**NEW** Starting Chemo March 2009

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  • sakura73
    sakura73 Member Posts: 467
    edited April 2009

    MIchelle - what a scary episode at the fundraiser! I am glad you are feeling better. I do think of things by percentages. I have also decided that the best description for the post chemo fuzz (that my friends can understand!) is that it is like the day after a really bad hangover. Your body has recovered but it remembers the horrors of the day before! I have found this description helps people understand that although I am able to function, I don't feel that great. Perhaps I just have a lot of boozing friends!

    Buddy - thank you for your nice comments, and I am so sorry to read you are still in hospital and now dealing with cysts. I pray there is nothing sinister and that all is resolved soon.

    Diane - how are you? What was the result of the tests?

    Everyone - I do agree that some people mean well but just don't know how to respond to bad news of things like cancer. I have been fortunate, but there are some people who have found it too scary I think, that their friend/relative "has cancer" and have backed off. I hope you have all had a lovely weekend. My brother has been here cooking up a storm and taking great care of me. I am going to gain weight for sure this time around!

  • Janet0527
    Janet0527 Member Posts: 141
    edited April 2009

    Ah yes, percentages indeed.  Every day that's how I think of myself - what percent of normal do I feel?  This 3rd round of AC for me has brought me down a bit more than before, but nothing I can complain about in light of what some of you are going through.  Buddy - A couple years ago I was stuck in the hospital for a week with an infection, while every day my infectious disease doctor said maybe I could go home the next day, and then it didn't happen.  Hang in there.  Diane - Are you feeling better?  Michelle - Congrats for getting caught up on all the posts, lol.  You must have been relieved not to be carted away from the fundraiser in an ambulance, and I'm sure the fresh air on your drive did you a world of good.  I agree completely with your take on expressing concern to people.  I adjusted my approach some years ago when my brother died.  I had always reached out to close friends, but someone I worked with or didn't know well, I would probably not approach for not wanting to say the wrong thing.  Well, when friends and acquaintances were offering me support, I realized that I so appreciated the act of someone approaching me in any way, regardless of what they said or if they fumbled.  Since then, I have always come forward to offer support, and then I base any followup conversations or actions on how the person responds.  I think just the acknowledgement is important, rather than acting like the most important thing that's going on in someone's life isn't worthy of conversation.  I know "isn't worthy" isn't the right way to explain it, but that's how it can seem.  On the flip side, I remember being very concerned about someone, but not wanting to intrude, so I try to remember that some people in my life must feel that way about me, and I just try not to take any reaction personally. 

  • marshall2000
    marshall2000 Member Posts: 110
    edited April 2009

    Buddy1: So Sorry that you aren't feeling well, i hope they take your ovaries and that you are home soon. I will be thinking of you.

    Diddle:

    same to you, I hope you feel better soon.

    all ladies: have decided that the claritin just doesn't work for me. I have had a miserable painful last few days after treatment. I do not like taking so many drugs that i can't function, besides they don't control the pain, they just make you not care that you are still hurting. Anyway, for anyone else who the claritin doesn't seem to help much, I took 2 dayquil cold tablets and a hydrocodone(lortab) this morning , and my pain is finally tolerabl;e. I hope the taxol is easier.

    The weather is beautiful here today, it has been all weekend, hoping i can be somewhat productive today. Wishing all a side effect free day.

    zi get lost in all the posts and don't always respond individually, but just wanted to let you all know that i think of each and everyone of you everyday.  ]

    Love to all, Michelle

  • Janet0527
    Janet0527 Member Posts: 141
    edited April 2009

    I just realized that I haven't had to shave my legs or under my arms for like a week now.  Finally, a side effect I can appreciate. =)

  • PattiB
    PattiB Member Posts: 421
    edited April 2009
    Buddy & Diane - Sending well wishes, and hope you are both feeling a better.  Buddy - I really admire you and wish you the best diagnosis for you this week.
  • maidmarion
    maidmarion Member Posts: 45
    edited April 2009

    Morning ladies...The fog is lifting and I'm at 70% Laughing  so will be back at work tomorrow I guess. I Know I have read that some of you had cravings for salt, I didn't first time round but sure did this time, and for mashed potato and gravy! So along with that I had the junk food you all said you had wanted, I actually had MacDonald's, something I don't usually buy, not a burger but a fillet -o-fish sandwhich and the fries were so good!  Se's were about the same as last time just seem to hit a little quicker, I do have a ongoing problem with skin issues though in that I suffer with psoriasis, I don't have too many patches thankfully at the minute, but the ones I do have are like burns after the chemo and are really sore, my Onc gave me some cream that helps and usually takes about 10 days to Calm it down.

    Friends.....well I had an experience before this pathway about four years ago that kind of sorted out who my true friends were which is another story and would fit on another forum if I ever felt the need for it, which I can say I don't. Anyway I am not in touch with those so called friends and I am left with a few close and dear friends that have been a constant support through both of my life changing times these last four years even though they are miles away in the UK. And since moving here I have made a few more friends that have been very caring and offered help in whatever way they can. I am equally touched by people that I have come across at work (clients) that have been supportive too either because BC has touched their lives or someone they know of. I do think that some people don't know how to handle certain situations until they see how you are dealing with it, so I decided to be out there and open about it, even bringing humor into it, especially at work. One young colleague even said I was her Hero the other day, I was touched, but you just do what you have to do to beat this B*****d disease.

    Janet...yes I'm liking the not shaving bit too!

    Well it's another beautiful day so I am going to make the most of it, some errands to do , fog permitting, then R&R with a bit of Vit D. Have a great Sunday everyone.

    Sending healing thoughts as always

    Julie

  • Janet0527
    Janet0527 Member Posts: 141
    edited April 2009

    Do you ever just forget for a minute and do something really stupid?  I just took a shower, and after I dried off I started to put my hair up in the towel like a turban, when I remembered I don't have to do that because I have no hair.  Duh. 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited April 2009

    I am sorry.  I apologize.  I did let my anger get the better of me.

    Sessna1

  • theredheadamy
    theredheadamy Member Posts: 43
    edited April 2009

    Oh my gosh---I still try to squeeze the water out of my hair before I get out of the shower---and it's been gone for over a month!

  • kellerka
    kellerka Member Posts: 49
    edited April 2009

    Buddy and Diane I hope you are both feeling better today. Sending good karma. So far #3 has been much easier than #2. SE's are very different. Bad bone pain (even with Claritin) and bad insomnia. So tired but can't sleep even with drugs. I know it could be worse so I won't complain too much. Cool and grey in the NW. I miss the sun of last week.

  • ginagina
    ginagina Member Posts: 327
    edited April 2009

    Thank you Sessna.

    Hope everybody is managing SEs today. Enjoy what's left of the weekend.

    gina

  • Dawnmrn1
    Dawnmrn1 Member Posts: 446
    edited April 2009

    Hi Everyone!  Hope you all had a great weekend!

    Buddy 1~  Hope you are feeling better and get good results

    Diane~ I wish your symptoms go away!

    To all!  Your true friends carry you thru the rough times, I have found in my 50 years that people who are no comfort and don't no how to handle situations ,usually have not had the opportunity to get thru bad times themselves, most have just bounced thru life and they are the center of everything, too bad they miss so much. They do not share themselves with anyone and often times end up alone,  The bad times make you strong and you learn to cope and you find all the gifts that you did not realize you have.  I feel very fortunate my family and friends are SOOOOOO

    Supportive,we had a yard sale for Breast Ca yesterday and 25 families donated stuff and we made alot of money,I am so proud of them!! We were there from 6 to 3:00, a long day in the sun, but worth it! We also had a great human interest story.  This woman about 40 walked to the Garage Sale on a busy street 3 times with a beautiful 4 yo girl, it was her daughters boyfriends child, of whom she was the primary caretaker. The grand mother kept coming and buying a few things, she was very quiet, until we noticed that she kept coming back, at the end of the sale she was there and we gave her everthing for that little girl , snow boots and snow pants, a bike with a helmet, a brass bed, books, videos and anything else she wanted, we loaded up a van and took her home. She cried and wished me good luck with my treatment and insisted we take her last$6 for BC.  We had a fit, but she wanted to contribute.  We were all breathless, we are all mothers of girls and have so much and our girls have so much! We couldn't help but admire this womans courage!  A feel good story for a Sunday pm. Much luck to all this week, we are all making progress in this journey!  Dawn

  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009

    MichelleinSJ... Got to get out and actually exercise before I decide if I can do it sans wig.  Soooo very sorry about your incident.  BUT, I'm happy you had friends there to help.

    marshall2000... I hope the new drugs work for your Neulasta pain

    maidmarion... Is there EVER a time when McDonald's fries DON'T taste good?  LOL...

    janet0527... Glad you admitted it first!  Yep, I've done that several times.  I actually laugh out loud at myself!

    kellerka... I would agree about the Neulasta pain after the 3 tx. The third tx pain was like a stabbing pain in between my shoulders.  It would go away fairly quickly, though.

    Dawn... What a wonderful story surrounding your garage sale.

    AND... Sessna1... it takes big person to come back and apologize.  Thank you for your apology and I personally accept.  I hope your treatments go well.

  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009
    IowaDiva has been MIA for a while now.  I'm worried.  Has anyone heard from her?
  • didle20Diane
    didle20Diane Member Posts: 404
    edited April 2009

    Jan mom of boys, I just put a note on Carol (Iowa Diva's) FB page....looks like she is doing great though.

    Well, my 48 hours are up and my antibiotic is FINALLY kicking in.  Wow was that the crappiest sinus infection in my life.  My head and teeth hurt like crazy....I now have an appreciation for all those sufferers out there.  I have minor allergy and sinus issues but this infection kicked me in the a**.  My NP told me Friday that it would take 48 hours for the anitbiotics to kick in....WOW was she exactly right.

    I still don't know if I have any other lingering infections but suppose that the levaquin will tackle whatever else is going on if there is anything.  I am finally feeling like myself again and plan on going into the office tomorrow.

    Thank you everyone for thinking of me and wishing my symptoms away.......I think I went through 10 boxes of tissues blowing my nose.

    I am also finally caught up on the past few days posts.......Dawn, what a wonderful garage sale tale.  I went to a golddoesgood.com party last night at 5....I only stayed to sell my mom's gold since my HEAD wouldn't allow me to stand upright....but wanted to let everyone know that my wonderful neighbor 2 doors down who hosted the party chose the Susan G Komen Foundation for her charity!  The party was a huge success and I think over $100 got donated!

    I also put some items on Craiglist and Ebay with all proceeds going to the Susan G Foundation, too.  I hope to raise awareness to the cause.  I may even sponser our own neighborhood yard sale if I can get enough interest. 

    Buddy..........hope you are doing well.....

    As far as support from friends........I am very surprised how many of my "friends" on FB that I haven't talked to since HS have sent wonderful emails letting me know that they are thinking of me and if I need anything to let them know.  I was curioius how some would respond since cancer scares so many people.  So far all has been very positive. I am very open with my disease and most people I have encountered have been wonderful.

    Wishing everyone with treatment this week a speedy recovery and no SE's......

    hugs

    Diane

  • PattiB
    PattiB Member Posts: 421
    edited April 2009

    Dawnmom - your story really touched me.

    Diane - Glad your feeling better.

    Hope everyone has an SE minimal/free week or is on the mend.  BUddy - still sending well wishes to you for the week, especially ?Wednesday?.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited April 2009

    Wow, haven't been near the computer to read posts in about 4 days.  Lots going on with everyone.  I'm not even going to try to respond to posts.  EXCEPT, that I am so impressed with Buddy.  You have the best outlook and "chemocentric"  - get a patent on that word!! 

  • crusader1
    crusader1 Member Posts: 1,222
    edited April 2009

    Hi All,

    Diane- sounds like you are finally feeling better. That  is great. The donations at the gold party sound great.Every little bit helps in this battle.

    Buddy- Hope you are  doing okay. I don't think we have heard from you today. Is everything okay. Are you coming home ? What is happening with your surgery.

    Marion- Glad you are getting better. I understand about making decisions which feel right to you. If you are comfortable with a decision it is a good one. Strong people are not concerned with what others feel. Some people are just ignorant.

    Michelle- Sorry to hear about your unfortunate incident. Glad friends helped you out.You must have been nervous.

    Let's hope everyone on this board sticks to their word.

     At a birthday party today two women admired my lovely hair. They did not know it was a wig. The funniest part was that a friend said she liked my eyebrows,They seem to be getting smaller each day. She thought I had a nice wax job. I could have told her it was done by chemo but I kept quiet...

    Tomorrow is an onco appt. One week from tomorrow is my last TC.

    Hope all had a good weekend...

    Hugs to all...

    Francine

  • didle20Diane
    didle20Diane Member Posts: 404
    edited April 2009

    Francine, Always good to see you on the board.......congrats on being the first from the March Chemo board to be through with chemo ..... Next Monday I know BUT let's start celebrating now!!!!!!

     I too have noticed a little thinning of the eyebrows but mine were so thick to begin with I hope I can pull it off.  Smile I did get a wax job before my chemo started and so far that hair has not grown back in so I guess I got a great "deal"......

    Patti, I sent you my number through FB.....I am doing MUCH better.

    All......I think I need to do my hair every morning *sigh*.......My daughter  picked up some brown thread on the floor the other day and told me she "found" some of my hair......too cute.  She is not crazy about her mom looking like a baby monkey so I have to wear my buffs around her.  We had 90 degree weather this weekend and I could not imagine how hot I would have been with my old head of hair......

    hugs

    Diane

  • sakura73
    sakura73 Member Posts: 467
    edited April 2009

    I still wrap my head in a towel when I get out of the shower - it is sheer force of habit! Plus my head gets cold. Like Diane I already can't imgaine what it was like 2 months ago when I had my hair. Waist  length! What was I thinking?

    I am soooo hungry this time around - and the steroids must have worn off by now so they are not my excuse. I feel like my metabolism has got faster or something. Let's hope that means I won't gain weight. Julie I am craving potato too -I love gravy!!!!

    Can I ask how long it took for your port to settle down? My neck and shoulder are really sore - I think I must be tensing them to compensate or something.

    Diane glad the sinuses are improving.

    Ricki I forgot to say yesterday that my right boob has a funky looking scar around the nipple, but courtesy of my breast surgeon is perkier than my left, so  I am happy to submit it to the Team Australia boob squad.

    Sessna thank you for your gracious note.

    Love to all.

  • Janet0527
    Janet0527 Member Posts: 141
    edited April 2009

    Diane - So good to know you're feeling better.  I'm glad to hear that you think you have to do your hair every morning, and that MOB also tries to wrap it up in a towel.  Sometimes I just laugh at myself, and sometimes I look at myself in the mirror and wonder WTF, and I feel sorry for myself for just a second, and then I get over it, and then I move on.  

    What a terrific weekend, but I might have overdone it just a little bit today.  It was so warm and sunny and beautiful, I spent a couple hours working in the yard this morning, in the DC heat (because when it's cold and we wish for Spring in DC, we get weather in the 90s), and then I took a shower and went to dance practice.  I stayed hydrated and I felt okay, but when I got home, I took a 2 hour nap, got up and fed the dog, took another two hour nap, and now I'm ready to go to bed for the night.  Sleeping all evening was not how I had intended to spend the end of my weekend, and I'm pissed at my pathetic tired body for needing to do that.

    I signed up for the Global Race for the Cure in DC on June 6, and I set my goal at $500 for donations.  After sending out an email yesterday morning, I've raised $400 through donations from just 7 friends already.  Many of the people I emailed have no idea that I have such a personal stake in this cause, though I did personalize my donation page to say that I'm a survivor (I didn't feel comfortable mentioning it directly in the email, though I can't exactly explain why).

    One more friend story.  At the studio where I had practice this afternoon, I ran into some people I know, one of whom I haven't seen since or talked to since my dx, but I know the word is out in this circle of friends.  He came up to me, gave me a big huge hug, told me he loved me and that he knew I was a strong woman and that I was going to be just fine.  Sometimes people just say exactly the right thing.

    I wish that hug and acknowledgement of everyone's strength right back at all of you.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited April 2009

    Rachel, it took 2 weeks for my port to "settle" down.....no real pain but just annoying feeling, now I have to remind myself it is there.  I have had no problems with it.

    Janet, I want some of your energy......you amaze me with all you get accomplished. I think that sometimes I use my DX to rest all the time when I know that I need to get out there and take longer walks with the kids.......no more excuses, I need to get with the program and really start exercising consistently again.

    hugs,

    Diane

  • NanaA
    NanaA Member Posts: 293
    edited April 2009

    sakura 73 - It took a couple weeks for port to feel more comfortable, but even now if i sit too long with that shoulder raised it will be uncomfortable again for a while.  I find if i sit in a chair or sofa with a high arm this happens, so have been a little more careful about  how i sit.  The more my port has been used the more comfortable it has become, most of the time i don't even know it is there any more.  It was put in last week of Feb, so it has been in 2 months, but since I will be doing herceptin for a year it will be used for a long time.  Hope this helped.  Best wishes for a good week.  Annette

  • crusader1
    crusader1 Member Posts: 1,222
    edited April 2009

    Dawn and others,

    I totally agree that adversity makes one strong. Both my parents died when I was in my twenties. I have always felt that this made me a much stronger person.I always knew what was important and what was not. Maybe this attitude toward life enabled me to accept my DX and move on.

    Diane..I am not the first to end from the Warrior Princesses.. I believe MOB ends this Wednesday and Chick finished this past Friday. She had problems with her TC's so her last one was a AC. She took many meds and is doing okay. I am sure we will see Chick on this board during the week.

    Diane- I also had very thick eyebrows before the chemo. My last wax was just before the chemo also. I did read on the TC board that a women lost her eyebrows a month after her 4 TC's. I guess we have some surprises to look forward to.

    Good Night all,

    Hugs,

    Francine

  • didle20Diane
    didle20Diane Member Posts: 404
    edited April 2009

    Oh, YAY for Chick and Jan......!!!!!!!

  • Ricki13
    Ricki13 Member Posts: 80
    edited April 2009

    I still have about half a dozen hair bands sitting on my bedside table for tying up my long hair when I get out of bed!  I hadn't even thought about it until now but I can probably put them away for a while.

  • ChrisC433
    ChrisC433 Member Posts: 553
    edited April 2009

    I got to tell you...you ladies put things in perspective for me.  This weekend was gorgeous.  I got into such a funk...I didn't want to do anything.  I was pissed that I had to cover my head when it was so hot.  It has only been a month since I lost my hair and I've had it already!  I went from the chair to bed all day.   Hubby tried to get me to go for a walk and I refused.  I don't think it was that I felt bad as much as I felt bad for myself.

    Then I read these posts and it kicks me back into action.  You ladies have such energy and seem to hit things head on (no pun intended).  I told DH that next time I get like that throw me out the front door and make me do something.  It can be a slippery slope and I dont' want to get too far down the other side of it!

    Does anyone have ideas for light headcoverings for the summer months?  The scarves I wear seem to heavy.  Hot flashes don't help!!  Seems like my thermostat is always overheated...

    Congrat's to those finishing.  Hugs to all experiencing SE's today!

    Chris

  • Janet0527
    Janet0527 Member Posts: 141
    edited April 2009

    Diane - I just try to keep moving, because if I stop, I'm not sure I'll be able to get started again.  In the interest of full disclosure, though, I do spend plenty of time just resting in between everything else, and this morning, I hit the wall.  I got up at 5:30 to get ready for work and I just could *not* do it.  I sent an email, took some Tylenol (had a slamming headache, probably from too much time in the heat yesterday), and went back to sleep for three more hours.  The head is better at the moment, but I guess my doc wasn't lying when he said the fatigue would increase with each round of AC.  Yep.

    Chris - So far the best I've found for comfort in the heat is a plain old cotton bandana - it feels lighter on my head than a silky scarf or a hat.  A suggestion from a friend though was to look for something in a sports store made of a fabric that wicks moisture, like a buff by UnderArmour or some such brand that uses the kinds of fabric they use to make shirts for running and biking.  I would think Sports Authority or that type of place would be a place to look.  And, if you're pissed that you have to cover your head, heck, go for a walk bald.  Who cares?  Do use sunscreen though! =)

  • Dawnmrn1
    Dawnmrn1 Member Posts: 446
    edited April 2009

    Chris!  I have one of those underarmour beanies, from Olympia sports!  Wonderful, Isleep in it and walk around the house with it.  I also have some cotton hats that are comfortable, I got those at Marshall's. I like something that doesn't stick to my head I find scarfs uncomfortable.You can also get those hair halos that velcroe inside a hat much cooler but no one knows you are bald!  I am self conscience, and have too many people around my house to go bald.  So I have these solutions!  Good Luck! Dawn

  • 7timewinner
    7timewinner Member Posts: 183
    edited April 2009

    Hi, all!

    Rachel...for the first 2 weeks after having my port placed, it felt like I had bad whiplash. But it does get better, I promise! Now, it only hurts for a couple of days after I've had it accessed...like a dry, pinching feeling. I'm also kind of bony, so that doesn't help.

    Well, it's Tx #3 out of 6 for me this Thursday! When it's over, I'm half way there, yay! I spent this past weekend (glorious weather in the NE) in the garden...finally! It felt like heaven. And just this morning, I packed up my little ones in the stroller and took a 1 mile walk. Not even close to what I used to be able to do, but it was something. And between the 2 kids and a double stroller, I was probably pushing a good 75 pounds. It felt good to sweat again!

    And that reminded me just how important it is to live fully on those weeks when I am feeling good. Chemo week comes around again too quickly.

    Blessings for all...especially those of us having hard days.

    Nadine

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