A large part of a Social Work assessment is to ask about how the patient and family are coping. There is no right or wrong way to cope. I tell patients and families, “However you are coping or feeling is called “normal”.
Today I went out to admit, “Lily”, seventy years old, to hospice. She was diagnosed with ALS or Lou Gehrig’s Disease over three years ago. She lives with her husband, “Eddie”, who is so focused on how he can help her. He recently retired and is home to help her as needed. Fortunately, the couple have funds to pay for hired caregiver support.
Lily is totally dependent with all of her needs. She can only move her head. She is no longer able to speak and can only communicate using head movements. She appeared calm and relaxed which represents her strength. One must feel so trapped into their own body.
Eddie was a matter-of-fact person. He wanted the truth and accepted whatever came his way. He has researched ALS thoroughly as wants to know what to expect and also how he can help her. He accepts reality as stated, “It is what it is”. He may have no control over ALS’s power, but he looks to what he does have power over.
When I asked him what helps him cope, he spoke about life after her death. He honestly shared, “I would love to learn how to play the piano”. Then quickly adding, “I must get a new hobby.”
I so admired his honesty. When one tells you their truth, it so gives you ways to help him back. It struck me today when he said, “It is what it is”. I am never surprised when I hear that statement as I do hear it a lot. I view it as one looking at ways that can be helpful and not trying to knock down a brick wall.
I cannot even imagine, but I
know Lily and Eddie’s journey is so challenging. I hope we can help both of them the best way
we, as an agency, can; because to us too, “It is what it is”.
IT IS WHAT IT IS
Three years ago, she heard,
“It is Lou Gehrig’s Disease.
There is no cure, only
decline.
So heartlessly, it impacts
everything
but your brain.”
Her decline has been constant
since then,
with precious moments of stability.
He feels the more he knows,
the better he can support her
during her expected downhill
ride
He’s researched the disease.
He is a realistic while
grasping the truth.
He wants to know all about
it;
while accepting the grim
facts.
She is totally dependent.
Now only able to move her
head.
She is alert and oriented,
but no longer able to speak.
When asked how he is coping,
he honestly replied;
“It is what it is.
I have no control.
I don’t dwell on
it.”
He is also realistic
regarding her needs.
“She was a very active
person.
This must be so hard for her."
Then one more time softly stating,
“It is what it is”.