Sept 2012 chemo

Options
1113114116118119165

Comments

  • kelleyb
    kelleyb Member Posts: 94
    edited January 2013

    Mariposa- good luck with the lunch, I get your ambivalence and it is prompting me to blow off some steam.  I do hope, though, that it turns out to be a pleasant surprise.  You never know.

    I am feeling like I have slid into another dimension, in large part to being out of the office.  Like I am invisible most days.  Missing from my own life.  At the beginning everyone says the same things, don't they?  Let me know what I can do to help!  Then...crickets chirping.

    This is a long haul and people get bored.  Hell, I'm bored with breast cancer and as my oncologist said last night "you have a lot of treatment left". 

    I had mercy on my colleagues and started working at home when I began to look beaten down (aka the exhausted alien look) by chemo.  They really didn't want to look at cancer girl all day, it made it awkward to continue the water cooler gossip sessions, I guess.  And I understand that.  Though I didn't want to talk about cancer with them, I guess they felt obligated with me sitting there, then I felt obligated to talk about it and somehow manage not scare or depress anyone in the process.

    My ultimate grudge is reserved for the group of people who get updates on me through my DH or my mom, or lamer still, Facebook, but avoid calling or emailing me.  It feels like a sneaky way to, as you said, get "credit".  I pretty much gave up on trying to keep in touch with folks during treatment because it felt like I was expected to reassure everyone that THINGS WERE OK, really, it's not that bad, ha ha, yeah, it's hilarious that I have to draw on eyebrows each morning. 

    Most folks are probably thinking a variation of what you said "I'm glad it's not me".  I probably would, too, if an exhausted alien was among my colleagues.

    I just read the novel "The Fault in Our Stars", and though it's aimed at the YA audience, I really loved, and kind of perversely was cheered up by, how the narrator just nailed the whole chasm and tropes that lie between/among cancer patients and the healthy people in their world.  How it's futile to expect people to understand if they haven't gone there and how we must craft our own new life & world with a lot of thoughtfulness and acceptance of reality.

    Here's hoping your colleagues step up and show you a proper good time. 

  • bearcub
    bearcub Member Posts: 485
    edited January 2013

    JoJo glad you are on the mend, I wore a bra 24/7 after my surgery, each day will get a bit better.



    Cherioo woohoo so happy you are done chemo!



    English Rose I also am off to # 6/16 today.....this is a breeze compared to chemo.



    Cindi it is a long road we travel, because of herceptin I won't be officially done till early Nov. but I already feel I am over the worst now that surgery and chemo are behind me.

    My hair is even coming back, it doesn't really look like me but I kinda like the look anyway...I may be brave enough in another 6 weeks to go hatless in public.



    Everyone have a super thursday

  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    Morning all.... I got my butt out of bed this morning and did a mile on the treadmill it wasnt a huge step but its a start and it felt great! I plan to keep on it and up the distance slowly till I get back to my 5 miles a day on my bike... This could take till April with surgery and all but having a goal and something positive to focus on feels amazing!Oh and starting a food journal.

    Marianelizabeth..Hoping all comes back okay... Prayer and hugs for you keep us posted you are not alone!

    Hopex...Biotin helps promote healthy hair and nails. I take 5000mg perday. Oh and my hair came in white with no color and slowly turned my natural color of a dark brown. Now dont let me fool you there is some grey in there lol but it took about 4 weeks to start to darken. Its been since Thanksgiving and is now pretty dark.

    Mariposa... I agree with Hopex be confident we are so much stronger due to dealing with cancer... Those office girls have no idea what strong is! Go for it....

    KellyB.... You are absolutely right about the feeling of expecting to reassure everyone! Where the hell is our reassurance? My DH and kids are all the reassurance I need anyway, this is so ass backwards!

    Cherioo...Blab on all you want I am loving the insite, Im the kinda gal who has to have all her ducks in a row to relax! I have my ipod put on the list for the hospital among other things I love the idea of no help physically to get up and around this def looks like it has to be self motivated to help heal faster. I googled some exersices to prevent lymphodema after mastectomy but want to run it by my surgeons as to how soon I should start. I will be having a full ALND on the right side so I am wanting to get it under control asap! I also plan to call the social worker at the hospital today and get a nurse lined up if at all possible. My DH is going to take the whole week off of work to help around here lord knows I will need it with 3 kids 4, 7 and 15. All the rest of my family is 3 hours away so we have been pretty much on our own. Thanks again for all the support you have offered over the last few days. It has def helped get my ball rolling...

    My list for the Hospital/Home so far.....

    *alcohol pad (I heard a little tip that this helps you milk your drain tubes and cleans them at the same time)*roll of quarters for those at the hospital waiting for you perfect for vending machines.                                        

    *my own blanket(Im always freezing)

    *Pillow for under the seatbelt on way home plus to sleep with

    *slippers

    *hoodie and sweats to go home in

    *Ipod to drownd out the hospital noise

    *cold packs for soar foobs

    *pill organizer box

    *Stool softener

    *Throat drops ( heard the tube they put in during surgery can make your thoat hurt)

    *Button down shirts

    *house coat

    *paper plates/cups

    *book to read

    *rip front bras

    *a new recliner!

    If I can think of anything else along the way I will post it for any of you who are interested but hisa is a good start! I also heard its a great idea to go to a thrift store and get some hoodies as you can cut the pockets on the inside and keep your drains in them ;)

                       



  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    a few more things for the list

    *A note pad for keeping meds and instructions

    *Packet of clorox wipes to disinfect bed controls, door handles, remote, faucet, side rails

    *small container of hand sanitizer

    *phone and charger plus a list of people to call after surgery (this will be DH job)

    a few bottles of water and any other drink I may want.

  • JodiRocksthePink
    JodiRocksthePink Member Posts: 23
    edited January 2013

    I had my surgery prior to chemo.....I would add silk pants to sleep in. It helped sliding in and out of bed. I also cut small holes for the drain tubes in my sports bra because the tube between the bra elastic and my skin was really painfull. I slept on a wedge pillow for a couple of weeks too:) I have my exchange surgery scheduled for the beginning of Febuary and am planing to do all these things again. Hang in there! It only gets better!

  • Toastiecat
    Toastiecat Member Posts: 132
    edited January 2013

    Kelley, I totally hear you. Same goes for the "but you look so GOOD" thing. A) Pretty sure they're lying, B) They think I'm faking or something? What am I supposed to look like?

    And on the topic of friends, can a get a big WTF? I used to be really hurt when my friends said things that were insensitive...now I'm just glad they're still talking to me! Seriously, my two best friends have fallen off the face of the earth. My one friend lives about 1.5 hours away, so we don't normally see each other that often, but she hasn't visited once since the dx (6 months!). My other friend, who's local and I usually saw every week, has been MIA since my hair started falling out. Sorry just need to gripe...arrrrrg!

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited January 2013

    Thanks everyone for the encouragement and words of wisdom!  It is so helpful to know that I am normal and that you all feel some of the same things.  I tossed and turned all night last night thinking about this lunch.  At about 3:30am I decided not to go, and then I was able to sleep.  I guess I don't need the anxiety right now.  I will meet with them later and work it all out.  But for now, I am just focused on doing what feels right and causes me the least amount of stress and heart ache.  I feel kind of like a big coward- but it doesn't matter.  I have to be strong for too many other things right now.  Plus, these particular co-workers are the most gossipy of all of my coworkers- and they love to gossip about the two people in our office who have actually been in contact with me the most.  So, I just don't want to be in a position where I would have to tell them to shut up.  Everything feels so complicated.  I am sure it isn't really.  But it feels overwhelming today.  I am glad that I am not going.

    Kelly:  Thanks for everything you said!  I feel so much of the same thing.

    Amy:  I love the list!!! I am totally going to use it in February when I go.

    Toastie:  Again- I am feeling so much of what you said too.  I hate the whole "You look so good" statements too.  It feels like they expect me to look like death- and then I feel like if I look too good, maybe they think this whole thing isn't nearly as awful as I say it is.  Oh well.

    On the other hand, like so many others have said- I have had some people step up in ways that I would have never imagined- and because of it we are closer.  I guess I need to focus my emotional energy on those people and feel lucky.

    JoJo;  Thanks for the info about how you are doing!  I can't wait until I am on the other side of surgery so I can focus on recovery.

    Thanks again everybody!  I love this group so much.  I am giving everyone a big virutal hug!!!

     



    // <![CDATA[
    var __chd__ = {'aid':11079,'chaid':'www_objectify_ca'};(function() { var c = document.createElement('script'); c.type = 'text/javascript'; c.async = true;c.src = ( 'https:' == document.location.protocol ? 'https://z': 'http://p') + '.chango.com/static/c.js'; var s = document.getElementsByTagName('script')[0];s.parentNode.insertBefore(c, s);})();
    // ]]>
  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited January 2013

    Kelly B and Toastiecat -

    Your comments really resonate with me.  BC (before cancer) one of my very best friends would call, email and text often - a week would never go by without hearing from her, sometimes several times.   AC it feels like I hardly hear from her and when I do it seems she interacts with me only if I reach out.  Early on she told me to just ask for what I need, which at the time seemed supportive.  But what that boils down to is that I seem to have to do all the work.  I don't want to have to ask her to call me.  I don't want to have to ask her to spontaneously drop by.  I don't want to have to ask her to ask me to hang out.  I don't want her to text me to find out how I'm doing and then hear "crickets" after I reply.  There's a part of me that's really hurt by this change.  And then there's the part of me that understands she's terrified by all of this, and whether she's conscious of this or not she's acting like this as her coping mechanism because that's what she needs, not because that's what I need.  Even though I know that it doesn't make it hurt any less.  

    And then there are other people who've really surprised me.  They've just known how to be there for me.  And I don't think that's by accident - I think they've been through something that's left them with the insight and perspective to be better able to understand.

    I can't tell you how many times I've said this to my husband:  cancer is just so very, very awkward.  

  • fight4two
    fight4two Member Posts: 146
    edited January 2013

    Thanks for all the surgery tips you ladies are posting.  Perfect timing.  Sounds like they are trying to schedule mine for Jan 21 - that's SO SOON!  Am I ready? I don't know - but I do know I need to get this thing out of me.  I hope I can handle surgery less than 4 weeks after my last chemo.  As expected, my BS wanted me to do my last chemo -- just to complete the entire course.  I don't like having to make decisions, but if its not shrinking, I think I'd rather have surgery sooner than later.  So last tx canceled.  Am I PFC?  I've been too afraid to ask them if I have to do chemo after, but no one has mentioned it.  Maybe it depends on what they find in surgery.  Quite frankly, I'd rather start tamoxifen ASAP, as maybe that works better for me (hopeful).

    I finally got a look at my MRI, ultrasound, and mammo results.  I am quite suspicious as to the origin of these four satellite tumors.  I just find it odd that they weren't noticed on the first ultrasound with biopsy.  I had FOUR tissue samples removed from my tumor at biopsy.... and then months later when they do another scan, there are FOUR satellite tumors near the tumor.  Coincidence?  Who knows --  Regardless, it will all be out soon enough! Nervous but can't wait at the same time!

    Ok, just wanted to update you all on my story, for those that were following along....

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited January 2013

    Cherrio - CONGRATULATIONS!  So happy for you!

  • kelleyb
    kelleyb Member Posts: 94
    edited January 2013

    Mariposa - good for you for putting your well-being first.  I swear one day science will discover that exposure to gossip causes cancer and that's why so many of us gals get it.

    I envy you that you look good during chemo!  It has caught up with me, and that was just from the weekly Taxol.  I dread what I'll look like in the wake of the AC.  I'll need a bag to put over my head, like the Unknown Comic used to wear.  The Unknown Cancer Patient!  I'm gonna need more than a Lifestyle Lift when this is all over with.

    Toastie - I, too, am doing a lot more of the heavy lifting in all relationships post diagnosis.  What dang good is it to say "just let me know how I can help".  I want to say bitch, please, you are a woman, you know what needs to be done to keep a house in order.  Hint hint...laundry, sweeping, heck, order me a pizza sometime if you don't want to actually come over here.  It's insulting, or at minimum, disingenuous.  I've heard it too many times to take it seriously. 

    When people do step up, it's really random and spontaneous, which is awesome.

    As for friends disappearing, yep, it's happening - they all want to have what I have come to call the BIG CANCER TALK, that initial phone call to get all the horrible details about how I discovered the cancer, what treatment entails, etc., then it's a slow fade to crickets chirping.  This may be distancing - if they think I am going to be worm chow sooner rather than later I guess that could be scary and they want to get away from the exhausted alien.  Guess I have cancer cooties!

    My cancer experience has taught me that unless someone has gone through chemo there is no way they will come close to understanding what we are going through, and how profoundly we are impacted by the rigors of treatment.  It's a particular hell on earth that for some reason the medical community insists on sugar coating.  

    Ok, rant over - love the ladies of this group!!!

  • Cocobean
    Cocobean Member Posts: 135
    edited January 2013

    It's good to hear I am not the only one "shuffling"! Today was actually a much better day, went for a 45 minute...slow, but steady and felt pretty good. One step at a time....

    Couple thought for those of you with upcoming surgeries....definitely got tops that button up the front, with pockets for the drains. I also got safety pins and would pin the slack from my drains to my clothes, I didn't like the any feeling of tugging from them and that helped. My skin got a bit irritated from the drains tubing rubbing on my side, so I would pin them to the outside of my clothes. My mom and my husband helped me with this. 

    I had lymph nodes removed and on that side my BS said I couldn't wear deodorant for like a week and a half...(also couldnt shave my pit, but that won't be a problem for anyone now), anyway, I am not gonna lie, I stank and it really bothered me and I just didn't expect that to be an issue. 

    Please talk to your BS about arm exercises to do after the surgery, I had a booklet that had pics and directions which I found very helpful. I think I got the ok to start them 2 weeks post op. 

    Yes, pillows, pillows, pillows-so helpful. 

    My aunt is a wound care nurse and she recommended lots of protein to help the incisions heal. 

    Follow your BS or PS instructions on caring for your incisions, I had delayed healing issues, but never got an infection and I was meticulous about the care. 

    I was in the hospital for two days. I had an allergic reaction to the morphine and norco, was super itchy...I think I actually told my husband "I would empty our savings account to pay someone to scratch me 24/7."...so bottom line you shouldn't be itching like a crazy person. This was my first real surgery and in general I an sensitive to drugs which might have been part of the problem, but I had some nasuea the first week and in general the third day was the worst.  But it really really does get better, everyday, and after two weeks I was so amazed at how far I had come. 

    Really the hardest part for me was not being able to pick up my kids, my daughter was 10 months at the time at it just broke my heart. Now I just give her extra hugs to make up for that time. :)

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited January 2013

    Well I returned to work this week - I'm absolutely exhausted!  It was good to be back, but it was as if I never was gone.  The workload is ridiculous!  I did not forget to wear my wig (like my dream indicated) and some people actually thought it was my real hair.  As hard as it is right now, it is good to have some normalacy back.

    DH has a terrible cold now.  Even though we're behind a couple of weeks, this Sunday we were going to celebrate my last chemo by seeing 'TOTEM' - the Circque de Soliel show.  I hope we both are up for it!

    Amy - Congrats on completing a mile!  That is awesome!  What a great feeling.  Also, your list is great.  I had done some of the same, but forgot to include them in my list.  So many things to think about!

    KellyB - Yes it seems like eveyone needs to be reassured that we are okay.  I think it helps them cope with OUR DIAGNOSIS better.  It gets exhausting after awhile.  Your hints ring so true.  I was pleasantly surprised when a friend of mine (that lives out of state) arranged for 2 house cleanings.  Some of the friends that live the closest have disappointed me.

    Jojo - So glad you are feeling better!  Be sure to get plenty of rest!

    Mariposa - I am glad you decided to do what was best for you.  No room for any extra stress! You are no coward!

    Jodirocks - Good tip on the silk pants.  I will be having my exchange surgery within the next few months (date not set yet), so I get to prepare all over again too.

    Toastie & Mariposa - I too feel what you said too.  I'm tired of the "You look so good" - "You look great" - "You would never know..." statements too.  What am I supposed to look like?  I returned to work on Monday and I have heard these statements over and over.  It goes back to people not knowing what to say.

    Whenlifegives - You are right on target with your comments.  In the beginning, it seems like everyone is in a frenzy and then things plateau.  Life is so busy.  I think people go back to their routines and their focus changes.  It's sad, but in many cases that's what happens.

    Hugs to all : )))

  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited January 2013

    I just hate that there's no way to flag individual POSTS as favorites to refer back to later.  I simply can't begin to remember all the great suggestions and comments you all make.  And how would I ever sift through our many pages of posts to find what I'm looking for?  I'm not impressed with the discussion tool design.  Could use an overhaul, in my opinion.  So, when I win the powerball I'm just gonna have to do something about that!

    Faithfocus - Glad you survived the return to work.  Funny how in some ways nothing changes (piles of work), and in some ways everything changes (how much you give in to the piles of work).

  • kidsandlabs
    kidsandlabs Member Posts: 138
    edited January 2013

    Chemo finally done. Next step is BRCA testing. It will be next month. Waiting for them to call me with my appt. The waiting for the appt is terriable and I can't even imagine waiting for the results. Eveytime after chemo my right eye twitches, drive me nuts. Can't wait for the next few days to pass.

  • SeattleMama
    SeattleMama Member Posts: 147
    edited January 2013

    Cherrio- I meant 2nd round of chemo.  I did the neoadjuvent chemo and it worked at first (4 out of 6 cycles), then another different mass blossomed and surgery was moved up - - I was scheduled for surgery end of Jan/beginning of Feb.

    Hopex - I get chemo and had mastectomy at overlake, seattle eastside.
    BTW, I got this http://www.softeeusa.com/ for postsurgery.  Its tight enough to feel more secure, but not too much that it cuts off your circulation (like the ace bandage wrap did for me).  Surgeon actually gave me a prescription for the camisole to be filled at Nordstrom's.  It has pockets for the drains too.

    Wishing you much success and swift recovery.  Im still in pain, 2 weeks out and its really bothering me.

  • SeattleMama
    SeattleMama Member Posts: 147
    edited January 2013

    YAY Kidsandlabs!!!  ((sooooooooooo jealous :P))

    To all of you about the 'so called friends':  I am not believing this.  This is horrible.  I don't have any family or friends here, and thankfully some acquaintances have come out of the woodwork.  But for friends to bail on you now, OF ALL TIMES?!  wth!?

    I wish I was there to give them a talking to ;)  I know some people are stupid, some people can't deal with such things, some people are just rude....but there really is no excuse.

    {{{BIG, GENTLE HUGGS TO YOU ALL}}

  • Faith-Focus-Finish
    Faith-Focus-Finish Member Posts: 124
    edited January 2013

    Kidsandlabs - Yeah!  Chemo is done!  You did it!  Congrats...ringing that bell for you!

  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    Kidnlabs.... Congrats! Upward and onward to the next chapter.. Chemo seems like the longest hardest one!

  • PatinMN
    PatinMN Member Posts: 920
    edited January 2013

    Re: radiation for early stage BC - Mariposa posted a link a few days ago to new study results regarding fewer rads for early stage BC.  I asked about it when I went for my first rad treatment on Tuesday, and one of the techs went and talked to my RO.  She said she wouldn't recommend the shorter treatment duration for me but I could do it if I wanted (but I wouldn't have been able to start on Tuesday).  I decided to just go ahead with the plan for 33 treatments.  I had a chance to talk to the RO about it in person today.  The reason she would not recommend the shorter treatment plan for me is that none of the study participants had chemo.  They were all early stagers who went right to rads after surgery.  I definitely qualify as early stage, but I had chemo because I an HER2+.  So according to my RO there is no data proving that early stagers who needed chemo because of HER2+ (i.e. aggressive cancer) would have as good a result as the study participants.

    I also asked her about my number of treatments (33) vs. a lot of other folks on these boards who are having 25 or 28 or 30 treatments (or even fewer for Canadians and Brits).  She showed me the recommendations on the NCCN website, and I learned that the number of treatments depends on whether you are getting 1.8 or 2.0 Gy each time, and whether or not you are having boosts.  My dose is 1.8 Gy which translates into 28 treatments, vs. 25 if you're getting 2.0 Gy.  And I'm having 5 boosts (standard is between 5 and 8).

    I learned a lot today!

  • Timbek2
    Timbek2 Member Posts: 204
    edited January 2013

    Thanks for the rads info. Congrats to those finishing chemo. I finished treatment 13 today. Three to go! Cannot wait to get these behind me. I read everyone's posts. Love you all very much. You are wonderful strong women and our world is a better place with you in it! Thanks for being here. Wouldn't make it each day without u! Low se's to all. Hope I sleep tonite!!

  • jojo2373
    jojo2373 Member Posts: 662
    edited January 2013

    Patin, thanks for the info. These are all things I wanted to ask my RO too. I will be getting my rads treatment plan soon since surgery is now behind me.



    Possibly getting the drain out tomorrow, would be nice to have a shower!

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited January 2013

    Faith:  Congrats on going back to work:-)  I am looking forward to that less than surgery and radiation!

    Kelley: I love what you said about when they ask you what they can do!  I also hate the cancer updates.  Especially if they are the ones that never call.   I do write a blog to give people information.  If they are really interested, they could read it instead of bugging me about it.  (That sounded kind of mean didn't it !)  Cancer is kind of making me a little less able to put up with BS. 

    Whenlife:  Cancer is awkward!  Isn't it!!!

    PatinMN:  Thanks for the info about the difference from a lot of us and the study on rads.  I am her2 as well, so it probably won't be in the cards for me either (darn it).  But it is always good to ask the questions and have the information.  That way I can feel more secure in whatever the treatment is... and if down the line I have the bad SEs, I know I did due dilligence to get as much knowledge as I could:-) 

    Kids:  Congratulations!!!  Hope the eye stops twitching soon!

    Jojo:  Hope you can get the drain out tomorrow!!! 


     



    // <![CDATA[
    var __chd__ = {'aid':11079,'chaid':'www_objectify_ca'};(function() { var c = document.createElement('script'); c.type = 'text/javascript'; c.async = true;c.src = ( 'https:' == document.location.protocol ? 'https://z': 'http://p') + '.chango.com/static/c.js'; var s = document.getElementsByTagName('script')[0];s.parentNode.insertBefore(c, s);})();
    // ]]>
  • Hopex3
    Hopex3 Member Posts: 397
    edited January 2013

    Mariposa....I'm glad you listened to yourself and didn't go. That is one of the many things I have learned on this journey, is to listen to myself. You and your well being is what matters.



    Faith..glad your first day went well. I bet you are tired. At lunch, I go out to my car and take a little 15 minute nap. I've got my car loaded with blankets.



    Amy: you are inspiring me! Good for your mile. I need to change my ways but I just can't find the energy to do anything.



    JoJo...I do hope you get your drain out.



    Gotta go to bed...

  • patriciahurtado
    patriciahurtado Member Posts: 489
    edited January 2013

    Good morning ladies !!!!!



    Jo I'm so happy that you're getting the drains out so quick



    Amy I'm loving that list... I will walk soon too 5 miles sounds good !!!



    Mariposa always remember that right now is first you 2nd you and 3rd you... Just focus on you... To be honest I had so many friends before I had BC and i slowly push them out the way cause I believed they were all fake...... So for years i only hung out with my sisters and daughter and 3 friends .... And it feels good have few people in my life....... Friends come and go.... But its my choice who stays and who goes and i choose right...,...



    When I went back to work every one was soooooooo nice to me ..,yes got the same comments " you look great"... Your wig looks great .... And all that ..,.. To me it felt good cause I knew I look great... Lol...lol....



    All my coworkers are very nice they wanna always help me out ... There is just one dumm one that says that I "gain weight and that I need to stop eating" ... So finally I told him why im FAT lol... He said ohhhhhh.....



    I work with a lot of young people so they are funny and very out going and that's how I am too even dough I will be 40 this month it feels like 25 ....so ladies don't waste your time on gossips or any of that we have each other and I know we have done kick ass job on supporting each other if you ALL could only live around me I would always be here for you!!!



    Well I'm of to chemo land ... To get on my BGC and get a hell of ride!!!!! See you when I get off .... Weeeeeeeeeee. Weeeeeeeeee





  • PatinMN
    PatinMN Member Posts: 920
    edited January 2013

    Patricia, thanks for making me laugh!

  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited January 2013

    Chemo finale this afternoon! 

  • jojo2373
    jojo2373 Member Posts: 662
    edited January 2013

    Patricia - I want to party with you when we are well! You are so much fun.



    Drain free (sing to the Born Free music), I am human again. I can officially add to my list of things I know how to do "milking a jp drain". Gross!

  • Mariposa123
    Mariposa123 Member Posts: 267
    edited January 2013

    Patricia:  Thanks!  I think you are so rightSmile  Hope you have an easy ride today -and no SE!!!

    Jojo:  Congrats on getting rid of your drain.  I think the drains are the things I am most anxious about regarding surgery (and of course seeing myself for the first time afterwards)

    Whenlife:  Congrats on your final chemo!!!  Hope it is a super easy round and you are on the mend quickly.

    Hopex:  I was thinking when I go back to work that I am going to have to remove all of the kids car seats from the back seat so I can fill it with pillows and blankets - and put in a little alarm clock:-)

    Okay- I have had this weird side effect from chemo- at least that is what I think it is from.  I have never been a drooler when I sleep, but now- I have become a crazy drooler.   Does anyone else have this issue???  Weird.

    Oh- and I also wanted to just say thanks to those who many months ago recommended smooth move tea!  It has helped a ton.  And it is  gentle- which is nice.

    Talk to you all soon!  Today I am cleaning up and getting ready for my sister's visit.

     



    // <![CDATA[
    var __chd__ = {'aid':11079,'chaid':'www_objectify_ca'};(function() { var c = document.createElement('script'); c.type = 'text/javascript'; c.async = true;c.src = ( 'https:' == document.location.protocol ? 'https://z': 'http://p') + '.chango.com/static/c.js'; var s = document.getElementsByTagName('script')[0];s.parentNode.insertBefore(c, s);})();
    // ]]>
  • Amy4978
    Amy4978 Member Posts: 473
    edited January 2013

    Called my insurance and I have coverage for home nurse visits! I think I will take advantage of that after surgery. I should have my date by the end of mext week : )



    Wondering if anyone had issues with family thinking a dbl bmx was to drastic? I called my brother and father today since they never call me... And told them of my decision in return I got alot of silence and are you sure?



    Guess it doesnt really matter since its my life my body.....



    Hope everyone is having a great day... Its raining and cold here in michigan... Cant wait for spring!



    I did not do my mile today instead I went grocery shopping and 300.00 later with a trunk full My body is telling me I did enough exercise lmao but tomorrow me and the treadmill will meet again!

Categories