Melissa’s Story

Melissa's Story

Hi, my name is Melissa, and I am from Jacksonville, Florida in the United States of America. I am Stage 3a and I was diagnosed in January 2024.  

About Me

I’m 48 years old. I’m a wife, mother of 3, mother-in-law to one. I’m a preschool teacher. I’m a faithful Catholic and my faith has played a huge part in my journey with FL.  My Catholic faith is something I have grown up with, and prayer is what my family turns to in times of need.  After my initial diagnosis my family gathered for rosaries, and I had people doing mass intentions and requesting prayer from all over the world.  God is with me through this. 

I enjoy spending time with my family.  Living in Florida we frequently take trips to Disney.  I enjoy antique & thrift shopping. I love spending time with my family. 

Melissa

Finding Out I have FL

I had a swelling in my right groin; it wasn’t painful but it that lasted for weeks. I saw my doctor, and she ordered an ultrasound and CT scan. The CT scan showed it was an enlarged lymph node, two to be exact.  

I had a biopsy removing the larger if the two and that’s when I learned I had Follicular Lymphoma. When I was first told I had cancer I don’t think it registered with me.  The surgeon said, ‘so the diagnosis is follicular lymphoma’ and I just sat there listening to him talk.  It was a few minutes later that I was like wait isn’t lymphoma cancer!?!? Then I asked what kind of doctor I would see and when he said ‘an oncologist’ that’s when it hit.  Oh wow.  That’s a cancer doctor.  I have cancer. 

I then had a PET scan and bone marrow biopsy. The only thing that showed was the other lymph node in my groin. I received 12 rounds of radiation on that area.  

A year or so went by until I had another CT scan which showed two enlarged lymph nodes under my left arm. I had to have a needle biopsy for that, and it was discovered that it was also follicular lymphoma. 

For me researching and getting all the information I can find helps.  I like to be informed.  I found the FLF (Follicular Lymphoma Foundation) and various FB groups and it helped to read other people’s stories. 

I asked what kind of doctor I would see and when he said ‘an oncologist’ that’s when it hit.  Oh wow.  That’s a cancer doctor.  I have cancer.

Treatment & Support

My initial treatment was radiation followed by Watch and Wait.  My family is very supportive.  My mother helped with picking my kids up from school so I could go to treatments.  My boss and co teacher were understanding with me missing work.  My husband was supportive and helped where he could.    

I had a PET scan early January 2026, and it found a few more swollen lymph nodes.  It also saw a mass near my liver.  I had a CT scan to check on the mass and thank goodness the mass is nothing to worry about.  More than likely was intestine that showed up on the PET. 

I will talk to my Dr shortly about the new lymph nodes. 

Challenges

When I learned of the enlarged lymph nodes under my arm, I felt defeated. I had hoped it would stay gone. I was worried about treatment options. The idea of Watch & Wait concerned me but after speaking to my doctor and understanding it better I now feel at peace. 

I was very nervous in the beginning. Lymphoma is scary and I immediately worried about death. I trust my doctors though and I feel good about my treatment plan.  

One thing that weighs on my mind occasionally is if this lymphoma will change into a more aggressive type. I pray and tell myself that we’ll cross that bridge when and if we get there! 

Watch & Wait concerned me but after speaking to my doctor and understanding it better I now feel at peace. 

Support & guidance to others

I learned on the last webinar that we’re more likely to die with follicular lymphoma than from follicular lymphoma and that statement has brought me great peace.

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If Melissa's story has inspired you and you wish to share your own personal FL journey or experiences, please complete our patient stories request form.