MI Survivors

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  • carollynn79
    carollynn79 Member Posts: 654
    edited November 2009

    Hello to all, I am form Port Hope MI, raised in Huntington Woods, moved the Deckerville in the thumb of Michigan my junior year of high school and then re-married and moved to Port Hope 8+ years ago.  Love rural Michigan living.  I am am avid gardener, cook, wine maker, canner, my husband and I do a lot of things ourselves.  We are still picking herbs, broccoli, leeks and parsnips from our garden.  I was diagnosed in May, had lumpectomy, onco score 21, decided against chemo, had radiation had to drive 78 miles one way but thanks to good friends and family got thru it.  Finished August 26, still struggle with fatigue, redness, swelling, fuzzy brain and insomnia, but am really doing fine.  I started tamox in July due to agreeing to a enter the Tailorx trial, said I would drop out if chosen for chemo becasue I felt the risk was not worth the benifit.  Glad to meet all of you, hate the reason. I receive my treatments from the group in Port Huron.

  • neesie
    neesie Member Posts: 1,924
    edited November 2009

    Note to self:   Remember to send Dianne something from U of M ........ Wolverines! (jk)

    Hi Carrolyn, love the thumb area, quite a drive but well worth it for the beauty!

    Sure seems like we're getting alot of new MI girls.................glad to meet all, but geez this beast has to be stopped.

    Hugs,

    Denise

  • ICanDoThis
    ICanDoThis Member Posts: 1,473
    edited November 2009

    Hello, all.

    We had a very quiet Thanksgiving, but we had it at home, with DH actually eating some of my good Bell & Evans turkey breast. Cut up real small, with lots of gravy, and homemade mashed potatoes. Today, he and DD walked the dog to the mailbox. Monday, his stitches come out, and I go back to work.

    Path report said - 17 nodes taken, along with an esophagus with a 2 cm dead tumor - NED! Personally, I believe that it was the second round of cisplatin that did it - we had to beg, as his creatinine level was 2 points too low - but he agreed to come in for hydration every day for a week after treatment was done, so they gave him the treatment.

    So now, we are both in monitoring and maintenance mode. It's my turn, but I'm willing for neither of us ever to get cancer again.

    Thank you all for being there for us throughout this process.

    F...K CANCER!

  • faithandfifty
    faithandfifty Member Posts: 10,007
    edited December 2009

    It was great to get to go lunch with our very own nEEsie:

    Here's the two of us @ Panera on Monday. Sorry that I didn't plan further ahead...... next time I'll attempt to let you know so that we can make plans.

    xx00xx00xx00xx

  • neesie
    neesie Member Posts: 1,924
    edited December 2009

    Geesh, I just came here to check on all and what do I see but ME!  By the way, that is Faiths New Book and it is Beautiful!!!!

    I've been thinking about Terry, Sue...........how's it going with him?

    I'm still flapping in the wind and getting no where, but I was ditzy before all this, so you can only imagine my brillance now.

    Was kinda hoping we could do a Holiday lunch....but thinking Christmas will be here before we can set it up.  Thought about a Cookie Exchange......but I don't bake.  Was going to have you over here, but I don't clean either..(kidding), and it doesn't look to Christmasy here................Maybe we can all get together the first of the year.

    I'm pretty free with time right now, so let me know what and when the rest can.

    Denise

  • susieloutoo
    susieloutoo Member Posts: 107
    edited December 2009
    Wink Hello My friends - it has been way to long since I have been in touch or been on the site...I hope everyone is doing well   - love to all!!!
  • SEI
    SEI Member Posts: 191
    edited December 2009

    Hi Everyone!

    Thought I'd stop in and see how everyone's doing.  Welcome to the new girls!

    Sue - I'm glad Terry's doing well - I've been keeping you guys in my thoughts.

    Hope everyone had a nice Thanksgiving.  Ours was quiet.  Just the DH and my Dad and football.

    I'd be up for a get together either before or after Christmas.  Sundays are best for me during football season, but could make it on a Saturday.

    Hope to see you guys soon!

    Irene

  • winggirl2
    winggirl2 Member Posts: 332
    edited December 2009

    Hi Girls,

    Welcome to the newcomers.

    Sue - I have been thinking of you. Thanks for the update on Terry. Glad that he is improving each day.

    Neesie and Faith - Great picture. Sorry I missed up the date and could not join you.

    Susielou - Nice to see you back. How are you doing?

    Are we going to try for a get together or wait until after holidays?

    Will try posting picture of Grandson. Neesie I had trouble too took me forever to post picture.

    Preview shows 2 pictures posted will see if one shows up.

    Hugs

    Wings

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  • peg119
    peg119 Member Posts: 281
    edited December 2009
  • michlady
    michlady Member Posts: 77
    edited December 2009

    Hi...I'm pretty new to this MI site, but wondered if this group did get together for support, lunch, etc. I'm from the Flint area and the only support group I've found meets on the day of my chemo. It might be nice to join one...???    It seems like everyone knows each other here...??

    Had my 2nd chemo a week ago.   (U of M)    Days 5 and 6 after chemo were very difficult.   Numb from head to toe, greatly fatigued, achey (not sleepy, just didn't want to move)  Getting better, but still not myself.   Has anyone had this?   Five days out seems strange to have such a difficult after-effect.  Worried that it might be even worse after the treatment next week and need suggesions on how to cope (emotionally and physically) with it!   Maybe I did too much the first few days after chemo?   (I did a bit of shopping each day...felt great-then day 5 hit!   Not good.) 

    Any suggestions would be SO appreciated  Laughing      Thanks!   

  • Leslie1962
    Leslie1962 Member Posts: 233
    edited December 2009

    michlady - I had my first chemo at U of M Ann Arbor on Tuesday of this week. I had AC and seemed to have tolerated it well. Could your pain be related to the Neulasta shot - are you getting them? I don't know about feeling so poorly 5-6 days after the chemo, maybe others can chime in. I gave myself the Neulasta shot on Wednesday and have not really noticed anything. Wondering when I may see something other than a slight redness to the face, which is listed in the U of M packet as a side effect I might see that is not life-threatening.

  • michlady
    michlady Member Posts: 77
    edited December 2009

    Hi Leslie,

    It looks like we're the opposite Tuesdays from each other.   Too bad ... it would be "fun" to meet!   I do go there for PT on my off Tuesdays..???    I really didn't have any side effects until Sunday-and it wasn't good.   I hope you do better!  I'll talk to the doctor about it when I go on Tuesday.   Let me know how you're doing :)      Today I feel great!  Went shopping, had my wig trimmed a bit, and out to lunch.   It feels  SO good to feel goodSmile   

  • neesie
    neesie Member Posts: 1,924
    edited December 2009

    Hi Michlady and Leslie............just wanted to say HI and let you know that you have found a great group of girls!  We all know how confused, dazed and scared you are just starting treatment. Just keep up the fight........you can do it.

    Most of us here do know each other.........and we can be kinda crazy sometimes, but we have a good time getting together and yet I know first hand the support the MI sisters give.

    We do get together for lunches every now and again and always get together and do the Komen walk in May.  Looking doubtful that we will be able to pull a luncheon off this close to Christmas, but hoping the first of the year.  We come from all over.........I was actually raised in Flint, raised my kids in Flushing and now live just south of Fenton.

    Everyone stay warm...............

    Denise

  • michlady
    michlady Member Posts: 77
    edited December 2009

    Neesie-I live in Grand Blanc so put me down for a get together anytime! 

     Leslie-how is the redness to the face?  I don't have that, but this morning woke up with the bottome of my left foot very tender, feeling like a blister -  but there seems to be nothing there, just some redness and very sore.   This is crazy!  My chemo was on Dec. 1 and now this?!   Going in Tuesday for my next treatment.  Lots of questions for the doctors!    

  • carollynn79
    carollynn79 Member Posts: 654
    edited December 2009

    I did not go thru chemo so cannot help.  I do know that a few months out of radiation you can get some things happening, have flare-ups that come and go.  All part of this roller coaster, and I do not like roller coasters.  I would love to see if I can make one of the meetings.  I live in the thumb of Michigan so it will be a jaunt but we will see wher the next one is.  Winter is here, brrrr cold.  Well better get dressed have some shopiing to do and pick up my "special" expensive shoes to help with my walking.  Had a hip replacement Oct 2008, Diagnosed BC May so now I have to get serious and learn to walk right, still very uneven so will get shoes and start PT.  2010 is getting closer!!

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    Hi everyone and welcome to the new ladies.  I thought it would be nice for a get together too, what about Sunday the 20th?  Would anyone like to do that? 

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    Oh, Faith and Denise, nice pciture of you two!  And Wings...he is beautiful.  It will be a fun Christmas for you. 

    Our two week vacation was spent partially upnorth at my parents, and then on a road trip to Niagara Falls, NY, MA, CT, RI, and NYC.  We got to see out little grand daguther Riley, who is 4 months old, and attend her baptism. 

  • Leslie1962
    Leslie1962 Member Posts: 233
    edited December 2009

    michlady - I decided to call U of M yesterday and was told the face flushing/redness is from the steroid. The nurse said I could take Benedryl and it would help. I did, and it worked. Now this morning rolls around and is my first day of not taking the steroid. My face is red so just took some more Benedryl. All seems well at the moment, thanks for asking.

  • neesie
    neesie Member Posts: 1,924
    edited December 2009

    Hi all,

    Leslie......glad you made contact with the U of M.......I didn't have chemo so don't know alot of the side effects.  My DH had Chemo and that is ONE SE he didn't have.  Hoping good things for you.

    Carollynn........Boy, you do live in the thumb!  Beautiful area.  We do have one girl that comes in from Imlay City.......yes, Irene....I'm talking about you!

    Chris........Sounds like a great vacation!  Was that the first time you saw Riley?  It's killing me, as I have still not gone to AZ to see my new Granddaughter.

    I'm sure I can do lunch on the 20th.  Hopefully we'll get some takers.  I know the Grands will be here on the 19th., but I'll send them packing before lunch on the 20th!

    Hopefully some of the girls will check here..........I'll send a email to some that I have addy's for.

    Hugs,

    Denise

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    Well this might work out for us then.  We have at least 2 for the 20th!  I was thinking of either Canterbury which we did a few years ago and was very nice or something in that area???

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    This is the second time we have seen her, once at 2 weeks and then now.  We want to keep in touch by Skype and webcam, but so far this has not worked.  How old is your gran baby in AZ?

  • michlady
    michlady Member Posts: 77
    edited December 2009

    Not-Me,

    I could do lunch on the 20th.   Canterbury Village in Lake Orion?   Put me down!  It is the Sunday after my chemo, which is usually a bad day for me, but I'm going to check with the oncologist on Tuesday to see if he can tweek things a bit so it's not so bad.   If he can, I'd love to come! 

     Sue 

  • winggirl2
    winggirl2 Member Posts: 332
    edited December 2009

    Hi Girls,

    Sorry I will have to pass on this lunch. Canterbury well over 2 hour drive for me. Will have to catch you on the next one. Eat something yummie for me and take pictures.

    Hugs

    Wings

  • carollynn79
    carollynn79 Member Posts: 654
    edited December 2009

    Count me out on the 20th, just too busy right now, need Sunday to rest and it is too far.

    Carol

  • neesie
    neesie Member Posts: 1,924
    edited December 2009

    Chris,Can you believe my Granddaughter is 2 months old and I have not seen her yet? It's killing me....just the timing.  She was born on the 5th and Fred died on the 9th., I will get there soon.....just have to force myself to put one foot in front of the other and do it.

    Not sure where Cantebury is.....................thinking it might be better if we wait until after Christmas for a luncheon?  It would be fun, but so many have alot going on...............majority rules, just keep us posted!

    Hugs,

    Denise

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    Denise,

    Do you have a webcam?  If so, you should try Skype so that you can see her.  It is free.  We connected with out German exchange student, it was like he was in the same room.  

    So sorry about the timing of events.  At least Fred knew that he had a new grand baby brought into the world. 

    Well. lets see if we can get a few ladies and then make a call on the lunch. 

    Not Me 

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    Well maybe we should wait for a get together???

  • michlady
    michlady Member Posts: 77
    edited December 2009

    Maybe...not too many responses.    The 20th will be the Sunday after my Tuesday chemo...and both times I've had TERRIBLE Sundays...so chances are (although I'm trying to stay postive) that I wouldn't be able to make it, either.    So that could narrow it down to two...not enough.    

    It was a nice thought, though!    Thanks for trying to pull it together!   Glad we have this forum to help out, though! 

    Sue 

  • Not-Me
    Not-Me Member Posts: 198
    edited December 2009

    I hope you are doing okay michlady.  I visit your town each week, for my Toastmasters meetings.  They are held at the hospital.  

    Maybe with the holidays we should wait.  How about January 11th?

  • michlady
    michlady Member Posts: 77
    edited December 2009

    Not-Me:     Jan. 11 should work fine for me.   It's the day before my chemo, so I should be feeling great!    If you get enough responses, just let me know where  :)    

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