition for Patients With Cystic FibrosisDiane L. Olson, RD, CSP, CNSD and W. Frederick Schwenk, II, MD Mayo Clinic College of Medicine, Rochester, Minnesota Cystic fibrosis (CF) is the most frequent, lethal genetic disorder among northern Europeans. The etiology of this autosomal recessive disease is known to be a defect in the cAMP activation of chloride (Cl—) channels in secretory cells in many organs of the body. Although this defect usually leads to severe lung disease, many of these patients also have nutritional deficiencies. Nutrition is one of the key components in the management of CF. Patients are at high risk for malnutrition, which may result in accelerated progression of the disease and increased morbidity. This review will discuss nutrition recommendations for calories, protein, vitamins and minerals, and enteral and parenteral nutrition support practices. Food FitnessAll kids need to eat well to grow up healthy and strong. But kids with CF need to eat more than most other kids, so they and their parents often work with a CF dietitian (say: dy-uh-tih-shun) to plan what they should eat. A dietitian is someone who knows all about food and nutrition. SAME GOES AS ADULTS2008 Pub MedIn adults with cystic fibrosis, percentage of ideal body weight based on the Metropolitan Life Insurance reference weights for medium/large frames overestimates the severity of underweight. Body-mass-index percentile for children and body mass index for adults as underweight indices have been proven to be valid. Strong associations between body mass index and lung function are also observed, but cutoff values to maintain a desirable level of lung function can vary. SUMMARY: Body mass index should replace the use of percentage of ideal body weight for classifying underweight in cystic fibrosis patients. More research is needed to identify appropriate indicators to classify short stature in children with cystic fibrosis.provided by www.CFF.orgNutrition & Cystic Fibrosis: Changes Through Life Good nutrition is crucial for people with cystic fibrosis (CF). For all ages, there appears to be a connection between good lung function and a higher body weight. A balanced, high-calorie diet with salt, fat, and protein gives the body what it needs to grow normally and live well. Normal gains in weight and height help build strong lungs and preserve lung function. Good nutrition also helps to build and keep a strong immune system to fight infections. Less infections and stronger lungs mean a longer, healthier life.Oh I can add many more refences if you like
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Yes he has CF, so a little weight is not going to harm him if he puts it on slowly and builts it as muscle. It will strenghten his lungs actually. So here is data backing my statementsnow I will accept apologies you morons, you think you know it all.Minocycline in the Antibiotic Regimen of Cystic Fibrosis Patients: Weight Gain and Clinical ImprovementIncreased weight gain and some clinical improvement was seen during treatment with minocyclineThose patients with severe disease gained more weight than those with mild or moderate disease, and males gained more than females. When minocycline hydro chloride was not the drug in use, patients lost weight and their health declined. Nutrition for Patients With Cystic FibrosisDiane L. Olson, RD, CSP, CNSD and W. Frederick Schwenk, II, MD Mayo Clinic College of Medicine, Rochester, Minnesota Cystic fibrosis (CF) is the most frequent, lethal genetic disorder among northern Europeans. The etiology of this autosomal recessive disease is known to be a defect in the cAMP activation of chloride (Cl—) channels in secretory cells in many organs of the body. Although this defect usually leads to severe lung disease, many of these patients also have nutritional deficiencies. Nutrition is one of the key components in the management of CF. Patients are at high risk for malnutrition, which may result in accelerated progression of the disease and increased morbidity. This review will discuss nutrition recommendations for calories, protein, vitamins and minerals, and enteral and parenteral nutrition support practices. Food FitnessAll kids need to eat well to grow up healthy and strong. But kids with CF need to eat more than most other kids, so they and their parents often work with a CF dietitian (say: dy-uh-tih-shun) to plan what they should eat. A dietitian is someone who knows all about food and nutrition. SAME GOES AS ADULTS2008 Pub MedIn adults with cystic fibrosis, percentage of ideal body weight based on the Metropolitan Life Insurance reference weights for medium/large frames overestimates the severity of underweight. Body-mass-index percentile for children and body mass index for adults as underweight indices have been proven to be valid. Strong associations between body mass index and lung function are also observed, but cutoff values to maintain a desirable level of lung function can vary. SUMMARY: Body mass index should replace the use of percentage of ideal body weight for classifying underweight in cystic fibrosis patients. More research is needed to identify appropriate indicators to classify short stature in children with cystic fibrosis.provided by www.CFF.orgNutrition & Cystic Fibrosis: Changes Through Life Good nutrition is crucial for people with cystic fibrosis (CF). For all ages, there appears to be a connection between good lung function and a higher body weight. A balanced, high-calorie diet with salt, fat, and protein gives the body what it needs to grow normally and live well. Normal gains in weight and height help build strong lungs and preserve lung function. Good nutrition also helps to build and keep a strong immune system to fight infections. Less infections and stronger lungs mean a longer, healthier life.Oh I can add many more refences if you like
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