kimcirucci

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Viewing 15 posts - 16 through 30 (of 43 total)
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  • in reply to: Mom turned 83 yesterday! #45918
    kimcirucci
    Spectator

    Hi Sharon, so happy to hear! Happy birthday to her. I told you that your mom would be here to celebrate her birthday. I never had a doubt. When you have a strong will, anything is possible. Get ready to ring in 2011 with you mom because she will reach her next goal. Wishing you & your family the happiest & healthiest of New Year’s. May you have many more magical moments with your mom. Stay strong. Hugs!!

    in reply to: We made it through Christmas #45898
    kimcirucci
    Spectator

    Kim, what can I say? Your quotes speak mouthfuls. I’ve lost many close loved ones and unfortunately we don’t have a choice but to continue on our journey without them. It is so very difficult however. With each loss, I have grown, become stronger and built up a strong will and determination. Now I’m fighting the battle, but this time for myself. There is nothing harder I have ever had to face. As a single mother, the thought of leaving my daughters is something I refuse to dwell on, or to ever allow to become an option. As for you, I am sure your mom never left your side and never will. I am so happy that your holiday was joyous, and I am sure your mother was smiling on all of you. Have a wonderful New Year filled with much joy, laughter & memories of your mom until you meet again.

    Kim

    in reply to: Luke 8:50–Day of Prayer #45547
    kimcirucci
    Spectator

    Wherever I am & whatever I am doing, you can count on me to join in the prayer on 12/29. I will also pray for your grandma today & every other day. Wishing much health & healing for her & all of us who are suffering from this nasty disease. Keep up the good work John.

    in reply to: Wanted: Survivor Stories #38090
    kimcirucci
    Spectator

    I’ve read all of your posts & want to respond to everyone. First of all, Kristin, I totally agree with what you’ve said and yes you are a survivor since you are surviving. My story is listed under the Intro section as “My inspirational story”. Since it’s so long, I won’t reiterate. As I’ve mentioned before, I don’t know if I will ever believe I am a cc survivor or even cancer-free, but to date, I have undergone ex vivo resection with a lot of reconstruction. This is a very rare type of surgery. I believe my surgery was the 6th one performed by my miracle worker surgeon, Dr. Kato. Although I was told in July following my surgery that I was cancer-free, I will forever be looking over my shoulder. As a matter of fact, I have a CT Scan scheduled for 12/28 & I must admit that I am a bit nervous to know of the results. I just keep positive & won’t allow my mind to drift onto negative thoughts. I have fought quite a few battles during the past year & I’m certainly not about to stop now. Regardless of what this next CT Scan shows, I will face it with my eyes wide open & fight with all of my might as I always do. It truly saddens me when I hear of people who begin to “give up”. I know all too well what it feels like to not be able to get out of bed, or to feel like you’re not going to make it, but through it all, I never allowed giving up to be an option. If anything, the more I was told that I was inoperable, the madder I got & the more I found the strength to fight even harder. As I mentioned, I will know in about another week if my CT Scan is still clear, but all I can say is I am alive today & feeling very well. I was able to Christmas shop for my children, partake in Christmas festivities, eat like a pig, and hug my daughters on Christmas morning. My current oncologist said that I should not be alive right now and that he believes someone took me by the hand. I truly believe that as well. He never even heard of the type of surgery I had, but he said he is certainly going to tell other doctors about it. During my recuperation period from my extensive surgery (5 months ago), I have even designed a pendant/bracelet for cancer patients. It is currently being made in China. I should have the finished product in a few weeks. The purpose of my pendant is to provide cancer patients with a sense of empowerment. Although we don’t have much control over this nasty disease, we do have control over our ability to fight. If anyone is interested in seeing my design, I would love to share it with you. To anyone who feels as though they want to give up, I would like to leave you with the words of one of my favorite quotes by Jack Dempsey which states: “A Champion is Someone Who Gets up Even When He Can’t”. Please never give up. Get up & keep on fighting!! This disease can be conquered, but you must fight to win. Best wishes & God bless to all!!

    in reply to: Uncomfortable Discussion #45865
    kimcirucci
    Spectator

    When it comes to those we love, I don’t think awkward, uncomfortable, inappropriate or anything of the like should even be a thought. You had a son, whom I sure was the light of your life, so why not talk about him. When those we love are gone & we can no longer display and express our affection toward them, the only thing we have left is to talk about them every minute we can. What better way to honor their memory. No matter how uncomfortable others may have felt, I’m sure it couldn’t come close to how badly you felt, so never feel bad about letting others know how wonderful your son was. No one likes to hear of sad things, but ignoring them does not mean they don’t exist. You shouldn’t ever regret keeping John’s memory alive regardless of who may feel uneasy about it. I understand blocking things out. When I was 3 yrs old, I lost my best friend/sister to leukemia. She was just about to turn 5. As young as I was, I never talked about it because I saw the pain in my mother’s eyes. Now I realize that keeping it in really doesn’t make the memory go away & certainly does not help anything. Over 40 yrs later, not a day goes by when I don’t think of my sister & I speak about her to anyone or anything that will listen. I think she deserves at least that much. We don’t have control over dying, but we do have control over keeping memories alive. Now dealing with cancer myself, I could only hope that when I am gone, I will be spoken of fondly by many, even if over a Christmas dinner. I wish you the strength to be able to think of your son & face the reality with courage & love. I think he would want that. I am sure he will never leave your heart, so allow your mind to join in as well. You will be together again some day. Until then, keep talking about John. I know I’m sure glad you did, and I truly believe others would feel honored to know of him as well. Continue to grace others with the life of your son. Wishing you a wonderful New Year filled with much joy, health, sunshine & laughter!

    in reply to: Good news- I guess #45854
    kimcirucci
    Spectator

    Hi Julie, I can definitely relate to your situation. I also have two children, ages 15 & 12, and the thought of ever leaving them is something I choose not to think about. I just tell myself that it is not an option in my world and I’m sticking to it. I am glad to hear of your “stable” news. We would love to hear that the tumors have gotten smaller or, better yet, have disappeared, but stable is something positive. Don’t ever give up on total disappearance. It may sound cliche, but miracles do happen. I’m told that I’m a miracle, but I don’t think I’ll ever feel confident enough to believe I am cancer-free. I had very extensive surgery to remove my tumor, 3/4 of my liver & much reconstruction, but due to the recurrent nature of this disease, I’ll always be looking over my shoulder. I have a scheduled CT Scan on 12/28 and I’m a little nervous to see what it shows, but I just let my mind stay strong & guide me. Continue to stay positive & fight with every ounce of power you have. Don’t let fear & negativity cloud your focus. If you believe that you can conquer this, then it can be done. I hope your treatment begins to shrink your tumors, or that a new treatment comes your way that brings you closer to becoming cancer-free. You are in my prayers. Please stay strong. Wishing you much health, happiness, sunshine & laughter in the New Year.

    Kim

    in reply to: Happy Holidays to all! #45836
    kimcirucci
    Spectator

    So happy for you Randi and, yes, may you have many, many more happy, cancer-free years ahead. Wishing you the happiest of holidays. May they be filled with joy, sunshine & much laughter!! Happy 55th….may all your wishes come true! Hugs to you.

    Kim

    in reply to: home for the hollidays I pray #45681
    kimcirucci
    Spectator

    Great to hear that things are moving right along. I agree, the tests should also be forwarded. My doctor won’t even read reports. He wants to see the actually films at all times. Maybe they can make arrangements to have that done. You really have to be persistent with these facilities. Well at least the ball is rolling. I will be anxiously awaiting your news. Keep the chin up my friend. Once again, have a wonderful holiday Mr. J.

    Kim

    in reply to: home for the hollidays I pray #45679
    kimcirucci
    Spectator

    Sounds like a great game plan Mr. J. I agree that you need to be closer to people, physicians, etc. It is true, even though we walk around with this horrid disease, others still feel compelled to complain about their issues, some often quite trivial. However, it is truly a gift to be able to listen & help others. It also helps to keep your mind off of your own problems. Those who are too self-consumed rarely have time to even notice others who are in need, but that’s why there are givers & takers in the world. We can’t all be the same…life would be too boring if that were the case So hats off to the givers! I hope you start crossing paths with more givers than takers. Good luck with relocating hospitals. I’ll be checking in on you. Wishing you a very Merry Christmas & a New Year filled with joy!

    in reply to: Steriods #45841
    kimcirucci
    Spectator

    Hi Lily. I don’t think a decrease in appetite is a side-effect of steroids. To the contrary, one of their purposes is to stimulate your appetite. Also, they tend to make you gain weight. They also cause mood changes, which can make some people a bit nasty. Therefore, I would not attribute your MIL’s weight loss & loss of appetite to the steroids. Perhaps the chemo is causing her loss of appetite. The shortness of breath could be due to a number of things, but one reason could be anemia. Do you know what her hemoglobin level is? Anemia could cause shortness of breath, as well as exhaustion. The chemo can also make you feel very tired. If she is not eating much, that could explain her weight loss, but once again, that could be from a number of reasons. Cancer itself causes weight loss as the cancer does steal nutrition from the body, which is why weight loss is one of the major indicators of having cancer. Are the doctors aware of your MIL’s symptoms? The weight loss is concerning. I’m not an expert, but I would mention this to the doctors. I hope this info is somewhat helpful. Please keep us posted. You & your family are in my prayers Lily.

    in reply to: home for the hollidays I pray #45675
    kimcirucci
    Spectator

    So sorry to hear about your loss of “friends” Mr. J. Some people don’t know how to handle illness, so they run. I have been extremely fortunate in that regard. I have so many people who have stepped up to the plate & have really gotten me thru this. Sometimes you have to open your heart in order for others to come in. Maybe that’s why I’ve been so blessed…that’s a door I always leave open. Please know that you have many friends on here & I don’t think any one of us would leave you out in the cold. No one truly knows what symptoms you will experience next. This disease has a mind of its own. All you can do is keep as mentally & physically strong as you can. You’d be surprised what the mind can do. I will pray that your strength remains high & that things start moving in a positive way for you. Just follow your body & don’t let anyone make you do anything that you think you can’t handle drug wise. If the medications make you too sick or weak, then take a break from them. In the meantime, we are all here for you. If I can help you in any way, please don’t hesitate to call upon me. Even if you need help finding home care nurses, etc. I think it would be a good idea to have a nurse check in on you periodically. Hopefully your insurance will allow it. If not, let me know. I’ll help you fight that too. Please take care of yourself & don’t hesitate to ask for anything. We all must stick together in order to beat that nasty demon. Don’t get down & don’t lose hope. You’re not alone. Keep us posted Mr. J.

    Kim

    in reply to: Just finished cycle 1 of 8 of gem/cis #43642
    kimcirucci
    Spectator

    Hi Shari. I must say, keep that attitude. It truly helps. I’ve always had an upbeat attitude & tried to laugh as much as I could through many adversities. I was also on the same chemo as you. The only side-effect I had was fevers. I didn’t really have any hair thinning until the end of my treatment, which I believe was when I approached the 4th month. I didn’t even take the anti-nausea meds. They made me feel sicker. I never had any nausea or vomitting. They said it was a harsh type of chemo, but other than a few days with fever & exhaustion, I would bounce right back. I wish you luck with it. I certainly don’t want to make you lose your focus, but the regimen didn’t work for me. Luckily I found a surgeon who removed my tumor when no one else would, so I feel blessed. I’ve been told that I’m a miracle. I’ll believe that when all of my scans come back normal. I don’t think I’ll ever feel completely cancer-free even if they say I am. I don’t think the feeling ever leaves you. However, I know I’m alive today & not many believed I would be, so here’s to miracles. May you be one of those miracles too, along with everyone else on this site. Keep up the great work. I know you will receive good news! Just keep fighting all the way!! My prayers are with you. Keep us posted.

    in reply to: What to do for Christmas? #45827
    kimcirucci
    Spectator

    Hi Sharon, I wish I had some exciting suggestion for you, but unfortunately I don’t. As a mother of two daughters, ages 12 & 15, the only thing I can say is simply spending time with my girls is a blessing in itself. I’m not sure what type of person your mom is. Maybe the slides would be too depressing for her. Perhaps you can just tell her how much having her as a mother has meant to you, and maybe just reminiscing. I’m sure whatever you do, your mother will be happy just to be with you. Just do whatever is in your heart. You certainly can’t go wrong with that. Wishing her a very happy birthday….I know she will be blowing out her candles. Please enjoy your time together, which I hope will last for a long time. Prayers for you & your family. Have the happiest of holidays ever. Hugs!!

    in reply to: Chemo Resistant #45794
    kimcirucci
    Spectator

    Hi Peony, I believe we have “spoken” before, so I apologize if I say anything that seems redundant. Your husband’s case hits home for me, as I too was on the exact treatment. Your husband is also the same age as I am. Unfortunately, Gemzar & Cisplatin did not work for me, as I believe I explained to you previously. I was wondering if you have attempted to contact Dr. Kato in NY. He will review your husband’s scans without having to meet him. If he feels he can perform his magic, he will ask you to come to his office. I can certainly relate to your husband’s frustration, fear, disgust, depression, etc. I also went from being a healthy woman attending nursing school, taking care of patients one day to lying in a hospital bed, now as a patient, the next. This disease will carry many emotions, but giving up should not be an option. The unfortunate reality is that this disease is a very difficult one to cure, but it is not impossible. As long as the possibility exists, you must never give up until you find it. If I can help you in any way, please let me know. My prayers are coming your way. This disease can be conquered, so together with all of us on here, let’s fight with every ounce of power we have. I’m not ready to give up & I sure hope your husband isn’t either. Good luck & please keep us posted. Hugs!!!!

    Kim

    P.S. If you would ever like to talk, please email me at kcirucci@msn.com & I will give you my phone #. Sometimes you can’t explain things in writing as you could via phone.

    in reply to: anniversary gift #45812
    kimcirucci
    Spectator

    That is certainly the best news I’ve heard in a while. Nothing like “meeting” someone who kicked this disease’s butt. Keep on that healthy journey. Have the happiest of holidays ever. Thanks for being a ray of hope for so many.

Viewing 15 posts - 16 through 30 (of 43 total)