Childhood Cancer Outcomes

Debate between Zarah Sultana and Anum Qaisar

Tuesday 26th April 2022 Commons Chamber

[Ms Anum Qaisar (Airdrie and Shotts) (SNP)]

I begin my contribution to this important debate by extending my sincere congratulations to the hon. Member for Gosport (Dame Caroline Dinenage). She was very eloquent in speaking of Sophie’s legacy.

In the past few weeks I have been speaking to my constituent Nadia Mahjid, who lives in Airdrie and whose son Rayhan sadly died from a brain tumour. I asked Nadia what she wanted me to say, and she asked me to tell his story. These are her words:

“Rayhan Majid was a happy, sweet and caring four-year-old boy… He loved sports and all things yellow including the Transformers Bumblebee and the Minions.

Rayhan was born in June 2013 in the midst of a heatwave and when he arrived, everybody remarked that he had brought the sunshine with him.”

Rayhan was

“always an active and healthy boy who was rarely unwell however, in October 2017, he started having severe headaches and sporadic episodes of vomiting.”

As with Sophie, GPs did not detect anything and it was not until Rayhan was taken to A&E, in his case six weeks later, that the decision was taken to conduct further tests. Sadly, an aggressive and cancerous tumour was detected in his brain:

“At that point the tumour had already grown…and as a result it was not able to be completely removed during surgery.”

Nadia says that,

“the aggressive surgery left our son Rayhan unable to talk, walk or swallow”,

and that he

“had to have a second surgery to have a shunt permanently inserted into his brain to prevent fluid build up.”

Devastatingly, however,

“the tumour re-grew and spread immediately after surgery even before radiotherapy and chemotherapy was commenced…it was decided to press on with the original treatment plan. Our Rayhan underwent 6 weeks of radiotherapy at the highest dose permitted for a child his age.”

The radiotherapy

“had no positive impact on Rayhan’s cancer either, a post treatment MRI scan showed the disease to be present and even more widespread than it was to begin with. The final treatment offered for our son Rayhan was high dose chemotherapy… A few hours after receiving his first dose of chemotherapy drugs, Rayhan’s heart rate and breathing started to be negatively impacted as well as him developing an allergic reaction to one of the many drugs he had received that day.

Rayhan tragically died a cruel, slow and painful death over the course of the 5 days of chemotherapy treatment, at the end our son was completely paralysed and unable to talk or even blink his eyes.

Rayhan was our ‘little ray of sunshine’. His light was cruelly extinguished by a relentless disease”.

I have a number of questions for the Minister, but she graciously offered to meet me after I wrote to the Prime Minister, so I will ask just one as I am pressed for time right now. Does she accept calls from Cancer Research UK that the UK Government should commit to maintaining a regulatory environment that facilitates international cancer studies, including a commitment to maintain the UK-EU data adequacy agreement and the compatibility of UK and EU trial regulations?

[Zarah Sultana (Coventry South) (Lab)]

I thank the hon. Lady for giving way, especially as she is giving such a heartfelt, passionate speech on behalf of her constituents. Ben was a young Coventrian who tragically passed away aged seven after just one year following his diagnosis with a rare childhood cancer—alveolar rhabdomyosarcoma. In his memory, his parents set up Pass The Smile For Ben, raising funds for treatment and research into rare childhood cancers. Will the hon. Lady join me in paying tribute to Ben’s parents, Sarah and Scott, and echoing their call for more funding and better treatment for children with rhabdomyosarcoma?

[Ms Qaisar]

I thank the hon. Lady for her intervention and I completely agree.

Every year in April, the month that Rayhan died, the neighbours of Rayhan’s family decorate their street in yellow, his favourite colour. His nursery has a bench to commemorate him. Rayhan was, and is, a much-loved boy. He died four years ago this month. This was a tribute from his mum, Nadia, on the anniversary of his death:

“When you were born you brought the sunshine with you and when you left, the colours drained out of our lives and this world has not been the same since.

You had to experience many things in your short life here that no child should ever have to, and many adults do not even experience in a lifetime.

We hope wherever you are it is worlds apart from all the pain, procedures and trauma you had to endure here and that we couldn’t protect you from.

We hope that in your new world, you are healed, happy and free to play, run and be a child again.

We are sure that you will be lighting up the heavens with your brilliance, that your laughter is echoing through the gardens of Jannah, that you are surrounded by friends aplenty and that you are having the most amazing, wondrous time, seeing and doing things that we cannot even imagine.

We love and miss you beyond measure Rayhan. Your Dad, your big brother, your little sister, all your family and I.

We include, remember and honour you everyday and we will never let you be forgotten. You are still our boy and the heart of our family even though you are not in the same world.

Our beautiful little Ray of Sunshine, our darling child, we miss you always, we love you forever.

4 years with you didn’t feel like enough, yet 4 years without you has felt like a lifetime.

Rest in Peace our darling boy.”