Levi's Star Shine On

Supporting Children With Brain Tumours

We are only too aware that the diagnosis of a brain tumour is absolutely devastating. 

 

Life for children with brain tumours and their families is changed in an instant.  It isn’t just the horror of the diagnosis, it’s the realisation that brain tumours and their treatment can cause physical and mental changes that could be permanent.  In fact some parents of children with brain tumours may even have to become full time carers.

 

Such changes could include:

 

·         Weakness down one side of the body

·         Poor balance, or shakes

·         Fits/blackouts

·         Headaches/migraines

·         Some may lose the sight of one, or both eyes

·         Some may have hearing difficulties

·         Growth problems

·         Early, or late puberty & fertility problems

·         Educational problems – problems with new learning (skills, or ideas), poor short term memory, problem solving

·         Learning difficulties – needing extra support at school, or in a special unit

·         Behavioural problems

 

With all these issues in mind we are only too happy to help as many children with brain tumours as possible, for as long as possible.

 

Children and young adults we have helped so far

 

James     was diagnosed with a brain tumour 5 years ago

aged 24   and has had frequent surgery, radiotherapy

            and chemotherapy.  His condition is

            non-curative.  We contributed financially

            towards a much needed family holiday

            for James, his wife and their little girl.

 

Jane       has a relapsed glioma (brain and spine).  She

aged 10   experiences decreased mobility as a result of

            her diagnosis and side effects. Jane can no

            longer walk to school, to town or to her friends

            houses or clubs. As no-one in her family

            drives, we paid for taxis to enable Jane to

            continue to participate in school and leisure

            activities with her peers as much as she is

            able.

 

Liam       was diagnosed with a medulloblastoma in 2008.

aged 17   He was coming to the end of a long course of

            treatment and feeling quite low. Due to his

            diagnosis, Liam had to put an apprenticeship on

            hold and needed something positive to focus on.

            We therefore helped to fund his motorbike

            restoration hobby.

 

Harry      was diagnosed in 2007 and now has a relapsed

aged 13   medulloblastoma. Due to his condition, extreme

            tiredness and access issues, Harry had missed

            a lot of school.  We helped towards the cost

            of a laptop that Harry could use both at home

            and school that would make life easier for him.

 

Alex       has a medullablastoma and was diagnosed in  

aged 9    2007.  Her mum cares for Alex full time and

            so money is understandably short. Alex loves

            to watch TV and they needed help to pay for

            the licence.  We bought this for Alex and her

            mum, as well as some extra treats for the

            little lady.

 

Nathan    was diagnosed with a medulloblastoma in 2006

aged 4    and relapsed in 2007. His family wanted to

            take Nathan on holiday to the Isle of Mull

            (Balamoray!!).  We helped to fund this very

            special trip for Nathan and his family.

                   After Nathans trip to Balamoray we funded

            several outings & treats for him and his

            sister, as sadly he began to receive

            palliative care.

 

Katie      was diagnosed in 2008 with a medulloblastoma.

aged 3    After Katy had finished her treatment, her

           family wanted to take her on holiday the first

           opportunity they got. We helped with the cost

           of their holiday, so that Katy could have some

           much deserved treats.

 

Carl       was diagnosed with a brain tumour in July

aged 20  2009.  He had to take time off work to

           undergo and recover from surgery.  Carl

           wanted to go on holiday with friends

           before starting radiotherapy.  We were

           happy to help fund this much needed

           holiday.

 

Luke      was first diagnosed with a brain tumour

aged 23  in September 2003.  He now has a

           relapsed brain tumour which sadly is

           non-curative.  Luke needed to be cared

           for in a hospice and his family needed

           help towards the cost of travelling to

           visit him regularly.  We were happy to

           help with these expenses.

 

Arslan    was diagnosed with a high grade glioma.

aged 3   Unfortunately Arslan is now receiving

           palliative care, following disease

           progression.  He has never seen his

           grandparents who live in Nigeria

           and his parents were desperately

           trying to raise the money to fly them

           over.  It was our pleasure to contribute

           towards the cost of this – Arslan is

           very excited at the thought of seeing

           them.

 

Jennifer  was diagnosed with a grade 3 ependymoma in

aged 3   September 2009. She is undergoing 18 months

           of gruelling chemotherapy in the hope of

           preventing the need for radiotherapy.  Her

           family desperately wanted to treat Jennifer

           and her five year old sister at this difficult

           time, but were struggling financially to meet

           essential bills.  We were happy to send them

           a grant to cover both of these areas, as we

           understand the very real pressures families

           are under when they receive such a devastating

           diagnosis.

 

Robert    was diagnosed with a brain tumour in September

aged 3    2009 and is undergoing 18 months of baby brain

            chemotherapy.  This will put huge pressure on

            his family, as they will be separated frequently

            during treatment.  We sent a grant to go

            towards treats and days out together for 

            Robert, his parents and younger siblings.

 

Ethane     was diagnosed with a metastatic

aged 18   meduloblastomain May 2009.  He is undergoing

            an 18 month course of treatment which is very

            debilitating.  This is particularly difficult for

            Ethan as he was very sport and active, but now

            spends a lot of time in bed.  Ethan wanted

            funds to buy a laptop, to help him stay in

            touch with his friends.  We were very happy

            to help.