Metformin (Glucophage) is currently the only biguanide oral antidiabetic drug. It works by inhibiting hepatic glucose production and increasing the sensitivity of peripheral tissue to insulin. Because its mechanism of action differs from that of sulfonylurea drugs, it may be given along with these drugs.
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Cystic Fibrosis (Reading & Sharing Part 2)
Bronchiectasis develops early in the course of cystic fibrosis, being detectable in infants as young as 10 weeks of age, and is persistent and progressive. Recent data reveal that neutrophil elastase activity in BAL fluid in early life is associated with early bronchiectasis in children with cystic fibrosis.
Nursing Assessment
Continue reading “Cystic Fibrosis (Reading & Sharing Part 2)”All Kinds of Mothers- Happy Mother’s Day
@ 1969 By Cecily Brownstone
There are all kinds of mothers in the world.
They come in different shapes and sizes.
Some mothers are tall.
Some mothers are short.
Some mothers are nice and roly-poly.
Some mothers are nice and slim.
And some mothers are soft and furry.
Does your mother feel nice and roly-poly? nice and slim? Which mother is soft and furry?
The Points of Light we see with our eyes
When we look up at the sky on a fine cloudless night, we see hundreds upon hundreds of twinkling points of light, some faint, others much brighter. We can see them best standing on a hill or high ground in the country; in towns, because of the smoke and the bright lights, we cannot see so many. Though most of these starts seem to flicker and twinkle, there are a few which are steady. These are not really stars but planets, quite near when compared with the stars, which are far away in space.
Cystic Fibrosis (Reading & Sharing)
Systic fibrosis is an inherited autosomal recessive disease in which abnormally thick mucus affects the reproductive, gastrointestinal, and respiratory tracts. Cystic fibrosis causes respiratory disease, characterized by chronic infection, obstructive airway disease, and progressive decline in lung function. Death is most commonly the result of respiratory failure. The life expectancy of patients with cystic fibrosis has increased to the mid-30s as a result of advances in treatment. Adult palliative care providers will be caring for more patient with cystic fibrosis as life expectancy of these patients continues to increase.
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