Quantitative Study Burdens among Parkinson’s disease...

Introduction â€Å"Parkinson’s is the second most common neurological disease after Alzheimer’s. It has been described as a chronic, progressive, neurological disorder, which generally not life-threatening but is incurable (Magennis Corry, 2013). Parkinson disease has no antidote but has altered treatments. Patients require caregivers help when PD gradually starts to affects motor, cognitive and emotional functioning. Patients are hindered from fulfilling their daily needs, thus necessitating the caregiver’s assistance. Care givers can be the PD patients relative, friends or non-professional caregivers (Martinez-Martin, Benito-Leon, Alonso, Catalan, Pondal, Zamarbide, †¦ Pedro, 2005). There are formal caregivers, paid helpers (Cifu, Carne,†¦show more content†¦This burdens a female caregiver. It would be an ultimately difficult transformation for a female caregiver as they will need to assist the PD patient in ways like bathing, getting dressed and getting their daily household chores done. Caregivers have to sacrifice their leisure time, their mental and physical health (Martinez-Martin et al., 2005). According to a data research from Spain, Martinez-Martin, Forjaz, Frades-Payo, Rusinol, Fernandez-Garcia, Benito-Leon, †¦ Catalan (2007), 77.5% of the caregivers are females. Only 21.25% of the caregivers are males. This is evident that there are relatively more female caregivers then males. The data further says 76.25% of the caregivers are spouse and 55% of caregivers do house works. 18.75% of the caregivers are children. This research is evident enough to show that many of the care givers are females and most likely PD patients are being taken care of by their spouses. Significantly, another data analysis from Spain, Carod-Artal, Mesquita, Ziomkowski Martinez-Martin (2013) shows that 80% of PD patients are males, 88% of caregivers are females and mostly these caregivers are their spouses. Another such Danish data analysis has similar results. Patients diagnosed with PD are assisted by their spouses. According to the data, 10 such caregivers were put under research. In this research female caregivers have been their primary source of research. These caregivers feel frustration as they