CarolLHRN's Avatar

CarolLHRN

Pittsburgh, PA

  • Patient: Colorectal (Colon) Cancer
    Patient Info: Currently in active treatment (initial surgery, receiving chemo rounds/radiation), Diagnosed: 11 months ago, Female, Age: 38
  • CarolLHRN's Avatar  

    Update about 17 hours ago

    CarolLHRN posted an update

    CT Scan this morning. I am hoping everything comes back clean. I won't get tests on Fridays anymore because I don't want to wait out the weekend waiting for results!

    • ttisme's Avatar

      Comment about 9 hours ago

      ttisme

      carol I had to wait 2 weeks, it was worse than getting my diganosis alone...

  • KendallHHC's Avatar  

    Wall Post 3 days ago

    KendallHHC wrote on CarolLHRN's wall

    Yay for finishing chemo! Give yourself time to heal - your body has been through a lot! What helped me most in recovering was sleep/rest, lots of water and lots of leafy green veggies!

  • CarolLHRN's Avatar  

    Experience 8 days ago

    CarolLHRN

    Celebration (Finished treatment): It feels so good to be done with treatment but still dealing with fatigue. I know that the last treatment has side effects too. It's just so hard because I am so ready to move on but the fatigue is holding me back. I know another 2 weeks or so I will start to feel better but it feels so far away!

    • StunnedMike's Avatar

      Comment 8 days ago

      StunnedMike

      Great news. You will bounce back in no time.

    • ttisme's Avatar

      Comment 5 days ago

      ttisme

      So happy for you. Don't push the fatigue issue!

  • CarolLHRN's Avatar  

    Blog Post 11 days ago

    CarolLHRN posted a blog post

    One Step Closer

    I had my last chemo treatment yesterday.  It was a great day.  I was nervous that my blood levels would not be good enough but they were.  The nurses started to do a dance in the hallway they were so excited.  I was excited too.  As much as I dreaded getting chemo and not feeling well, I just wanted to be done.  I was able to have a great weekend feeling well and knowing that I'll be feeling well again made it OK.  I was also able to get my surgery scheduled.  I actually called for the appointment as I was sitting getting my chemo.  I'm all set for June 14.  It's just a little over 5 months away.  It's hard to believe that this journey will soon be over.  I'm am super excited to get my life back and pursue the things I love again.  I miss swimming and hiking and kayaking and cycling so much.  I can't wait to jump back in the pool in a couple of weeks and take a nice ride on the trails.

    • RuthAnne's Avatar

      Comment 9 days ago

      RuthAnne

      Congratulations is a big enough word. So happy for you!

    • ttisme's Avatar

      Comment 8 days ago

      ttisme

      I didn't get to see my nurse when I was disconnected, cuz he doesn't work weekends....made me sad. I need to see him! Going to take him and my chemo buddy balloons next week!

  • CarolLHRN's Avatar  

    Update 11 days ago

    CarolLHRN posted an update

    Had my last chemo yesterday. I get disconnected tomorrow and will be done with all these chemicals being dumped into my body. Surgery scheduled for June 14. Finally seeing the finish line!

    • DaveWaz's Avatar

      Comment 9 days ago

      DaveWaz

      Oh wow - that is awesome news!!!!! Hope you did something good for yourself to celebrate!

  • CarolLHRN's Avatar  

    Blog Post 15 days ago

    CarolLHRN posted a blog post

    Good to Go for Monday

    Yesterday I went to the dermatologist to figure out what the mysterious red spots were.  Well, they didn't know what they were either.  They decided to do a biopsy just to make sure all was OK.  I told the doctor she could do whatever treatment she wanted as long as she cleared me for chemo on Monday.  She told me she has never had a patient who actually wanted chemo treatment.  Once I explained it was the last one, she understood and cleared me. I had a punch biopsy of one of the spots on my neck.  I don't really think it was necessary as the spots are fading but if that's what it took to be cleared for chemo then so be it.  It didn't hurt much.  I got numbed up and the 2 stitches were in before I knew it.  I'll go back next week to have the stitches out so no biggie.  I'm a professional with using Glad Press and Seal to cover wounds so even my shower was easy today. So now I just need to hope that my platelets are high enough on Monday to get my last treatment.  I'm hoping these 5 extra days make the difference.  Hopefully Monday I will have my chemo, be disconnected on Wednesday and be done with this phase of treatment.  Then it's just the reversal surgery and I am done.  I can't wait.  If I get my chemo on Monday I will be calling the surgeon's office to get a date for my surgery while getting chemo!

  • CarolLHRN's Avatar  

    Blog Post 17 days ago

    CarolLHRN posted a blog post

    Mysterious Spots

    So I got the bloody nose taken care of.  I went to the ENT on Monday afternoon and he removed the packing and indicated no further care was need.  Yea!  I hope I never have to get my nose packed again.  It is not a pleasant experience.  With the nose thing behind me, a new issue has appeared: I have spots on my shoulders and neck. The first spot was noticed Sunday night.  I figured it was just a bug bite.  On Tuesday morning, I woke up with 5 additional spots on my other shoulder and my neck.  I'm not sure if they are spots or welts or what they are but they are red and raised.  I went to my PCP yesterday and she didn't know what they were either but after consulting with my oncologist, it was decided I need to see a dermatologist and hold off on chemo today.  Sigh.  So tomorrow I am off to the dermatologist who will hopefully solve the mystery of the spots. I am disappointed I am not finishing chemo today but there was a good chance my counts weren't good enough to get chemo anyway.  I'm trying to look at the bright side of things.  I'm going to a concert tonight and I'll be able to feel good.  Tomorrow I'm going to the wine festival.  Even though I can't drink a lot, it will be fun to sip a few good wines.  Perhaps a BBQ is in order this weekend.  I'm trying to stay focused on enjoying time with my friends, something I really haven't felt up to in a while. If all goes well with the dermatologist tomorrow, she will OK me to continue with chemo.  I'll get my final treatment on Monday and disconnected on Wednesday.  It will so nice to finally be done.  It just seems like it's taking forever to just finish up!

    • agrogan's Avatar

      Comment 16 days ago

      agrogan

      Hi I'm sorry you couldn't get your last treatment yesterday. My nineth quimo treatment was cancelled yesterday because of my platelet count been 79, my oncologist likes it to be close to 100. I wonder why your oncologist has a lower standard when it comes to the platelet count. I can't wait to be done also 4 more to go. Best wishes and God bless you.

    • ttisme's Avatar

      Comment 15 days ago

      ttisme

      Sorry your last treatment has been postponed. This week was meant for healing! Enjoy your weekend off and look forward to all that are to come!

  • CarolLHRN's Avatar  

    Update 18 days ago

    CarolLHRN posted an update

    Developed some red spots on my neck and shoulders and feel a bit run down. Highly doubt I will get chemo tomorrow and it's the last one! Waiting for the nurse to call back for next steps. Sigh. I just want to be done!

    • StunnedMike's Avatar

      Comment 17 days ago

      StunnedMike

      Fingers crossed! Starting my down hill slide today. 6 more to go!

  • CarolLHRN's Avatar  

    Blog Post 22 days ago

    CarolLHRN posted a blog post

    Bloody Nose Woes

    Growing up, my brother was the one with the bloody noses.  I never had a bloody nose.  That was until yesterday.  Being on chemo, it is common to have some blood in your nasal discharge.  It's sort of a strange thing.  You lose your nasal hair and have drainage all the time, sometimes a little blood tinged.  Your eyes tear a lot as well so you basically look like a toddler who just had a big cry.  But I have managed to deal with these side effects until yesterday.  After blowing my nose in the morning when I woke up, I noticed that my nose was continuing to ooze blood and wasn't really stopping.  It wasn't pouring out but it required constant attention. So, before I went out the door to go to work, I called my oncologist office and of course they told me to go to the ER.  I knew they were going to say that and part of me wishes I never called.  So, I drove to the ER with a tissue up my nose.  By the time I got to the ER, the oozing had calmed down a bit but I proceeded to get care.  I had my labs drawn and it was no surprise that my platelets were low (26).  The doctor attempted to cauterize my nose but that was unsuccessful (and painful!).  So they decided to pack my nose.  To say the least, it is not a pleasant experience and it's  not pleasant to have my nose packed for the next couple of days. Luckily I have been able to work from home today so no one had to see this packing hanging out of my nose.  When I go out this weekend, I will be sure to cover it better than it is now so I don't have snot dripping out of my nose in public.  That would be a sight to see!  On Monday afternoon I got to the ENT to have the packing removed and hopefully that will be the end of this. With my platelets being so low, my last chemo will probably be delayed a week.  They told me to go and have my labs done and see what happens.  I don't have high hopes that I will finish on May 2 but instead May 9.  I can see the finish line but I just can't get to it.  Tripped up right before getting there.  People say almost done but there is still a lot to get through.  I just keep plugging along and one day, it will all be done.  Oh, I can't wait for that day!

    • ttisme's Avatar

      Comment 19 days ago

      ttisme

      Sorry about the nose bleeds! sucks. "All most done and OHHH your finished" are two comments that are as irksome as folks asking how are you...Hang in there Carol, you can do this. Prayers!

    • StunnedMike's Avatar

      Comment 18 days ago

      StunnedMike

      My nose hasn't stopped bleeding since I started treatments. Sometimes swallowing the blood makes my stomach upset. But mine is not as bad as yours. Glad you are reaching the end. I start 7 today. Down hill now.

  • ttisme's Avatar  

    Wall Post 28 days ago

    ttisme wrote on CarolLHRN's wall

    Carol, wanted to share this with you....my friend had a temp Ilosotomy(sp) due to years of suffering from ulceritis colitis (sure can't spell tonight). she had the j-pouch procedure done at the same time. Wednesday they reversed the bag and hooked up the pouch...she's eating soft foods two days later! with minimal pain!

  • CarolLHRN's Avatar  

    Update 29 days ago

    CarolLHRN posted an update

    Had my 7 of 8 chemo treatment this week. It was a roller coaster of an appointment. My platelets were 56 which met the cut off point but my hemoglobin, potassium, white cells and albumin were all low. After my nurse worked with my oncologist, I got my treatment. But... They told me not to count on getting my next treatment on time. I have been told this once before but my labs were OK. I really want them to be OK the next time because the next treatment is my last!

    • StunnedMike's Avatar

      Comment 29 days ago

      StunnedMike

      My white cells where low this time too. Any thing we can do to make them higher?

    • RuthAnne's Avatar

      Comment 28 days ago

      RuthAnne

      Keeping our fingers crossed - hang in there!

    • steve70x7's Avatar

      Comment 26 days ago

      steve70x7

      I hate the word "Waiting!" That really is the worse part for me. Waiting for labs, waiting for radiologist's reports, waiting, waiting, waiting!

      Don't you just hate those computerized phone messages that say, "Your approximate wait time for the next agent is three years."

      On the other hand, thank God I'm still around to wait! ;)

      I hope you wait time is short.

  • CarolLHRN's Avatar  

    Blog Post about 1 month ago

    CarolLHRN posted a blog post

    My New Best Friend

    Hello blog followers.  I apologize for not updating the blog lately but my new best friend, my couch,  has gotten in the way.  Chemo is definitely taking it's toll on me and I have become a couch potato.  Once I am home from work, I put on my comfy PJ's, sit on the couch with my remote and chill.  I think perhaps, my body is permanently indented in the couch.  An important thing to note however, is my couch is not my best friend forever.  In fact, I am thinking once this journey is over, a new couch is in order.  I think I have spent more time on my couch in the last 3-4 weeks than I have the entire time I have owned it.  But I know once the chemo has ended (25 days but who is counting!) that I will need some recovery time.  But after that, who will need a couch?!?!  I will hopefully be riding my bike and golfing and generally, not at home to be sitting on my couch. Although it has been a comfort these last couple weeks and will continue to be so for another couple weeks, couch and Carol just don't fit well in the same sentence.  At first it was hard to get comfortable on my couch.  I was almost like Sheldon from the Big Bang Theory trying to find a place to sit at Penny's.  None were comfortable at all.  But I have developed a love hate relationship with my couch.  The couch is beloved right now but I think it knows that in a short time, it will be once again forgotten and never used. On a serious note, I do have 25 more days until chemo is over.  I cannot wait as the chemo has taken every ounce of energy I have.  I continue to work and I think that's good for me.  I think it's good to have to get up and get dressed and get out the door every  morning, even if it means taking short breaks in the process.  At work I get engrossed in my projects and forget about chemo, and being tired, and even my dear friend couch.  My boss has been amazing understanding if I need to work from home, not that I have done that too much.  I'm tired of being tired but it's part of the journey and knowing the end is nearing makes it tolerable.  I have already started to plan when I can start golfing again as well as going on trips with Venture Outdoors.  I envision that last day of chemo, emailing the surgeon to schedule my surgery.  The finish line is near and even when I feel I can't go anymore, time just keeps passing by whether I am ready or not.  I know I can hang in there just a couple more weeks and then look forward to better times.

  • CarolLHRN's Avatar  

    Update about 1 month ago

    CarolLHRN posted an update

    I accomplished a lot of sleep this weekend and feel better today for allowing myself the time to get much needed rest. Still tired but not as bad as the weekend. I had my Neulasta shot on Saturday and I have no side effects. I have been taking Claritin as many suggested and I guess it did the trick. Still doing my platelet chant as I need to keep them up to keep on schedule. Just 2 more treatments; 25 days. But who's counting!

  • CarolLHRN's Avatar  

    Update about 1 month ago

    CarolLHRN posted an update

    Platelets were up to 72 today but white count was low. Getting my chemo as scheduled but adding Neulasta on Saturday. Happy the chemo is still on schedule but I haven't heard good things about Neulasta. Will try the Clartin before the shot and keep plenty of Tylenol on hand.

    • ttisme's Avatar

      Comment about 1 month ago

      ttisme

      Glad you were able to go on with treatment! Only thing my chemo buddy complianed about was sore muscles. She took claritin and tylenol too!

    • StunnedMike's Avatar

      Comment about 1 month ago

      StunnedMike

      Started 5 today myself. Need to stay on track. I will have to cancel fiights if is miss a treatment.

  • ttisme's Avatar  

    Wall Post about 1 month ago

    ttisme wrote on CarolLHRN's wall

    Girl I was so happy that I didn't have to shave my legs for the first three months! I too lost alot if not all on arms and such! but when my eye lashes looked like kid cut them off, I quit wearing make up! Glad to say that things are growing back

  • CarolLHRN's Avatar  

    Update about 1 month ago

    CarolLHRN posted an update

    Getting nervous about my chemo appointment this week. My platelets have to be above 50,000. Last time they were 69,000. I really don't want to skip a week. I just want to be finished. This will be treatment 6 of 8 and if I keep on schedule I will be done in 5 weeks. I know I will still need time to recover but knowing there is no more chemo will be a huge emotional booster.

  • Emily6040's Avatar  

    Wall Post about 1 month ago

    Emily6040 wrote on CarolLHRN's wall

    Thanks Carol. The FU is distributing slowly through my pump now , I am home relaxing, I am sneezing a lot today Hope I am not getting sick. Does that ever happen to you. Did you have a PETSCAN after your 4th Chemo and was it good? They told me they will check me for stability or a reduction and know this cocktail is working.... Let me knoiw your experience that will be great!!!

    Thanks so much!!
    Emily

    • ttisme's Avatar

      Comment about 1 month ago

      ttisme

      all of the drugs we are on can "dry" you out! I start the sneezing on Monday after treatment and will continue sneezing all week. Onc nurse recommended i use saline nasal spray to "put moisture" back in my nose. It works, just have to do it three or four times a day.
      I can deal with the sneezing, its the dry mouth, split lips and tongue that I am having ISSUES with!

    • CarolLHRN's Avatar

      Comment about 1 month ago

      CarolLHRN

      I didn't have a PetScan because my case is different than yours. I do know that is is the usual regimen to have the PetScan to see how things are progressing.

      I have a very dry nose and mouth. I am constantly blowing my nose and because my platelets have dropped significantly, if I blow too hard, I get a bit of a bloody nose. I use Biotene toothpaste to help with the dry mouth. I mostly only sneeze when I am exposed to cool air. I am so happy it is warming up because having chemo in January and February was really painful.

      The best advice I can give you is to "ride the wave". If you feel tired, take a nap. If you feel good, take advantage and go for a walk. Eat what you can and what you want. Hang in there and before you know it, you'll be through it.

      I just have 3 more infusions left. I have a feeling I won't get one next time because my platelets are so low but I won't know until I go. I try to see the silver lining in it. If I don't get the chemo I will have a better Passover and Easter.

      Keep us posted!

  • CarolLHRN's Avatar  

    Wall Post about 1 month ago

    CarolLHRN wrote on Emily6040's wall

    Hi Emily,
    There are lots of us going through the same cocktail you are. I am 5/8 through. I had chemo/radiation prior to surgery so I only need 8 treatments of FOLFOX instead of 12. The side effects are weird but manageable. We were have a run of warm weather where we live and then suddenly a cold day. I forgot how much it hurt to breath cold air. Nothing a scarf couldn't fix though. We'll get you through this!

  • Emily6040's Avatar  

    Wall Post about 1 month ago

    Emily6040 wrote on CarolLHRN's wall

    Hi Carol,

    My only surgery thus far has been the hysterectomy. They didn't know it was Colon till afterwards. I have a legion about 4 cm that they are hping Chemo will shrink. I am on 5 FU and the Oxaliplatin and the fusilov booster. They said they may treat the mass legion with radiation - they want o see the effect that chemo has on it first. Second round of 12 tomorrow.

    Is that the same treatment you are on?

    • ttisme's Avatar

      Comment about 1 month ago

      ttisme

      HI Emily,
      I am finishing up the same chemo regime as you. I have 2 more treatments left. I should be finished end of April. Had a mass removed and resection of my ascending colon in October.
      Holler if you have questions, Like Carol I check in here daily. Good luck and rest when you need to!
      T

  • Emily6040's Avatar  

    Wall Post about 1 month ago

    Emily6040 wrote on CarolLHRN's wall

    Hi Carol,

    I have also been diagnosed with Colon Cancer and want to connect up so we can learn from each other.I started treatment with my second round of Chemo tomorrow. Hope you are doing great!

    Emily

    • CarolLHRN's Avatar

      Comment about 1 month ago

      CarolLHRN

      Absolutely. I am on the site everyday. What type of chemo are you getting? Have you had any surgery?