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Sickle Cell & Thalassaemia Service Anndeloris Chacon R.G.N. Clinical Coordinator Thursday 29 th October 2009. Psychosocial Aspects of Sickle Cell and Thalassaemia.
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Sickle Cell & Thalassaemia Service Anndeloris Chacon R.G.N.Clinical Coordinator Thursday 29th October 2009
Aim: To look at how Sickle Cell and Thalassaemia affect the lives of those with the disorder, their family, education and other aspects.
Major themes identified after • listening to the clients were and are: • Fear Death Stigma Disruption
Continuous education for the clients Conditions Medication Complications Self Management
Raising awareness of the clients’ perceptions with professionals and families Professionals/family disbelief Labels (lazy, drug addict, etc)
How physical and socio-economic stressors affect these disorders Housing Education Employment Socialising
These themes were addressed through 1. Educational sessions for clients, families/carers, professionals and others
2. Psychological Support Psychotherapy [1 to 1 and a group session] Reflexology Aqua massage (dry hydrotherapy) Psychology
3. Trial of home care support when managing crises at home alone Cleaning of the home Collection of medication Someone to visit after discharge
How can we help the clients to live to their optimum level of well-being? LISTEN DISCUSS
ASK QUESTIONS do not ASSUMEBE MINDFUL OF THE LABELS we give to the clients – this stays with them for life
Solution: Provide individualised, client centred holistic care
Vision: Sickle Cell and Thalassaemia Services will provide for each client with coordinated services which deliver access and support to maintain/increase their optimum level of well-being.
Outcome: An empowered client with excellent self management who receives support and advice for the service.
Coordination of Hierarchy of Needs Client at the centre Services around to support well-being