Comments on: The Most Invisible Family Caregivers /invisible-family-caregivers/ Future of Nursing Tue, 26 Nov 2019 14:46:15 +0000 hourly 1 https://wordpress.org/?v=6.0.10 By: campaignforaction /invisible-family-caregivers/#comment-51 Fri, 23 Sep 2016 17:54:00 +0000 /?p=8736#comment-51 In reply to Yeonette G..

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By: Yeonette G. /invisible-family-caregivers/#comment-45 Thu, 22 Sep 2016 21:51:00 +0000 /?p=8736#comment-45 Very Interesting post for as you so aptly named it an “invisible” issue. It is saddening to know that in 2016 given the thought process changes that have taken place in our society in other areas of taboo topics of life that mental illness continues to be stigmatized across cultures. People are usually ashamed to confirm that they have a family member who is mentally ill so to disclose that they are the caregiver of these individuals comes with a greater cloak of secrecy. This is especially alarming because the stresses of care giving are multifaceted and it takes a toll on the person proving the care financially, emotionally and physically. So its of utmost importance that we don’t create a situation in which the caregiver needs a caregiver to take care of them.

There definitely needs to be a change in the mindset of how people view mental illness so that caregivers can be more open in discussing
the struggles that comes with their responsibility. I feel that this change can occur now as compared to years past because of the Millennial generation that we currently live in. There have been shifts in the public’s views about what were once deemed taboo subjects in society so I feel that the same can be done for mental illness. May is mental illness month so conversations such as these should be highlighted to bring awareness. I am in total agreement that individuals who care for their mentally ill family members need to speak up and out. Sharing their experiences will help to unveil the cloak of secrecy and stigma that causes caregivers and the individual to be isolated and ostracized.

To add to your point of how can we help, there are the support services out there that provides information, assistance, respite, counseling, and support groups for caregivers and many of these programs and services are available through local government agencies, service organizations, faith-based organizations, employers’ programs and some grass roots organizations. And because we now live in a tech savvy society, lets not forget blogging, so many ideas and forums that share creative real life ideas by caregivers with similar circumstances are also available. The internet has a wealth of information on such topics, with the legitimate ones aiming to improve caregiver depression, anxiety and anger. At the end of the day, lets continue to work at reducing this already stressful environment and bring acceptance and visibility to a sensitive topic.

Yeonette G.

RU-ABSN – Newark

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