Taylor Morgan Rivera, 14, was called home to glory on Monday, April 26, 2010. She fought a courageous three-year battle with cancer. She was born Nov. 21, 1995, to the union of Thomas and Tammy (Montelongo) Rivera. She was an eigth-grade student at Roncolli Middle School. She enjoyed softball, music, movies, games, was an avid Colorado Rockies fan, but most of all enjoyed spending time with her family, who she loved so dearly. Taylor is survived by her loving parents, Thomas and Tammy; her brothers, Matthew Rivera and Landon Rivera; her grandparents, Paul and Gloria Rivera, Frank and Arlene Montelongo; godparents, Frank Montelongo and Lisa Garcia; uncle, Willie (Debbie) Rivera; aunts, Elaine (Charles) Jacobs, Pauline Rivera, Loretta Rivera, Lucille Osteen and Sylvia (Donnie) Coghill; numerous cousins, other relatives and friends. Special thank you to the doctors and nurses at Children's Hospital. Special doctors, Dr. Lia Gore, Dr. Kerry Moss, Dr. Meg Macy and Dr. Arthur Lui. Special nurses, Deb, Molly, Lauren, Kristen and Beth. Memorial contributions may be made to any U.S. Bank location, in the name of Taylor Morgan Rivera Memorial Fund.
Monday, April 26, 2010
One more angel, watching over us tonight...
Taylor Morgan Rivera, 14, was called home to glory on Monday, April 26, 2010. She fought a courageous three-year battle with cancer. She was born Nov. 21, 1995, to the union of Thomas and Tammy (Montelongo) Rivera. She was an eigth-grade student at Roncolli Middle School. She enjoyed softball, music, movies, games, was an avid Colorado Rockies fan, but most of all enjoyed spending time with her family, who she loved so dearly. Taylor is survived by her loving parents, Thomas and Tammy; her brothers, Matthew Rivera and Landon Rivera; her grandparents, Paul and Gloria Rivera, Frank and Arlene Montelongo; godparents, Frank Montelongo and Lisa Garcia; uncle, Willie (Debbie) Rivera; aunts, Elaine (Charles) Jacobs, Pauline Rivera, Loretta Rivera, Lucille Osteen and Sylvia (Donnie) Coghill; numerous cousins, other relatives and friends. Special thank you to the doctors and nurses at Children's Hospital. Special doctors, Dr. Lia Gore, Dr. Kerry Moss, Dr. Meg Macy and Dr. Arthur Lui. Special nurses, Deb, Molly, Lauren, Kristen and Beth. Memorial contributions may be made to any U.S. Bank location, in the name of Taylor Morgan Rivera Memorial Fund.
Thursday, March 25, 2010
Any excuse to celebrate...
Here I am again. One more round since you know when. At least, I know when - always will.I celebrated my 38th birthday in February. Today I will celebrate my 2 year anniversary of remission. I sorta feel like it's my 2nd birthday.
I know - any excuse to celebrate Tommy...
And you know what? YES. Any excuse to celebrate life. And even more than that - quality of life. I know I'm lucky for where I've been and for where I'm at and I know it could be gone in a minute.
Well, not much else to say than that. Next week is Spring Break and I will spending time having a check-up and probably a CT scan or an ultrasound. Good. Times. *wink*
Cheers!
Monday, March 1, 2010
Happy National Colorectal Cancer Awareness Month to You!!

March is National Colorectal Cancer Awareness Month.
And since this happens to be the exact type of cancer I have, I am plugging it here.
The American Cancer Society encourages all Americans at average risk to begin screening starting at age 50.
Despite progress, colon cancer remains the third leading cause of cancer death in both men and women in the United States.
"Colon cancer is one of only a few cancers that can be prevented through screening," said Al Stabilito, Northeast Ohio Public Relations Director of the American Cancer Society. "Precancerous polyps, from which colon cancers often develop, can be identified and removed before they become cancerous."
The American Cancer Society recommends that men and women at average risk for colon cancer begin screening at age 50. People at increased or high risk should talk to their doctor about the appropriate screening test and schedule for them.
Monday, November 16, 2009
And whadaya know. The world just keeps spinning...
Next check-up set for mid-February. Just short of my two year "birthday".
I also met with the Genetic Testing Counselor. She doesn't feel like my family history screams that my particular case was due to genetics. Not ruling it out, she says testing wouldn't hurt. The thing is, tested or not - not matter what the results - my family would still be urged to test at the very latest, 10 years prior to my diagnosis (so at age 26). If the testing came up to positive, then testing would be even sooner. Maybe age 20. Yikes.
I told her I would think about it. Probably won't do anything right now for financial reasons more than anything. Maybe next year when I am starting out brand new racking up my Maximum Out of Pocket Expenses. Heck, they still haven't even billed me for my CT. I can't wait to see that one. Kinda shady if you ask me - this whole new insurance business. I have not had much fun with it. At least with Kaiser I knew how everything worked and, for the most part, I knew how much it was all gonna cost. They (insurance companies) sure know how to get you when you're down, don't they.
Speaking of being down...
My friend Cindy K. Not doin' so well. She had a bad reaction to her first round of chemo and has been in the hospital for a few days. Send extra prayers and good vibes in general her way please.
Sunday, October 4, 2009
I don't think you should be able to call that a Berry Smoothie...
Let's see. Where do I start?
New Doctor
At the end of July I met my new Oncologist. Dr. Cohn with the RMCC. So far, so good. I didn't think the receptionist was especially remarkable - but the nurse that took me back for my vitals was really nice. I wish I could remember her name. She was very personable. A PA came in and talked over my history with me and I was extremely impressed when Dr. Cohn came in later on and it was obvious that the PA related information that I had just given to her and that Dr. Cohn had listened. It reminded me of that telephone game you played when you were a kid and you whisper something to your neighbor down the line and at the end the message has nothing to do with what it started out as. Except this time it actually came out the same way I told it in the beginning. It sounds like Dr. Cohn wants me to come in every 4 months for a CT scan and also recommended some genetic gene testing.
New Insurance
That all would have been peachy keen with me but before I went in for my CT scan I got a letter from my new insurance company (Anthem) saying that I was not approved due to my pre-existing condition and that I needed to provide a certificate of creditable coverage (CCC). You know, this is the one condition that I made sure I would be good to go on before I quit Sun. I wasn't going to make the move if it would mean that I would lose my healthcare coverage. I was assured that I wouldn't because I had coverage with Kaiser for such an extended period of time, I wasn't supposed to have to go throught he wait period. Well, by the time I got a response on the CCC stating that I was approved - something that I finally had to fax, call on and remain on the phone until the fax was reviewed and my status was changed - it had already been two months gone by. This really makes me pretty angry. I feel like I should be reimbursed for two months worth of insurance that I was not able to use! Yeah, I guess I could wish in one hand and...
CT Scan
So since things finally cleared up, I was able to reschedule my CT scan. Friday 9/25 I had to go back in for bloodwork since so much time had passed, but I saw that intake nurse again and again she was super nice. I didn't see Dr. Cohn. Just the lab and the scheduler to pick up the Berry flavored ReadyCat super yummy prep drink (that is sarcasm for any of you who have never had the pleasure). My CT scan was in the LoveHeals mobile unit. It's a semi-trailer that visits several sites in the metro area for people needing CT or PET scans. Also a very cool crew.
Genetic Testing
On November 16th, I will be going in for a genetic counseling review. Because of my unusual age of diagnosis and the fact that three out of my four siblings have had polyps found, Dr C thought it would be a good idea. Actually, my mom finally went in for her colonoscopy and they also found 2 benign polyps in her. Still trying to get dad in there. I will also be seeing Dr C after/during that appointment to review the results of my scan. I know that's a long time in between, but I am sure if they see anything concerning, they will contact me sooner.
Peeps & Prayers
Jeanine...
My last day of chemo will have been one year ago on October 8th-10th. Do you remember that big ol' end of chemo party I had to celebrate? Well, I remember how ready I was to celebrate. My friend Jeanine had her end of chemo party last night. I was so happy to be able to celebrate with her! She had six rounds of chemo for her recently diagnosed breast cancer. Jeanine is looking great, still has the most positive attitude ever and is getting ready for surgery, which she is happy so say will be a lumpectomy instead of a masectomy. After that, she is anticipating 30 days of radiation. Go Jeanine! In the words of your beautiful sister - You kicked chemo's ass! Keep up the fight!
Cindy Kay...
One more friend diagnosed with breast cancer. I know that she had surgery already and from what I understand, she should have already begun radiation. I haven't had a chance to talk to her, but I know that she has faith, friends and family - which is the true miracle cocktail to fight this nasty beast. Sending you my love Cindy Kay.
Taylor...
My little cousin Tay who I have talked about a lot on this blog has come to another crossroad in her cancer journey. Taylor is now 13 years old. She's been battling this disease for 2 years now. Unimaginable, but real. She had been doing so much better, on a clinical trial treatment receiving chemo for 5 days on alternate weeks. Discussion was going on about the possibility of getting the medication in an oral form. Her hair was growing back and she was feeling back to normal - even ready to maybe play some sports. She was receiving scans every 8 weeks to mark her results. Recently Taylor found out that her tumor growth had surpassed what was allowed by the clinical trial (this was her second plan of treatment) and that she would no longer be able to participate. I know, I can't imagine. I saw Tay and her family at the Miracle Party this year and she appropriately was dressed as a super hero. Tay has begun radiation - I think she'll have 35 consecutive days of treatment (minus the weekends). She still has her fighting attitude and she is always in my thoughts and prayers.
And, Life In General...
Things are going really well for me. I am really liking my new job. Love the people I work with. I am shocked at how much my son has grown over the summer. He thinks he's 5' 5", but I am having a hard time believing it. I am 5' 2" and think he might be as tall as me, but mostly - people are telling me I am out of my mind and to deal with it. My baby is growing up. He's doing awesome in school. Reading like crazy (they're doing a reading challenge and he's docked about 5,000 pages) and will be going to Washington DC for their school trip in May. I'll be going to Oregon next week for a friend's wedding and am very much looking forward to that.
Well, it's been nice catching up with anyone who still checks this site out ;)
Hope you're well.
