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Lymphoma and Pets
Life after cancer.
But what I am just now beginning to sense, what I am beginning to find, is that life after cancer is anything but "normal". I can understand and appreciate many of the physical processes and changes that have taken place. I can still feel some of the residual effects of my treatments when I am called upon to physically exert myself. My endurance and stamina are still a long way from "normal"and I am told that the more I exercise and push myself, the quicker will be my recovery. But what is just now beginning to come into focus is the impact that this ordeal has had on my emotional and psychological well being.
Up to this point the primary goal of the medical community, as relates to cancer, has been to find new and better ways to treat cancer, and hopefully eventually find a cure. It has only been recently that they have begun to appreciate and address the need for developing a program to benefit cancer survivors. It is being recognized that after the physical treatment ends, there is a distinct phase of the cancer experience, and those who study cancer survivors have suggested a strategy for the ongoing clinical care of cancer survivors. At the heart of this strategy is a survivorship care plan (SCP), a document that includes details not only about the patient's diagnosis and treatment but also essential information needed for long-term health care. Designed for discussion at the end of treatment, the SCP should include summaries of the key diagnostic and staging results, treatments and dosages received, as well as the potential later effects of those treatments. It should prompt discussion about recurrent and new cancers; genetic implications; possible long-term and late effects; explanation of legal rights affecting employment and insurance; recommendations for nutrition, exercise, lifestyle changes and rehabilitation; and referrals for psychological and support assessments. But because the recognition of this need is so new, most cancer treatment centers do not yet have SCP's in active use.
Unfortunately this whole new field is just now being studied and guidelines developed. That is not much help for someone like me, already designated as a survivor, and beginning to discover areas of need as they develop. Rather reactive in nature, and unfortunately not especially proactive. In my own personal case, I am beginning to sense a feeling of deepening depression setting in. Holly has also detected this (as you would naturally expect she would) and suggests that it could well be a result of the 12+ months of intense emotional stress and strain, the ongoing conscious efforts to stay positive and upbeat (a drain in itself), dealing with the more recent fatigue and who knows what other unseen burdens. I have an appointment shortly with my regular family doctor and will discuss it with him, and will probably ask for a prescription for an antidepressant as an assist.
My fatigue and my depression seem to be the only two latent symptoms that I sense at this point. But in my reading I find a wealth of information about this area of cancer survivorship and many of the other symptoms or side effects, covering such areas as worry, feeling stress, depression and anxiety, anger, feeling alone, religion and spirituality, etc. I am listing a few links here to give anyone interested a place to start.
After Treatment: Developing a Survivorship Care Plan
Facing Forward: Life After Cancer Treatment
Cancer survivors: Managing your emotions after cancer treatment
Your Emotions after Treatment
I am adding this post to my blog to acknowledge that life after cancer can, and very probably will, involve previously unseen and unexpected aspects that everyone should be aware of. Being a cancer survivor is wonderful beyond description. But being an informed and aware cancer survivor is even better. God bless.