Transcript What CHOC contributes - 1

Presentation to the
Parliamentary Committee
on Health
CHOC Childhood Cancer Foundation
South Africa
24th August 2011
Attendees
From CHOC
Mzwandile Khanya
Parent, whose daughter died of Acute Myloid Leukaemia in 2005.
Chair of CHOC
Francois Peenz
Parent, whose daughter survived Acute Lymphoblastic Leukaemia
CEO of CHOC.
Julian Cutland
Parent, whose daughter survived Aplastic Anaemia.
Former Chair of CHOC;
Former Board Member (2001-8) of the International Confederation
of Childhood Cancer Parent Organisations (ICCCPO).
Attendees
South African Children’s Cancer Study Group (SACCSG)
Prof Mariana Kruger
Executive Head of Paediatrics, Tygerberg Childrens Hospital
Continental President for Africa, International Society for Paediatric
Oncology (SIOP)
Member of Executive Committee of SACCSG
Prof Alan Davidson
Head of Paediatric Oncology, Red Cross Children’s Hospital
Former Chair of SACCSG
Ms Tiisetso Tshehle
Social Worker
Presentation outline
• Myths and facts
• About childhood cancer
• What CHOC contributes
• Cultural Challenges in Oncology
• Going forward
Myths and Facts - 1
• Myth: Children don’t get cancer
• Facts:
• Worldwide, 1 child in 600 gets cancer before
age 16
• In SA, should have 2100 children diagnosed
• Actual: ~700 pa reported
• Thus > 1000 children go undiagnosed and
untreated
Myths and Facts - 2
• Myth: Cancer is a death sentence
• Facts:
• With early diagnosis and correct
treatment, ~75% of children can be cured,
and lead full & normal lives.
• Survival rate in SA is lower, especially due
to non-recognition and late diagnosis
Myths and Facts - 3
• Myth: Cancer is a “white man’s illness”
• Facts:
• Cancer has no respect for ethnic origin,
wealth or social status
• Children with cancer are fully
representative of population demographics
About Childhood Cancer -1
• Childhood cancers are different from adult
ones
– in types and frequency
– not “lifestyle-related”
– not preventable
• Different treatment protocols from adults
About Childhood Cancer -2
• Proven and accepted worldwide that
children must be treated:
– in paediatric oncology units (POUs),
– by paediatric oncologists
– using paediatric protocols
• Treatment centres in major tertiary /
academic hospitals
• SA has world class treatment centres,
using international protocols
– but struggle with limited resources
About Childhood Cancer -3
• Treatment consists of combination of
chemotherapy, radiation, surgery
• Treatment is intensive and long (1 – 3 years)
– requires regular visits to treatment centre
– places a wide range of demands on whole family
• time, financial, emotional, spiritual, information
– extra pressures when child is from “out of town”
• Important to treat the whole child, and not
just the illness
About Childhood Cancer - 4
• Teenagers and adolescents present
special issues
– Proven that they do better on paediatric
protocols in paediatric units
– Different social, psychological needs
– Trend in many countries for specialist teenage
cancer units
• Children should be nursed in wards suited for their
developmental needs and similar age
CHOC Background
• Traumatic event to have a child diagnosed
with a life threatening illness
• CHOC is an organisation of parents who
have been through this
• Started in Jhb in 1979
• Became a national organisation in 2000
– Now have divisions in all major centres
• Emphasis on working with medical staff
What CHOC contributes - 1
Provide wide range of services for families
• Psychosocial & emotional support
– From other parents; from volunteers
– Now have our own social workers
• Funding for transport
– To prevent abandonment of treatment for
financial reasons
What CHOC contributes - 2
CHOC houses
• A “home away from home” for families
from out of town
• For parents to stay when child is being
treated, or in hospital
• CHOC owns 7 houses (5 from Danone
project), and rent 2 more
What CHOC contributes - 3
• Child-friendly wards
– Hospitals are frightening places
– Age-appropriate decorations, toys, games,
TVs, etc
– Volunteers, to support children and parents
• Information
– Understanding the illnesses, treatments
– And how best to cope with things
What CHOC contributes - 4
Primary focus on public sector hospitals
• Medical equipment
• Support for doctors & nurses to attend
conferences
• Improvements in the treatment centres (eg
revamp at Bara)
• Funding staff to maintain childhood cancer
registry since 2000
What CHOC contributes - 5
• Advocacy & awareness
– Medical and nursing; general public
– Aim is early diagnosis and effective treatment
– Warning Signs from SACCSG – lead to critical
improvement in early diagnosis
• Cooperation with other role-players
– Government
– NGOs
• Cancer-related; Hospices; Just Footprints; TGO
• International connections (ICCCPO)
What CHOC doesn’t contribute
• CHOC does not fund treatment
– Responsibility of the Government and Medical
Aids
• But we do a lot of other things to support
the children and families!
– Major financial support for child to attend
treatment
Challenges of Culture in Oncology
• Cancer is increasing in prevalence and incidence
• Most indigenous languages do not include a word
for Cancer
• It affects patient’s notion of disease and response to
treatment
• The use of tonic and herbs to strengthen resistance
(traditional healing)
• Educational attainment and functional literacy (goldfish syndrome)
• Relationship of culture to health is complex and still
poorly understood
• Cancer is associated with social stigmatisation in
some cultures.
Overcoming the challenges
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Communication
Listening
Value diversity
Cultural self-assessment
Consciousness of dynamics inherent when
cultures interact
• Institutionalise cultural knowledge
• Develop programs and services that reflect an
understanding of diversity between and within
cultures
• Acknowledge how fears and ignorance
influence attitudes, beliefs and feelings.
Benefits of Cultural Competence
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Improved therapeutic outcome and relationship
Decline in disparities in medical care
Survival and improved well-being
Effective cross-cultural negotiation
BUT logic and human behaviour seldom walk
the same road (Bar-on; 2001:299).
Going forward 1: What is a child?
• SA Constitution - <18 years of age
• Norm: upper age limit in hospitals is 12 yrs
– So a child of 13 is often treated in an adult
ward!!
– Most under 15 do end up in paediatric units
• Proven that teenagers do better on
paediatric protocols, in paediatric units
• All children up to 16 at least treated in
paediatric units – Need adolescent units
2: Funding of Childhood Cancer
• Not all provinces have treatment centres
– Some specialist treatments only done at one
centre
• Tertiary grants to provinces to fund various
things, including cancer
• In theory, funds paid to province / hospital
which provides treatment
• In practice, it doesn’t work
• International patients also a problem
3: National Cancer Control Plan
& Policies for Childhood Cancer
• Move to make cancer a “reportable
illness” is a very positive step
– No national statistics for cancer since 2000
– SACCSG childhood cancer registry – 1987
till current (incomplete data but available)
3: National Cancer Control Plan
& Policies for Childhood Cancer
• “Call for Action” from survivors (May 11)
– Burden of cancer not well recognised
• Priority to produce coherent plan (NCCP)
• Policy for childhood cancer must be part
of the NCCP
4: UN Summit on NCDs
• Only illness prioritised by UN is HIV/AIDS
– Implications on international funding
• Summit on Non-communicable diseases
– UN. New York, Sept 2011
• Hope to have cancer as one of illnesses
“recognised” by UN as priority
– Including childhood cancer
5: Awareness of Childhood
Cancer
• Lack of knowledge in medical and nursing
professions
• Many cases not recognised, or only at
advanced stages
• Need to create awareness at primary care
level, and up referral chain
• Incorporate childhood cancer into IMCI
process (Integrated Management of
Childhood Illnesses)
6: Hospital Schools
• All children have a right to education
• Children who are hospitalised for a long
period lose out on their schooling
• Some hospitals provide good schools in the
hospital
• But many have nothing, or of poor quality
• Responsibility of Dept of Education, but not
happening well
Concluding remarks
• CHOC is established as the voice of
children with cancer, and their families
• We focus on ensuring that all children are
diagnosed, are treated effectively, and are
provided with all the support they need.
• We work cooperatively with all role-players
Concluding remarks
• There is still much to be done
• NEED PUBLIC-PRIVATE PARTNERSHIP
between Health and Education
Departments and CHOC
Thank you for the opportunity to
talk to the committee