Most, if not all, of us, when confronted with
a medical condition in a loved one want to know what we can do to fix it. We don’t like to see someone else have to
endure pain and discomfort or grueling treatments or remedies. We want to know exactly what it is that we can
DO to make things better. More often than not, there is nothing we can DO to make things better and that makes
us frustrated because of perceived ineffectiveness.
So,
how do we navigate the times we may find ourselves in the role of a caregiver?
For
one, the caregiver must realize the importance they play in the day to day life
of the patient. At the Hope Lodge, each
patient is strongly encouraged to have a caregiver with them at all times
during their treatment and time spent at the lodge. It’s not mandatory, but it is highly
recommended as the lodge does not provide 24 hour cares. The caregiver is there to attend to the physical,
mental and spiritual needs of the patient.
And,
it certainly doesn’t need to be much. Many
are the times when simply a touch from someone is all that’s required to soothe
a particularly rough day. Just knowing
that someone is there is blessedly comforting.
And, there is healing in the physical touch provided from one individual
to another.
When
faced with the challenges of life-threatening disease the burden upon the mind
can be overwhelming. The care-giver
serves as a companion to listen to the thoughts and feelings expressed and to
offer comfort through reassuring words.
Don’t
forget caregivers; during this journey, you have to take time for
yourself. You will feel drained. What you are going through is physically,
emotionally and spiritually draining and you will feel it. You must recognize your own limitations and
be prepared to seek respite when the time is right. And you know what? It’s okay to say I recognize my limits. It’s not just okay, it’s required. If you don’t recognize your own limitations,
it can impact the care and well-being of the patient.
And
don’t forget to pray. If you’re inclined
to pray out loud, do so. The patient
will draw solace from your words. But
even if you don’t pray out loud, pray nonetheless. It makes a world of difference.
So,
although we cannot DO anything to make the patient well, there are myriad ways
we can serve the patient and things that we can DO to make the journey
tolerable. It is in that doing that the
caregiver receives reward in a sense of an important job well done. The words may come from others, or from the
patient in the form of emotional and heartfelt words of gratitude. The caregiver can come away from this
experience enriched in the knowing that another individual’s life and comfort
has been positively impacted by one’s own actions. I’m pretty sure there aren’t very many things
that get any better than that!
Thanks for recognizing the caregivers! It most certainly is a frustrating place to be...the attitude of the patient can make the experience less frustrating though. Thanks, Ken, for your positive outlook, care and concern for the other side of cancer. Love you, brother!!
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