I have suffered PD for about 11 years. In 2018, I was diagnosed with dysphagia and had to be fed via PEG.This year saw me back to nearly fully eating normally only to contract pneumonia and return to be fed by PEG once more.
Has anyone experienced this problem?
Is there anyone out there who has used CBD in a form usable via a PEG.
Regards
G Morrison
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Written by
Jmorri567
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I’m sorry you have dysphagia. Many of us have swallowing problems to some degree. As soon as I notice the muscles in my throat being less strong I remind myself to sing. One uses the same muscles to swallow as one does to sing, therefore singing, however badly, quickly strengthens the swallow. I have a section on helping dysphagia in my book “Music as medicine, particularly in Parkinson’s” amazon.co.uk/Music-as-Medic...
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