Saturday, August 30, 2014

What a day!



I am worn out BUT for good reason.  I woke up rested this morning after a good night's sleep. The kiddos ended the week on high notes - YIPEE!!!  I'm easing my way back into work and, I'm happy to say, I was able to put in a few hours today. That may not sound like much to you, maybe not even anything to get excited about, but it gave me such a lift!  For me, it's a good thing to feel like I'm contributing - even on a very small scale at this point. I'm using my brain and I'm (hopefully/eventually) helping my co-workers. I'm really excited at the prospect of spending a few hours a week checking off a to do list and maybe, just maybe, returning as a real contributor to the team. Don't worry, per the doc, the husband, and the boss, I'm not permitted to stress or overdo it. I'm listening...promise. 
Now I need a nap!


Back tomorrow.
Love to all!
Andee

Wednesday, August 27, 2014

It's been a good day

We had a good time today. We stopped by Poppy's Donuts in Richmond to pick up some goodies for the clinic staff - front desk, nurses, lab folks, etc. This was our little way of saying thanks and to let them in our anniversary celebration. The doughnuts were yummy!!
Treatment went smoothly. Today was one of my short days. I got to go straight to infusion - no doctor visit today - and it's an off day for Herceptin. That means my morning looked a like this.

  • Arrive - check in with the front desk, get my paperwork, distribute doughnuts and napkins.
  • Wait for a few minutes
  • Get called back to the infusion area
  • Deliver doughnuts to staff
  • Weight and blood pressure checked. Sent to MY chair.  ;-)
  • Port area cleaned and sterilized
  • Port accessed (stuck with big needle)
  • Blood drawn
  • Wait on blood test results
  • All clear on the blood tests, Pre-meds administered (including steroid and Benadryl)
  • Once pre-meds completed, Taxol hooked up with 1 hour infusion.
  • Chat with the nurses a bit.
  • Exit stage right.
We laughed A LOT! Short days are good.  We were out by 11 ( with an 8:30 start). I was even able to sneak in about 45 minutes of sleep before the kids got home. 
Next week will be a bit longer since I will see the doc first but no herceptin so that knocks off some time. We're getting closer my friends!!

Love to all,
Andee

Treatment Update


Tuesday, August 26, 2014

Let's celebrate our anniversary with chemo...

...said no one, ever! But, you know what we're gonna do? We're going to laugh like we always do. Look at those faces! Tomorrow's festivities could never match the joy and fun of that day but for a chemo day, it will be pretty spectacular.
August 27, 2005
Since I have the privilege to be married to the most fabulous man ever, he's taking off work and coming along to hang out with us even though it's not his week in the rotation. That means I get to spend the day with my hubby and my sissy. THAT means that there will be smiles and laughter and we can try to help everyone else forget where we all are and why we're there...even if it's just for a few hours. We're going to share some joy!  Be sure to dance and laugh along with us!

A recent TBT cover project. AWWWW
Love to all!
Andee

No Jinx, PLEEEEASE

I have presented myself with a challenge this evening - to write a post without really going into detail on the topic. I fear the jinx, you know. I fear that if I say it aloud I will somehow cause a disturbance in The Force and make it all fall apart. Example: yesterday I wrote about my hair and the fact that I had seen a few silver strands coming through - well today I found a whole crop of those suckers! So, I'm going to give this a try while doing all I can to maintain the balance of the universe. .


So, I look at the calendar today, as I often do, and I realize that (1) my baby girl is turning 5 in a month (WHAT?!) and (2) the day before her birthday, something that has been a fixture in my life since May is supposed to come to an end...assuming there are no delays (KNOCKING ON WOOD WITH ALL MY MIGHT). Just think about that for a minute...ok, that's enough. Let's move on before the jinx fairies show up...and if they do, just act normal. 
While (briefly) considering this next milestone, it hit me. Now is the time to start planning ahead for Andrea 2.0. Physical, emotional, personal, professional, spiritual...all of it. I need to work on fitness plan (starting slow), tighten up on a nutrition plan, make sure that I'm balancing work and home in such a way that neither suffers, find new and exciting ways to manage stress, basically I need to figure out how to take care of everything, do it all perfectly and not stress out in the process. Easy, right??  

Even when "it" comes to an end, my journey does not. I'll be dealing with treatment right up until the holidays but the fun doesn't even stop there, I'll be going for Herceptin infusions every three weeks for the next year, at some point I'll start a 5 year regimen of Tamoxifen. I still have a few surgeries ahead of me and, I'm sure, more poking, prodding and testing. All this while trying to get back to a "normal" life.  Whew, I'm tired just thinking about it. Wait...I'm tired all the time. ha!  The reality is that things won't go "back to normal", this is a new normal and I'm OK with it. I have so much to be thankful for and I'm going to figure it all out.  I can manage my health, be a good wife and mom, an asset to my employer and an over-sharing blogger. Right?  That's all part of the journey so at some point we'll move away from discussing treatments and symptoms and discuss the "what's next" and I'm looking forward to it.

Love to all,
Andee

Sunday, August 24, 2014

My head looks like a dirty peach

There is definitely some activity happening on top of the ol' chrome dome. It's not so "chrome" anymore. It's fuzzy. I'm so used to having nothing up there that it looks funny to me...it's as if my head is dirty. The shadow just keeps getting darker. It still appears to be coming in dark...well, mostly dark. I've spotted a couple of silver sprouts but at least it's hair...right?



The side effect list this week is essentially the same but I feel like I've needed more sleep this time than in recent weeks. I've just accepted that fact that I'm rolling the dice each week in this round. It has not been the same from week to week to so just wait and see what's going to happen. Tingly feet seem to be a regular thing but some weeks it's worse than others. Heartburn on days 4-6, post treatment, continues to show up and be nasty. The dark coloring on my fingers seems to be lightening a bit but toes seem to remain darker.  Did I mention I'm sleepy all the time? Well, I'd hoped to write more but I'm sleepy (go figure) and 6 AM will be here before I know it. 

Night all. Back tomorrow.

Love to all,
Andee

Thursday, August 21, 2014

Reality Bites

Let me begin by saying that I'm still OK. Other than some bothersome (to me) weight gain (thanks to the steroids), the standard fatigue and the other nuisance side effects, I'm doing great! I had an echo on Monday and everything looked good. Overall, I can't complain. My attitude is still good, I'm still a complete dork and goofball and I've laughed so hard today that my sides hurt. Also, I'm thrilled to say that we are now officially beyond the halfway point in the second round of chemo!

 



 
With all of that good news, you're probably wondering what about this reality actually bites. Well, I'm still angered by the horror of cancer in general. Just since my diagnosis in March I've heard of several others and I've experienced the loss of a fantastic woman who was diagnosed only a couple of weeks before me (that one REALLY pisses me off). I'm a very empathetic person so I tend to get more emotional about the situations of others. Yesterday turned out to be particularly rough for a treatment day. We kept it light and we laughed a lot. We spent some quality time with one of our favorite roomies but there were a couple of moments - very brief, but powerful - that Bobby and I were reminded of how it can be.
 
Oddly, the topic of specific diagnoses does not often come up with between patients during chemo, at least not in my experience. We have had at least 4 (I think) sessions with our roomie from yesterday so she finally asked me about the type of cancer I had, etc. You know me, no hesitation about sharing my business. I told her my story and she then proceeded to share hers. Let me start by saying, if you were to see her on the street, you probably would not guess that was battling cancer. She's in her late 60s and quite thin, but not "sickly" looking. She speaks softly, she lost her voice as a result of treatment, but with a light and lovely German accent. She said her sister was diagnosed with colon cancer and passed from it. Then, in October of last year she, herself, was diagnosed. She said it was inoperable and by the time they found it, it had already spread to her liver and her lungs...stage 4. She will continue with Chemo for the rest of her life. As if that was not sobering enough, she said that in all her life prior to her diagnosis, she had never been sick, never hospitalized, no surgeries, she hadn't taken many, if any, medications. That sounds great but apparently, when it comes to treatment, it's not so great. She has been allergic to every medication she's been given and has experienced every side effect in the books. On top of that, the chemo they were giving her yesterday was so strong that the onset of nausea was only 15 minutes. It can cause bad cramping immediately. Of course, the medical staff did everything they could to reduce the symptoms and the reactions to the meds. She seemed comfortable but before we left you could tell she was getting uncomfortable. As she was telling us about her treatment she said she would probably be dead by now if not for the treatment but she's not sure she would have agreed to it had she known what the treatment itself would do to her. It just broke my heart. She is such a sweet woman and we so enjoy our time with her (outside of the whole chemo part).
 
My usual seat is in a room with 2 chairs and I end up in the one by the door so, as a result, I can see out into the hall and the nurses' area. As we were talking yesterday I noticed someone new walking into the infusion area. This isn't unusual and yesterday was pretty busy. Obviously, I looked up when the new arrival came in but something was different about this one. There is a routine. If you aren't seeing the doctor that day, you get weighed in and have your blood pressure checked before proceeding to your chair. If you have seen the doc, there's usually some brief chit chat with the nurses in their area and then off to your room. The person who came in didn't get any vitals checked and didn't move on to a room. At first she had her back to me as she talked to one of the nurses. Then she headed toward the restroom but turned around before going in...she was sobbing. I instantly hurt for her. You can jump to a few conclusions based on the location and the audience and it's not good. I didn't stare, I didn't try to overhear. She went into the restroom for a couple of minutes and then came back out. She was still upset but was a little better. She gave the nurse and long hug and then prepared to leave. All I heard the nurse say to her before she left was, "Please don't go on the internet and look it up."  My heart sank. That was the extent of the visit and all I know but it was so painful to watch and it reminds you just how serious things can get and how hard it can be to realize you are NOT in control of the outcomes.  Have I mentioned that cancer sucks??!!
 
This is very real and very challenging. I deal with something similar to survivor guilt. I had the same experience in the NICU. Gabriel is a great example of a success story but he's not the norm. I was very conflicted about sharing our story because there are so many families who deal with the long term effects of premature birth. You worry that people will look at someone like Gabriel and think "Wow, preemies do great now. Modern medicine has gotten over the hump so maybe I don't need to support organizations like the March of Dimes..." You get the idea. I'm now dealing with the same type of feelings in my current situation. Now I worry that I might make chemo seem like a breeze. It's not a breeze but, for me, it was not anywhere near as bad as I expected. Not even close. I was prepared for every side effect, every horror story I'd ever heard about any chemo was fresh on my mind. It just hasn't happened for me. Yes, I feel guilty because my head is not over the toilet for days at a time, because my fingernails haven't fallen off, because I don't really care that my hair fell out, my eyebrows are disappearing and my lashes are thin. I feel guilty because I could tell the doctor to just take the boobs! What about people who have cancer in organ which can't be removed or have cancer that is inoperable, for one reason or another. I know I'm probably oversharing and I know it probably sounds like I'm depressed but I'm not. I'm just sharing in hopes that others can understand that there is so much more to cancer and all that goes with in than you might expect. My attitude remains positive, my laughter is still loud and frequent, and my love of life is stronger than ever but I have a different perspective on life. Cherish is, embrace it, and don't take anything for granted. Even on my worst day, I'm thrilled to be alive. I will continue through treatment and be thrilled that I have had good reports and clean scans showing no evidence of disease but I will never refer to myself as a survivor. If you know me well, you probably already knew that was coming. I have a thing about jinxes. Don't worry, I'll save that story for another post. I will get through treatment, pray for additional clean scans and good reports but I will forever have that little person in the back of mind wondering if it's going to show up somewhere else. The treatment itself can result in leukemia and other cancers down the road so this will forever be a part of my life. That's no joke! I will continue to laugh, enjoy life and just carry on. I am tougher than I ever imagined I could be, I am more positive than I expected and I have received so many positives as a result of this experience that it is, in some way, a blessing.
 
I promise, I'll keep it light for a while after a post like this. Now smile with me as we check out some Phteven!  I am an animal lover and I have a big crush on little Tuna the Chiweenie AKA Phteven.  There is a story behind how I came to fall for Phteven but, again, we'll save that for another post. In the meantime, check him out!!
 
Have a laugh today and don't forget to "Just Say It!"
Love to all,
Andee
 


Tuesday, August 19, 2014

I see a post a comin'...(sung to to the tune of Orange Blossom Special)

Image from classictrainsongs.com


I thought I should post a brief comment about my FB page status from earlier. There will be a full post coming but I wanted to let you know that I'm not knocking ribbons and wrist bands, I have them and wear them, too. I'm just having another "cancer really sucks" day today because of, what seems to be, a constantly growing list of cancer scares and diagnoses in the past few weeks. There is so much that goes on and goes with a cancer diagnosis. I choose to put my experience out into the world but there are so many families who deal with this, and other illnesses/challenges alone. UGH!!  It's EVERYWHERE, people and if you haven't been touched by it yet, sadly, the odds are that you will be. I wish cancer had a face so I could punch it in the nose!

Sunday, August 17, 2014

It's time the get the ticker checked & all about my chemo meds

Good Sunday evening to you, friends. Well, what's left of it anyway. In about 30 minutes it will be Monday. That means I get to make the trip to "town" to have my second heart echo done. The first one was completed just prior to the start of treatment. It has been 3 months already, do you believe that?????  I started treatment on May 15. How time flies when you're having fun.
So the first echo was done to check my heart pre-treatment. Now they're checking to see how it's holding up. Chemo drugs can do a number on it so they check every 3 months to make sure everything is working as it should. The damage done, if there is any, will reverse once treatment ends...that's what I hear, anyway. So if you get a chance, say a little prayer for a strong heart and no treatment delays.  

I've been threatening to post information on my chemo drugs for a while now but have never gotten around to it. Since we're talking side effects of said drugs, I thought I would just post them here.  I am posting links in the order in which the meds were received. A/C was round 1 and that includes Adriamycin aka The Red Devil (Doxorubicin) and Cytoxan (Cyclophosphamide). Round 2 consists of Taxol and Herceptin. Note that Herceptin isn't considered chemotherapy and has few side effects. Once chemotherapy ends, I will continue to receive Herceptin infusions every 3 weeks until I have completed 1 year. Good times! Feel free to follow the links below and see how much fun chemotherapy can be. 

Goodnight and love to all,
Andee

Where in the world have you been?


I'm still here and kickin'. I've been doing the sleep thing, as you might expect. I didn't get much last weekend so I'm trying to be sure I get enough this weekend. 
Side effects this week have been annoying. Now dealing with some arm pain/possible cording so that stinks but I'm working through it. I'll be contacting my PT this week to see if there is anything extra I should be doing. Good times. Other than that I still have tingling feet, raging heartburn, and a super dry nose. Ready to get the last 6 chemo sessions out of the way and move on to phase 3. I'm looking forward to the day that I have ZERO side effects to report and I can be somewhat normal again. Don't worry. I'm still all smiles but speaking the truth. That's what you come here for, right??  

Love to all!
Andee

Friday, August 15, 2014

It's 2:22 and I'm awake

I didn't just wake up, I haven't been to sleep yet. I hate steroid induced insomnia day! Luckily, I was able to get a few bonus hours of sleep this morning after Bobby took the kids to school. It doesn't seem like much right now but it helped.
To stay awake or try to sleep and hope I wake up on time, that is the question.

***On a side note, I think my dark fingers are getting lighter. WOOHOO!! Also, the shadow of hair on my head is getting darker by the day. WOOHOO!!

Tuesday, August 12, 2014

Just say it

If you love someone, do you tell them? I tell Bobby and the kids I love them every opportunity I get. Same with the rest of the family. It's sincere every time I say it. I wouldn't say it if I didn't mean it and I think everyone knows that. The question I'm asking though is really about your friends. Are there people in your life that you love and you just don't think it's appropriate to say it or it's not comfortable to say it?  This topic has always fascinated me and it is brought to mind especially when I or someone close to me experiences a loss. Even with the passing of Robin Williams, as I read all of the tributes I wonder whether he was aware of all of this love while he was alive. Do you tell friends you love them? I have a very small group of close friends and I can tell you that I do! I'm sure it might make some people uncomfortable. It's a statement of fact. If I love ya, I'm going to tell you. I never want to regret not letting someone know they are important to me. If it makes them uncomfortable for a few minutes, oh well.   ;-) It's not a romantic thing folks - I've been with my Prince Charming for a quarter century.

I feel like we should also share appreciation. Each of us walk this earth and wonder if we've made a difference. Have we positively impacted the world? From personal experience I can tell you that I found some peace during the most difficult times of my life because someone simply said, "thank you for sharing your story". I was very open when we lost Christian, again with life in the NICU and now with the cancer diagnosis. It means to the world to know that at least 3 women, none of whom I know personally, heard my story and scheduled a mammogram as a result. A couple of those led to the early detection of issues. There it is!  I don't need anything more than that. My goal is to try to make a difference, no matter how small, while I grace this earth.

My point is this, if someone has made a difference in your life, tell them now. If it's just for being your friend, your mentor, or an inspiration of some kind, I'm sure they would love to hear about it themselves...now...you can tell the story over and over after their gone too but take a moment to say "Hey, I just want to say thank you for..."

Just a thought....

Love to all,
Andee

I'm a little slow and I'm having trouble keeping count

8/11/14
Most days, I'm satisfied with my level of smarts. Other days, like today, I wonder if I have any at all. I've been going through chemo since the middle of May, I've tracked meds, side effects...blah blah blah.  One of those side effects has been raging heartburn for a few days per week. I'm talking the kind of heartburn that is triggered by EVERYTHING, including water. I had a similar experience when I was pregnant with Mattie - not with Gabriel because I was only pregnant with him for about 15 minutes - well, 24 for weeks...same thing. ***Stay with me here. It's going to seem like I'm derailing but I promise I'll bring it all together....you may proceed***
 Anyway, on the heartburn days I try to eat and drink milder stuff. It doesn't really help but I keep doing it.  As I've mentioned somewhere, there are days that milk and mashed potatoes feel like battery acid. Now, with this round of chemo, I was lead to believe that the nausea would be milder if not nonexistent. My oncologist said that he doubted I would even need any medication. I have been too chicken to stop because the one time I did stop the meds just a little early and got sick, it was not pleasant. Plus, it seemed like the mild nausea I was experiencing was hitting well after treatment. I could not understand why I was feeling nauseated at the end of the cycle...that is, until today. Let's walk through the treatment week, shall we?


  • Wednesday (AKA Treatment Day) - Side effect: Benadryl haze  (sleep)
  • Thursday - Side effect: Steroid insomnia
  • Friday - Side effect: fatigue (sleep!!!)
  • Saturday - Side effect: fatigue (sleep!!!)
  • Sunday - Side effect: mild fatigue, mild heartburn, mild nausea
  • Monday - Side effect: heartburn, mild nausea with meds, moderate nausea without meds
  • Tuesday - Side effect: heartburn,  mild nausea with meds, moderate nausea without meds
I just could not figure out why the nausea came on so late but I didn't spend too much time trying to figure it out because so much about this experience just defies logic. For some reason, though, today it hit me. On days that I'm dealing with heartburn, I try to drink only water and milk. I didn't drink any milk until later in the day and within just a few minutes my stomach was protesting. EUREKA!! It's not the chemo that's making me nauseous on those days, it's DAIRY PRODUCTS!!!! DUH DUH DUH DUH DUH DUH DUH DUH.  I know that the general rule is that dairy makes nausea worse but since I wasn't already nauseated, it didn't occur to me. Now, the chemo may make the dairy experience worse but it wasn't directly causing the nausea. The lesson here, folks, is to pay close attention to the side effects during your treatment cycle. Just tracking it isn't enough, you have to pay attention to the details so you don't cause yourself unnecessary discomfort. Lesson learned a little late in the game, but learned. 

Now, sticking with the "I'm a dork" theme, not only am I slow to pick up on patterns, I'm also having trouble remembering where I am in the treatment schedule. The transition to weekly treatment has actually made it seem like things are moving along more quickly than they are. At one point this weekend I told someone I had 5 treatments left...wait, that's not right...I have 7. How in the world do you get messed up on something like that??  Luckily, I keep my trusty Post It on my bathroom mirror and mark off each treatment. After tomorrow's treatment I'll be halfway through round 2.  When I mentioned this to my oncologist last week he quickly corrected me and said that if I looked at round 1 and 2 combined, I was more than halfway through treatment. Yes, this is true but I prefer to handle them individually. Why, you ask? Because if I were to do that with chemo and radiation, I wouldn't be anywhere near halfway. It's all about the positives!

Back later!
Love to all,
Andee

Monday, August 11, 2014

That kid...

This evening, I made my "famous" chocolate chip cookies (from scratch, thank you very much). The following conversation took place in the kitchen shortly after the first batch came out of the oven.

Mattie: (after her first bite) I know why they are called chocolate chip cookies!!
Mommy: Really? Why?
Mattie: Because they have chocolate chips in them.
Mommy: WOW!  Daddy, did you hear that? Mattie thinks they are called chocolate chip cookies because they have chocolate chips in them.
Daddy: I don't think so, are you sure, Mattie?
Mattie: Yes, I am an expert.

I believe...

...that during treatment, there really isn't such a thing as too much sleep. Yes, it's disruptive to normal life and you feel like you might be perceived as lazy but GET OVER IT!  In this round of treatment I don't need to sleep for a week, like I did the last round but a good amount of extra sleep over 2-4 days has been the trend. Right up until last week. With the kids going to back to school and all that needed to be done around the house (see other blog for details on that), I was afraid to sleep. I haven't slept well at night and no naps at all after treatment day. Now I'm paying for it. The good news is that I think I can get myself back on track with some slight adjustments. I'm going to have to schedule a daily nap time or I'm going to crash.  Now where's my blankie?

Gotta run, it's time to get the munchkins up and ready. 
Love to all,
Andee

Friday, August 8, 2014

Just when you think you have it all figured out

Sometimes things can move along a certain way and you think, "I've got this under control!" and than WHACK, life slaps you in the back of the head, as if to say, "Nope, not so much."  No, this is not going to be a Debbie Downer post. It is yet another educational post. Just to let you know, in case you ever have to go through Chemo, the side effects change from one drug to another (duh) and sometimes from the start of one treatment to the middle. Yep, this time around it seems like I'm getting new and interesting side effects every week. They nuisance type things but it's still crazy to think each week something else takes the lead in the side effect race. The tip here, don't ever assume that you have everything figured out. Be prepared to go with the flow and be flexible so you don't drive yourself crazy. Here's a bit of the latest (no TMI, don't worry).

  • My nose is still driving me crazy. Desert dry. Still working with the saline and Vaseline to cope. It helps but it takes a lot of upkeep. 
  • Nausea has lessened/improved each week so far. I'm still too chicken to go completely off my nausea meds but I'm down to the minimim.
  • Heartburn is still baaaaaaad for a few days each week.
  • Neuropathy was very irritating with last week's treatment. My toes were tingling for days. Oddly, this week, the tingling has been minimal since treatment. I'm not sure what's up with that.
  • Hands still look dirty. Nothing to see here, move on.  ;-)
  • Sleep cycle seems to have no pattern anymore. Fatigue is still an issue but better than round 1, for certain! Last week I slept pretty well and at night...like when normal people sleep. This week has been a little more random. That doesn't work well when you need to help get small children up and out the door for the first two days of school. I'll spare you the story but I slept through 3 alarms this morning. They still got to school on time but DANG!!!
  • I have a hairline...that's about all I have but I do have a hairline! It's not really filling in yet but what's there seems to be growing and, so far, it's dark. I was expecting some crazy silver/blonde monstrosity but I see no signs of that as of yet. I know you're on the edge of your seat so I'll keep you posted.
I'm cutting this short because I actually think I might be able to get some sleep right now. The kids will be up searching for Mommy in a few hours so I need to sleep while I can. Hopefully my 5:00PM cup of coffee won't interfere.

Catch ya later!
Love to all,
Andee

Thursday, August 7, 2014

Jinx

I should not have made any mention of  having a "relatively normal" sleep cycle last week. Ugh! I've had a whopping 3 1/2 hours of sleep since 5 AM Wednesday. I'm out, my friends. I have to be up by 6 to get the kiddos ready for school. Thankfully they both fell asleep quickly after baths and a bedtime story so I have a good chance if getting to sleep by 10:30. Wish me luck.

Back tomorrow!
Love to all,
Andee

And....breathe


Wednesday, August 6, 2014

Fun times at treatment

Today was TREATMENT DAY!!!  My darling husband (DH) was my treatment buddy today (we have a rotation with the weekly visits) and we had one of our regular roommates today. That means we could share the joy!  Numbing cream was on nice and early again so I felt absolutely nothing (woohoo!). Met with the doctor to discuss side effects, etc. Nothing worth delaying treatment over so he gave me the thumbs up an sent me on for the juice.  Blood work came back good. My nurses said the numbers looked great but I didn't get the exact numbers. They were going to print out a report for me but we all forgot before I left.  Oh, my echo is scheduled for the 18th so we can check on the ol' ticker.


So, we arrived at 8 AM, waited a bit, saw the doc, waited a bit, went in for infusion, I was plugged in, blood drawn, blood tested (waited some more), got the all clear, started pre-meds and then Taxol started at about 10:15 and that takes about an hour. No Herceptin today so that saved us about another 40 minutes. Being there for so long you have to be able to entertain yourself. We chatted with the nurses, like always, played our tunes (today's Pandora stations were Journey Radio and Dean Martin Radio), puzzle books and today we added a game. We played Heads Up. If you're not familiar with Heads Up, it's pretty fun. I have included a clip from Ellen of her playing with Sean Hayes. You can download it on iPhone, iPad and Android.  We played on the Kindle today because it's easier to see. Everybody got into it - nurses and all. Good times!




I was able to sleep for a bit after we got home today (bonus!) but I need to try to get some extra rest because my babies, BOTH of them, start school tomorrow. I can't even talk about it. Gabriel has moved on to 1st grade and my little baby girl is rolling her ginormous personality into Kindergarten. WHAT?  Thanks to my folks for helping with supplies, they are all packed up and ready for their first day. Supply bag is packed, Backpacks are loaded and ready to go. Clothes are ready, first day of school signs printed for pics, camera battery charged, and a little pack of Kleenex all ready to roll. I can't believe how fast the time goes. Wish us luck! I'll be back tomorrow....promise.

Love to all,
Andee

Monday, August 4, 2014

RRT Post - Eyebrows & Eyelashes

Welcome back to The Really Real Truth Series. It's been a while so I thought I would pull a topic from the list and compose a quick post.
As you might have heard, most (not all) chemotherapy drugs result in hair loss. All hair is at risk (woohoo!). It seems that wild card areas are the eyebrows and the eyelashes. This can be particularly difficult since your eyebrows and lashes (or lack thereof) can significantly change your appearance, and not necessarily in a good way. For me, I've kind of fallen in the middle - my eyebrows have thinned a good amount but there are still some there to work with. My lashes thinned slightly but mascara seems to be enough to make them look normal. I have false lashes but have not yet worn them...haven't really felt the need. The thinning brows have taken a tiny bit more effort. So far, a little dark shadow and some brow sealer has been enough. I'll post the info on the brow sealer on the Products page. If you need some guidance for building up remaining brows or starting with blank slate, I have a link to a great instructional video on the Links  & Resources page from a blogger with alopecia. She makes it look easy but with practice, it doesn't take too long.
As always, the key here is to remember that this is all temporary. I'm sure I'll soon be complaining and about my eyebrows looking like caterpillars, but for now, I'll continue to try to bulk them up.  ;-)

Hello again

Good...um..morning?  The midnight hour is very confusing for me. Seems early enough to still be considered "night" but, technically, the start of another day.  Oh, how 'bout this...
Good day, friends.
Yes, I'm back. I needed to take a break for a couple of days. I missed posting, actually. As I've said many times, the blog is part therapy and, boy, I could use some therapy...and some laughs. So here I am, back again. I will resume regular posting tomorr...uhh...later today.
Until then, I leave you with this...



Love to all,
Andee

Friday, August 1, 2014