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Fighting cerebral palsy in Africa Cerebral palsy aff ects children across Africa. Prevention is difficult since we know little about its aetiology in African countries, and efforts to help those affected are hampered by a lack of resources. But individuals and organisations are rising to the challenge. Adrian Burton reports.
Strengthening links between researchers, clinicians, therapists, and those providing specialist training and care is vital if we are to make headway against CP
In February, 2013, a working group of the African Child Neurology Association met in Cape Town to try to build a picture of CP across the continent, to determine how well equipped diff erent countries are to deal with it, and to identify the steps needed to improve the situation. Its fi ndings reveal the scale of the problem. The delegates, from 22 African nations, reported that a large proportion of children seem to be aff ected through postnatal insults, such as meningitis or cerebral malaria, yet no system of surveillance of at-risk babies was available in nine of these countries. Specialist services were often absent. In some countries, traditional healers were still the fi rst point of contact for medical help, and South Africa and Egypt were the only countries to have any guidelines for managing CP. And while all the countries represented reported physiotherapy to be available, about half could off er no occupational, speech, or language therapy, and many could provide no orthopaedic support.
"And remember, just because a country reports having certain facilities, that does not at all mean they are ubiquitously available or of the best quality", explains Jo Wilmshurst, head of paediatric neurology at the Red Cross War Memorial Children's Hospital. "For example, even in South Africa, the most developed of the nations represented [in the working group], CP can be a huge burden in rural areas, where resources and help can be sorely limited. Indeed, in most African countries, the help available outside the major cities may be minimal. Staffi ng capacity and training are inadequate to support focused disability care, let alone multidisciplinary services, and equipment is typically lacking or outdated."
The delegates agreed that further research was needed to clarify aetiologies and outcomes, and 2 years later the results are beginning to come in. "In Botswana, we recently found perinatal hypoxia (28%), prematurity (21%), postnatal infections (15%), and prenatal TORCH [toxoplasmosis, rubella, cytomegalovirus, and herpes] infections (10%) to be the most common aetiologies", says David Bearden of the Division of Child Neurology, Children's Hospital of Philadelphia, PA, USA, who reported the results of a study of 68 children at the April, 2015, meeting of the American Academy of Neurology in Washington DC, USA. Co-investigator Baphaleng Monokwane, of the Department of Paediatrics, University of Botswana, Gabarone, Botswana, explains that CP was often the consequence of delayed referral to a tertiary hospital. "Unfortunately, we see cases of complicated meningitis due to delays in seeking medical interventions because of traditional beliefs. Addressing this could make a diff erence. In terms of prematurity, we could do a lot by working on prevention."
The same research group also reported that 41% of aff ected children fell into the most severe motor impairment category, while 84% suff ered intellectual disability, 77% had epilepsy, 46% were visually impaired, 16% had hearing problems, 31% had contractures, and 28% showed orthopaedic complications. Refl ecting the delegates' recognition of the need for innovative solutions to maximise access to health care, Bearden emphasises the potential of "appropriate, low-cost, communitybased classes in which we could teach parents basic rehabilitation techniques for these problems. This, in combination with regular check-ups by community health workers, may be better than a system that demands parents regularly bring children to a hospital, which can be very challenging for families in most parts of Africa."
Malamulele Onward, a nongovernmental organisation based at the Children's Memorial Institute, Braamfontein, South Africa, may be ahead of the game in this respect. "Many dedicated therapists and midlevel staff work at hospitals across the continent, but don't have specialised training in CP", explains Gillian Saloojee, the organisation's executive director. "Over the past 9 years, our work with over 700 children and their families in deeply rural areas of South Africa, Lesotho, and Rwanda has shown that a sustainable intervention model not only has to include training for rehabilitation therapists, but also for parents and families, along with the provision and fi tting of postural equipment, hands-on therapy, and regular mentoring visits."
"Parents are an untapped resource in rural areas", adds Misty Weyer, Malamulele Onward's training coordinator, "one that we mobilise through our Carer-2-Carer Facilitator Course or through blocks of residential intensive therapy. We developed the Carer-2-Carer programme ... with 20 parents representing five languages and cultures, and it's now the fi rst CP programme in South Africa to be taught by rural parents themselves. Parents are trained in CP care, shown how to support other parents and facilitate peer-learning, and work in partnership with their local CP clinics. This provides other families [with] access to information about CP in ways they understand, in their own language, from someone living similar experiences."
"We assess our programmes through feedback from the parents, plus annual follow-up visits to the rural hospitals, where we have trained therapists and mid-level workers, and through home visits to children we've treated", explains Saloojee. "As we've learned about the realities of daily life for caregivers and families, the more appropriate our training courses have become. The burden remains huge, but we've seen that the strategies we follow can change the quality of care children with CP receive in rural areas."
Malamulele Onward, however, is not alone in its eff orts. Cerebral Palsy Africa, a non-governmental organisation based in Duns, Scotland, UK, is involved in similar projects in Ghana, Zambia, Malawi, Kenya, and Uganda. "We provide training to rehabilitation workers [involved in] community-based projects, which allows access to children and families and helps win their trust", explains co-founder Archie Hinchcliff e. "In addition, we train specialist therapists in [guaranteed] long-term paediatric employment; this boosts the eff orts of rehabilitation workers, [to] help avoid children developing contractures, and ensures their continued progress. And we help set up self-sustaining workshops in which the workers we train make assistive, supportive devices from waste paper and cardboard available at hospital pharmacies. Using appropriate paper-based technology methods, chairs and standing frames can be made to measure, facilitating each child's development and social participation."
Other organisations are working on the ground too, such as the Cheshire Foundation (Botswana), Benola (Nigeria), Handicap International (Burundi), and the Ronald Trust for Cerebral Palsy and Autism Children (Zimbabwe). The African Paediatric Fellowship Program at the University of Cape Town is also off ering special training for African doctors, nurses, and rehabilitation practitioners. "We've trained doctors in Ghana, Kenya, Tanzania, and Zimbabwe in neurology patient care", explains Wilmshurst, "and training courses have been run in Ghana and Zimbabwe, developing rehabilitation awareness in these regions".
"Strengthening links between researchers, clinicians, therapists, and those providing specialist training and care is vital if we are to make headway against CP", concludes Donald. "Our meeting in Cape Town brought together clinicians often working in isolation who can now support each other. Creating links with organisations like Malamulele Onward can only increase our chances of taking on this problem that makes life so difficult for all who are touched by it. African nations may be hampered by low resource levels for years to come, but by pooling our minds and hearts, and by pulling together, we can begin to make a difference."
Adrian Burton
Burton, A. (2015). Fighting cerebral palsy in Africa. The Lancet. Neurology, 14(9), 876–7. doi:10.1016/S1474-4422(15)00189-1
In memory of Bafokeng Mohamoe March 18, 2010–June 10, 2015
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The founding father of Turkish Child Neurology, Professor Yavuz Renda (b.1932) has passed away peacefully on the 24th of July, 2015 after a long illness. His family roots aided Mustapha Kemal Atatürk in the construction of Modern Turkey in 1923. Professor Renda established the backbones of our discipline in Turkey starting from early 1960s. This was parallel to the blossoming of Child Neurology worldwide. Professor Renda was a great teacher and a spirit to his pupils. He had deep concerns for the benefit of his patients and their families. He was a considerate man to his colleagues and juniors. We shall deeply miss him. His principles will be followed in generations.
Haluk Topaloglu, Ankara
On behalf of the Turkish Child Neurology Society

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We are deeply saddened to hear the passing of Professor Jean François Marie Aicardi in Paris. A world-renowned physician and child neurologist, Professor Aicardi had friends, students and patients from all over the world . A true giant of Paediatric Neurology, his passing is indeed a great loss to the world of child neurology and to the countless friends and colleagues all over the world. The International Child Neurology Association express it's deepest condolence on the demise of this truly inspirational Child Neurologist.
Jean François Marie Aicardi studied at the Paris Medical School and became an Interne des Hôpitaux de Paris in 1951. He trained at Hôpital de la Salpêtrière under Raymond Garcin (1897-1971)under Raymond Garcin (1897-1971)and at Hôspital des Enfants Malades in Paris under Stéphane Thieffry. He received his doctorate from the University of Paris in 1955 on convulsive disorders in the first year of life . From 1955-1956 as a research fellow at the Harvard Medical School and the Children's Hospital Medical Center in Bostn. On returning to Paris, Aicardi joined the Department of Infantile Surgery at the Hôpital des Enfants Malades as a Paediatrician, where he remained until 1964 while continuing his interest in child neurology. He then worked as an assistant to Thieffry from 1964 to 1979 in the Department of Child Neurology at the Hôpital Saint Vincent de Paul. In 1968 he joined the Institut National de la Santé et de la Recherche Médicale (INSERM). He returned with his team to the Hôpital des Enfants Malades in 1979 to create and run a new unit of child neurology.
In 1970 Aicardi was invited to Oxford, England, by Ronald MacKeith (1908-1977) in order to participate in the first meeting of the European Study Group in Child Neurology, an exclusive group of The Spastics Society, an organisation that has played an important role in the development of child neurology in Europe. This group became the European Federation of Child Neurology Societies in 1973 and has branches in most European countries. Following his retirement in 1991, Jean Aicardi was appointed honorary professor of child neurology at the Institute of Child Health and honorary consultant at the Hospital for Sick Children, London. In March 1999 he became the founding editor of the journal Epileptic Disorders.
Aicardi was awarded the Cornelia de Lange Medallion from the Dutch Society of Child Neurology in 1985 and the Hower Award from the American Child Neurology Society in 1986. In 1995 he received the Epilepsy research Award from the American Epilepsy Society. Professor Aicardi is known throughout the world through his encyclopaedic text books and scientific works. He has authored more than 250 original papers which deals with childhood epilepsy, while many are devoted to brain malformations, progressive encephalopathies, and other aspects of child neurology.
Biography source: Aicardi, J. (2013). Jean Aicardi: my circuitous path to becoming a French child neurologist and epileptologist. Journal of Child Neurology, 28(3), 409–15. doi:10.1177/0883073812470212 J_Child_Neurol-2013-Aicardi-409-15_b640f.pdf
Also see:
Krägeloh-Mann I, Board of the Society of Neuropediatrics (2015) Prof. Jean François Marie Aicardi (1926-2015). Neuropediatrics ():. DOI: 10.1055/s-0035-1566445 PMID: 26535874.
Stephenson J, Professor Jean Aicardi (1926-2015) https://www.childneurologysociety.org/about/in-memoriam/professor-jean-aicard

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The 13th Nigeria Society of Neuroscience (NSN) Conference will be held in AFE BABALOLA UNIVERSITY ADO EKITI (ABUAD) in from 11-14 November 2015. The theme of the conference is "Nervous system disorders: African Challenge".
The venue of the meeting is the College of Medicine and Health Sciences, Afe Babalola University, Ado-Ekiti, Nigeria. Ado Ekiti is a a city in southwest Nigeria, the state capital and headquarters of the Ekiti. It is also known as Ado. The people of Ado Ekiti are mainly of the Ekiti sub-thnic group of the Yoruba. Ado Ekiti city has a state owned university, the University of Ado Ekiti, now Ekiti state university, Ado-Ekiti, a privately owned University. The Afe Babalola University, Ado-Ekiti, a Polytechnic- the Federal Polytechnic, Ado-Ekiti. Various commercial enterprises operate in Ado Ekiti. The city is the trade centre for a farming region where yams, cassava, grain and tobacco are grown. Cotton is also grown for weaving..
Call for abstracts
Submission of abstracts opens April 1, 2015 and closes October 30, 2015. Submitted abstracts should not exceed 300 words and must include Background, Aims and Objectives, Methodology, Results and Conclusion. A maximum of three relevant references should also be included. Please send your abstracts to This email address is being protected from spambots. You need JavaScript enabled to view it.
Categories | Early Registration | Late Registration |
Undergrad students |
N1,500.00 |
N2,500.00 |
Postgrad students | N8,000.00 | N10,000.00 |
Professionals | N20,000.00 | N25,000.00 |
Local Organising Committee
Chairman
Laofe Ogundipe
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Secretary
Babwale Olatunji
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Scientifc Subcommittee Chair
Olalekan Ogundele
+2348153324284
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Media & Pub. Subcommittee Chair
Philip Adeniyi
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Professor Helen Cross, Executive board member of the ICNA, The Prince of Wales's Chair of Childhood Epilepsy, Deputy Head of Developmental Neurosciences Programme of the UCL Institute of Child Health and Honorary Consultant in Paediatric Neurology at Great Ormond Street Hospital NHS Trust, London and Young Epilepsy, Lingfield, received an OBE (Officer of the Most Excellent Order of the British Empire) in the Queen of England's Birthday Honours for her services to Children with Epilepsy.
Professor Cross said
Huge progress has been made in the diagnosis and management of epilepsy over the past 20 years. This has required national and international collaboration, as well as constant translation to clinical practice. This award is a great honour, and which I dedicate to all the children with epilepsy with whom I have had contact over the years, who continue to teach us so much more and for whom we strive for better outcome".!
Professor Cross has published widely on seizure, neuropsychological and behavioural outcomes in children who have undergone surgical resection for treatment of their epilepsy.
Her research has focused on improving outcomes for children with early onset epilepsy. Her early research was into improving imaging techniques to determine areas of likely seizure onset in children with drug resistant focal epilepsy and has developed an epilepsy surgery programme based on her research.
She conducted the first randomized controlled trial of the ketogenic diet in the treatment of children with drug resistant focal epilepsy and is endeavouring to conduct the same in the very young and adults. Recognising there was little in the way of control data with regard to neurodevelopmental progress, she initiated the North London Epilepsy in Infancy study, where a cohort of children was recruited at diagnosis in the first two years of life, and has been followed to at least three years. She is now aiming to conduct a similar study over a wider geographical area, also examining phenotypes and genotypes.
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