Afraid 2, Huntington's Disease and My Family- for the Spouse, Caregiver or Family Member -Prologue



 

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Afraid 2:
Huntington’s Disease
and My Family;
for the Spouse,
Caregiver or Family Member


By: Michelle Hardt Thompson


Prologue:
My family used to have fun all of the time. We would go camping together, swim together, play games together, or have picnics and BBQ’s together. We were far from perfect, but my family was definitely having a very great time along the way. We were also very religious together. Our faith kept us strong, and our love and hope moved us forward.

Then things changed. Dad was forgetting things all of the time. At his office or at home, there were post-it notes everywhere, even in his shirt pocket. We thought that he had just been too stressed and needed a little more support. But soon thereafter he started to forget how to shift the gears in his car, to stop at red lights, and how to back up the car straight. He was very confused and troubled about his newfound situation.

He also started yelling and having angry outbursts all of the time. Any little thing could spark a raging voice. It was easier to avoid his path then to possibly encounter his unpredictable wrath. He never seemed happy anymore. And we never knew when his Jeckel/Hyde complex would switch. It was that simple. He was nice and fun, or mean and hurtful.

Then it was time. There had been rumors in the family that both my grandpa and my grandpa’s brother had a disease. The family had been very quiet about it and we hadn’t heard much because my grandpa and grandma had divorced a short time before my dad was born. Consequently, we did not have a whole lot of contact with my grandpa’s family. After taking into consideration many suspicions, my dad soon decided to see a neurologist. Then, a few months and a few more doctors later came the diagnosis: he had Huntington’s disease, a degenerative brain disease. This was only the beginning.

Mom and dad sat my brothers, sisters and I down to tell us about the disease. They also explained that they decided to rewrite their wills and create a new trust. They planned for when my dad would leave work and go on disability, adjusting his life insurance and other tedious things. But I remember the conversation vividly when they mentioned how my mom had planned to care for my dad when he was no longer able to care for himself.
They did not want this disease to change our family at all. Everything would be taken care of, the plans were made, and there would be little worry about. We were agreed up until they told us that we each (of the biological children) had a 50% chance of inheriting this disease.

I admit we were moderately afraid. My sister and I were both engaged with plans to be married, and start our own families. Ok, this news was a little more than disturbing. It was then that we understood how real this disease was. If we had this disease, we could possibly pass it on to our children as well. For days there were a lot of thoughts, prayers and concerns that were voiced, but nothing could have prepared us as well as witnessing my father struggle with the disease first hand.

We started noticing his physical symptoms. While sitting still he was unable to keep his head steady. It would bob back and forth to a silent rhythm. Sometimes out of nowhere his hand would fly up from rest at his side, to up in front of his face. It became very clear that he could not control the sharp or the subtle muscle twitches that very often were outwardly visible. He also seemed to loose his balance very easily and decided to start using a cane.

We quickly realized that the reduction of stress played a very large roll in how his physical symptoms manifested themselves. He left his work and gave up driving. He in some ways felt that he was abandoning his manhood and freedom, and resulting emotions were twisted as well. Everything was very hard on him. Most of all he was obviously frustrated with the new person he had physically become. Depression became very evident, enough so that he opted to go on medication to ease his ‘lows’. And after witnessing all of these things, we soon realized that it wasn’t the physical or emotional symptoms that were the most menacing and hardest for us to face.

We watched as our once moral and compassionate father, showed sides that we had never seen. His inhibitions, moral conscience, and logical thinking were vanishing. He became very selfish and the only emotion he displayed was anger. He became promiscuous, devious, rude, chaotic and unpredictable. We very rarely saw rational behavior, especially when he was spending money. And he never displayed any kind of remorse for anything he did that was obviously hurtful to others, including thoughts of suicide. The dad that we all new and loved had been replaced with a new person: one that we couldn’t respect or trust. It was very hard to have sympathy for someone who very openly, didn’t seem to care. The behavior changes came so quickly that we could barely contemplate mourning for the loss of a certain aspect in our father, when the realization of another loss would interfere, over and over again.

And then the ‘plan’ that had been so carefully constructed before everything had come to the point that it had come to, changed. My mom could not function with the realization of my dad’s new lifestyle. She could not work, raise children, and stay emotionally stable, by constantly being aware of his latest antics. He was unknowingly making it very hard on her by disrespecting her and her efforts to maintain a healthy, caring relationship with him. And this was all so much out of his character that she really didn’t even know how to react to him any more. She painfully decided that they needed to divorce.

There haven’t been very many happy family outings in a while. Being in the same room with my father would leave you vulnerable for an unexpected verbal attack. Being in the same room with my mother would leave you vulnerable for an unexpected emotional breakdown. It was hard, and we knew our family would never be the same. I found that the faith that my father had taught us children when we were young was barely holding the broken pieces of our family together. And hope seemed distant: hope that things might be different, hope that things might be like they were before the disease, hope that things might get easier, hope that we would stand triumphant and honorable at the end of this trial.

I find myself telling everyone, if you could have only known the dad that I grew up with, the dad that taught me to play the piano, that drove me to soccer games and cheered me on in the cold, that swiftly came to apologize in tears after an argument, that would buy special junk food for our slumber parties, that would honor and cherish my mother and their relationship, that taught others about faith and Jesus Christ, that would invite the local transient home for a warm dinner and a job opportunity, that would sacrifice wearing holes in his clothes so that everyone else in the family could afford new clothing, that would work hard day and night to provide for his family (sometimes holding 3 jobs at once), that would edit my English papers, that showed us how to be patriotic, that taught us the sanctity of marriage and being chaste, that taught us how to set up tents and cook foil dinners, that taught us how to drive a stick shift, that was a night in shining armor for his little girl that adored and admired him.

I know there is a purpose and a season for everything. But that doesn’t make reality of the present any easier, especially when trying to explain to someone that my dad’s Huntington’s behaviors are not who my dad really is, or was. Or when trying to understand why I tested negative for the disease, while others will test positive. And there isn’t hardly enough information out there to prepare you for and to lessen the blow of this disease. Each case is different as well as each family. Though I still experience fear, and because any kind of change is hard, I strive every day to learn more and prepare myself better for the things yet to come. And through my experience, this is what I have learned thus far:

Hope lies in the past, with fond memories. Hope lies in the present with your knowledge and in your support system. Hope lies in the future, with a cure. Hope lies in our faith, and in the love that will pull us through.


Huntington’s disease and the Family; for the Spouse, Caregiver or Family Member

By Michelle Hardt Thompson

 

Things I have learned from Huntington’s disease:

 

Laugh a Little

Even when you have to be serious, a sense of humor can salvage an almost broken day.  When tension and stress are maximized, the light tug of humor can soften and ease the pain.  When my dad’s arm would fly up uncontrollably, he would wave his hand and say that he just wanted to say “hi”.  We couldn’t help but chuckle and smile.  Don’t forget to laugh, and look at things with a light-hearted perspective.

 

Pray a Lot

Your faith, however perceived, can fill in the gaps where you fall short.  I believe that faith is hope, and hope can save a lot of things.  After all you can do, pray and truly believe that things will get better.  Our spiritual side can correlate with our emotional health.  And a higher power helps by filling in the gaps, strengthening our drive, motive and resolve.  I believe that a loving Heavenly Father, hears and answers our prayers, and will comfort and lighten our burdens in his own way and timeframe.

 

Network of Support

No one can handle everything alone.  If we were meant to, we probably wouldn’t have been born into families, or have naturally come together in societies and groups.  Humans are social, and we help lift each other up and support each other.  Family is obviously crucial.  Parents, children, siblings, aunts, uncles, grandparents all serve supportive rolls in some way.  Friends, neighbors and others we associate with also support in distinct ways.  The web of support that we spin around ourselves can be our lifeline.  It can carry us when we feel we don’t have the strength for another day.  It can encourage us, strengthen us, guide us and applaud our strengths.  Professional counselors can also help us put our struggles into perspective.  And support groups help us to understand that others share in our grief and pain, in their own ways.

 

Constructive Outlet

Keep busy.  When you are working creatively or constructively on what ever project you choose, it will help you to resist from focusing on the mere difficult side of your life, and will open up your heart to positive alternatives.  And some times you just have to walk away:  everyone can use a little break now and again.  It is ok to leave your struggles for an evening, a day, or even a week.  Having a favorite place, activity, etc. can recharge your emotional batteries.  So if you are feeling empty and vulnerable to anger or other negative emotions, arrange to have your own personal uplifting time.

 

 Personal History

Write it now:  where you were born, your family and friends, where you have lived, fun experiences and special occasions.  Add photographs.  A family who has happy visual memories to fall back on will be better equipped to endure the worst.  And it is a great family history opportunity to be passed on through generations.  It’s also important to understand who you are before Huntington’s disease, so that you have a clearer picture of who you will become with Huntington’s disease (even as the caregiver or family member).  If you were prone to angry outbursts, they may increase.  If you were anxious and timid, you may now be aggressive and forceful.  Stress usually changes most of us for the worst, so figure out what kind of person you are, so you can prepare yourself for the kind of person you may become. 

 

For Better or for Worse

Why do you think a marriage commitment brings this up?  HD definitely falls under the “worse” category.  The hard will get harder.  The pain will increase and emotional tension and heartache will test your bond.  Have good communication now.  Write things down, and strive to make every day the best that your relationship has seen.  And don’t forget your goals and strengths.

 

Unconditional Love

It is hard to love someone that is hateful, hurtful, deceitful and unfaithful.  This disease takes away an individual’s personality, but not their soul.  Dig deep into their whole being and love that soul, that person that you knew before the disease.  Love the person and overlook their actions because nagging and contention will only make you forget who this individual once was, and the ability to treasure that memory.


Reaching Out

Reach out to other families like yours who are suffering.  Find strength in numbers and in serving others.  Again, it is an opportunity to forget yourself and your woes for a moment, and think about what others are trudging through as well.

 

Giving Support

Be there for each other.  Voice your frustrations, but more often voice your love and affection towards your family and to those you care about and who are struggling the most.  Just like we depend on others for strength and support, we can also be that foundation to someone else.

 

Be Strong, Hang on to Hope, and Don’t Give Up

Patience can wear thin, but your strength comes from every fiber of your being.  Be strong for your family.  Be strong for the HD affected person in your life.  Be strong for those who grow from your experience and your strength – including yourself. 


 Phillip Hardt     phardt1@cox.net    602-309-3118
 

 

 
 
         
   

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