Beautiful. Thank you Skipper & Jim. Very much appreciated.
Dad will have as much time with me as he desires while I'm there, even though he can't talk, I will be with him. We're very English/unemotional "solider on" is how it's being dealt with and expression of emotion is warned against, but I...
Hello lovely people,
I'm looking forward to flying back to the UK to spend Christmas with my family. I am really stuck about what to get dad for a gift.
Dad relies 100% on a feeding tube and can't get around on his own any more. He has a little iPad to type into but next year is getting a...
Thanks so much Hollister, Nikki & Donna. Looking into flights as we speak. Dad is very underweight (has a feeding tube) and has been in hospital with this for a week now (although only just diagnosed with pneumonia) so it sounds like I should go for sure.
Thank you. xxxx
I'm not sure where this should go so I apologize if it's in the wrong forum.
I am in the US, my dad is in the UK. I just heard this morning that he has pneumonia - he's in the hospital. Both mum & dad have repeatedly told the doctors that they want to take one day at a time and don't want to...
This is very encouraging Janeg - thank you for posting about it. I've convinced my dad to go gluten free for 3 weeks but he wouldn't commit to the ketogenic. I'm hoping that he feels enough of an improvement to keep going on in and then I'll try to convince him to remove foods with high...
Hi everyone,
I'm a newbie here. My dad just got diagnosed with MND 2 days ago but has been experiencing the symptoms for over 2 years. He is 69 and his voice is starting to be affected. His muscles have been twitching and are atrophying. I think we're all somewhat in a state of disbelief.
The...