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View Full Version : Newly Retrached due to Vocal cord injuries


emcclary
01-25-2009, 04:51 PM
Hello

I was just retrached Jan 20th due to vocal cord problems caused by extended intubation during Sept 08 after a motorcycle accident. The reason for the second trach is because I have vocal cord fixation from scar tissue caused by the intubation which lasted three weeks. I am learning to adjust to living with the trach and had some questions. I was able to speak perfectly fine after one day because my vocal cords are in a midline position and they close perfectly they just wont open. I had to get the trach because they wanted me to have a viable airway before they started exploring my vocal cords because if they swelled I could lose my airway. I have a portex size 8 fenestrated cuffless trach. The fenestrations arent really doing anything since I never remove the inner cannula. While in the hospital I was rarely suctioned since my lungs are very strong and my cough reflex clears the mucous easily. I run a humidifier while I sleep at night but thats it they gave me a humidifier with a trach mask but I dont feel I need it am I wrong? How long did most of you wait to return to daily activities? I tried the speaking valve but have in issue with controlling my breathhs. I breath to deeply and end up stacking my breaths due to the vocal cords restriction not allowing to exhale as fast as I inhale. I also have to learn to slwo doen my speech rate and volume which before the accident ws fast and on the loud side. Any adive you guys could give me would be appreciated. Hopefully I will only have to keep the trach for 4-6 months but I need to return to my company as soon as possible.

Kate
01-25-2009, 05:25 PM
Welcome-most of us are parents of kids who are trached-but there are a good number of adults-hopefully they will help out. I think as far as the humidifier and trach mask--if you feel comfortable without it-then don't use it-but if you are feeling dry without it-use it. I know that probably sounds just so generic, but really that is what we do with Mitchell-if he's dry I give him nebs but other than that he isn't on any humidity and we live in the midwest where it is super cold and dry.
Hopefully they'll get the vocal cords figured out-good luck. Again, I'm sure some of the adults w/trachs will chime in too.

emcclary
01-25-2009, 06:36 PM
Thanks Kate I know most people here have children with trachs and I really feel for you seeing as I have one now at 46 yrs old. I cant imagine how a child would feel waking up with one of these and I was awake for the whole surgery with just a local because they didnt want to risk intubation again. It feels real funny in my throat at times especially when I have my head turned or not straight up. Fortunately I can eat and drink fine but I have gotten chest and back pains from coughing in the beginning right after surgery that are still with me yet. Hopefully after another week or so I will get used to it all until they can do my surgery and see how I progress from there.

Lisa and peewee
01-25-2009, 09:23 PM
My husband has been trached for 1 year and 3 months now and still has a funny feeling in his throat at times but of course he has a differnt type of trach and has it for Obstructive Sleep Apnea so things are a little differnt for him... He was back at work with 2 weeks I belive and has been going strong every since....He too also uses only a room humidifer a vicks and it works fine! he hated the trach collar! But when is is getting dry he uses Simply Saline Nasal Spray one squirt and he is good to go...but coughs alot after (I dont know if that is something other people use or recomend but our ENT told us about it) Good luck with everything and if you have any more questions feel free to ask!

Kate
01-25-2009, 10:00 PM
But when is is getting dry he uses Simply Saline Nasal Spray one squirt and he is good to go...but coughs alot after (I dont know if that is something other people use or recomend but our ENT told us about it) Good luck with everything and if you have any more questions feel free to ask!

That is what we do for Mitchell too-but we get saline from our DME-same stuff basically--or we give him a saline neb--I like that better because I feel it goes deeper.