Welcome!

This is a journal of our lives with my mom, affectionately known as Little Mama. In her 90's, she is a sweet, spunky, spirited, sometimes exasperating, tiny little lady that now lives with moderate dementia and macular degeneration. These journal entries show the good times and the not-so-good times.

Little Mama's type of dementia is age-related and is not hereditary. Sometimes, she appears to be perfectly normal. Other times, it is obvious that something is amiss. It is her desire to remain in our home rather than live out her days in an assisted living facility. It is my prayer that we will be able to honor her in this way. We feel blessed...and challenged...that she lives in our home. This is not easy, and important things rarely are easy. It takes an emotional and physical toll on the caregivers. I've been through the 7 stages of grief at least once if not more! If you are in a similar situation, you understand what I mean! Fortunately, our family helps a lot both physically and emotionally. It takes a team.

The fourth commandment tells us to honor our parents. That is done in many different ways. If you are struggling with a decision, please pray and ask for guidance and wisdom. Our Lord will let you know how He wants you to honor them. Regardless of the way you honor your loved ones, you will need support. So build your team, whether it is from members of your family or a support group.

I am finally learning that: I can't fix it. I can't change it. All I can do is accept it, trust God, and roll with it. (My condensed version of the Serenity Prayer.) We are learning to relax, laugh, and savor every moment we have with my mom on this side of Heaven.

So, scroll down.... read the entries...laugh and cry with us.

Blessings!
Lisa

















Saturday, September 14, 2013

Do you often wonder what you can do to help a friend or loved one that is ill or infirmed or a caregiver?  Someone recently asked me “Anything we can do?”  I realized that people are truly at a loss when helping a family with a disabled or ill family member. We are doubly at a loss!  Unless you have had that experience, you are likely limited in your understanding of what a day in the life of a caregiver is like.  I am equally unaccustomed to asking for help or even being able to articulate how others can help.  So, I described a little of our situation to this individual, which helped me to figure out what we need.  We need community and we need spiritual nourishment.  We must remain connected to those that we love and that love us – especially God!  I am confident that others in a similar or even worse situation need the same thing in varying degrees. 

In answer to the question “Anything we can do?”, here are a few suggestions:
  • ·         Stop by for a visit, but please call first.  Chat about any topic. 
  • ·         Offer to come over and visit with the patient so the caregiver can either get out of the house for a few minutes…or take a nap…or clean….or whatever else they need to do but can’t because they must sit RIGHT THERE with their loved one.
  • ·         Send a “thinking of you” card.
  • ·         Call.  Talk with the caregiver.  Talk with the patient.  The patient – if still able to talk – might not know who you are.  That’s okay.  The good feeling from getting a phone call from someone will remain for a while!  If they can’t talk anymore, that’s okay, too!  They can listen…..and feel good.
  • ·         Pray.  Prayer is powerful.  Then send an email or a card to say, “I prayed for you and your loved one.”  Powerful.