My name if Jennifer Ponce and I am a 38 year old 4 year Lymphoma cancer survivor!
Four years ago on August 22, 2006 I rang the bell. The bell that was to signify the end of my cancer treatment. Not the journey...just the treatment. This day was far more emotional then I ever could have anticipated. I thought it would really be no big deal, I would ring the bell because Keith and a few of my friends insisted. Heck - I didn't even know the bell existed until a couple of days before my last zap of radiation.
Ringing Out
Ring this bell
three times well
Its toll to clearly say,
My treatment's done
This course is run
And, I am on my way!
REAR ADMIRAL IRVE C. Le MOYNE, USN
JANUARY 4, 1996
I can tell you that I rang that bell way more then three times well... I took a hold of that string and rang that bell with every ounce of my being...with warm tears streaming down my face that could be seen flooding the floor beneath. In fact everyone around us was crying. Not just me, not just Keith and my friends, but there was not a dry eye in the lobby... I don't think this is something that is special just to me...I think anyone that witnesses a patient ringing that bell is overwhelmed with emotion.
My hair started growing back just before my last round of chemo (the doctor told me it was because my body was past the insult of the chemo...nice Dr. Sam...nice....). So I promised Keith that I would remove my "security blanket" after ringing the bell. I promised not just for the day, but for good. This was a hard one for me. With no hair and no bandanna I felt ugly. But I was officially no longer sick and it was time to move past this chapter, so I hesitantly agreed. The significance was strong so I knew I had to get past my self consciousness.
A glimpse into my cancer story.
It all started on Thursday January 05, 2006. I went to see my primary care physician, Dr. Lincoln. My left ear hurt and I had a little cough. Dr. Lincoln listened to my breathing and asked if I had been short of breath, when I told her a little she decided to do a chest x-ray. She was being thorough and wanted to make sure that I did not have phenomena.
Needless to say when she came back with the x-ray results she explained that I did not have phenomena but that I did have a large mass on my left lung that appeared to be a tumor. {Can we go back to that phenomena thing…I think I am okay with that now…haha}. I remember her drawing a picture of my lungs, the location of my tumor and the location of my heart with a blue marker on the white paper that lined the examining table like it was yesterday. She gave me a list of a few different tumors (because I told her that Keith was going to ask a lot of questions that I was not going to be able to answer). Then she asked asked if I could make myself available to have a CT scan that same afternoon… Ahhh Doc, you just told me I have a large mass on my left lung, of course I have time!
I called Keith once I got in my truck and asked him to please call in sick to work. Telling him was probably the hardest thing to do. He of course asked why and for the first time, I started crying so hard I do know how he could have understood me…but I got it out…”I have a large mass on my left lung and I need to go for CT scans. Can you please take me”? I told him everything the doc told me and gave him the list of the tumors that the doctor had given me, which he had information on before I got home.
I called Keith once I got in my truck and asked him to please call in sick to work. Telling him was probably the hardest thing to do. He of course asked why and for the first time, I started crying so hard I do know how he could have understood me…but I got it out…”I have a large mass on my left lung and I need to go for CT scans. Can you please take me”? I told him everything the doc told me and gave him the list of the tumors that the doctor had given me, which he had information on before I got home.
The CT scans were set for around 4:30 and Dr Lincoln finally called around 7:00 …I say finally because I think those were the longest hours of my life. She was very thorough in her explanation but really the only thing she was able to clarify was that it was definitely a tumor.
My co-worker and good friend Kristen and I were hoping it was just Slim Jims that were stuck to my lung (I had been eating a lot of them. Scott, our other co-worker brought a tub of them to work after Christmas). So glad I had Kristen there, to help lighten things up...she was scared and she was worried but together we laughed.
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| Kristen - I love my Lymphoma awareness bracelet... I will cherish it always ~ ♥ |
On Monday the 9th we saw the Pulmonary Dr. and on Tuesday the 10th the biopsy was done. We got the final diagnosis on Thursday the 12th when the Pulmonary doctor called me at work to tell my I had Lymphoma. I remember being so naive that I asked the Dr. "Lymphoma, what does that mean? Is it benign?" And I remember the voice on the other end saying "No dear, it's cancer". I must have been in a bit of shock because I hung up the phone called Keith, shared the news and continued to work.
It was all happening so fast and I was scared and I really did not know how to reassure everyone that I was going to be okay. It was inevitable ... I was going to get through this. I never doubted that!
In the middle of the night while Keith was sleeping I remember sneaking out of bed and going to the kitchen. In the middle of the night I cried. I cried alone. I cried loud. I cried hard. I buried my face into the palms of my hands and sobbed. In the middle of the night I picked up the phone and I called MDAnderson. I left a message requesting an appointment in the Lymphoma department. On my way to work just a few hours later, I had to keep my mind busy, I got a call from MDAnderson. The soonest they could get me in would be the 25th due to the MLK holiday.... How was I going to wait 12 whole days knowing I had cancer and not knowing how we were going to get rid of it...
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| In good spirits before my doctors appointment |
My doctors appointment on the 25th was overwhelming. Dr. Samaniego, was my Oncologist. I remember thinking how serious he was, not funny but very serious. It was like he was calculating in his head how to make my cancer go away. I knew after meeting him that I was in good hands.
The next step was to undergo several different tests to determine stage and treatment of my cancer. Dr. Samaniego informed me that I would lose my hair. It was going to happen and that I should accept it. That was when I started crying uncontrollably. Not because I am vain,. Not because I care that much about my hair. But because now EVERYONE would know I was sick. The funny part was that even through my tears and obvious dismay I looked at him and said "no, not my hair" and it sounded like "no, not the gum drop buttons" (you know Shrek - the gingerbread man)... I was also told in this appointment that all chemo would be administered through a central line catheter. Leaving that day I was a little unclear as to what a central line catheter really was.
The next step was to undergo several different tests to determine stage and treatment of my cancer. Dr. Samaniego informed me that I would lose my hair. It was going to happen and that I should accept it. That was when I started crying uncontrollably. Not because I am vain,. Not because I care that much about my hair. But because now EVERYONE would know I was sick. The funny part was that even through my tears and obvious dismay I looked at him and said "no, not my hair" and it sounded like "no, not the gum drop buttons" (you know Shrek - the gingerbread man)... I was also told in this appointment that all chemo would be administered through a central line catheter. Leaving that day I was a little unclear as to what a central line catheter really was.
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| Together we will conquer!! ~ ♥ |
On February 2, 2006, I had a bone marrow aspiration/biopsy done. I am not going to lie, this was not a fun procedure it left me a little sore. Keith said I handled it like a champ!!! Only a couple of tears but no yelling. YEAH JEN!!
The next step was to have my catheter inserted, okay no lies…this sucked! We referred to the catheter as Jenney’s Predators Patch or simply JP2. It was inserted right below my collar bone on the right side of my chest, it was very awkward having this gadget with two tubes sticking out of my chest. I can honestly say I learned to adapt. Keith had to take classes to learn how change the dressing and how to simply care for the catheter. He is such a wonderful hubby and watching him go through this with me and his unbelievable strength just made me love him that much more.…like I thought that was even possible!! The first time the dressing was changed I had it done at the hospital and I nearly fainted for the first time in my life...but it got easier.
The next step was to have my catheter inserted, okay no lies…this sucked! We referred to the catheter as Jenney’s Predators Patch or simply JP2. It was inserted right below my collar bone on the right side of my chest, it was very awkward having this gadget with two tubes sticking out of my chest. I can honestly say I learned to adapt. Keith had to take classes to learn how change the dressing and how to simply care for the catheter. He is such a wonderful hubby and watching him go through this with me and his unbelievable strength just made me love him that much more.…like I thought that was even possible!! The first time the dressing was changed I had it done at the hospital and I nearly fainted for the first time in my life...but it got easier.
On Friday Feb. 10th we started our first round of chemo and received our staging results. {I use the words we and our because I did not go through this alone, Keith was very much apart of every diagnosis or treatment that I went through}. The staging results showed that I had Stage II, Large B-Cell, Non Hodgkin's Lymphoma. I had a mass on my left lung (9.5cm) and little popcorn size masses in the base of my neck near my left lung. The chemo regimen that I took was called RCHOP (all the initials of the meds). The first 4 are administered through the catheter and then there was one that I took orally. I spent a day in the hospital and then was able to bring a chemo bag (which was hooked to the catheter) home. I had to stay hooked to the bag for 48 hours. The chemo made me a little loopy, forgetful, and achy but other then that I really didn't have any major side effects.
I started to lose my hair shortly after my first round of chemo. It was as dramatic as you see in the movies. I could not even run my fingers through my hair without big clumps getting stuck between my fingers. I decided that this was the one thing that I did have control of so I called my friend Kathy and told her that I was ready. I was freaked out and I think my dear friend was freaked out too. She told me that she had to stop on the side of the road before getting to my house to cry...she did not know how she was going to keep it together for me. We moved the truck out of the garage and Kathy started her master piece. To see ALL of my hair on the ground was a bit humbling. My one regret is that my hair was not long enough to donate to locks of love (Locks of Love is a public non-profit organization that provides hairpieces to financially disadvantaged children under age 18 suffering from long-term medical hair loss). I held it together and Kathy was shocked at how pretty my head was??? So we found laughter.
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| Kathy (with Kade in her belly) & Jackie (with Ryder in her belly) ~ ♥ |
After weekly fast track visits (to check blood counts). Six rounds of chemo every 21 days (2 of which were delayed due to low blood counts). Neulasta injections, given in the stomach, 24 hrs after every chemo cycle to help boost white blood cell count. Numerous X-Rays,CT, &, PET Scans and several trips to the Dr. for consultations later on June 30th we received the wonderful news. I no longer had cancer. There was no longer evidence of the disease (NED-no evidence of disease). I was able to get my catheter removed and I no longer needed chemo...This is of course where the 5 weeks of daily radiation began...but I can now proudly say that the rest is history!
Every year I try to go back and re-read the updates that we sent out to all of our loving family and friends. They bring back such a range of emotions. I can openly admit that the biggest being the overwhelming amount of love and support that we received thought our journey.
I am not sad that I had cancer. I am glad to be a survivor. Cancer DID change my life. It made me less careless about how I live it. It made me slow down and appreciate all that I have around me. These are not changes that happened overnight but happened non the less. This sound like something Kelle Hampton would say but I am drinking it all in and I am sucking the bee-jee-sus out of it...savoring every little sip. Life is beautiful! It is good! It is precious and I am living it baby!!!
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| Demetra... Could not have done it with out you! ~♥ |
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| Just a picture to prove that I did own something other then that orange shirt...lol |















