Vikki’s Story

Vikki's Story

My name is Vikki, and I live in England, and I was diagnosed with FL in 2015.

Vikki 2

About Me

I am a company director and a mum to twin sons aged 23. I regularly go to the gym.

Finding Out I have FL

I remember everything about the day I was diagnosed with FL. I can shut my eyes and see the room; the desk, the window, and hear the birds tweeting. And I can still hear the consultant telling me that unfortunately I have a form of blood cancer. And I remember my husband crying for the first time since our sons’ births.

The months following were a blur of hospital appointments, scans, and blood tests. There is a misconception that once a cancer diagnosis is made things move quickly, but the reality is they don’t.

“I remember everything about the day I was diagnosed with FL….”

Treatment & Support

It was finally decided that I would go on watch and wait. This is when my mental health took a significant drop. I felt no one understood and I hated burdening my family and friends. This is when i found the Facebook Living with Follicular Lymphoma page. Thousands of people like me with the same diagnosis – all who understood. They could give advice and support.

In 2017 I started treatment. The nodes in my neck got slightly bigger and I was generally not coping with watch and wait. I read an article in the waiting room stating that NICE were recommending Rituximab as a first line treatment for FL so I asked my consultant, and they thought it was a good idea. I got total NED on the second scan after treatment and on the last scan in October 24; still showing I was in remission. No symptoms and bloods were all ok as of September 2025, so the consultant feels I’m still in remission.

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The LWFL group was a lifeline helping with lots of information on treatments and support when in treatment. I then found myself supporting other members by sharing my journey and experiences.

The Follicular Lymphoma Foundation (FLF) was set up, and I have been a super supporter for the charity for some time giving the LWFL Facebook page a voice to the charity.

Challenges

Accepting my diagnosis. I think once you can do that life does become easier.

“The LWFL Facebook Group was a lifeline…with lots of support.”

Triumphs

I’m happy to say I am 8 years in remission and life is good. I’m recently single and know that my cancer will return at some point, but I don’t feel alone. I know even if I’m still single, I will have the full support of the LWFL FB group. Every member is truly part of my FL family.

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Support & guidance to others

Stay positive. Look after your mental health.

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