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Kelly

Kelly

I am so grateful for the grant which I received. It has helped me financially during such a difficult time. 

I was diagnosed with pseudomyxoma peritonei (or PMP) in 2019. I have had a full hysterectomy, cytoreductive surgery and HIPEC (also know by patients as MOAS – mother of all surgeries!), and recently received numerous rounds of chemotherapy. I applied for a family grant from Pseudomyxoma Survivor and was able to use the money I received towards my bills which had increased due to being at home 24/7, purchasing new pyjamas and bedding which I needed and still need due to severe night sweats.

I’m now under palliative care and received a prognosis of six to eight months. With money I had left over, I have been able to enjoy days out with my family and friends. Time is precious and I aim to make the most of what time I have left. The picture of me on a recent family mini staycation in Llandudno.

Find out more about our family grants and how they might help you here.

In memory of Kelly

#CytoreductiveSurgery, #HIPEC, #inmemory, #pseudomyxomaperitonei

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I didn’t have endometriosis, I had PMP

I didn’t have endometriosis, I had PMP

My story began a few months after I got married. My first symptom was the sudden onset of intense pain while I was at work one day. After a few hours, the pain subsided but I decided to make an appointment with my family doctor a few days later.

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I thought I had a hernia

I thought I had a hernia

John went into hospital for a hernia operation. Afterwards, he was told that it wasn’t a hernia but a ‘small, bloody mass’. The pathology came back as pseudomyxoma peritonei (PMP).

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A grant from Pseudomyxoma Survivor helped me