scott-sibley

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Viewing 15 posts - 16 through 30 (of 70 total)
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  • in reply to: physical restrictions with port a cath #91847
    scott-sibley
    Member

    Thanks very much, that is very kind. I’ll just be glad to lose this picc line. I have to wear one of those gloves that farmers wear over their arms to have artifical sexy time with cows. The line has bled a lot too, so I spend lots of time either at outpatients or calling the von trying to get the dressing changed.

    in reply to: 2nd line treatment. #91547
    scott-sibley
    Member

    Picc line is in. I was there for less than an hour. Other than the initial iv line which hurt, and all the blood I could feel running down my arm, it was a breeze.

    in reply to: new member first post #91576
    scott-sibley
    Member

    Hello David, it was great to make contact with you guys last night. I’m still blown away that 2 guys close in age that live minutes apart have the same rare disease. We even have the same name. My first name is David, but I go by my middle name. I added you guys on FB, so message me anytime you would like.

    in reply to: Cholestyramine Resin #91534
    scott-sibley
    Member

    The best way I’ve found to mix the powder is with just enough water that you can swallow it all at once. The chalky residue is the problem for me. I have not itched in a bit now, but Ive made a very conscious effort to not scratch. I’ve found all along that if I dont scratch the itch, it goes away in a minute or so. If I do scratch however, eventually I’m itchy all over and I got crazy.
    I have also read to use the same cup for the medication and don’t let others use it. The reason being is that some of the residue remains in the cup.

    in reply to: 2nd line treatment. #91545
    scott-sibley
    Member

    I’m not going to lie, the more I research or see pictures of this picc line, the more anxious I’m getting. I’m sure they will inform me and ease my mind tomorrow when I get it installed, but right now, I’m scared shitless. I think the thought of it interfering with coaching my son’s foitball team is the biggest problem. It also looks kinda gross.

    in reply to: Hello i m newbie #91489
    scott-sibley
    Member

    Hello Robert and welcome to our group.

    in reply to: 2016 CCF Annual Conference #91554
    scott-sibley
    Member

    The wife and I actually laughed at the prognosis when we got it, but it upsets so many friends and family if they search for cc on the internet and see the prognosis. We have had many very upset people come to the door or on the phone the first few months after my diagnosis. The good thing is most of them brought me great things to eat.
    I do not have that book nor have I ever heard of it. I hope its available here in Canada. I will definitely ask, and thanks for letting me know about it.

    in reply to: 2016 CCF Annual Conference #91551
    scott-sibley
    Member

    Wow, 8 years!!!! That gives so much hope to someone like me who is 4 months into this fight, and Im only supposed to get a year. I’m sure many others feel the exact same way.

    in reply to: 2nd line treatment. #91542
    scott-sibley
    Member

    Yep, I’m a definite hillbilly. not a bit of yuppy city slicker in me. I’ve read so far that I need to clean the picc line constantly and I can’t swim with it. Im gonna ask for the one that is under the skin. I’d have to wait a bit to get it though. Im sure there is a decent waiting list.

    in reply to: Cholestyramine Resin #91530
    scott-sibley
    Member

    Thanks for that link Gavin, it was exactly what I was looking for. I just did a search on google myself for shits and giggles and that link didn’t come up. I dont know if its because I use my phone instead of my pc, but my searches seem to be very limited.

    in reply to: Looking for other Canadians #91539
    scott-sibley
    Member

    I have never really looked for literature while in Halifax, but I will. The specialist in Halifax is coaching my onc here in Kentville. He seems to have quite a bit of experience with cc, and Im going to try and meet him next trip down.

    in reply to: Cholestyramine Resin #91529
    scott-sibley
    Member

    Im thinking my itching is more winter/woodstove related. I’ve been showering a few extra times in cooler water, and using moisturizer. It seems to make the itch go away. Also, If I can fight the urge to scratch, the itch goes away. If I scratch, it spreads and drives me nuts

    in reply to: Looking for other Canadians #91537
    scott-sibley
    Member

    I do receive chemo right here in Kentville. I have to travel to Halifax for PET scans. If I ever need radiation or any other treatment I’ll need to travel to Halifax for those as well. Its only an hour away, so that’s ok.
    I used to have a stop in Baddeck when I had a sales route many years ago. Its nice there. All of Cape Breton Island is nice.
    Are you from Toronto? I lived there for a few months when I worked for Futureshop when I was out of school. I worked at the store on Weston Rd. I’m too much of a hillbilly for the big city, but I had some good times there.
    I have not met any other canucks with cc. I don’t know if my onc has ever dealt with a cc case. She always finds the right specialist to get the right answer though.

    in reply to: Looking for other Canadians #91535
    scott-sibley
    Member

    Nova Scotia here. I live in Kentville, Located in the Annapolis Valley.

    in reply to: 1st Check up PET scan #91498
    scott-sibley
    Member

    ah ha, the phrase Im looking for is “second line treatment” now Im finding stuff.

Viewing 15 posts - 16 through 30 (of 70 total)