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Welcome To My Blog...

This blog follows my journey of 2 different cochlear implants and my condition: Multiple mitochondrial DNA deletions I have started this blog 15 yrs too late but ill try my best to fit it all in! I have packed a lot of medical jargon into my life since I was 8.

There has been happiness and tears but I've come through it all with my family and my friends.I'm profoundly deaf as a result of a condition called Multiple mitochondrial DNA deletions which I have had since birth but I didnt find out this til I was 19. I have had 2 cochlear implants (at the age of 8 and then 15) I lost the 1st cochlear implant in my right ear after 7 years due to a bad, accuring ear infection (which I couldnt fight off because of my mitochondrial condition) at the age of 15 and had a 2nd one implanted in my left ear that same year which I have now.

My Story


10 May 2010

New purple pump...!

Next week, I will be getting a snazzy new purple pump for my PEG! I've been checking it out online and it looks really cool! It looks smaller and I will be have better feed packs as at the moment we get BOTTLES of feed and on the new pump, they have these tinfoil bags now that u can just throw in the bin. Next monday, me and my mum will be trained how to use the pump as we did with the current one I have now. I'm sure it will be simple enough to do. When i looked online, they show you videos of how you use it and the beeps it comes with if there's a problem. When I heard them, i kinda thought they sounded like the beeps I get on the maps on the CI! It was very strange!

So I get the new pump next monday, but the new feed packets come later, so I will have to keep using the current pump I have at the moment and I will eventually start using the new one!

It comes with its own little rucksack to take it places if need be and you can walk about with it which is better because with the wire on the pump i have now i cant really walk far unless I drag the pump around with me!

Bring on the Feed!
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