Starting Chemo Aug 09

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  • Scoobydoo
    Scoobydoo Member Posts: 499
    edited August 2009

    Happy Friday!

    Well I go for my port on Wednesday.  My employer has told me I can work from home the entire 4 months on chemotherapy and on days that I feel good I am welcome to come in.  That is just the best news ever!  I start AC/T on 9/3, but the date still needs to be completely finalized.

    Manue - I have really good insurance too and I dont know what I would have done without it.  We would be financially devastated.

    Jenn - I know what you mean about worried of catching germs in crowds.  I will start chemo pretty much right at the start of flu season and am worried about swine flu.  Sorry to hear your throat is still hurting, but happy that it seems to going away.  Let us know if there is any connection to folic acid.  Enjoy your weekend!

    Yasmiv - yes we are both blessed that we have such flexible jobs.  But I also agree that it is very empowering to be able to go in to work when we are feeling good.

     Kim - I am going to have my hubby buzz shave me.  I go to the wig place on Sunday to get fitted.  I decided on a custom lace front wig.  It's a little pricey but worth it.  My insurance will pick up half the cost.  Glad to hear you are home.  I hate hospitals.  Did they find out if the rash was chicken pox? 

     Karen - oh your kitty story is so sweet.  I hope you get to keep it.  I have two doggies who are so sweet and loving. 

     SusanFL- that is so awesome that your hair will probably not fall out.  That is definitely something to be thankful for. 

    Mainecon- that is great that you are feeling well!  I pray I have the same experience. 

    Anita

  • buccaneersdj
    buccaneersdj Member Posts: 241
    edited August 2009

    Hi everyone TGIF!!! Well the port is in, so far so good a little sore today I am taking Advil the Doc gave me Darvacit wow no thanks those things knocked me right out. My third eye (mole) is also gone can't wait to take the bandaid off tomorrow and see it. Today is day 16 and hair is coming out big time oh yea; "all my hair everywhere"! Good new at least one of my friends cancelled plans and will be here for the big shave along with 1 son and my DH.

    Kristen, I was told my chemo facility does not have wifi, I am bringing my netbook anyway because I find it hard to believe that in that huge busy building there is no wifi.

    I hope everyone has a SE free weekend!!!!!!!

    Thanks for being there for my head shaving drama.......(((HUGS)))) Donna

  • buccaneersdj
    buccaneersdj Member Posts: 241
    edited August 2009

    Good news, I to have reached my $1000. deductable and plus my $5000. max out of pocket that didn't take long about 2 months! Hope they can get my rads in by the end of the calendar year!! Gotta love an HMO...NOT!

  • Karen09
    Karen09 Member Posts: 320
    edited August 2009

    Oh Jenn I'm so sorry your throat is sore!  Take it easy!  You haven't had an easy time of this.  I really admire your attitude though.

    Thanks for the cat comments ladies.  He's a he, thought he was a she but no.  It was going well but he has very stinky urine.  I don't know if it just that I am more sensitive to bad smells right now but I had to clean the litterbox and almost threw up several times.  Ugh!  Hopefully I'll get used to it or I may get my dad to take him for a little while.  I did put an ad on the radio so maybe his owner will come out of hiding.  He is a very sweet little guy though and nice to have around.  I live alone so it is especially nice.  Not sure about a name yet....

    I washed my hair this morning and there was a lot more hair in the sink at the end of it.  And tons more when I blrew it dry.  Oh well.  I'm getting to the point that I was before my chemo started, I'm tired of thinking about it and just want to get it over with I think.  At least we will all be bald together and I will be in good company!

    I think I might be going out to breakfast tomorrow and I'm going to try to see if a friend of mine might want to go to a matinee on Sunday when less people are around, like you Jenn.  We've been wanting to see "The Ugly Truth" so we may see that.

  • NavyMom
    NavyMom Member Posts: 1,099
    edited August 2009

    Hi everybody! Buccaneer thanks for the chuckle regarding your third eye.  I was laughing out loud. I have some very good news.  My Navy son called to say he finally got his orders.  He will be stationed in Jacksonville,FL fot the next 3 years! Yea!   He will be going to school for the first 6 months.  More advanced training to work on P-3 Orion planes(radar/electrical stuff)  He reports to his new base on October 14 and is planning a visit home sometime between now and then!  Another yea! 

    Next bit of good news: one night when I couldn't sleep (again) I was surfing the net looking for chemo hats and the like.  Came across this site www.heavenlyhats.com   They offered a free hat to people that have lost their hair due to medical reasons.  So I filled in the form and today in the mail I got a package from them with FIVE hats inside!  All brand new with the tags still on.  All different solid colors the same style of winter ski cap. It really made my day!  Five Hats! I just couldn't believe the generosity.  Got that nice warm fuzzy feeling.

    Next bit of good news:  I got the call today that my wig is in.  Her name is miranda!  Only down side is, now that I am sporting a short hairdo I am not so sure about my selection.  I am liking the short hair after all.  But the lady said I could send this one back a pick out something else if I changed my mind.  So no problem!

    My hub and I are going to the local Italian fest on Sunday afternoon.  Neither of us are Italian but we love the food and they will have entertainment.  A Rat Pack band that plays Sinatra and Dean Martin stuff.  We like to dance and even have taken ballroom lessons!  So it will be fun and something to look forward to before all the "Cancer Crap" starts again.  LET THE BATTLE BEGIN!

    Sorry to so blabbery today.  Just had a lot to share.  I am glad you are here to listen.  I wish everyone a good weekend.  Remember to laugh, laugh and laugh some more.  If someone thinks you're nuts, just blame it on the chemo

  • YoYo44
    YoYo44 Member Posts: 203
    edited August 2009

    Hi ladies,

    Sounds like lots of good news out there, I am so glad.  Just read all the news and it is all a blur.  Just thought I'd sign in quickly.  Fridays are always super busy since I am off every Thursday, only check e-mails at the end of the day.

    Kristin-LOL about the book title.  Too funny. Scalp is still itchy but the hair is hanging in.  But I bought a great wig that is"me" yesterday so I feel ready.  Not really sure about wearing it since I have never been bald before!!!! but we shall see.

    Kim-how are you-sounds better so not chicken pox?

    Karen-glad to hear about the kitty.  We have 2 cats and they are very sweet.  Especially appreciated now.

    I read about your insurance situation and it makes me sad.  I am in the Montreal area in Canada (Quebec has it's quirks with the medical situation compared to the rest of the country) and have a great private coverage as well for meds.  I am at a great medical facility too so feel very well taken care of.  I have not gotten my scans etc as quickly as you ladies but if they were of immediate medical necessity it would have happened.  We are very fortunate here. I wish you all luck with the current government discussions.  It really seems a pity that everyone cannot have a high level of care and not be harmed financially.

    My news is TX3 was uneventful and I feel great today!  The SE's might start to accumulate but I'll deal with that as it comes.  I met my onc yesterday and he confirmed what I thought, but was afraid to think, my tumour is responding to the Taxol (or the Zoladex?!)!!  We were not sure if chemo would have a great effect hence the neo-adjuvant treatment.  I have ILC (which only has 20-30% response rate to chemo) and the tumour is large, 3.5-4 cm (hard to judge due to how the tumours grow).  So I am greatly relieved and feeling like I am progressing.  He said we might be able to do surgery after the 12xTaxol.  Will cross that bridge later-but also want this lump out!!

    I was debating about sharing the other bad news I have but think I will.  My father in law had a massive stroke this past Monday.  He has been on machines and under heavy sedation all week but weekend or early next week will probably be decision time.  While this is hard for me my poor DH is obviously getting the brunt of it.  First me and now this.  My good friend and I, who both seem to have lots of familty suffering lately, came to the conclusion that God does not operate under the quota system and we just have to take what comes with the most amount of grace we can muster.  So we have our prayers for the least amount of suffering for the FIL.  Sorry to end on a sad note.  But there has been a mixture of good and bad-just like life in general and we have a very tight and blessed family.

    I hope everyone has a great weekend and gets the maximum enjoyment that you can get from it! Cool 

  • NavyMom
    NavyMom Member Posts: 1,099
    edited August 2009

    YoYo -Peaceful thoughts for you and your family.   Your thoughts about God not having a quota really rang true for me, too.  Hugs to you.  Hang in there and God bless your husband.

    Navy

  • jenn3
    jenn3 Member Posts: 3,316
    edited August 2009

    It's the afternoon and my voice is still not there, but my throat feels much much better - I may be crazy, but I really think it's the folic acid.  DH just came home and said we had in invite to go watch the Saints pre-season game at a friends - I think I'll go, as I don't want to pass up enjoying the good days. I just won't be able to scream....... I've been lucky on the insurance thing - so far I've only had to pay one $200 co-pay for my surgery and one $30 office visit, according the the clinic I have 100% for the rest (as of now).   My mother in-law came over said it looked like I lost weight.  I stood on the scale and I did - 7lbs. I'm really not trying during chemo and quite honestly I thought I had been eating too much on the good days.   Anyone else losing weight?  I don't want the dr to get upset with me, but I am eating!

    YoYo - I am so sorry to hear about your father in-law, there are no words except I'll be thinking and praying for you and your family during this tough time.

    Donna- so glad to hear the port went in well and you found a friend to come over for the buzzzzz.....

    Karen - As a child I grew up with cats and some male cats do have very strong odor on top of which your senses are probably sensitive.

    Navymom - I am so glad to hear you son will stay put in Jacksonville for the next three years!! I know it can be hard wondering if they're leaving the county, we have one nephew that just got back from Iraq and another is getting ready to leave for Afganistan.  Thanks for the heavenlyhats website, I think I'll check them out.  I did get with Laurie @ FranceLuxe for the free scarf she offered.

    Scoobydoo - I'm so glad to hear your office will be flexible. Mine is too - they've told me I can pretty much set my hours, come in on good days, stay home on bad days and if I come in feeling good, then feel bad I can leave.  I'm hoping to go in week after next and get back into the swing of things - I am so tired of being home everyday. 

    Well I think I'll go shower and figure out what outfit will work on my newly flattened chest, complimented by my extremely short hair cut and get ready for the Saints game. 

  • Karen09
    Karen09 Member Posts: 320
    edited August 2009

    YoYo - I'm so very sorry for your loss!  You'll be in my thoughts.

    Jenn - have fun with your friends.  I'm sure you will look beautiful my dear!

    Hugs everyone! 

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    Hi ladies

    Welcome to our new Amazons.

    I'v been a bit miserable the past couple of days but today is much better. I have mouth sores (again) despite all my brushing and rinsing and I've had indigestion to the point where I don't want to eat as I know I'll be miserable. But started taking prilosec today and a prescription for "magic mouthwash" so all in all much better.

    Sorry to hear of nasty SEs in  others and if you're feeling good - enjoy!!

    Jenn - I have lost weight, but not particularly from the chemo, just the whole thing, from worry and surgery onwards.  I am now in the range of normal - not having been there for probably 15 years plus! So it's certainly not that I'm wasting away.

    Still have some hair but it's at the point where I wear a hat or something when I go out. Had lunch with a friend yesterday and wore a little turban with a scarf tied round it. Looked quite good.

    I am not ready to wear my wig. Not sure when I will be. I too have enjoyed my really short haircut and the wig doesn't seem like me now. Oh well. I'll wait till I'm truly bald and maybe will like it then.

  • Luddy
    Luddy Member Posts: 11
    edited August 2009

    Hi everyboby...

    Went wig shopping last Saturday and also had my long hair cut short this week to match the wig length.  This is the first time in 25 years I had have short hair.  I plan on having some fun it. You know what they say about lemons and lemonade.

    Had my port put in yesterday.  Old student - I agree with you. My port surgery was more uncomfortable than my lumpectomy.  Little stiffness, bruising, and swelling. I hope this subsides before Tuesday when I get my first treatment.

    Kristen09 - I too am doing TCH. I am sooooo glad to hear that you are feeling fairly well and that the exercising helps.  I am going to try to keep walking throughout.

    I am getting very nervous about my first treatment.  The uncertainty of how bad I may feel is hard.  I cried last evening on my husband's shoulder about the fear of feeling sick for the next 4 months.  Like so many of you, I have never really been sick in my life and it is hard to accept at times.  Very difficult to slow down and LET people take care of me! 

    Talk later....  

  • Kim09
    Kim09 Member Posts: 100
    edited August 2009

    Well the rash is pretty much gone and the eye infection seems to have clear up also.  I have not heard back about whether it was chicken pox or not.  But the anti-viral medicine seems to be knocking out whatever it was.

    The hair is really coming out this evening.  So glad I am getting the buzz tomorrow afternoon.

    YoYo44 - Sorry to hear about your father-in-law.  Your family will be in my thoughts and prayers.

    Luddy - Try not to worry about how bad the treatment will be.  I have found that nothing is ever as bad as I can imagine it to be.  What I did to stop myself from worrying was everytime I worried about the chemo treatment I thought of the chemo as a pacman going after all bad cells.  That way I had a little inside joke with myself.

  • eliz46
    eliz46 Member Posts: 71
    edited August 2009

    Hi everyone im from the group of july chemo starters im on my second treatment, all is well. My treatment is Taxatere/cytoxan every 21 days for 4 rounds ...The waiting for all of the information is the worst..... if i didnt find this site who know how i would be its great to chat to others and get pointers and information. 

  • lindal52809
    lindal52809 Member Posts: 25
    edited August 2009

    Hi sister Amazons

    1 down 5 to go. Lots to read up on again. Thinking of all you are all going thru, and keeping a positive outlooks for everyone.

    I got my port stiches off this morning, and everything looks great with that. Went to my teaching session for my Chemo treatments, got my binder (whoo hoo) more stuff to keep organized and keep track of. Blood tests looked great too. Port is so excellent. No poking all over my arms trying to find a spot. Then we began my CAT treatment. It all went very well. I feel good - today

    It felt so good to get started. I drank lots of water all day yesterday, at my Company baseball game and I didn't think about today all day. It was a fun day. Even got myself a Pink Baseball hat. I took my pills after dinner last night and went to sleep early too! 

    We got our grocery shopping done afterwards and went to dinner. Then my husband bought me an IPOD to listen to during my sessions. We are not in private rooms and the may be times I just want to zone out and not listen to what everyone else it doing.

    I am scheduled for the 6x's unless anything changes, so I'll be done by December.  Am going for my neulasta shot monday morning. What ever SE's I have I know I can get thru them. I have to!  Like all of you. Keep sharing. I'll let you know how I'm doing tomorrow.  

    Better tomorrows!!!  Linda

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    Linda - great attitude. You'll do just fine.

  • Karen09
    Karen09 Member Posts: 320
    edited August 2009

    If it makes you feel any better Linda I did fine with the Neulasta.  First chemo - not so great.  First Neulasta - no SE that I noticed.  I hope that doesn't mean it didn't work. 

  • pshelton
    pshelton Member Posts: 140
    edited August 2009

    Hi Yasmin,

    Still feeling pretty good, I feel a little churning in the tummy but the meds are doing their thing and I go ahead and eat a small meal...going to go for my walk in a few minutes...I get tired earlier in the evening and ready for bed earlier than usual but so far, knock on wood, that's been the worst of it...drink that water girls, tons of it and take those meds....I think that is the secret, hope its that easy...

    Hugs,

    Paula 

  • jenn3
    jenn3 Member Posts: 3,316
    edited August 2009

    Good morning - Woke up feeling lazy, but rather than let lazy take over the day I took the dogs for a good long walk.  Now I have energy!!!  My throat still very sore and still no voice, but I don't feel bad.

    Gill -sorry you had a rough couple of days.  My sister in-law told me to get "chemo" mouthwash from the dr for my throat.  I wonder if that's the same as "magic" mouthwash you got. 

    Linda/Luddy- you'll do fine once you get started.  The waiting is so hard.

    Karen - Did the dr tell you anything about losing weight?  Mine really stressed they didn't want me to lose weight during chemo.

    eliz46-thanks for visiting - we love to hear from positive people. 

    Hope everyone has a wonderful Saturday.  Laughing

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    karen and Linda - I have had 2 neulasta shots so far and no side effects at all. My blood work was good for my second tx so it must be working!

    Some of us here have started treatment, others are waiting to begin. I often go back and read the June chemo thread - so many of them have the end in sight! I just wanted to remind everyone that we WILL get through this and before long, future chemo groups will be reading our thread (getting lots of useful info) and marvelling that the end of chemo is in sight for us too.

  • yasminv1
    yasminv1 Member Posts: 238
    edited August 2009

    Good Afternoon everyone. I hope all of you are doing well.

    I am on Day 3 and feeling very good. I worked out yesterday and ran for 30 minutes this morning. I have had an upset stomach. I feel mild cramps and diarrhea but staying hydrated. I have lost 2 pounds since Thursday but I am sure it is the stomach issues and lots of fluids. I have noticed I begin to get tired around 5PM and don't feel like doing much.

    Paula - I am so glad you are doing well. Hang in there...staying positive and hope does help! Smile

    jenn3 - I hope your throat feels better soon. I am glad the walk with the dogs gave you an energy boost.

    Have a great weekend everyone. Take Care and be well.

    Yasmin

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    DH buzzed my head today. I am so glad it is gone. Tried my wig on - gave us a good laugh. I got some fake bangs, and with a scarf or turban, I really like the look. I just look so weird with a bare forehead.

    So another milestone done.

  • Kim09
    Kim09 Member Posts: 100
    edited August 2009

    Well I ended up getting an extemely short hair cut instead of the buzz cut.  I then tried on the my wig.  The hairdresser was actually very impressesd with the quality of the wig.  He said it looked very natrual on me.  It was so hot today that I took the wig back off.  I am getting more comfortable being out in public with the new cut.

    My friends called and invited me to a pool party tomorrow and I am going.  I think my surgical sites should be okay getting wet. (Its been a month since the lumpechtomy and 2 weeks since the port was put in.)

    Like Gillyone says another milestone has now passed.

    Now I have to decide if I want to wear the wig to work Monday or just a headscarf.

  • Karen09
    Karen09 Member Posts: 320
    edited August 2009

    Jenn - I hope you are feeling better!  Yes, my oncologist did talk to me about not losing weight right now.  I don't know how some of us couldn't though with being sick and mouth sores.  I'm eating really well now and trying to eat a lot but I'm sure I did lose a few pounds in the first couple days. 

    Good for all you ladies who are shaving/getting short hair cuts.  I'm noticing more hair in the sink when I wash my hair too so won't be long for me too. 

    My mouth is getting sore now too - lovely.  I have a prescription mouth wash - nystatin.  And I've been gargling with salt water too.  I don't know if they helped today or if it was the popsicle and frozen yogourt but I felt better tonight than this morning. 

    I had a great breakfast out with friends this morning and really enjoyed my omelette and home fries!  I was in heaven!  Tomorrow I'm going to see The Ugly Truth matinee with a gf and looking forward to that too. 

    I finally named my stray cat - Luke.  for luck.  A friend of mine suggested it and it sounded like a cute name for my cute little black&white friend.

    Hope you are all having a good weekend!

  • jenn3
    jenn3 Member Posts: 3,316
    edited August 2009

    Good morning - sounds like we're hitting some expected milestones.  My throat is still sore and still can't talk, but I did notice my tounge looks like it has a film on it towards the back.  I think it's thrush and maybe it's further down my throat.  I'll call the dr later this morning and see if they can give me something.  I'm tired of not speaking.  I was going to tell y'all this morning that my hair stopped shedding yesterday, but my scalp is very sensitive.  However, when I got out of the shower earlier it was full of hair.  Guess I just didn't notice it yesterday

    Gill - thanks for positive words and glad you're past the hair thing, we're all in line to be next.  

    Karen - I agree, how can we not lose weight, upset stomachs, mouth pain and things taste different. 

    Kim - a wonderful time at the pool party, much deserved!

    Yasmin - how are you today?

    This morning a friend is coming for coffee and I think I'm going to attempt homemade blueberry muffins.  Then later DH and I may go to the show.  Hope everyone has a wonderful Sunday.

  • Kayel
    Kayel Member Posts: 28
    edited August 2009
    • Hello Ladies~

    I am new to the board but not  to my DX.  I actually started my BC journey in Feb. when I found out I had DCIS.  It was hard to hear the "c" word but I felt comforted that it was stage 0 very earliest stage, slow growing, etc.  I had a lumpectomy Feb. 18 and results came back without clear margins .  Over the next 4 months I had 3 re-excisions and the last time on June 15th a sentinal node biopsy.  New DX, as I had lymph node involvement.  I ended up having a bilateral Mx and Reconstruction on July 16th with further lymph node removal.  My DX changed to stage 3.  There were 3 small tumors and 6 total affected lymph nodes.  Now on to chemo and radiation.  I begin my treatment on with AC this week on Aug. 19th.  I am also participating in the clinical trial for Avastin.  Is anyone else in this group involved with this trial? 

    I am finding a great deal of information from reading the posts.  I am new to posting but think this group will be a great source of support for me. I had my chemo teach session last week and boy what alot of information to digest.   Good luck to everyone

  • yasminv1
    yasminv1 Member Posts: 238
    edited August 2009

    gillyone - you sound so positive about the buzz cut. I think I will shave as soon as I notice a good amount of hair out.

    Kim09 - I hope you have a great time at the pool party.

    jenn3 - I am feeling Ok. I feel more tired today than yesterday. I had enough energy to run yesterday but not today..just going to take it easy on the couch. Still suffering from diarrhea and stomach aches here and there. It is not too bad though. Today I am noticing a tiny bit of an ear ache, my tongue feels weird and I have a little sore throat. I have that metallic taste in my mouth too. I am going to stay positive because it could be worse. I feel lucky to have manageable side effects so far. Jenn, I hope the doctor is able to give you something for your throat. I can only imagine how uncomfortable you feel. Let us know what they give you. Take care of yourself and take it easy. I hope your blueberry muffin and coffee party was fun.

    Kayel - Welcome. I just joined this thread too. The ladies here are wonderful and have provided tons of positivity and information in their posts. Good Luck to you.

    Take care everyone and be well.

  • yasminv1
    yasminv1 Member Posts: 238
    edited August 2009

    Ack! Just noticed my tongue has a white film on it. No wonder it is feeling weird this morning. Bummer!

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    I have a suggestion for those about to start tx - things I wish I had done!

    KEEP A GOOD RECORD - of everything that happens to your bady and what you do in response. For example, when you go for tx (#2 for me) the onc nurse asks all kind of questions about how you have been - SEs etc, when you had your last bowel movement etc. I wish I had kept track of how many days after tx I started with heartburn, so that I can pro-active at the right time,  or when I was constipated and prevent it this time, and which day I was most fatigued and not plan anything for that day. I know not everything is cut and dried, but I wish I had written everything down and not relied upon my memory!!.

  • NavyMom
    NavyMom Member Posts: 1,099
    edited August 2009

    Great advise, Gilly.  I have TX #1 on Tuesday. 

    Thanks

    Navy

  • sheila888
    sheila888 Member Posts: 25,634
    edited August 2009

    Gill, You touched a very important subject. I kept a journal every day from diagnosis to 18 months after. I used to write every thing every night including my own thoughts. That was a great comfort for me. And here i am 4 y ears later i know exactly what was happening to me then.

    Good suggestion.

    To all August Amazon's don't forget next year this time everything you are going through will be behind you.

    Good Luck and Best Wishes to all AMAZON's.

    Wink Sheila

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