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We have found that by being present and through the practice of
active listening families ask questions they would not otherwise
ask. Some want to know worst-case scenarios. Many want to
know what it is like to die and how it will be for them. Of course
some of these questions do not have answers. But by relating to
families and sharing stories of how other families have coped,
by understanding the unique dynamics of a family, and by connecting
them to appropriate resources, Compassionate Care ALS provides
a different kind of service. We fill a vital niche for those
challenged by ALS in ways that are not aptly handled through faceless
documents.
Click here if you are a family member of
an ALS patient in need of support
“I will not forget your compassion and
caring. Because you had gone through it with many other families,
you knew of our pain. You were always ready to help. I remember,
towards the end, I called you to ask how much longer would she
have to live. You came to the house, evaluated Brenda’s condition,
and helped me prepare for her death.”
- Russ Cisek, spouse
of ALS patient |
CCALS has provided services, support,
durable goods and educational workshops to clients, their families
and caregivers in the following shaded states:
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