Is There A September 2011 Chemo Group?

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  • PinkShirtNow
    PinkShirtNow Member Posts: 134
    edited September 2011

    Hi everyone!  I start 12 weeks of weekly taxol tomorrow.  I'm in the ISPY2 trial so I will also get ABT-888 (pill twice per day).  I will also get carboplatin every 3 weeks.  When that is finished, I'll have bi-weekly AC for 8-12 weeks.  It is all very overwhelming to think about right now. My surgery will be at the completion of my chemo.

    You all inspire me to be brave.  

  • Lowrider54
    Lowrider54 Member Posts: 2,721
    edited September 2011

    Wow, this Sept group sure did grow!  It was growing before I started and then I got to post my first treatment and wow...4 pages already!

    It feels a little funny being here - I started chemo on Friday.  Abraxane and Avastin.  As a stage iv, I don't count the rounds...I am on it for as long as I can tolerate it. 

    Today...after 5 days post treatment, I am pondering when I will start to feel a little better.  Do I have to wait until it knocks back the new progression?  Is there a time frame post treatment when things start to not make me feel so crappy?   This will really suck if it only gets worse with each treatment (I know my blood counts will drop).  Anybody?

    Thanks

    LowRider

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2011

    Hello! I don't post very much, but do read a lot on this Forum. As I write this, I'm in my chemo chair, receiving the first infusion of the Gemzar/Taxotere regimen I'm now starting.



    I've already had Taxol/Avastin, which took me to NED after 8 cycles, then on Avastin only for 5 mo when there was progression. Then started on clinical trial with Ixempra/Sprycel, which failed after 4 months, when I had more progression and addition of skim mets around my neck.



    With my stage IV status, I have no set number of cycles, I just continue on this until either there is progression, or, my body gets too worn down by this regimen. Nevertheless, I'm hopeful this will take me back to NED, and "maintenance" thereafter.



    Wishing all you ladies successful chemo with minimal SE and discomfort.



    God Bless us, everyone.

  • ovbru
    ovbru Member Posts: 4
    edited September 2011

    rjbaby69 - I meant slow making words. I don't feel any reduced capacity of the brain.

  • findingsolace
    findingsolace Member Posts: 17
    edited September 2011

    Hi Everyone- Hope you don't mind I would like to join the group. It is tough keeping everyone's name straight! I start 6 rounds of TCH Sept 16th, along with the port placement the same day.  I am getting a bit nervous but reading all the posts makes me feel I am not alone.  I am ready with my claritin, immodium, etc.  Here's to a good journey for all of us.

  • westieluv
    westieluv Member Posts: 303
    edited September 2011

    I am hosting a party for my Mom, who has TN, in recovery from BMX and starts chemo later this month.  I am thinking about a Chemo Pamper Party.  Anyone have ideas for this?  I want it to be a loving, nuturing, fun time with friends/family bringing Mom stuff to pamper herself before she starts Chemo in the 3rd week of September.  I need invitation ideas and party favor ideas plus some games to throw in there maybe concerning breast cancer awareness??? 

    I know you ladies have good ideas....so help me out!

  • Shawna77
    Shawna77 Member Posts: 28
    edited September 2011

    Thanks Bluejay!

  • Suz39
    Suz39 Member Posts: 125
    edited September 2011

    Hi All,

    Day 5 for me.  Nothing new to report.  I was able to do a long walk this morning, and actually found that I felt better when I was on the move, rather than sitting still.  I think that I might have thrush, so got the mouthwash for it.  Since I can't taste much, it doesn't taste bad at all.

    Westieluv, I was at Pier 1 the other day, and they had a little corner of stuff that looked like it was for a breast cancer party - not that it would have occurred to me to throw a party for breast cancer, but that is just me.  My favourite thing was the bell.  I kind of wish that I bought it, because sometimes my husband can't hear when I am calling him ;-)  It was bright pink, and had some encouraging words written on it.  It is very nice that you are doing that for your mother.  Have fun! 

  • FieryRed42
    FieryRed42 Member Posts: 15
    edited September 2011

    So I start tomorrow - took my first dose of steroids today and so far it's kind of fun, I have so much energy! :)

    I bought a gorgeous wig yesterday, it's the Spotlight by Raquel Welch - I got to try on a ton of different ones and hers were all pretty nice. The color I picked is called "Fiery" which I thought was perfect for me!

    Westieluv: my friend is throwing me a party in a couple of weeks, we're calling it a Hat Party and having everyone bring me a hat/scarf/headcovering - nothing expensive, mostly just fun and silly stuff so people can show their support without making the whole thing too serious or depressing. I think it will be during the day and we'll serve cupcakes and champagne, something fun and girly.

    I can't remember who asked me but I took Tamoxifen for 8 months before surgery to try to shrink my tumors so I could have a lumpectomy - it's not standard but some people do it if they don't want to do chemo (obviously since I'm on this thread that plan didn't work out for me - I got an oncotype of 38 so it made it a pretty clear choice). It did shrink my tumors a good bit, but I still ended up doing a mastectomy because my surgeon thought it would be safer and better cosmetically, and I'm actually really happy with how it's turning out (still have tissue expander in but it's already looking pretty good).

    Someone asked me what supplements I'm taking - I'm doing a multivitamin (source of life gold, it's awesome), glutamine, alpha-lipoic acid, and a probiotic. I was reading the Life Over Cancer book from the Block center and he recommends all those things (and my onc said it was ok too).

    Haha you can tell the steroids are making me hyper by how much I'm writing! Hope everyone has a great day, I'll report back after I get my treatment.

  • westieluv
    westieluv Member Posts: 303
    edited September 2011

    Thanks Suz39.  I hope to hold another party for her when she is done with the chemo.  This is really just a chance for all of her close friends to come together in a showing of support for her.  We aren't celebrating the chemo as much as we are celebrating her efforts to kick cancer's A@@ to the curb!  I'll check out the Pier 1 online site to see if they have items there.

    Thanks for the input!

  • keepitsimple63
    keepitsimple63 Member Posts: 4
    edited September 2011

    Hi, I just discovered this thread and boy I am so happy about that. I start Chemo today, 9/8/11. I'm heading out the door in 3 hours so I can't chat much right now but I will check back as soon as I can. Good luck to each and everyone of you! We can do this and together we will be stronger. Hugs!!!

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Hi everyone.  I finally got my 4 JP drains out yesterday, 3 weeks 5 days post BMX.  I feel like a freed woman.  I was doing the happy dance in the office.  No more freaky things popping out of my clothes.  Now they have scheduled chemo to start on 09/14, couldn't do it until the drainswere out.  MO switched regimen from dd AC x 4 plus Taxol x 12 to TC x 4.  That shortens my chemo program from 5 months to 3 months and means I do not have to worry about the Adriamycin cardiotoxicity. 

    Fiery red, you sure do make those steroids sound good.  I did not get a prescription for steroids so I suppose I will be getting that with the chemo pre-meds and that's all.  I like the idea of something to head off neuropathy, like the alpha-lipoic.  I thought antioxidants were a no-go during therapy but then saw a lot of information suggesting it is okay.  I'm going to google it a little more.  Thanks for tip.  Good day to all of you.  I am just here doing my happy dance without those drains.

  • PinkShirtNow
    PinkShirtNow Member Posts: 134
    edited September 2011

     I had my first chemo treatment yesterday - paclitaxel and carboplatin.  It was a longer process than I expected because it was my first treatment.  I met with my chemo nurse practitioner to discuss the process then I went to the chemo treatment area.  My chemo nurse drew blood from my port and sent it off for testing.  After the go ahead, she started my IV anti-nausea drugs, benadryl, and dexamethasone (I'll take this the night before from now on).  Then I waited to make sure I didn't have any reactions to these drugs before they started the chemo drugs.

     It was wonderfully uneventful and I was mostly drowsy due to the Benadryl.  The part I didn't expect was that I had to urinate almost every half hour because of all the fluids pumping through me.  I also drank lots of fluids the day before so I was pretty hydrated anyway.  It was almost embarassing that I kept having to get up and go to the bathroom.  However, I am getting past being embarrassed about any of this.  

    I was nervous when I had to take my first oral dose of ABT-888 (stud drug on ISPY2 trial) at home.  It is a pill that I take every 12 hours.  I've had 2 doses so far and things are okay.

    Today I feel pretty much like normal.  My body is feeling "heavy" like it does when I am really tired which is to be expected.  I also feel "drugged" but not sick.

     So, the infusion wasn't as bad as I imagined it would be.  I think I will appreciate having my port although it still give me the willies to know it is in there.

     I hope my experience helps anyone who is nervous about their first treatment (or scared to death like I was!).

     Take care of yourselves.

  • bluejay58
    bluejay58 Member Posts: 62
    edited September 2011

    Heh, PinkShirt, I had to go to the restroom too during my treatment, and I felt embarrassed at first wheeling my IV down the hall.  :)

    I had my first treatment two days ago (Tuesday), and so far my reactions have not been TOO bad.  I did have what I'll call "brain fog" late Tuesday afternoon and evening and yesterday, but today seems to be much better on that front.  I really hit a Wall of Fatigue yesterday.  Very mild nausea (took one phenergan to be safe).  Felt "heavy" and slow along with the brain fog.  Tongue feels a little funny, almost like I've burned it on spicy/hot food, but so far food and water doesn't taste too different.  No constipation or diarrhea.  Had a night sweat last night, but I honestly don't know if that was due to the drugs or to the fact that I'm in menopause (I'm 53).

     *hugs* and strength to all.  <3

  • shelley2011
    shelley2011 Member Posts: 199
    edited September 2011

    Can't help but laugh, but I was also dragging my IV pole to the restroom every 1/2 hour.  Pretty funny.   I am day 13 of TCx4.  My hair is thinning out, guessing the clumps will start later today or tomorrow.  Otherwise, I feel pretty darn good!  Third full day at work this week, a little tired when I get home.  But amazingly well, and glad of it. 

    I am working on building myself up for the next round.  According to MO, with the TC regimen days 7 - 9 are the worst blood count days.  Then everything starts to build back up.  So, I'm taking my multi-vitamin, drinking Ensure, and eating lots of yogurt.  I am also continuing to drink more water or Gatorade.  I was told not to take any anti-oxidant supplements too - MO said they work against the chemo.  But that's just my guy. 

    Guess I better brush out that wig tonight!  Best of luck, strength, courage and health to all!

  • sdw4158
    sdw4158 Member Posts: 5
    edited September 2011

    Hi Everyone,

    I had my first treatment this morning (TCx4) and the worst part so far was the stick.  The nurse finally made it on the 3rd try. 

    Pink Shirt Now: Don't feel bad about using the bathroom.  I also drug my pole with me 2 times to the bathroom.  Even when I got home I had to go but now, even though I am drinking plenty of water, it is nothing like this morning,

    bluejay58: My tongue also feels like burned or sand papered.  While food does not taste different I am having a little heartburn from yogart.   I also have a strange feeling. 

    Now tomorrow on to the shot.  My cousin stated that was worse for her than the chemo.  She took advil but still in a lot of pain.

    Take Care Everyone

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011

    Hello!!

    I had my DMX & sentinel node biopsy on August 16th and axillary node dissection on August 30th. I got my last drain pulled today as well as meeting with my oncologist. I start chemo September 14th. I'm getting Taxotere, Carboplatin & Herceptin. I'm so glad to finally be getting started!! I'm not worried about losing my hair and probably won't wear a wig - it's just too hot here in Florida. I'm more concerned about my nails. Losing them just sounds painful!! 

    Best of luck to everyone!!

    Goodnight =) 

  • Kimberly1961
    Kimberly1961 Member Posts: 407
    edited September 2011

    Maybe this would be better addressed on LE thread.  So far I do not have lymphedema.  I had BMX with two nodes checked on cancer side and one on noncancer side.  The noncancer side has less range of motion.  Now twice it has been excruciating when they take my blood pressure with automated machine at the MO's office.  It was bad enough last time that when she said, do you need me to release it, I said yes.  She attached a smaller cuff to the machine and took my pressure from the forearm and it was fine.  I wouldn't think one lousy lymph node would cause such a ruckus on that arm.  Blood draws are fine.  Have any of you had a reaction to the blood pressure cuff post op.  Thanks, Kimberly.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Hello ladies.  I had my first treatment today.  Everything went very well.  One minor problem.  The pump quit pumping and we tried everything.  They even sent me next door to do an x-ray to see if the port had moved.  Nope.  It was good.  So they prepared to finish my treatment in my vein in my arm.  One of the nurses came over and said I want to try one other thing before we do that.  I already had the IV and was ready.  They nurse changed the entire tubing from the drug bag to where it goes into my port.  And guess what?  Yep.  Worked like a charm from then on.  We kept the IV in my arm too in case the pump failed.  Thankfully it did not and I finished treament just fine.

    They called me into the dr.'s office.  So here I go in to see the doctor wheeling my port down the hall.  He came in and asked how I was.  He told me that he got the oncotype test score back.  I started sweating a little then.  Was expect a high number.  Well, my oncotype number is.........14!  Yeah!  He said that I had a 90% chance of this NEVER coming back.  I'll take that any day!!  Still doing the chemo and rads.  Not willing to take any chances with the beast! 

    So far no SE.  The nurse said I would probably do fine today and tomorrow would be really good but Saturday and Sunday would be the days to watch for.  Thankfully I do not work those days so I will be at home resting.

    I have to go back to the dr. tomorrow and get the nuelasta shot and some fluids.  They also called in some scripts at the drug store for antibiotics and nausea.  They told me that I could not take ativan and xanax together and I had to choose between then.  I chose xanax because I use them to control my panic attacks.  She said if I took ativan and xanax together I would wind up in the hospital!  That's good to know!

    I went to the American Cancer Society today and I chose a wig and a toboggan.  I really like the wig.  I got the toboggan to wear at night or on cold days when I'm out side or whatever.  The I went over the Breast Center and I got another wig and a wrap.  I liked all of them.  And best thing of all.......they were all free!  Talked to my hairstylist tonight and he is ready to shape the wigs to make them more "me" and he will have his clippers ready to do the deed when the time comes. 

     other than that, I packed way too much stuff!  We had all kinds of snacks and books and stuff to do and ended up talking to my little group of people more than anything.  There was a 91 year old lady next to me.  She didn't have cancer but was being treated for something different.  She was so sweet.  I enjoyed our conversation very much. 

    The lady that did my stick in the port did an awesome job.  The used some cold numbing spray and I didn't feel a thing.  She was very good!  They did leave the needle in my port today because I am going back tomorrow to get fluids.  It really isn't bothering me at all and you  really can't even tell it's there.

    Well, starting to get a little tired and I am working tomorrow.  So that was my day at chemo.

    Good luck everyone and welcome to all the new ladies. 

    Hugs!

  • CJRT
    CJRT Member Posts: 524
    edited September 2011

    Hi Ladies- Glad to hear everyone is doing well thus far with the first round of chemo. I started off well but ended up dehydrated which was tough. Between feeling so terrible and the young kids, it made for a rough holiday weekend. Feeling better now though. Getting fluid infusions has helped immensely, and I am hoping to be proactive next cycle to avoid it.

     RJ- Sorry to hear about the drama with the pump but glad the rest of the day went well. Fluid infusion today should be great with warding off a lot of side effects. 

     Kelli- We are on the same combo- Taxotere, Carbo, and Herceptin. I go every 3 weeks for 6 cycles. If you don't mind me asking, what is your schedule like? A chemo nurse told me the carbo was a bit easier on the hair and nails than some of the others, so hopefully the nails won't be as bad as you fear. I'm in Florida too and know what you mean about the heat. Good luck!

  • findingsolace
    findingsolace Member Posts: 17
    edited September 2011

    Hi Everyone. I am so jealous (if you want to call it that), that everyone has started their treatment and I am still waiting until Sept 16th! I am going out with my girlfriends for a "get-ready-for-chemo party". Kelliregiand CJRT- I am also doing TCH, 6 cycles. Are you icing your nails? I don't think I will.   PinkShirt and Bluejay58- thanks for the details about your first time. I am worried because I never hydrate myself and when I do, I have to rush to the bathroom like I can't hold it in! Now I know I have to drink a lot and you say you are going to the bathroom every half hour- what if I have an accident, like if someone else is using the bathroom and here I am hopping around with my legs crossed with my IV pole- what a site. Ugh! No one besides me it seems is getting a port the same day as their first chemo. Does that sound wierd to you or not? They say they do it all the time. So I go in at 7am and they said not to expect to leave until 5pm. I guess I will be somewhat drugged up from the port placement during the first half of my chemo, right? Take care everyone.

  • Kelliregi
    Kelliregi Member Posts: 138
    edited September 2011

    Good morning!

    CJRT - I get the T & C every 3 weeks and the H every week for the first 18 weeks, then just the H every 3 weeks for the remainder of the year. It took me until yesterday to mentally process that I will have chemo treatments every week for 18 weeks! I'm just a little slow =). I'm just grateful that I get to skip rads!!! I'm most worried about the Taxotere. That's the one I've heard the most difficult side effect from. I know everyone is different, so I'm staying positive and keeping an open mind. Sorry about the dehydration problems. Hopefully it will be a 1 time thing.

    findingsolace - My treatment only starts 2 days before yours. I was a little jealous of everyone starting on the 8th =). I don't think I'm going to ice my fingers, at least for the first treatment. We'll see how it goes after.

    And so the insurance battle begins!! Found out yesterday, my insurance company had denied my coverage for my DMX. They agree its a covered procedure and are looking in to it. It seems to be a problem that I had it done as an outpatient and didn't require pre-authorization.  

    Today I get a call from my Onc office ad get told they are haveing problems because our COBRA coverage has been cancelled!! Funny, they cashed our COBRA payment check!!!

    I know this will all get straightened out, but what a pain in the a$$!! I need to be gratefull that I have insurance =)

  • bluejay58
    bluejay58 Member Posts: 62
    edited September 2011

    Hi findingsolace!  I do know what you mean about the restrooms -- my center has one in the same area as the treatment room, but it was occupied when I had to go.  There was another one (and there may be a third, for all I know), but it was down the hall, so that was the embarrassing part, pushing my IV ahead of me like it was my dog leading me on her walk. Plus the pump was beeping because the bag was empty.  :D  I'm willing to bet wherever you're going for treatment has two restrooms also.  Here's hoping!

    Also, I know I've seen a few other posts (maybe in the August 2011 chemo thread?) about women getting their ports and having their first treatment the same day.  So it does happen.  I was pretty tired/still drugged-out from my placement that afternoon (I had mine done at 7 a.m.), but it was nowhere near as bad as I felt after my lumpectomy.

  • PinkShirtNow
    PinkShirtNow Member Posts: 134
    edited September 2011

    Finding Solace - My chemo center had 4 bathrooms so I never had to wait.   I just couldn't believe that I had to go so many times!  I  went as soon as I felt I needed to so I was never in danger of an accident if I had to wait.  Like Bluejay58, I was a little embarrassed to be pushing my beeping pole ahead of me down the hall,  Then I realized that nobody was really paying much attention to what I was doing anyway.  They were all concentrating on their own chemo treatment.

    I did walk in on someone who didn't lock the door or answer my knock, though.  Oh well, I've seen bare butts before.

  • olgah34
    olgah34 Member Posts: 407
    edited September 2011

    Hello, I am new here and scared .I already had 3 operations back-to-back ( 2 lumpectomies, PORT insertion and BMX with reconstruction on Sptember 1).Still having my drains till may be, Monday?

     I start my chemo on September 15-Carboplatin, Taxotere and Herceptin.I will have 6 treatments every 3 weeks and Herceptin for a year.

    rj baby, I like your attitude...What is the onco type number? When do they do it?

  • Rockym
    Rockym Member Posts: 1,261
    edited September 2011

    olgah34, Oncotype dx is a specialized test test for ER+ women.  They usually do this test before a decision is made to do chemo.  It will tell the patient the chances of chemo actually helping with each person's particular cancer traits.  A score of 1 - 18 says with no node involvement and a low grade/size you can skip chemo.  A score of 18 - 31 puts you in a grey area and above 31 says chemo is a given.

    Since you are HER2+, you were getting chemo regardless (at least that is what I've been told).  My situation was such that I was looking for any way out of chemo.  I had two MOs give me their opinions.  I had my pathology sent out to Johns Hopkins to get a better understanding of the lymph node involvement and I spent time conversing with a NP on the Johns Hopkins website. Each person had a different take on why I needed chemo.  My current MO said age (47 next month), the other MO said lymph nodes trump everything and the NP said that my oncotype being a 22 was too questionable.  Okay, so here I am.  My TCx4 will start 9/19 @ 9:00.

    Good thing my lucky numbers are 9 and 19.
  • CJRT
    CJRT Member Posts: 524
    edited September 2011

    Kelli- Good luck with your insurance battles. Just what you need what juggling everything else!

    Findingsolace- Wasn't planning on icing the nails but I honestly didn't research it much.

    Olgah- Looks like we have the same treatment schedule. My first infusion took a while because they did the Taxotere very slowly and a loaded dose of Herceptin, but I was told the future ones take much less time.

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    olgah34 I think rockym explained the test pretty well.  I had 2 of 4 node involvement so there was no question I was getting chemo.  I am just so glad my score came back low.  It's a good sign, but I also think with cancer, you never know.  Hang in there and visit with us often.  Lots of smart and knowledgeable ladies here.

    I have taken some of the ladies advice and got my supply of immodium AD, ex-lax, clariton and flushable moist wipes.  So I am ready!  My MO advises Tylenol.  He does not want me taking anything with aspirin in it.  Okay, got my stock of Tylenol ready too!  LOL!  I am just trying to be ready for any and every thing.  Of course, I have only had my first treatment and I feel just fine.  I feel like myself, but we shall see the further I go, the worse it will probably get.  I am trying to get mentally and emotionally prepared for that if it happens.

    Hugs!

  • belleeast
    belleeast Member Posts: 653
    edited September 2011

    hi all, i am supposed to start chemo this month, had my port put in on wed. couldn't sleep last nite because of pain, this morning redness had spread. long story short,port was taken out because of infection,was put on antibiotics for 10 days,have to go back mon so dr can check and change bandage!

    i am already so tired of this,feel like i'm on the rollercoaster again!

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited September 2011

    Hello Ladies!  Hope you are all well today.  Let me share my new "drama" with you.  Things like this only happen to me, I swear!!!

    So I hope you have read the post about yesterday's chemo fiasco.  So today, I had to go back for fluids and my neulasta shot.  Supposed to not take a long time.  They do not have to draw blood or nothing.  Just blood pressure and weight.  My appointment time is 10:00 a.m.  So I arrive and check in at about 9:36 or so.  Several people come in after me and I'm just sitting there waiting.  The nurse comes out and remind me that when I get my vitals to come on back and they would be ready for me to begin.  Okay.  I understand and know what to do.  I wait, and I wait, and I wait.  The people that came in after me are all going in for vitals and blood draws and still I'm waiting.   The nurse comes back out and I shrug my shoulders and say I don't know!  She finds the guy calling the names and asks him why I haven't had my vitals yet and they were waiting on me.  She motions me on back.  Whew.  She was good!  Of course by this time it is 11:00.  Hour past my appointment time.  Get the vitals and go back and get in my little chair.  They hook me up and all goes very well.  The nurse that gave me the shot asked me if I wanted it in my belly or the back of my arm.  I guess I gave her a puzzled look and she said it is less painful in the belly.  I lifted my shirt and said go for it! 

    Things like this only happen to me, I swear!  Hopefully next treatment will go fine.

    I do have a question for the doctor when I see him on Tuesday.  Yes I have another check up on Tuesday with the MO.  Not treatment just a check up.  I suspect he is wanting to know how my weekend went and how I am feeling.  But my question to him is this, when we first met with him, he was I would be getting Taxotere and Cytoxin for 6 treatments.  Of course this was before the oncotype test results were in.  But when I went in for treatment, I was given a folder with all the information on the treatment, side effects, drugs I would be taking, etc.  The nurse went over everything.  I also had a treatment calendar in there.  Showed when I would need treatments and shots.  The question I have for the doctor is my calendar only showed 4 treatments whereas he first told me 6.  So I am wondering if he cut it down because of my low score.  But that is one of the questions I do have for him when I see him on Tuesday.

    I also have to see my surgeon that day.  He is doing a post-op on the port.  It looks good and works just fine and of course the ex-ray showed it was fine.  I purposely made my appointments on the same day to try and save me some gas and time away from work.  Brought work home tonight for this weekend because I am falling so far behind.  Ugh!  At least I am not working at the convenience store tomorrow.  I am afraid tomorrow and Sunday will be rough days like the nurse said, so I am trying to be prepared.

    Okay, so much for the drama in my life the last two days.  I just kinda find it amusing.  At least it ain't boring!!

    Hope you guys have a wonderful weekend.  Talk to you soon.

    Hugs!

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