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Recovering and Article… August 26, 2009

Posted by loz121 in Uncategorized.
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I have just got back from the doc’s because of that wheeze in my chest. The doc told me that it should get better in time and I need lots of rest and I will be back to my normal self in no time!
Apart from coughing up all the time which is making my PEG area so sore. 😦 we got cream from the doc for it but I can’t use it til Friday til the nurse shows us how to use it! Every time i cough, it seems to hurt my PEG area but I can’t stop coughting… I also have the blood test to see if my liver function has gone back to normal from my time in hospital. I hope its back to normal!
On a good note, the article about my 15 yrs as a cochlear implantee has come up in the magazine “here and now”
here is the link if anyone would like to read it. HERE AND NOW page 16.
Now to rest!
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Comments»

1. Megan - August 27, 2009

Hey. I don't have my PEG anymore, i had it taken out in January. But its definatly more comfortable than the tube, and much more easily hidden and forgotten about it. I only had the tube for 3 months before changing to the button PEG. Xx


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