Does anyone else have experience with these? My mum is going to have one fitted as they have come to the conclusion she is now unable to swallow . We are hoping it improves her life going forward as her pd was a late diagnosis :disappointed:


My dad had an n tube for a while when in hospital then when they felt he will never be able to swallow again he was operated on and now has the tube in his stomach where we feed/meds through.
It takes getting used to and needs really strict care/timing/regime. Genuinely makes a world of difference and once you get used to it and find a system to suit your lifestyle/hers it gives you so much more freedom