I worked as a teacher and deputy headteacher in primary education for thirty seven years, many of those also as a Special Needs Co-ordinator with a specialism in Autism.
After having an ulcer on my tongue that refused to clear up, I was first diagnosed with a squamous cell carcinoma in 2015 which was treated with a small operation to remove it. Eighteen months later it returned and the same procedure was carried out. In 2019 it recurred again and this time I had a partial glossectomy, reconstruction with a free flap and a neck dissection. This was followed by six weeks of chemoradiation.
Following this wonderful experience I had to adjust to living with my ‘new normal’ which presented many problems. At this point I heard about The Swallows from my speech and language therapist as a new group was starting in Lincolnshire. The help and support I received was amazing and at this point my husband and I decided we would like to use our experiences and knowledge to help The Swallows support those who are going through, or have been through, treatment for head and neck cancer.
We have been active members and fundraisers for the last six years, regularly attending the national online meetings in order to keep our knowledge of new developments and advice up to date. For the last three years we have been leading the Lincolnshire group which meets online due to the huge size of our county.
I am a member of the Patient Advisory Group for the Petneck 2 project and a new study researching the need for support following the end of radiotherapy treatment. I am also a trial participant in the Aquax2 study which has seen a huge increase in my saliva production.
I am pleased to be an Advocate for this wonderful charity.