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You are here: Home1 / Retinoblastoma Resource2 / Living With Retinoblastoma3 / Focus on Hope4 / Alphabet of Hope 2018
A child life specialist uses a toy cat with removable eye to help a young girl receiving chemotherapy cope with eye removal and artificial eyes.

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Alphabet of Hope 2018

Hopefulness means different things to different people.

Hugs bring me comfort, security, reassurance. Please hug me often!

Overcoming cancer is our deepest desire, our journey and destination.

Photos saved my child’s life. I thank God that he is still with me.

Exams Under Anaesthetic – so long as we have EUAs, our children are alive, and life will be good again one day very soon.

A young girl poses with a bunch of daisies.

We produced this beautiful Alphabet of Hope with insights and reflections from families affected by retinoblastoma around the world.  The Alphabet was originally created in 2012 for the first One Retinoblastoma World meeting in London.

Every 2 weeks throughout 2018, we shared via social media a different word and accompanying thought from the Alphabet.  We hope you enjoy this video showcasing the complete Alphabet and all the images shared throughout the year.

A full text version of the alphabet can be found directly below the video.

Action is eloquence said Shakespeare.  Reach out today and hug your child, touch the world, contribute to the fabric of hope that brings life itself to those most in need across the globe.

Baby face, you light up my world, showing me the way forward.  Courage and peace flow through the tips of your fingers, flooding my entire being as your tiny hand clasps mine with complete trust and love.

Cancer has been my violent awakening to the fragility and beauty of life, I will never again let the day pass without appreciation for it, and for the people who bless my path through it.

Dying is a part of life. Even In her last days on this earth, I was able to help my child smile and embrace life.  In those minutes and hours together, we touched heaven and I rediscovered the meaning of love.

Exams Under Anaesthetic – I have lost count of them.  Some good, some bad, always stressful for all of us, but I am reminded that so long as we have EUAs, our children are alive, and life will be good again one day very soon.

Family and friends have been my saving grace.  They have been with me every step of the way.  They are my comfort and encouragement, sounding board, researcher and objective assessor, confidante and constant safe harbour.

Grief has been my pathway to healing.  I mourned the loss of my child’s eye for a long time.  Part of my hope for his life was removed along with it.  Grieving has helped me find peace, and the realisation that life can be normal even with only one seeing eye.

Hugs bring me comfort, security, reassurance.  Your silent expression of love heals my broken spirit and floods me with peace.  Please hug me often!

Imagine life after treatment.  This is my escape from present distress, from the minutiae of our sterile home on the oncology floor.  I dream of watching my child make mud pies In the sun, and I know all will be well.

Joy in the love and concern that others show.  Joy in knowing this present sorrow will not endure forever.  Joy for each child whose life or sight is saved.   Joy that cure is possible for all children with simple action.

Knowledge gives me strength.  When I know the routine or the possibilities I can be prepared and prepare my child.  When I know the benefits and risks, I can make decisions.  When I know I am not alone, I have courage and hope.

Love without boundaries, without fear or regret.  Be generous with your time.  Speak silent words of love with your comforting hugs.  No darkness will destroy me when love keeps my candle of hope alight.

Memories allow me to keep those I love beside me wherever I go.  You are just a thought away.  The joy of your presence in my heart helps me put one foot in front of the other.  Today I will smile for you.

Now is the time to be happy, to smile and enjoy life.  Yesterday has taken away her troubles, and tomorrow may not arrive.  All we ever have is this moment in time – make the most of it.

Overcoming cancer is our deepest desire, our journey and destination.  Chemo, radiation, surgery, prayer, love, courage, patience, even grief.  We will overcome!

Photos saved my child’s life.  Even though I mourn the loss of his beautiful eye, I thank God every day that he is still with me, cancer free and a delightful rogue.

Quiet time to reflect, process, think and be still.  To breathe deeply and fill my lungs with healing fresh air.  To find peace in this moment and know it is enough to sustain me.  To be engulfed by calm, cleansed and rejuvenated by rest.

Rollercoaster riding in the dark – that is what this experience is like.  One moment we are flying high and the next we plummet into the depths as new tumours appear.  I can’t see where we are heading.  My only comfort is that I am not riding this coaster alone.

Surgery has terrified us and been our salvation.  Signing the consent form is the hardest thing I have ever done, yet even though we had to remove both your eyes, I am thankful for these surgeries because they saved your life and the cancer is no more.

Therapy is hope itself – the possibility of cure or relief of suffering.  I cannot imagine experiencing retinoblastoma without the hope of treatment and emotional support.  We are truly blessed.

United in the quest to bring hope to every child with retinoblastoma.  Hope is not about who or what is first, best, strongest, richest, most well known or exciting.  Hope is the quiet joining together of many hands, hearts and minds in patient collaborative effort to provide the very best care possible..

Vision is more than opening my eyes.  Children blinded by this cancer have so much vision, more than many of us sighted people who spend too much time looking at the world and not really seeing.  I try to close my eyes at some point each day and find that capacity for vision inside myself.

Wisdom – so much wisdom I need on this journey.  Far more than my 22 brief and sheltered years have amassed.  I can only pray for God to show me the way, and for open eyes, ears and heart to receive His reply.  God grant me the serenity to accept the things I cannot change, courage to change the things I can, and wisdom to know the difference.

Xylophone – your little fist tightly gripping the stick as you contemplate this new gift.  Gently tapping, then enthusiastically banging the brightly coloured metal keys.  After an hour, the sound drives me crazy, but your play is music to my ears – today is a good day!

Yellow is the colour of the sun, of gold.  Some say it is the colour of cowardice – I say it is the colour of courage and hope.  Hope for sunshine and smiles, hope that suffering and death will be conquered by our Gold Ribbon Army, hope for a better tomorrow.  May we all be shining white petals of support around Daisy’s sunny, hopeful heart.

Zeal to fight back!  I am angry that I did not know about the simple sign of white pupil.  I am outraged that my child is one of less than 20% worldwide who survive.  I commit my indignant energy to the collective building of a better future for all children and families.

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  • Retinoblastoma Overview
    • How the Eye Works
    • Retinoblastoma Biology
    • Unilateral Retinoblastoma
    • Bilateral Retinoblastoma
    • Extraocular Retinoblastoma
    • Trilateral Retinoblastoma
    • Genetics of Retinoblastoma
    • Global Incidence
    • Signs and Symptoms
    • Referral and Diagnosis
    • Treatments
    • Care After Treatment
    • Prognosis
    • Retinoblastoma Glossary
  • Know the Glow
    • Fundal (Red Eye) Reflex and Red-Eye Reduction
    • White Eye Reflex
    • Photo Challenge
    • White Eye and Rb
    • White Eye after Rb Diagnosis
    • White Eye and Adults
    • PhotoRED Technique
    • Next Steps
    • Examining the Fundal / Red Reflex
  • Medical Care
    • Questions to Ask the Medical Team and Yourself
    • Diagnosis and Staging
      • Staging Systems
      • Multidisciplinary Team and Tumour Board
      • Treatment Plan and Care Pathway
      • Hospital Packing Tips
    • Retinoblastoma Genetics
      • Rb Genetics Explained
      • Mosaic Mutations
      • MYCNA Retinoblastoma
      • Genetic Counseling
      • Genetic Testing
      • Genetic Test Results
      • Pre-implantation Genetic Diagnosis (PGD)
      • Genetics Glossary
    • A Therapeutic Alliance
      • Your Child’s Doctors
      • Good Communication
      • Resolving Conflict
      • Second Opinions
      • Changing Doctors
      • Medical Staff
    • Medical Procedures
      • Informed Consent
      • Procedure Pain
      • Blood Draw
      • Bone Marrow Aspiration
      • Bone Scan
      • Chest X-ray
      • CT Scan
      • Echocardiogram
      • EUA
      • Eye Pressure Test
      • General Anaesthetic
      • Hearing Tests
      • Inserting an IV
      • Intrathecal Injection
      • Lumbar Puncture
      • MRI Scan
      • Radionuclide GFR
      • Subcutaneous Injection
      • Taking a Temperature
      • Transfusion
      • Ultrasound of the Eye
      • Vision Testing
      • Vision Testing – Support Your Child
      • Vision Testing – Just For Kids!
    • Treatment
      • Risk of Under-Treatment and Over-Treatment
        • Reduce Risk of Under-Treatment and Over-Treatment
      • Treatment Decision Making Guide
        • Step 1 – Acknowledge Your Thoughts and Feelings
        • Step 2 – Understand Your Decision-Making Style
        • Step 3 – Find Your Expert Team
        • Step 4 – Understand Shared Decision Making and Informed Consent
        • Step 5 – Set an Intention to Make Balanced Decisions
        • Step 6 – Learn About Retinoblastoma
        • Step 7 – Evaluate Your Options
        • Step 8 – Consider Your Values and Goals
        • Step 9 – Manage Disagreement and Conflict
        • Step 10 – Make Your Decision
        • Step 11 – Review Your Decision
        • Step 12 – Support Your Child and Yourself
        • Review the 12 Decision Making Steps
      • Enucleation
        • Making the Decision
        • Eye Removal Surgery
        • Orbital Implants
        • Types of Orbital Implant
        • Side Effects
        • Pathology
        • After Surgery
        • Coping with Other People
        • Artificial Eyes
        • Artificial Eye Care
      • Focal Therapy
        • Laser
        • Cryotherapy
        • Periocular Chemotherapy
        • Intravitreal Chemotherapy
      • Chemotherapy
        • Chemotherapy for Rb
        • Intra-Arterial Chemotherapy
        • Regimens and Protocols
        • During Treatment
        • Central Venous Catheter
        • CVC Care and Risks
        • Blood Test Results
        • When to Call the Doctor
      • Radiation Therapy
        • Radioactive Plaque
        • Coping With Isolation
        • Radiotherapy
        • Radiotherapy Planning
        • Treatment Process
        • EBRT Side Effects
        • Ask the Doctor
      • Transplant
        • Types of Transplant
        • Transplant Process
        • Coping With Transplant
        • Complications
        • Long-term side effects
        • Ask the Doctor
      • Side Effects
        • Low Blood Counts
        • Pneumonia and Chickenpox
        • Protect Your Neutropaenic Child
        • Pets and Infection Risk
        • Fatigue
        • Pain
        • Hair Loss
        • Nausea and Vomiting
        • Taste Changes
        • Oral Care
        • Skin and Nails
        • Diarrhoea
        • Constipation
        • Bed Wetting
        • When to Call the Doctor
      • Occlusion Therapy (Eye Patching)
        • Introduction to Eye Patching
        • Preparing to Patch
        • Support Your Patching Child
        • Eye Patching – Just For Kids!
    • Clinical Research
      • Clinical Research Introduction
      • Clinical Research Phases
      • Protocol Document
      • Monitoring and Safety
      • Rb Clinical Research
      • Informed Consent
      • Ask the Investigator
      • Ethnography Research
      • Patient-Led Research – A New Approach
      • Patient-Led Research – Challenges and Development
    • Surviving Hospital
      • Advocate for Your Child
      • Packing for Hospital
      • Hospital Life
      • Your Child’s Space
      • Record Keeping
      • Recreation
    • International Care
      • Contacting Doctors
      • Finances and Fundraising
      • Travel and Housing
      • Questions to Ask
    • End of Treatment
      • Celebration
      • Follow Up Care
      • Follow Up Schedule
      • Life-Long Follow Up
      • Removing the Central Line
      • A New Normal
      • Relapse
      • Second Primary Cancers
      • Symptoms of Second Primary Cancers
      • Ask the Doctors
    • End of Life Care
      • Changing Treatment Goals
      • Palliative Care
  • Child Life
    • Child Life is More Than Play
      • The Art of Child Life
    • Procedure Support
      • Stay Calm
      • Make a Plan
      • Medical Play
      • Distraction Play
      • Comfort Positions
      • Giving Eye Drops
      • Support for Needle Procedures
      • Anaesthetic Induction
      • Preparing for Surgery
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      • Imaging Scans
      • HandWashing for Kids
      • Reduce Face Touching
    • Pain Management
      • Know the Signs of Pain
      • Manage Pain
      • Mind-Body Strategies
    • Living With a Special Eye
      • Before Enucleation
      • Going to the Ocularist
      • Making an Artificial Eye
      • Handling the Special Eye
      • Keeping the Eye in Place
      • The Young Child Living With a Special Eye
      • The Older Child Living With a Special Eye
      • When There Is No Eye
    • Psychological Support
      • Reduce Your Stress
      • Infant Massage Training
      • Talking With Kids About Vision Loss
      • Talking About Vision Loss – For Kids!
      • Support and Encourage
      • Coping With Difference
      • Worry Eaters Guide
      • Personal Story Books
      • Youth Retinoblastoma Support at Upopolis
      • Camp Sunshine Rb Week
      • Activities for Isolating With Children
      • Post-Traumatic Stress Disorder in Childhood Cancer
  • Living With Retinoblastoma
    • Children
      • Children Learn From You
      • Sibling Responses
      • Support Siblings
      • Communicate
      • Reduce Stress
      • Tantrums
      • Discipline
    • Parents
      • Emotional Responses
      • Manage Anger
      • Depression and PTSD
      • Look After Yourself
      • Relationships
      • Sharing the News
      • Update People
      • Seek and Accept Help
    • Grandparents
      • Genetic Implications
      • How You Can Help
      • Look After Yourself
    • School Life
      • Effects of Treatment
      • Preparing For School
      • School Activities
      • Artificial Eye Care
      • Infection Control
      • Older Children
      • Advice for Teachers
    • Eye Care
      • Prevent Eye Injury
      • First Aid for the Eyes
      • Nutrition for the Eyes
    • Bereavement
      • End Of Life Care
      • Before the Funeral
      • Acts of Remembrance
      • Parental Grief
      • Sibling Grief
      • Carrying the Torch
    • Focus on Hope
      • False Hope
      • Encourage Hope
      • The First Alphabet of Hope
      • Alphabet of Hope 2018
      • Alphabet of Hope 2019 – #LifeBeyondRb
      • Alphabet of Hope 2020 – #FamilyInSight
      • Alphabet of Hope 2021 – #MindAndBody
      • Alphabet of Hope 2022 – #RbCare
      • Alphabet of Hope 2023 – #RbResearch
      • Alphabet of Hope 2024 – #RbEarlyDiagnosis
      • Alphabet of Hope 2025-2026 – #RbChildLife
  • Family and Friends
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    • Words That Help
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    • Help During the Holidays
  • Through Our Eyes
    • RAE of Hope
    • Unilateral Rb
      • John (Kenya)
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      • Ewan (England)
      • Rowan (USA)
      • Bisrat S (Ethiopia)
      • Alexa (Ireland)
      • Linda (Kenya)
      • Lele (China)
      • Katelyn (USA)
      • Jordan (USA)
      • Danielle (Canada)
      • Bright (Cameroon)
    • Bilateral Rb
      • Daisy (UK)
      • Aidan (Canada)
      • Libby and Ella (USA)
      • Angie, Kieran and Cameron (UK)
      • Bisrat E (Ethiopia)
      • Abby (USA)
      • Brady (USA)
      • Sera (Fiji)
      • Katy and Harry (UK)
      • Hope (South Africa)
      • Ross Richard (USA)
      • Bella (Philippines)
      • Peter (Kenya)
      • Jaymee (Australia)
      • Ella Nina (Burundi)
      • Ernest (Kenya)
    • Extraocular Rb
      • Rati (Botswana)
      • Ross Richard (USA)
      • Bella (Philippines)
      • Sera (Fiji)
      • Ella Nina (Burundi)
      • Ernest (Kenya)
      • Bright (Cameroon)
    • Trilateral Rb
      • Libby and Ella (USA)
  • Other Organizations
    • Rb Communities on Social Media
    • Retinoblastoma Organizations
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    • General Cancer Support
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    • Transport Providers
    • Hospital Housing
    • Support for Children
    • Support for Siblings
    • Support for Survivors
    • Cancer Camps
    • Wish Granting
    • Disability Support
    • Bereavement Support
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