November 2009-Starting Chemo

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  • Mouse6694
    Mouse6694 Member Posts: 88
    edited November 2009
    NEW MOON was great better than the first Twilight. Took my daughter out of school early had some lunch and enjoyed the movie it was a great day. I sat at the top row hoping to avoid any sneezing or coughing germs to filter down. I had been hiding in the house since tx2 and needed the break. I got tired of finding hair everywhere and shaved myself bald in the shower luckily I didnt cut myself but I was done and my head was hurting and now I feel refreshed. Today was a good day, through it all girls there are still some good days out there and we just need to hang on.
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  • SharaD
    SharaD Member Posts: 100
    edited November 2009

    Thanks doronet.   I've heard Vit D is not good for LYMPHOMA, but apparently a number of current chemotherapies have been shown to be greatly HELPED by vitamin D, in other words your chemo works better if taken along with vitamin D therapy.   I've heard no Vit C with chemo, but that's the first time I've heard no vitamin D.  I'll ask my Onc!  I've been pumping the Vit D in preparation for chemo but maybe I should have checked first.  This disease is not "one size fits all", that's for sure!

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  • mabelle
    mabelle Member Posts: 80
    edited November 2009

    Thanks to everyone for the words of welcome and support. I've now looked back on most of the previous posts and have taken away lots of great tips and advise.

    I don't have much news to report, I feel about the same as the last time I posted... still a bit queasy and quite tired. My taste buds are still doing weird things - but I think I've just gotten used to it.

    I would like to share something with you. I've signed up to be part of a trial - a "randomized controlled trial of combined aerobic and resistance exercise in breast cancer survivors receiving chemotherapy: or the CARE trial."

    I've only been to 2 exercise sessions so far, but have to say that during these sessions I have felt really good. I go into the gym feeling like crap, then halfway through the exercise, I feel really good with no queasiness and pumped with energy. I'm required to go mondays, wednesdays, and fridays for about an hour a day the whole time I'm on chemo (6 months). They've set up a small gym just for this trial, and all the women there are in the same boat. All you see is beautiful bald women huffing and puffing on treadmills and stair climbers. Its really quite fantastic. I feel really lucky to be a part of this and I think its going to be really good for both my spirit and my body. The women who I have spoken to who have been in the trial for 3 or 4 months are also very positive about their experiences - saying they always feel better after their exercise. 

    If anyone is offering this trial in any of your cities - I highly recommend looking into it. And if there's no trial, try and get out for a walk or a hike, or whatever, as much as you can. It really seems to help.

    I'll let you know how I feel after a few more treatments... I may be cursing the day I signed on (but I hope not!) 

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  • BeccaS
    BeccaS Member Posts: 19
    edited November 2009

    Hello to all sisters on this journey! I'm in the good week before the next tx and I find myself so happy to have energy, be free of SE. wow! The first two weeks were really rough and I wondered if I could actually do this, but this feeling of wellness is powerful medicine and boosts my confidence. Best wishes to all of us.

    The timing of this round is good for my Thanksgiving but will be lousy for Christmas. Oh well.

    I have a port and am so grateful for it. It makes the chemo infusions so much easier and when I went into the hospital (for neutropenia - low white blood cell count) they used it for the antibiotics etc. Leaves both hands free, saves my veins and doesn't hurt... it is just a bit odd feeling at times. With only one arm available for poking and my veins hard to access I figured I wasn't going to have any access left after a year's worth of treatments. So I am very happy for this invention.

    My hair follicles are all tingly and am shedding like a dog! In the morning after my shower I have to sweep the floor. I had my hair cut really short, shorter than I've ever had it (in August it was below my waist - then shoulder length - now an inch or two). I like it! Not a fan of its thinning and loss but... I was not planning to get a wig but all the advice seems to be to have the option... so I am rethinking whether I want one. It seems a hassle, but then there could be times when it would help others be at ease (and maybe me too). How did you decide which one and where?

    Thanks for the fine company. 

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  • BetsyBuzz
    BetsyBuzz Member Posts: 592
    edited November 2009

    Hi Ladies...just lurking on your site. I finished 4 DD A/C and 4 DD Taxol treatments in August. Then had 33 rads with 7 boosts. Finished up a month ago. One of the ladies on another thread suggested to some of us to share what worked for us with others as they go through treatment.

    So here goes:

    About day 17 my hair started falling out in clumps. My scalp started hurting. I buzzed it short but didn't shave it for another week or so. It was such a mess. My suggestion, shave it sooner...as soon as it starts coming out in clumps. It feels so much better not having the hair pulling on your follicles. I went without a wig the entire time and did just fine. But I know I was in the minority. Do what makes you feel the best. There is no right or wrong way to walk through this part of the treatment.

    I had terrible bone pain from neulasta shots and taxol. I learned when taking any pain meds along with chemo be sure to take a stool softener or two at the same time. If you are experience lots of bone pain talk with your onc., they will give you something to help. Also for the constipation, I used a morning cocktail the first week after chemo. 1/3 c OJ, 2/3 c prune juice heated (needs to be heated). I was able to drink it even when water started taste metallic (end of A/C beginning of Taxol).

    Lots of women on my thread said Claritan worked for pain. I did not have the same results.

    For neuropathy - I took glutamine and had very good results. Initially I was skeptical. Mostly cause I had difficulty getting it down. I finally figured out I could handle it with ginger ale. I took a tbsp in the am and one in the pm with about a cup of ginger ale, while on Taxol. I had a terrible time with finger pain and neuropathy and it really helped. I have no lingering neuropathy and I'm 4.5 months PFC.

    When food became an issue - which it did. I ate lots of fresh fruit, yogurt and egg salad. Cold food was easier on my mouth and stomach.

    Speaking of mouths - mouth sores...ask your onc for some magic mouth wash if it becomes a problem. I think its part lidocane, milanta and cherry flavor.

    Fatigue - Mine included heart palpitations. It was very scary to me. Actually I was totally freaked out by them. But it's part of the process. My RBC & WBC were very low. Listen to your body but get out of bed every day. I tried to walk each day..even though my dh laughed at me, he said I was moving at "walker pace", he was referring to elderly people walking with walkers not speed walking.

    Oh any one on the A/C T treatment plan...don't assume taxol is better. It's just different. It's better in some ways but worse in others.

    I know there is more...but that's all I can think of right now.  You can do this. These threads are a life line. It's a great place to whine, rant, encourage and learn. Plus it's truly amazing the friendships I've developed online. It's a wonderful support group. Good luck.

    Betsy

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  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    I JUST WENT TO PAGE BACK AND LOST MY WHOLE POST>>>>> grrrrr.

    Here goes again. 

    Betsy ~ thank you so much for popping in and giving us some great information.  I hope you are feeling good and getting on with life as best as one could after this awful blow of BC.

    Becca ~ I am glad you are feeling good !  :)  Yes, the wig is a good idea to have on hand.  Sometimes for you sometimes maybe to comfort another who is uncomfortable.  For example: my kids friends ~ when they come over I find 15 and 10 year olds get all nervous and don't want to see me sick.  Nor do I want my kids to feel uncomfortable.  So I plop one on my head.  They will help you at the Wig place pick one out that matches your hairstyle and color or you can have fun and go crazy too !

    Mouse ~ So happy you had a nice day with your daughter and enjoyed New Moon.  I love that whole series and have read every book.  (hence a 15 year old DD too) :)

    Shara ~ I hope you are feeling good.

    Mabelle ~ Your exercise class sounds wonderful !  I am sure it is good to keep the body strong while going through all of this.  I used to exercise all the time ~ now since I've been diagnosed with the dreaded "c" word, the depression just doesn't give me the will.  I do go for a walk now and then and clean the house that is like an aerobic workout for me !!!  :)  I may have to dust off the treadmill or bike, HECK full gym I have in my basement as chemo is just making me be one of the blessed girls that is gaining WEIGHT!

    I can't page back so to all my other sisters here, BrendaSharon you will always be our LEADER even if you don't feel good or are having a Whimpy DAY!  And Ccnani is always here to cheer us ON too ~ Mommy2two, Cafelovr, Doronet and everyone else I am forgetting.  I think of you all each day and am thankful to have your friendship and support here.

    Have a good day girls...

    :)

    Alicia

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  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    omasmom7,SLV/Sherri,LiveLife/Ntalie,jwick74

    We are all behind you today as you go for your first TX. may you ladies find the piece we did when we all went through our first in that the "Sheer Terror" of not knowing will finally be over. You will find a inner piece as you go thru this part of your journey. I hope each and every one of you have minimal side effects.  Get rest, drink plenty of fluids, then drink more!!!! Try not to have an empty tum-tum and remember to rinse with 1 tsp. ea. of saltwater and baking soda to a 16 oz. bottle of water to rinse well after each meal. Tylenol X-tra Strength for the headaches and remember never let the pain get ahead of you. Take what you need before you need it, this is the best rule of thumb. Some take Claritin for pain before chemo, but I'm not real up on that so read back on some of the posts.  I wish each and every one of you the best~~~your in my thoughts and prayers~~~ Happy Thanksgiving~~~~~

    SharD, You are lucky enough not to go for TX till Friday. Be sure to enjoy this Thanksgiving and be ready for TC on Friday.  I hope I got his right!!!~~~ Sorry for all my misunderstandings!! I hope you are not angry with me. The more this goes on the harder a time I am having, let alone my brain seems just a little fried. My boss has been good so far as he just chuckles at my silly mistakes but again I feel blessed to even be able to come to work.  So far I've only missed TX days or my surgery days at the beginning of my "Nightmare on Chemo Street" At least now I am not soooo scared of everything like I was at first. I've learned to roll with the punches!!

    To all until Monday, I'm signing off, to you and yours,

    To ALL                                       "WARRIOR SISTERS"

     (((((PEACE&HUGS)))))                         and YUMMY FOODS, I am Thankful to be here

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  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    WARRIOR CCnani Where are you???????????????????????????????????????

    CC CC CCNani, I'm calling out ot you~~~~~~~~~~CC CC CCNani, Where are you!!!????

    I am sooo worried about CC!!!She has not posted since November 21st!!! This is sooo not like her.  She was always on top of it and posted everyday.  she even picked up my slack when I couldn't post. I have even sent her 2 PM's and she didn't respond.  I just don't know what to think!~

    I hope she is just off having fun~~~relaxing somewhere~~~maybe at a concert yelling out to fave musician at the top of her lungs. She isn't even scheduled to have Chemo TX till December, but she still loved to catch up everyday. If anyone has heard anything from her, please let me know~

     Concerned ~~~~ for my "Warrior-CCnan"  (((((SAFE-HUGS)))))

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  • GrandmaMickey
    GrandmaMickey Member Posts: 41
    edited November 2009

    please add me too - Started Nov 5, 2009 Adriamycine/cytoxan - 2nd was to be 3 weeks later - then every 2 weeks - Then Hecepton/Taxol weekly for 12 weeks, followed by surgery and radiation.  Unfortunately, first chemo worked great on the tumor but ruined my white cell count and I've been postponed for my second chemo - blood tests will determine whether I can have it or not - anyone experience anything like this?

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  • Sherri_V
    Sherri_V Member Posts: 159
    edited November 2009

    I got my second treatment today but the cocktail was changed.  Now I am having treatment every 3-4 weeks instead of every 2.  Feeling okay but I've been drinking all day so hopefully that is helping :)

    I'm going to watch a movie with my girls now but I'll report back how I'm feeling later.

    Thanks for thinking of me today!

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  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    GrandmaMickey ~ Welcome, sorry you have to be here with us... but we are a fine bunch !  And yes your white blood count needs to be at a certain level to receive your next chemo treatment.  So wishing you lots of good blood cells growing .

    Sherri ~ glad to hear you are OK, sorry your cocktail was switched it seems to be a normal occurance of whatever our body will withstand.  Hang in there.  I hope you feel ok for tomorrow. 

    Thinking of you all.  Hoping everyone is enjoying their families ~

    Alicia

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  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Ccnani ~ WHERE ARE YOU???????  worried.........  Embarassed

    Hopefully just busy with holiday stuff.

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  • mommy2two
    mommy2two Member Posts: 130
    edited November 2009

    November WARRIORS....I'm back!  Whew, I felt like crap the last few days but I'm on the uphill climb now!  I'm thinking I will feel great tomorrow, just in time to enjoy my Nana's good cooking.  I'm a little behind in my posts but honestly, I can't keep everything on here straight anymore.  Unfortunately, it has grown so much.

    I hope everyone that had a tx today is doing okay.  My thoughts and prayers are with you and I hope you can enjoy the holiday tomorrow.

    Welcome to all the new Warriors - I'm sorry you have to be here but you'll find this to be a great place to get support, encouragement, and advice!  Even though we've never "met" each other, I feel I've found life-long friendships here.

    I too miss ccnani...where are you?  I hope all is well and that you check in soon.

    Brenda, Alicia, Shel, Pam, Kimmy, Sherri, Cafelovr, Littlebird, Mouse, Doronet & everyone else I'm forgetting....HAPPY THANKSGIVING!!!  Wishing you all a wonderful blessed holiday with your families  Laughing

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  • suzieq60
    suzieq60 Member Posts: 6,059
    edited November 2009

    1st TCH treatment 8 days ago. I am still really sick. Leg pains, headache, earache, stomach cramps, indigestion you name it. When will it get better? and my hair hasn't even started falling out. The docs should give you the stuff to take just in case you get a side effect, not make you suffer it first. Hopefully 2nd treatment will be better.

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  • kayh
    kayh Member Posts: 37
    edited November 2009

    On day 5  slowly ground to a halt, so that on day 6 could not get out of bed much at all.

    Day 7 was much improved, even cooked dinner and put some away in the freezer for DH later.

    Alas, when came time to eat I couldn't even look at it. 

     Day 8 woke at 2.30am with nasty headache. Went to see Onc Dr  and she said dose is worked out by body weight, which is not always accurate.( Especially when they weight with clothes & shoes)  If your metabolism is slow(which mine probably is) you  get an extra dose. So she has decreased the dose by 10% for next time. She has also upped the anti nausea drugs for next time. Getting Emend next time

     She said it should decrease the side effects. So sounds promising.

    Also heart test came back with excellent results.

    Feeling quite positive after Dr's visit, I'll send DH off to his fly tying with the boys tonight.(trout fishermen) 

    BetsyBuzz I too have a taste for cold things like egg salad and fruit. I haven't had a coffee since starting chemo and I can only face one cup of tea a day. It is very hot here I might feel differently if it was winter.

    Hugs to all and special Hugs to those getting TX tomorrow.

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  • livelife
    livelife Member Posts: 38
    edited November 2009

    Happy Thanksgiving to you all. I suppose even though we are in difficult circumstances that no onw would choose we do have alot to be thankful for- all the advances in the treatment of this disease-( that have given me an extra 20 years so far ,since my first diagnosis of lymphoma), all the love and care we have been receiving from our family and friends and of course the wonderful support we are getting from being in Brenda's gang. I always fancied being one of the Pink Ladies in the Grease film- now I feel that I have that with this group.

    I would like to thank the sister who mentioned taking a light sleeping tablet if needed- I took my steroids too late the other day and only had 2 hours sleep -so last night- chemo night took a light 'sleep helper'. 9 hours pure restorative sleep. Which was great as I have a very dear friend flying over from Ireland this afternoon -so want to be rested so I can enjoy our few days together. 

    Shara D could you let me  know abit more about vit D  and vit C or where to look for info, especially the lymphoma related stuff- i haven't heard that before- so am very interested.

    Mabelle- I have read fab things about exercising- 3-5 hours moderate exercise a week throughout our treatment -seems to increase our chance of survival by 50% -so dear sister warriors- get out there walking, skipping, dancingSmile 

    GrandmaMickey- quite a few of us are on white cell boosting injections- neupogen or neulasta- last time I had chemo- 6 years ago- I had to fail my blood test a couple of times before I got put on them- so this time I was 'lucky' to get them first time. I think they increase the nuetrophil count but not the lymphocyte count. Yesterday i found out that my lymphocyte count was low- so I just need to be alert for picking up a viral infextion. 

    Mouse 6694 good tip re sitting at back of cinema. We still have to live life don't we. 

    Becca S- I would definitely get a wig as an option- I wear a silk scarf at home but when i go out i wear one of my two wigs-same colour- completely different styles. They are chocolate brown so different to my normal colour- but that is one of the fun things about this journey we are on- there are some light hearted moments that we can make the most of. Yesterday at the hospital this woman thought that I was in my late 20's -i am 43- that is what a difference they can make.

    CCnani- I send you my love and look foward to hearing from you Mother Hen.

    Love to you all xxx

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  • MeNeverMind
    MeNeverMind Member Posts: 42
    edited November 2009

    Happy Thanksgiving!!!! 

    Welcome to all the new sisters.  How everyone is going OK.  I have been just drained latley.  My mouth has been raw for 3 days and even with all the rinsing it still hurts.  I left work early yesterday because it hurt to talk.  I am still looking forward to dinner tonight but most of it will be to salty. 

    God bless everyone and ((((((((((((((((HUGS)))))))))))))))))) to all.  Love Kimmy

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  • Melinda41
    Melinda41 Member Posts: 672
    edited November 2009

    Happy Thanksgiving Everyone!!!

    I was helping my 10DD make her first Thanksgiving dish yesterday, plus teaching her how to make one of my traditional side items. Realized that I am probably not the best judge of whether a dish has enough flavor as my taste is all screwed up. So my fingers are crossed that what we made will be edible for everyone else!

    I hope that everyone has a wonderful day!

    MeNeverMind: Sorry to hear you are having a tough time with your mouth, have you tried the half Milk of Magnesia, half liquid Benedryl mix to dab on the spots? I have one hole in my gums, I am still rinsing, dabbing hydrogen peroxide on it and using Numsit. I am going to try the MOM/Benedryl today.

    Kayh: Sorry you are having such a tough time, but glad to know that the Doctor "heard" you and will adjust your dosage next time.

    Suepen: Does your doctor know how bad this has been, hopefully, next cycle they will make the appropriate adjustments.

    Livelife: Enjoy your visit, glad you were able to get a good nights rest.

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  • Psalm121
    Psalm121 Member Posts: 238
    edited December 2009

    Good early morning ladies, and a very Happy Thanksgiving!

    I have read all posts and have thoroughly enjoyd "meeting" you all!! So much helpful information and support.  I can't remember all your post names to address individually yet, just had chemo #2 yesterday and foggy-brained...couldn't sleep last nite, up going to bathroom to flush system!! My chemo is Taxotere and Cytoxan (1st tx 11-5-09, 2nd 11-25-09).  My hair started falling out on my shoulders on day 13 following 1st tx, so I cut it really close with scissors and put my wig on and out the door to plastics appt!!  No other choice, didn't want to look like the Toy Story Barbie dolls or a mangy pup!!! I laugh and I cry when I read all your posts,but mostly, I relate. It's such a relief to know I am not alone.  I had severe bone/joint pain by day 2 after 1st chemo....took percocet (left over from mastectomy-which I stopped taking after 2 days!!) pain was really bad, I, too waited too long to take pain med, Tylenol didn't touch it!! Monday, called Onc office and nurse case manager recommended taking Aleve, (every 12 hours, which helps me get through the nite, as well).  Still took Tylenol by 6th hr after Aleve, kept running low-grade fever and needed exra relief fort that.  Already on Aleve after 2nd treatment, don't want to go down that road again!!  Does anyone get hiccups??!!  Dangdest thing!!  They don't last long, but happen frequently starting treatment day and through the nite even!!  I too use homemade mouth rinse of warm water, 2 tsp baking soda, 1 tsp salt....feels really good after brushing teeth, seems to add to the clean feeling and my mouth feels better for eating afterward.  Plastic utensils are the greatest!!  Mashed potatoes with some butter is bliss!! Not to mention Carnation Instant Breakfast, Applesauce and Orange/Vanilla milkshakes!!!  My darling husband and 13 year old precious son are keeping me in good spirits with much love and support.  Oh the many blessings and the realizations of the things once took for granted!!!  No more!!  I have so much appreciation for my family and friends and their prayers.  Here's hoping all is well with you wonderful ladies....keep inspiring us newbies....I so look forward to the new posts!!  

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  • Shel
    Shel Member Posts: 41
    edited November 2009

    Happy Thanksgiving, everyone.  Day 7 here.  Yesterday I worked more than a full day (so many people already gone for the holiday) that I am wiped out today.  I was really happy to do it because the people at work have been so incredible to me through this. And luckily, my sisters are taking care of dinner; my daugthers and I just have to show up.  Don't think much will taste good, but I look forward to the company.

    Welcome to GrandmaMickey and Psalm 121.  This is a great group of women and I know you will get the support and advice you need here.  Also, welcome to anyone else new.  I don't want to page back or I will lose the post.

    I hope everyone has a day full of family and maybe small good tastes of food.

    Shelley

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  • BoxerSue
    BoxerSue Member Posts: 16
    edited November 2009

    Happy Thanksgiving, Everyone.

    Much to be thankful for.

    Turkeys in the oven.  Did all the side dishes and pies yesterday so all we have to do is re-heat.

    Everythings always better the second day anyway, right?

    Still have the headache - just trying to ignore it.

    Thankful for all of you - it's somehow calming knowing all of you are out there.

    Sue

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  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Happy Thanksgiving girls.

    I am thankfull for all of you.

    Hugs ~

    Alicia

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  • SharaD
    SharaD Member Posts: 100
    edited November 2009

    Happy Thanksgiving everyone...I hope that you all have smiles the size of a turkey today, and frowns the size of a pea.



    livelife.....On October 9th, ScienceDaily.com had a report about Vitamin D from the San Francisco Symposium on breast cancer. You might start with that article. As for lymphoma, there should be the latest information at lymphomafoundation.org......Also, if you do a google search on "Can Vitamin C block Cancer Drugs?"....a few stories will come up about this topic.

    As far as vitamins in general...it gets confusing because you'll find lots of information about certain vitamins PREVENTING cancer, but this does not necessarily mean that this vitamin is good for you during cancer treatment because some large doses of vitamins can interfere with certain drugs

    . It's all pretty confusing so be sure and discuss with your onc as everyone's case is different. Also some people might benefit from Vitamin C, while certain forms of it such as abscorbic acid might be hard on the tummy during treatment. (ie might need to avoid juices with added citric acid ).

    There is lots of info on vitamins here on breastcancer.org as well, in the health section/ tips on treatments.



    P.S. For those of you developing mouth sores, if you can eat yogurt it always helps with most types of mouth sores...make sure it has "active cultures".

    Lastly I have a tip for anyone developing a rash....you may have already been told to use the "free and clear" detergents and no 'bounce' or perfumey-softeners....If you want to soften your laundry, use 1/2 cup of white distilled vinegar in the rinse water. It helps to soften the laundry and vinegar also protects against rashes. (no your clothes won't come out smelling like vinegar!)

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  • Mouse6694
    Mouse6694 Member Posts: 88
    edited November 2009
    Happy Thanksgiving to all my sisters out there hope your day is blessed. Innocent
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  • littlebird75
    littlebird75 Member Posts: 120
    edited November 2009

    Yesterday was day 5 out of first round of chemo of Cytoxen and Taxotere (you guys post so many abbreviations but I don't know what they all mean) and I was a zombie all day and night. Day 4 was the worst for pain - joint pain from my hips to my toes, but on day 4 it settled mostly in my ankles and feet. Other than yesterday when I was asleep every moment I could be (including on the potty) I hadn't had much sleep - the pain was keeping me awake.

    I started yesterday (day 5) as being constipated, but over night ended up with the opposite problem. I hadn't taken any laxatives, just fiber and a stool softener. 

    I just realized what a wonderful post this is for Thanksgiving morning. Sorry. *sheepish grin*

    Anyway - I am supposed to bring a green bean casserole to a friend's house for a pot luck dinner. I think I should be able to manage that. I feel like I've rounded the bend to the side of this chemotherapy round that side effects start to diminish. I have to say I was expecting very little side effects, so this was a bit of a suprise. 

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  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    Just wishing even one

    HAPPY THANKSGIVING!!



    I have been blessed with all my wonderful grandchildren, all in good in health, As well I feel good and have been able to enjoy the meal they all so lovingly prepared for me. Look forward another meal in a few more hours

    I give thanks to all my family,

    I give THANKS for all of you,

    My new found "Warrior Sisters"

    I will properly post + welcome all Newbies this coming Monday

    (((((HUGS))))). To ALL Love Brenda

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  • Sherri_V
    Sherri_V Member Posts: 159
    edited November 2009

    I had my 2nd chemo treatment yesterday.  My tumor was measured manually and the size has decreased in just 2 weeks from 3cm x 5 cm to 2cm x 3 cm - a drastic reduction!

    Happy to have good news!  Hopefully the side effects will be easy on me this time around :)

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  • mommy2two
    mommy2two Member Posts: 130
    edited November 2009

    GREAT NEWS Sherri!!!  I hope you feel okay and have no/few side effects this go round.

    I hope everyone had a great Thansgiving with their family/friends!  I really enjoyed being with my family, more so this year than ever before.  Hope everyone has a great side effect free weekend!

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  • Melinda41
    Melinda41 Member Posts: 672
    edited November 2009

    Sherri: That is impressive shrinkage!

    Hope everyone had a great, side effect free day!

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  • suzieq60
    suzieq60 Member Posts: 6,059
    edited November 2009

    I'm actually feeling human today (day 9),  I actually got out of bed.

    Went to see the oncologist with my husband for his annual checkup (bowel cancer, lung mets 3 yrs ago). He's all clear again!!! Hurray!!!

     So, while I was there I gave the doc an earful about how sick I've been. Got all the meds in place for next time so hopefully it won't be so bad. I told him about the sore throat and he had a look and said I don't have an infection so that's good. Really the stomach pain/grumbles have been the worst thing, so with the medication in place, I should be ok next time.

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