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Vital Info


Eddy (eddymejiajr)


August 17, 2010


Click here.


New York, New York


August 11, 1983


Cancer Fighter

Cancer Info


Multiple Myeloma


June 12, 2010


Radiation Therapy


The fatigue


I have great people in my life


Be around


Fatigue


Spine


Roosevelt Hospital


Keep smiling and laugh A LOT


Stay busy



coming soon


Stats


Posts: 2
Photos: 0
Events: 0
My Supporters: 3
I Support: 3
Comments: 1
Views: 3912
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Eddy's Cancer Blog

So much for being off this week

My doctor has me on a schedule that requires me to take 2 infusions a week for 2 weeks, then a week off. This was my 2nd week off when my doctor calls me and says that since he wasn’t around last Thursday I didn’t receive my Zometa infusion. So we made a schedule for me to come in on Friday to do it.

Silly of me to think I wasn’t going to have to deal with any needles this week.

I showed up a bit late. Walking with a cane sucks. When I walked into the infusion suite I was greeted by my nurse. I love my nurse. Her name is Gina and she has a very personable quality to her. She’s funny and always makes me laugh.

After checking in I was surprised at how few people were there that day. I wasn’t sure if this was a good or bad thing. Check in, blood pressure, temperature, but because i’m only taking the Zometa today, NO BLOOD! Even though i’ve gotten used to giving blood it still sucks.

Gina gets the Zometa, finds a vein, and we’re on our way. I watch Everybody Loves Raymond as I wait. 30 minutes later i’m done and telling Gina to have fun on her vacation. I will have a different nurse on Monday. All of them are nice so i’m not worried, although Gina helps me feel more comfortable with being the youngest person around. She’ll be back for the next cycle.

It was a good day after all.

Keep that sense of humor going..whatever happens you are going to beat this beast! Hope you have a nice needle-free weekend….

A hug.

Eddy, all of the darn procedures sucks, but cancer sucks more. I don’t know who invented the darn thing anyway, nobody wants it so we need to get rid of it. Maybe we could all get together and come up with some type of infusion to blow the darn thing off the face of the earth, then nobody would have to worry about it anymore. Everybody hates it anyway, and who wants to be around if you are hated anyway, so it should all just blow up and go away.

Eddy, it is to good to hear that your nurses are so pleasant, it certainly makes the process easier, and it is good that you have so much confidence in your medical team, it makes going through this madness much easier.

We wish you the best of luck as you continue through the procedures that are making you healthy. Hang in there and stay tuff!

Eddy you’re not only good at taking orders and your treatment but you are a LADIESMAN too! Well look out nurses cause Eddie’s on the prowl. Hey you kick the begeezes out of whatever is lurking cause we want more tales from the nurse’s station. Keep up your positive attitude Eddy. I know you are going to stomp this out.

How you doin’ Eddy?

Prayers and hugs.

Eddy, I am sorry I missed your birthday, how are you doing? Miss your posts…

A birthday hug, HM

Better late than never

I was in the hospital for 5 weeks, the longest weeks of my life. I had to give up my Yankees/Mets tickets because I was in the hospital! I was discharged on July 12th, 2010. I started Chemo on July 15th.

With one month of chemo under my belt I feel more positive about my progress. The doctor says my blood counts are up and my calcium levels are down. Due to my low white blood cell counts the doctor recommended I not start the Revlemid till my next cycle. It has me a bit worried. I feel like i’ve been doing so well and i’m afraid the Revlemid will kick my ass.

I want to take all the steps possible and attack this thing with everything we can. I hate feeling nauseous and fatigued as i’m usually a very active person. That’s my main concern. I’m young by Myeloma standards so the doctors feel it’s best to be as aggressive as possible, which I totally agree with.

The Revlemid cycle starts on the 23rd. I’m anxious to see the effect it makes on the cancer cells.

Louise threw a punch at your cancer.
Louise sent you a prayer.

I hope this is not a duplicate, I just wrote a comment but it has vanished…

So anyway, yes you are way too young, my father-in-law had MM but he was in his late 70s and had nothing like you have experienced. I know the chemo will be tough. You are right to think of it as an assault on the bad stuff.

My favorite baseball year is 1955 when the Dodgers, still in Brooklyn, won the Series…then a year later they sold out and moved to LA and I never was their fan again. I was 12 and I suddenly realized the world was not what I thought it was!

Hang in there..take every day, every hour, as it comes, and live long enough to see more of those Yankees/Mets games…

Hey, thanks for the comment.

I notice you spoke of your father-in-laws experience with MM in the past tense. Does that mean he is cancer free or has he passed?

The chemo has been surprisingly easy so far, I’m hoping it stays that way with the Revlemid.

So do you still follow baseball? I actually went to 2 Yankee games this week. It’s like it was meant to be after I wrote my blog. My friend was off from work and offered me a late birthday present, then the next day we were both bored so we went again. They won both games!

I am taking it day by day and have every intention of seeing the Yankees/Mets next season.

I was diagnosed with MM in April’08 and given 6 months to 1 yr to live. Praise God I’m still here. My initial (and current) treatment was Velcade, Revlimid, and Dexamethasone (RVD) a steroid. I have done a lot of research on treatment options and changed my diet completely. This has helped tolerate side effects. Revlimid is nothing to fear. The following is a small example of research.
A Gift of Time “If you want to do something, do it now. Don’t wait.” This advice come from a patient with end-stage pancreatic cancer who was given an unexpected gift of time, thanks to curcumin, the main ingredient in the spice tumeric. When Duane Jacobson first came to the Clinical Center for Targeted Therapy (CCTT) at M. D. Anderson, he had less than three months to live, estimated his oncologist Razelle Kurzrock, M.D., principal investigator of the curcumin trial and also chair of the Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program). More than two years later, he is traveling around the world with his wife Hildrud while enrolled in an NIH-sponsored, phase II clinical trial of curcumin in advanced pancreatic cancer.

God bless. There is Hope.

Eddy; Welcome to the blog. Yes, you sure are in for a fight but it sounds like you know how to tackle this. Just keep posting, you know your friends will grow along with you. Weezie







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