The next stage is usually depression; this is when the person or persons actually experiences the true mourning and grief of the death, they experience sad feelings, feel nonenergetic and are despondent to those around them. The final stage is acceptance; in this case Mike is at this stage and seems to want Sally to be there as well. This stage is when the person or persons have pulled out of their depression, and have accepted the death and are able to move on with their live (Kanel, K., 2007). There are many ways to deal with a death or the process of dying, but in the majority of cases these stages will be seen. Because
For instance, in this article the military states that when a soldier is experiencing sighs of mental trouble or PTSD they will move him to a location not far from the battle field to rest for a couple days and speak with someone about their traumatic experiences and probably receive some medication. I think it is good when mental issues like these are recognized by higher ranking officials and they realize that some help needs to be enforced; although I don’t think enough is being done to let the soldier properly heal before he is sent back into battle. I think it would be more useful to completely remove a soldier suffering from PTSD from any dangerous war like area, in order to help decrease their anxiety level. Give them a psychiatrist to speak with and help with their traumatic experiences. Then when they show signs of mental stability send them back.
After Sethe spent some time with Beloved, she felt guilty for what she did to her and began apologizing to her. Amir suffered more to gain his redemption. This will be made evident after analyzing how Amir and Sethe felt after doing what they had done and the pain they endured when gaining their redemption. Amir suffered more to gain redemption because he experienced guilt for a longer period of time. Although feeling guilt doesn’t accomplish redemption, it is the first step to it.
I have listed other possible effects below * Long term effects may be: * Loss of motivation * Restricted opportunities * Limited access to services * Long term depression * Increased behavior problems * Difficulty communicating * Lack of education * Lack of achievement The effects listed above are not only ones that affect the individual; they are effects that can be experienced by the individual’s family and friends too. The individual’s family can become isolated from society through trying to protect their family member and will often experience verbal abuse for having a family member that is perceived to be different. Family members can sometimes feel embarrassed about the shame
Family members feel helpless as they cannot do anything to help some days and feel very inadequate, as time goes on and things with the disease progress the family realise that they are losing a loved one even though they are still present. This is very distressing for the individual and family as the disease
I have often thought that it would be so much easier to just end it all rather than deal with the sometimes overwhelming anxiety that associates to the abuse. There are days that I have woken up and actually [Cliché: "actual" and "actually" are weak words whose meaning is nothing more than "in point of fact." They are often used as intensifiers but usually can be deleted with no change in meaning ] contemplated taking my own life. I do not, I know what that does to the people left to deal with the loss. Men are known to commit suicide more often than women, (Mironova, Rhodes, Bethell, Tonmyr, Boyle, Wekerle, & Leslie, ) (2011) (p1).
They fear becoming dependent on others or having a very poor quality of life. Sadly, our current health care system and its practices leave people suffering unreasonably and unnecessarily at the end of life. Too often, people suffer from avoidable pain and other symptoms in their final days. And such suffering can occur even with good care. People advocate for more reliable euthanasia/physician-assisted suicide to guard against these possibilities.
Author Jo Danna describes caretaker suffering to come in the forms of discouragement of being unable to stop the disease from progressing even with one on one care, resentment of the energy, time and money spent, self-loathing because of losing patience with an Alzheimer’s sufferer who means no intentional harm, frequent sicknesses such as colds or headaches, lack of time for oneself and the things one enjoys, cutting oneself off from friends and other family members to put the patient first, and severe depression due to a combination of these factors(90). This shows us that the caretaker’s attitudes, ideas and beliefs play a part in the problems that arise from caring for
Assisted Suicide Laurie Martin PHI 200 Christine Nortz Assisted Suicide After reading the story about the death of Susan Wolfs father and all that he went through prior to his death, I have some strong feelings on how I would feel and what I would do if put in the same situation. It is not a situation I would want to be in, but it is one that we all have to except the possibility of being in. Susan Wolf was in a very tough situation. I don’t know if I could handle the same, but if I were faced with a loved one in a lot of pain and being diagnosed as terminal, I think I would do the same thing. I don’t have a problem with assisted suicide and think it should be legalized.
In moderate to severe traumatic brain injury there could be permanent memory loss, trouble with speech and loss of coordination among other visible and invisible symptoms. Since the individual did not have these issues prior to the injury they will most likely have a negative effect at first. Due to the loss of abilities, they may experience mood changes, anger, depression or anxiousness. These internal psychological challenges may also be compounded by the social anxiety they may feel. Unfortunately, the general society is unforgiving toward those with special needs or differences.