GNT: During last two weeks we change the... - PSP Association

PSP Association

9,230 members11,333 posts

GNT

Fadwa profile image
8 Replies

During last two weeks we change the feeding tube for my father two times and he was admit in the hospital he remove the tube from his nose at night he is able to eat but very little amount can any one give me advice how he can live without eating it's very difficult for me to look at him and count the days any one can just tell me if he have experience about this period of disease thank you

Written by
Fadwa profile image
Fadwa
To view profiles and participate in discussions please or .
8 Replies
cabbagecottage profile image
cabbagecottage

My mother had a stroke and they had difficulty feeding and keeping tube in nose , at the same time uncertain that it was going into the lung or not so fitted a peg instead .

Luckily she had no problem with the tube and left the peg tube alone . She lived for three years after that and eventually was able to eat some orally . But the peg sustained her . good luck maybe your dad will come to Terms with it . hugs xx

Fadwa profile image
Fadwa in reply to cabbagecottage

Thank you cabbagecottage but can you please let me know if the peg need a local or full anesthesia regards

cabbagecottage profile image
cabbagecottage in reply to Fadwa

Sorry not to get back before . I believe my mum had full anasthetic but not really sure .

nomansland profile image
nomansland

Madeline did the same thing...that nose job is an additional, hell for your dad unless it is your dad,s wish to leave this earth a stomach tube should be looked at,Madeline has had one for 3 plus years,to us at least it was a Godsend,regards..Rollie...but do remember psp is progressive so as you extend life the illness goes to lower steps...

The main questioon seems to be: does your father want to be fed? If so, he will find the peg fitted direct into the stomach much less intrusive and uncomfortable than the nose route. My wife had one for over a year before she died; her main nourishment was pumped to her overnight while she slept, leaving the days free except for three 20 minute sessions with syringes providing essential water, and an additonal liquid food to restore her weight and strength (lost when she could no longer swallow food of any kind) and her medication. The whole process worked very well.

Very best wishes,

Christopher

Fadwa profile image
Fadwa in reply to

Thank you but did the peg need a local or full anesthesia in in my country at the present we have only one doctor he can do it , regards

jimandsharynp profile image
jimandsharynp

My wife just stopped eating and ate very, very little before her death. Don't know if it was on purpose or the disease. I didn't ask her. After a week of not eating much she took a turn and passed in two days. The end is a tough time for us all. She didn't struggle at all, took one peaceful last breath and passed on to heaven. Finally free from PSP and the trials and tribulations of this world. Stay strong and don't force your loved one to eat. Jimbo

Fadwa profile image
Fadwa

Thank you all and appreciate yr opinion best wishes to you all

You may also like...

Swallowing help pls...CBD

decision..feeding tube or not. He has said \\"if I can't do things for myself, then no feeding...

New here - my father has PSP

He finds it very hard to speak, but he can still understand, so the fitting of a tube is his...

Is this normal? Am I expecting too much?

Provale cup that releases one teaspoon of liquid per sip. The therapist had him eat his breakfast...

Getting a PEG tube - psychological setback

semi-advanced PSP patients? How can we reassure/help her? Any ideas will be very helpful.

Dad in late stage PSP

the PEG tube will help improve his health - later that day, after checking an MRI, he declared him...