Starting Chemo in March 2014

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  • megomendy
    megomendy Member Posts: 141
    edited March 2014

    So I had my first treatment today. It is surprising how easy it was. Saw the doctor first and didnt need blood work as I already had it. Then walked over to the treatment room. They give people a private room for their first treatment, so that was nice and there was a bed to relax on. FIrst, hydrating for 2 hours, which sounds long, but it zipped by. In betweeen the nurse was teaching you things, I was playing online, eating, texting, huby was doing work. Then she came in with the Adriamycin, which is in 2 large syringes and she sits there and pushes it into the port. That took about 15 minutes. (And yes, I am peeing red!)  I had a sweet young nurse who was easy to talk to. Then they hung the Cytoxan for half an hour. Just going over all the paperwork at the end takes a while too. So I got to chemo at 10:30 and left at 1:45. I really expected to be there all day. I feel perfectly fine now. But I am very suggestible, so I am going to try and keep busy and not pay attention to any aches and pains. Going for my neulasta shot tomorrow so I need to remember my Claritin.

    Laura, I live in Manalapan, right next to Freehold!! Small world.

    My insurance has no wig coverage either. Darn. I bought one though. 

  • megomendy
    megomendy Member Posts: 141
    edited March 2014

    I just had my port put in Wednesday, so I was told I couldnt put Emla cream on it because there is a glue over it and the cream could interfere with the glue. (My MO said she never heard of that.) But it really didnt hurt at all, and mine is still pretty sore. It was very nice to have both hands free.

  • mom2Bnegativex3
    mom2Bnegativex3 Member Posts: 221
    edited March 2014

    WOO HOO! Meg!! Make sur you drink plenty of water and take your senekot S tonight! Stay ahead of the game!! I am so happy for you!!

  • mom2Bnegativex3
    mom2Bnegativex3 Member Posts: 221
    edited March 2014

    Megomendy, when do you get you taxol/carbo? After these treatments? I am trying to find someone who has had these two. Thanks!

  • Xrayalli
    Xrayalli Member Posts: 237
    edited March 2014

    Welcome Mitzro, yes, that is similar to my story, sorry you have so many positive lymph nodes, ugh. I wish my chemo has started, I want to get this show on the road. My Mo is still consulting on what he wants to use! he's never had a patient with a tumor like mine. 

    Thanks to the Moderators, too, for the links. 

    I am going to go back to work Monday, even though I'm still dealing with some pain. But not before I have a girls weekend! They said they're gonna spoil me and I think I'm going to let them :)

  • Lovemyboysandlabs
    Lovemyboysandlabs Member Posts: 83
    edited March 2014

    Sending prayers your way cancerisnotmyhappyplace that the scans are okay. HUGS as you go through this.

  • megomendy
    megomendy Member Posts: 141
    edited March 2014

    Yes, Mom2B, I get the taxol and carbo after the AC. 8 weeks from now. The nurse said the taxol does not really have nausea as a side effect, but has the neuropathy, but the carbo can have some nausea. So I think they premedicate for it then too.

  • Kris103
    Kris103 Member Posts: 57
    edited March 2014

    Meg - Gratz on the uneventful infusion! Way to go! Like Mom2B said, stay ahead of the game on the meds, and you'll be fine. I just got back from my first Neulasta, and was surprised at how easy that went. They must use a very fine needle, as I barely felt anything at all. Of course, wilth me, they've got a good bit of tummy to work with. Now's the waiting game to see what SE's will be like. I've got my Claritin and Aleve on board, and my onc nurse said that if it actually does get bad, I've got the OK to hit the Norco that I didn't use after port surgery.

  • jmg58
    jmg58 Member Posts: 185
    edited March 2014

    Wow.  I'm glad to hear everything went well, Meg, and for you, too, Kris!  You are giving me hope.  I will only say this one more time because I don't want to bring anyone down...I am so scared.  I am just so scared I cannot imagine not crying the whole time.  I cannot imagine this going well for me when even a simple hot chocolate makes my heart race and skip beats and antidepressants give me chest pains that send me to the ER.  I just can't imagine doing this but the fact that you're all making it through relatively okay so far is giving me lots of hope.  

    Have a great time out with the girls, Alli!!!  I hope everyone has a great weekend with lots of peace and rest.  Sorry to be so freaked out about this...I'll try to get myself together over the weekend and put my big girl pants back on.

  • MedicMom2
    MedicMom2 Member Posts: 26
    edited March 2014

    Mitzro: here's what I found. I hope it helps. Are you in CT too? I'm northcentral CT going to St Fran's for my fun and excitement. 

    image

  • Lovemyboysandlabs
    Lovemyboysandlabs Member Posts: 83
    edited March 2014

    Aquala Bathtub Caddy

    Getting myself one of these for bath-time, I think they should give these out to all of the Cancer patients! :) 

    Just thought I would post something fun for a change...

  • lgoldie
    lgoldie Member Posts: 120
    edited March 2014

    You sound like a sister.   I have been terrified of the side effects.  Here's my take for today:  I have had ONE A/C eight days ago. So far I have had some nausea, diarrhea, dry icky mouth, dehydration, no appetite, palpitations, the absolute worst fatigue immagineable. weakness, shakiness, oh, and my hair is falling out.  The news is I lived to day 8.  I would not have bet on it.  Oh yeah, jitters and hot flashes from the streroid.   All was super scary and my anxiety has gone through the roof.  What have I learned, call your doc anytime you want.  Yup, there is nothing they have not heard.  They have been patient and helpful.   I have learned that I am no longer afraid to die.  Fifty five years old and just learned it.e  If I do not make it through chemo, I will go to heaven with my Savior which is my ultimate long term goal anyway.  So I didn't go today.  I am still alive He has a plan for me than included today  If you want to correspond, I would Love to cause nobody is a bigger chicken than I  Leah

  • CancerVixen
    CancerVixen Member Posts: 28
    edited March 2014

    Hi Ladies!!  I feel so behind with all of your progress but so happy to see all of the support in this group!!  It truly is amazing to see how people come together.  Please forgive me if I dont address all of you.  As far as for me yesterday was a horrible day but today has been the best day since my treatment last Wednesday!!! YEAH!!!!!!!!!  Finally things are turning around!!!  My energy is much improved.  One thing that hasnt gone away are the stomach pains.  Lovemyboys&labs since we are both on Perjeta and pretty sure that is the culprit lets see if we can compare and see how long this lasts.  These pains are definitely not from constipation or diarehha as they are constant and nothing seems to help.  I will try a bath tonight though to get some relief.

    JMG58 - I am worried about your lack of support.  I know how hard it is.  Im not sure what your financial situation is but it is worth paying someone to help you or ask your hospital social worker if there are any programs you may qualify for.  They are putting in an application for me with an outside organization to see if I can get help with childcare.  Please let us know what they say and we can help come up with some more ideas.  Maybe a volunteer through the church??

    lgoldie - I want you to know you are not alone in suffering with anxiety.  I developed severe anxiety and panic attacks the first time i went through this 7 years ago.  I have been taking Klonopin ever since.  Its very similar to xanax.  Before I was recently diagnosed i only had to take .25mg before bed.  That is half of a .5mg pill.  Well now that this all started I take 2 .5mg pills a day and still feel nervous and anxious!  I beat myself up because i am now taking 4x the dose I needed before and that seems like alot but then on the other hand I have to be able to function.  I really dont feel like I have emotional support from my team. They are great with the medical stuff but mentally and emotionally it really does take a toll and if you are prone to being an anxious person like me then its even worse. Being alone doesnt help either as there is no one there to comfort you (or me!)   Im not sure how i can help but I want you to know you are not alone!!  I am just as scared and anxious!!  I can say I got through it once and deep down no matter how scared or anxious know that I will again and so will you!! I promise!!!!!!!!!    Dawn

     

  • CancerVixen
    CancerVixen Member Posts: 28
    edited March 2014

    Almost forgot the best news of the day!!!  I can no longer feel my lump after one treatment!!!!!!!!  Im not sure how this is possible but I had my best friend over last night who is a nurse and she felt it before and it was big and hard and now cant find it!!!!!!!!!

  • Lovemyboysandlabs
    Lovemyboysandlabs Member Posts: 83
    edited March 2014

    YAY Dawn! I have to say I am afraid to feel mine... I am afraid I guess that it got bigger, so I just don't go there.

    From what I've read, it seems that Perjeta is the culprit. I thought I was over the pain this morning--I ate cereal, went for a walk, even went to La Madeleine for a chicken salad sandwich and soup because I was HUNGRY. Then, I felt so amazing that we actually went shopping for a bit! I was on a cloud! Then it hit. Now I have the big D. My pain started on Wednesday (had chemo on Monday) as just horrible cramping with no relief, then constipation, now the big D along with some general pain in my gut. So what do you take for it? I have no clue, since it seems I have everything going on in there. I meet with the PA on Thursday, so we will be discussing this because according to her I should not be uncomfortable. HA! Someone else said that they only experienced this the first time they took Perjeta, then it went away. We can only hope!

  • CaliKiwi
    CaliKiwi Member Posts: 98
    edited March 2014

    Well done Meg, great to get that first one under your belt.

    Jmg58, I wish there was a way I could help you. Honestly the infusion was so super easy, the nurse was so helpful, I hope that it will be the same way for you.

    Cancervixen - so glad that things are turning around for you!  And what exciting news about the lump!

    I'm feeling ok today. I felt pretty good this morning to decided to try a walk.  It was a very short one, just to the end of my block, started great, ended feeling nauseous, dizzy, swollen, and hot.  I was exhausted and had to take a nap, I think it stirred up all the remaning toxins, probably a good thing. A few hours later and I do feel much more recovered.

  • cancerisnotmyhappyplace
    cancerisnotmyhappyplace Member Posts: 49
    edited March 2014

    Just wanted to thank you all for sharing you ups and downs.  How you treat the SE and try co for measures benefits us all.  You all are doing great!

  • AKJ
    AKJ Member Posts: 190
    edited March 2014

    Wow, so much to keep up with! JMG, don't be ashamed of being scared. I bet every one of us feels that way. How could we not? 

    I made it through a full day of work today. Don't really know how I did it. I'm so exhausted at this moment. Thank heaven it's the weekend. I'm hoping it'll get easier since it's almost two weeks until my next treatment. 

    I hope nobody cares that I'm posting in the March thread since I actually began tx at the very end of Feb. I feel more part of the March group.

  • Jmenchaca78
    Jmenchaca78 Member Posts: 19
    edited March 2014

    hey girls just wanted to chime in and say that I have made it through my first treatment! And it was pretty easy. I didn't have a port placed so mine was through an IV. The taxotere did burn going in but it was tolerable and the cytoxin wasn't felt at all. I feel fine now just tired but no other symptoms yet. Tomorrow I will go in for my Neulasta  shot which I'm hoping will be tolerable as well, Claritin and Aleve are on hand. Thanks to these discussion boards I feel like I've been pretty prepared and my MO has been impressed by how much I know. Thanks ladies

  • CancerVixen
    CancerVixen Member Posts: 28
    edited March 2014

    Lovemyboys - Im glad to hear you felt amazing even if for a little while!  Please dont be afraid to feel your lump.  You may be surprised in a few days.  I have the big D too and take imodium here and there.  Not every time but nothing helps with the stomach pains.  i asked the nurse today if i could get a prescrip for muscle relaxers thinking that might help but of course she said no and Dr is out on Fri.  She tells me to go to the ER because I shouldnt be feeling this and maybe its an infection.  Well I know for sure its not and its from the darn Perjeta!  I see my MO on Tuesday so hopefully he will come up with something by then.  Either way we pray this is only a one time thing and then next time we dont have this side effect. 

    Kiwilady - Glad to hear you went for a walk today. Even though it brought on some side effects its good to keep things moving.  I have to do more of it myself now that I finally have some energy.  

  • Xrayalli
    Xrayalli Member Posts: 237
    edited March 2014

    Dawn, that's amazing about the lump feeling smaller! Chemo is so powerful, I can't even fathom....

    AKJ-of course you are welcome in the March group, at the rate I'm going I might have to switch to April! I hope not, geesh!

    I love to read how supportive and helpful everyone is to each other.

  • Lorbgoo
    Lorbgoo Member Posts: 213
    edited March 2014

    meg glad your chemo went well. That gives me hope. I am so nervous. I'm surprised I don't cry all day and night. 

    Alli enjoy your girls weekend. I'm jealous. 

    Welcome AKJ  I'm glad you were able to make it through work. Get plenty of rest this weekend. I had to stop work because I work at a preschool and I'm around over 100 kids and range from 5 months to 5 years. I was nervous to catch something that would delay chemo. 

    Cancervixon. That is great news about your lump! Wow. What powerful stuff chemo is. 

    Jmen. Glad your treatment went well too. 

    Jmg. I am so scars too. I just want to sleep the next 3 months away and wake up and this would be all over. I'm a big baby. I'm so frightened. 

    I have so much anxiety too. I have been taking Xanax. 

    I hope I didn't forgot anyone. Have a good night. 

    Lori

  • Maggiemay1220
    Maggiemay1220 Member Posts: 27
    edited March 2014

    I aced it, girls.  I had my first of 4 AC treatments today.  It took 3 hours.  As of right now I feel ok but have a touch of heartburn.  I am glad I have the port for the chemo.  I will fully admit it was a pain in the butt to have put in but but it made today pretty easy.  My husband and I are fighting to let us self inject the neupogen over 5 days instead of 1 shot.  I want it for 2 reasons, one the pain from it is less in smaller doses and two, it is less time I have to take off work.  They explained that the bone pain is worse the younger you are.  We'll see.  We thought everything was set and guess what...nope!  I have to go in Monday for the single shot for this round.  Bummer.  

  • Macintx
    Macintx Member Posts: 118
    edited March 2014

    Maggiemay, I didn't have any bone pain at all from the Neulasta shot, so it's not a guarantee that you will have it.  Just a thought.  Although, I am 49 and I don't know how old you are, but I also hadn't heard that the bone pain is worse the younger you are.

  • mom2Bnegativex3
    mom2Bnegativex3 Member Posts: 221
    edited March 2014

    CONGRATS to the ladies who made it through TX today!! We can do this!! (()) hugs to everyone:)

  • megomendy
    megomendy Member Posts: 141
    edited March 2014

    JMG58, Hey, it's okay if you cry! When I saw my Mo before the chemo my bp was high, for me. And I was worried and she said, hey if your bp wasnt high, I'd think that was strange. I am not a cryer, but I've cried! What helped me a lot was that they dont just hook you up to the chemo meds. THere is a long process and you get a saline drip for a while, so it was slow. Bring a laptop or tablet and distract yourself. 

    Hey, I wonder if anxiety is linked to breast cancer. I also have anxiety and take Effexor WR for the past 10 years maybe. I love it! Helps me so much. 

    Cancervixen, congrats! That is great news. I wish we could "like" each others posts or comment right on the post. Maybe we should think of starting a fb group so we can learn our "real " names and be able to stay on one topic better?

    AKJ, No, we insist you go back to the February group! lol Yes, stay with us. We're the fun group. I hope I can go to work at least a few days a week. Need the money!

    So tomorrow I am getting the neulasta. So I take the claritin in the morning, and thenonce a day for 7 days. Anything else? Aleve was mentioned, but the chemo nurse said to try and limit advil/aleve because it can affect your platelet count. She prefers tylenol, unless its just occasional. 

    Jmenchacha, so we are on the same treatment schedule,just diff meds. I feel sine so far too. I have a little headache, but I think it's just from being hungry earlier. My friend was bringing over food for us and she's always late lol I think it's best not to get too hungry. 

    Lorbgoo, I also work at a preschool, ages 3-5. My doctor said I could go to work. If I see a child and they look obviously sick, I'll just skip that kid. Or see them in the classroom. I feel like at my age, hopefully I've had most of those germs. I would love to just sleep the next few months away as well. But think about how fast time goes. I mean, it's March already and it feels like we just had New Years. So before we know it, we'll be looking back on this whole experience. Not fondly, but it'll be over.

  • Generation3
    Generation3 Member Posts: 45
    edited March 2014

    Congratulations to all of you who have made it through round 1!!!  I'm not really looking forward to starting but I do want to stop the travel of any cancer cells coarsing through my veins. Cancervixen, glad you're feeling better and yeah for the disappearing lump. Alli, how's yor arm feeling? Hope the swelling is going down. Megomendy thanks for your post. Next week I'm starting on adriamycin, cytoxin, and taxotere. Have been quite nervous about the cardiac effects of adriamycin. Glad to hear it went well foir you. Hugs to all of you and have a nice weekend!

  • Jmenchaca78
    Jmenchaca78 Member Posts: 19
    edited March 2014

    ok I'm struggling with some major heartburn now and my omeprazole is not helping! Gonna try drinking a milkshake cuz that's what my mom did when she was going through chemo, lets hope this works blah!

  • Maggiemay1220
    Maggiemay1220 Member Posts: 27
    edited March 2014

    jmenchaca, I am with you.  Thankful for no nausea but the heartburn is nasty. 

    Generation3, I was a basket case up until this morning and woke up amazingly calm. The whole first process of being a 1st timer only took 3 hours.  

    Macintx, I am right behind you at 43.  The nurse said that younger people get the leg pain over older ones because they reproduce the WBC more rapidly. I hope there is none, what a pleasant surprise it would be!  Did you take Claritin?

  • rosebud77
    rosebud77 Member Posts: 24
    edited March 2014

    Hi Everyone,   I am starting chemo either this month or early April so I thought I would get some good advice from you ladies. My story is somewhat similar to Nadia's and a couple of other ladies on this thread.  I was blindsided with a stiffer diagnosis than originally thought.  I woke up with breast pain January 15th which kept me up the rest of the night.  I was diagnosed Jan 30 and had a DMX with nodes removed, expanders in, and two drains left to go.   I will most likely be starting chemo either by the end of the month or early April.  I have been extremely stoic through this whole ordeal, but lost it a few times very unexpectantly.  For instance, I threw a dinner party for past co-workers a day before I left for the hospital, and had a fabulous time.  My husband thought I was nuts but it was a lot of fun and he admitted later that it had been a smart strategy to stay so busy cooking and cleaning.  I've been able to talk about breast cancer  without getting upset from the beginning.   My breast surgeon even told me that I should think about becoming a mentor because I have the right attitude. (very sensible) BUT>>>>>HA!  In the hospital I completely lost it because my roommate's husband was in the room all night and I felt very exposed.  I sobbed and sobbed in the bathroom.   What I was really upset about was finding out that I had pretty involved lymph nodes which was a total surprise.   A few days later, I lost it again when I couldn't get a sensible appointment with the medical oncologist as I live 3 hours away from the hospital.  I have  now been upgraded to a stage 3  and now have to have a bone scan and a total body cat scan on Tuesday to see if it is worse than a  III. At the beginning, they thought I was only  a stage 1.  Once those results are in, the medical oncologist will know what kind of plan to come up with. My healing should be pretty good by the end of March, and my appointment is in a couple of weeks, so I imagine this will roll out pretty fast.   Life can turn on a dime, can't it?  Anyhoo, I ordered a wig today and drove myself because I didn't trust myself to keep it together because  when I can't get appointments scheduled, it seems to upset me.  Today, when I called  this special salon lady about a wig appointment , she  could see I was really disappointed that they had no openings so they used called ID to find me and call me back to tell me to come in and the owner would work with me.  That was a nice surprise.The special salon I went to caters to hair loss, thinning  and wigs. The owner talked me into a wig that will look almost exactly like my own longish golden/reddish hair.  I was amazed that such a thing was possible.  Even the odd color she stuck on my head today looked like my own hair once she brushed it and fooled around with it. I will even  be able to tie it back !!!!!!!   I also ordered some bangs so I can wear a ball cap  and look like I have some hair under it.      In General, Waiting is the worst about this whole ordeal.  That, and having it completely wreck my schedule.  Can't plan anything.  Oh well.  I read all of your posts and I am going to make a list to ask the oncologist about baths and other great ideas you all have.  I may end up being an April Girl, but we'll see.     Sorry this posting is so long........  Feeling chatty and a tad depressed.

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