Canadians in British Columbia

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  • runor
    runor Member Posts: 1,798
    edited September 2019

    M.E., I will post a quick note on Micmel's thread saying you are needing down time to recover.

  • moth
    moth Member Posts: 4,800
    edited September 2019

    " I think we should find a date in November to meet at Cactus Club on Broadway. The second week of November is booked solid for me from Nov 9-15, otherwise it's all good"

    I can do Nov 16th or 23rd. Technically I can also make the 2nd but it's harder. I can make up a survey monkey if we want a poll? Or do we want to just pick a date and announce & just wing it?

    moth

  • DearLife
    DearLife Member Posts: 1,183
    edited September 2019

    Hi Moth. I could be there on Saturday Nov. 23. It would be nice to see everyone again. A potluck would be lovely but it is harder to organize.

  • moth
    moth Member Posts: 4,800
    edited September 2019

    Let's go with the 23rd then! :)

  • Pots
    Pots Member Posts: 186
    edited September 2019

    Nov 23 works for me too. Looking forward to seeing folks again!

    An

  • wrenn
    wrenn Member Posts: 2,707
    edited September 2019

    There's a silent retreat at Callanish on the 23rd but if that changes I will be there for sure.

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited September 2019

    Thanks for the responses everyone. I am dictating here as no way I could type with what I have going on. Everything went sideways last week, Wednesday I suppose when nausea and vomiting took over. I let my medical people know and was told to take Zofran and take it easy, ha ha. Friday it Got worse and I was in ER Saturday and I’m still here now though waiting for a bed. I am in a small quieter area thank goodness as the noise in the main area made me crazy and I almost went home. CT scans that night Showed a sub dural haematoma first then Scans of my spine showed cerebral spinal leakage. This may have gone back to the first surgery even but Wednesday I will have what is called a blood patch which will try to stop the leak.


  • wrenn
    wrenn Member Posts: 2,707
    edited October 2019

    Oh wow Marian. I can't believe what you have had to endure. it really seems endless for too damn long now. I would be cursing up a storm in your situation and to have to sleep in emerg this long just seems cruel. I am glad you went to emerg though. I hope they find you a bed very soon. And I hope the issue is resolved. Will be keeping you in my heart.

  • janky
    janky Member Posts: 500
    edited October 2019

    Oh Marian! I will be praying and sending positive energy your way - unbelieveable what you are going through :(

  • Pots
    Pots Member Posts: 186
    edited October 2019

    Marian, thanks for sending us an update. I’m in your pockets to keep you company while you wait. OMG you have sure had one thing after the next. At least you’re being watched in the ER...But it certainly is not a calm relaxed space.


  • DearLife
    DearLife Member Posts: 1,183
    edited October 2019

    Marian I am so sorry that you are having these complications. I hope they get everything under control soon and get you home again. We are all thinking of you!

    ❤️

    Pearl

  • stellamaris
    stellamaris Member Posts: 384
    edited October 2019

    Sending positive, healing thoughts your way Marian. So sorry you have to deal with these complications.

  • adagio
    adagio Member Posts: 982
    edited October 2019

    Marian - thinking of you while you go through this incredibly difficult time.

  • runor
    runor Member Posts: 1,798
    edited October 2019

    That is rotten news MarianE. I hope they get you straightened out quickly but man, you have got to be exhausted to the core from all of this. THinking of you and hoping for some improvement for you very soon!

  • Elderberry
    Elderberry Member Posts: 993
    edited October 2019

    Marian, I seldom go on the boards. I am so sorry you are in this situation. Getting the rug yanked out from under you. I am so hoping that you'll be posting soon saying "thumbs up -- I'm doing so much better" Hugs.

  • moth
    moth Member Posts: 4,800
    edited October 2019

    Marian, hang in there. Hope they get the spinal fluid leaks under control asap and I hope your pain is being well managed. gentle hugs

  • BlueSky1969
    BlueSky1969 Member Posts: 65
    edited October 2019

    Marian; I'm sorry to hear you are going through all this! I second Moth and hope your pain is being managed. And may this resolve quickly.

    I've been off the boards trying to get my life in order (?) Moved my mom into a facility, got my eldest off to U - although he's returning this wknd, a false start.

    Had an Onc appt the other morning. Was disappointed to learn they are now watching my L breast. Ugh.

    Hi to all...

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited October 2019

    Thanks everyone. I got a bed Tuesday and had the blood patch Wednesday. Headache gone right away almost but blood transfusion needed by then along wit IV potassium etc. has set me back. I am drained but on the way back.

    BlueSky, glad for the first things but not for the MO appointment with the watching/waiting again.

    Good night all. Early but needed.

    Marian

  • runor
    runor Member Posts: 1,798
    edited October 2019

    Sending you strength and speedy recovery, MarianElizabeth.

  • velo
    velo Member Posts: 44
    edited October 2019

    Thought I would say hi to the other BC women here. Waves! I am nervous right now as I go into a new and scary stage of my journey. CT scan appears to be mets to lung/bone. I get a lung biopsy this week and see my MO in Victoria Oct 25. Seems horribly too far away. Don't know what to expect at this stage and hope MO is on ball to latest/greatest/trials and everything. Hope not rushed, I hate feeling rushed through appt especially since its a few hours trip to come back.

  • moth
    moth Member Posts: 4,800
    edited October 2019

    Hi velo, welcome. Sucky news; I'm hoping you get some good reports later this month & a solid treatment plan. Hang in there.

    I do think that one really good thing about the BC Cancer Agency is that they do seem to be very evidence based and because it's a province wide program, you get the experience of the whole team behind your MO. They all seem to work collaboratively to arrive at treatment plans (or follow well established treatment protocols and clinical pathways).

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited October 2019

    Velo, I just wrote to you and everything started deleting. I want to welcome you here and know there are many with you. You and I were diagnosed in 2012 I see. I was in Vancouver them and move to Victoria in May 2017 just about when I found about my MBC. I really like the cancer team here and have a caring MO. Did you have your first treatments here in Victoria? Take lots of deep breaths and let's hope things move quickly so no long waiting games. The biopsy should tell the story but until then, there is no knowing.

    I am at BCCA often so let me know if ever you would like to meet.

    Hi Moth. How is it going now for you?

    🙏Marian

  • moth
    moth Member Posts: 4,800
    edited October 2019

    Marian - thx for asking, I am well. My MO agreed to put in a requisition for a breast MRI to do in between my annual mammograms. Apparently the BCCA changed some guidelines about who could qualify for them & now early stagers with certain density criteria may qualify. She initially wasn't sure it would get approved but it did & I'm scheduled for December.

    I'm half way through semester 4 out of 9 of the nursing program. I'm on a surgical rotation right now. I'm feeling fine and mostly enjoying myself though occasionally I worry that I'm not eating or sleeping as well as I should; always trying to find that magical balance between studying & the rest of life :)

  • velo
    velo Member Posts: 44
    edited October 2019

    Hi Moth and Marian -

    Thanks for the welcome. Yes I had my previous tx in Victoria. MO not very emphathetic. But he does return calls if I have questions.


  • wrenn
    wrenn Member Posts: 2,707
    edited October 2019

    Welcome back Velo and so sorry for your recent news. I am hoping for Dr. House diagnosis too. :-) Not funny though to have this worry. This is a great group to lean on.

    Marian I hope things continue to improve for you. You are so damn strong.

    Bluesky I hope the L breast is fine. What a worry. Feels like it never ends.

    Moth, You are already just about half way through the nursing program. Time goes so fast.

    Hi to everyone and I hope it is as sunny where you are. Kits is blue skies and leaves turning colour. Nirvana.

    Take care everyone.

  • cathy67
    cathy67 Member Posts: 514
    edited October 2019

    Hi ladies!

    I was referred by moth to this forum, so grateful we have this one in Vancouver.

    I will spend time to go through all what you were discussing, but it is holiday now, busy around.

    So, can anyone tell me your gathering details? Just in case, I don't have enough time to find it before the meeting time. By the way, I am in richmond BC,

    Catherine

  • moth
    moth Member Posts: 4,800
    edited October 2019

    Hi Catherine - yay you made it over!

    We're looking at Saturday Nov 23 1 pm at Cactus Club, Broadway & Ash.

    I'll be posting an RSVP surveymonkey in a second :)

  • moth
    moth Member Posts: 4,800
    edited October 2019

    Can everyone pls RSVP by clicking here https://www.surveymonkey.com/r/Z9N3LHQ

    I'll make reservations in a couple weeks once we have some numbers.


  • cathy67
    cathy67 Member Posts: 514
    edited October 2019

    Hi moth,

    I am preparing for chemo. Are we using port or picc for the chemo, if 8 rounds, do you pick up this option?

  • marianelizabeth
    marianelizabeth Member Posts: 1,735
    edited October 2019

    cathy67, I had a port for my round of 8 and loved it. I had a Bard Power port then (2012/13) and have now now. The Pics is more hassle though probably less costly. For showering, you have to cover or detach~~not sure as I never had one. The port can also be used for blood work, I have mine done through my port and am about to get that done. The lab tech leaves it accessed for my chemo tomorrow. Pokes are almost impossible so if your veins are also poor, then a port is a godsend.

    Marian

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