"OCF Canuck" Patient Advocate (1000+ posts) Joined: Sep 2006 Posts: 1,357 Likes: 5 | Breathe deeply and relax. You are at a great place for information. I agree with the others about getting alot more information about your surgery - I am surprised that they didn't explain more to you, and yes, you should contact the doctor or nurse for another appointment to again go over what they are planning. My advice is to take someone with you - family or friend - who - guaranteed - will hear more/different things than you will.
As far as what to expect at home post surgery? If you need it the hospital can arrange for a nurse to visit you - homecare - to deal with dressings and make sure that your tracheotomy is healing as expected. When I was in hospital in Winnipeg, I was also visited by a social worker who enquired as to who would be at home to assist, patient needs, etc. No doubt that will be the case for you as well.
I hear that is a great Cancer Centre in London so I'm sureyou will be in great hands. Keep posting.
From a fellow canuck!
Donna
Donna,69, SCC L Tongue T2N1MO Stg IV 4/04 w/partial gloss;32 radtx; T2N2M0 Stg IV; R tongue-2nd partial gloss w/graft 10/07; 30 radtx/2 cispl 2/08. 3rd Oral Cancer surgery 1/22 - Stage 1. 2022 surgery eliminated swallowing and bottom left jaw. Now a “Tubie for Life”.no food envy - Thank God! Surviving isn't easy!!!! .Proudly Canadian - YES, UNIVERSAL HEALTH CARE IS WONDERFUL! (Not perfect but definitely WONDERFUL)
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