Tag Archives: daughter

Struggling and Understanding

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Mom has developed trouble with a symptom called spasticity in her legs.  I don’t exactly understand what it is or means.  The only thing I do know is Sister K and I like to do a funny accent to make Mom laugh and say “spaaasticity.”   I did some scholarly research which amounted to googling and found this at the National Multiple Sclerosis Society website. I don’t know much about spasticity but I know when Mom is having issues with it she describes it as tightening and occasional feelings of shocks sent through her legs. 

I think her use of the word “shocks” is interesting because it is also a good word to describe how I feel about this too.  Shock because MS and the symptoms that come along with it are never ending.  Everything I read, everyone I talk to has a new one that I never knew existed.  No two people experience it the exact same way.  Personally, I hate this part of this disease.  I think it makes coping with it more difficult because there is no way to predict what will or won’t happen to Mom.  There is no direct path of what usually happens or which symptoms usually occur.  There are some symptoms Mom doesn’t have and others she has had for awhile.  Will other symptoms surface later or is this as bad as it could get?  All these questions make researching and reading scary too.  It makes it scary because sometimes I enjoy living in the “dark” on big issues like this.  So I struggle.  I struggle because people tell me to do the research and get informed.  I struggle with how to find a balance between the known and the unknown.  One of which is scarier for me than the other.

One thing I can do though is try to understand.  When mom talks to me at lunchtime and starts opening up about how she is feeling on a particular day I ask questions.  I try not to ask general/basic questions but specific questions.  What does that feel like, describe it to me, does it hurt, etc.  I am finding that by asking her these it is also getting her to talk about her MS and giving her a way to vent about it.  It is also making me more aware of what is affecting her.  I used to be inclined to think she was exaggerating things or making them sound worse.  I had a tendency to brush off her comments about not feeling well and change the subject.  I am not proud of that but if I am going to be honest it is true.  In trying harder to understand the specifics of Mom’s symptoms I hope to be able to help her through them better.

A few weeks ago when Mom was visiting we were hanging out at Sister K’s apartment and her lower back was really hurting.  In the past I might have just brushed this off but I really sat and listened and thought of ways to help.  I remembered my chiropractor is always telling me to use ice- 10 minutes on, 10 minutes off.  So I got up and headed to the fridge where I found a frozen bag of vegetables I knew full well would never be used by Sister K.  So I came back and put the ice behind Mom’s back as she sat on the couch.  For the rest of the evening while I was there I was taking it on and off to help her.  She later said it really helped and she felt so much better. It made me feel good because I knew I had made a difference in helping to ease her feelings of pain for an evening. 

I can’t help all the time but if I can every once in awhile it will make a big difference in helping not only Mom but also helping me not feel so helpless in our fight against MS.

25 Things

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As I write this blog about my experience dealing with Mom’s MS I am showing a glimpse into our relationship.  But this is a relationship that has existed for 27 years and is in no way rooted in memories of Mom having MS.  Thinking about that fact I came up with 25 things (based on the popular 25 things on facebook) I want to share about Mom and me that are unrelated to having MS:

25. We met for the first time in Europe.  I was born in Heidelberg, Germany where Dad was stationed in the Army.
24. Since I am the oldest I lived 2 1/2 years of my life having Mom all to myself.
23. Mom loves to dance just like me.  She danced in our dance recitals when we were little in an adult ladies class and when I was 7 we did a Mother/Daughter routine together.  I thought I was so cool.
22. Mom and Dad went on glamorous dates when we were little.  I remember them leaving in tuxedos, military dress uniforms and Mom in beautiful dresses and jewelry. 
21. When Sister K and I were little we did baton twirling.  Mom would help us practice our routines, recording music on cassette tapes and counting for us during practices outside in the backyard.
20. Mom let us take over the living room with our toys and our “dining room” was Barbie Central in our house.
19. Mom was the one who always pushed me when I was scared.  She pushed me on a plane to Washington, DC when I was 17; She pushed me into my dorm room when I was 18; She pushed me on a plane again when I was 21 to study abroad in Europe for a month.  She never shed a tear in front of me for any of this but Dad said she always did once I was gone. 
18. We had an amazing trip to San Diego one time while Dad was working at a conference there.  Mom, Sister K and I explored the city together not knowing where we were or and making up plans to see things as we went along.
17. Mom was room mom for my class every year in elementary school.
16. Mom attached all my sequins for dance recital costumes on with a hot glue gun.  She believed you could solve all of life’s issues using a glue gun. 
15. Mom threw some great birthday parties for us at Chuck E Cheese.  
14. Mom loved and still loves to buy us clothes.  We love this about her, so does her VISA card.  
13. During my wedding Mom was my biggest cheerleader.  She flawlessly planned it all.
12. I bought the wedding dress that made Mom cry.  That’s how I knew I made the right decision.
11. Mom loves silly stories.
10. Whenever I have a story or comment to share I know I can always call Mom and she will laugh and listen.
9. Mom is our biggest role model.  For Sister K and me the only reason we ever did certain things was because Mom did.  
8. Mom drove us everywhere in a blue Dodge Caravan.  We practically lived in that Caravan my entire childhood.  
7. Mom and I love to watch chick flicks.  No matter how cheesy, movie theater or tv, we love them all. 
6. Mom’s friends love her.  They want to be around her and include her in whatever they do.
5. Mom is always the best to cuddle with on flights.  That’s probably why Sister K usually always sits next to her.
4. Mom makes us listen to Christmas music nonstop when it’s on the radio at Christmastime.
3. Mom is thoughtful and always gives thoughtful gifts.  She loved making us care packages at college, buying us treats to take back after a visit home and even buying us a Christmas tree for our college dorm rooms.
2. Mom, Sister K and me are best friends.  You mess with one of us you mess with all of us. 
1. A hug from Mom makes everything better.  Always has. Always will.
 
I wrote these things down because I need to remember them.  I need to focus on them.  These things describe Mom and they have nothing to do with MS.  These are the stories, the memories, the moments that we have shared and continue to share that have molded and created our strong bond.  I need to focus more on who Mom is without allowing MS to cloud my every thought associated with us.   Because at her core she is not Mom with MS she is just Mom.  Mo

Mother/Daughter Movie Time

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I was home visiting one weekend and Dad was in the other room watching tv.  Mom and I were hanging out in my parents bedroom for some reason and I was flipping channels trying to find us a good chick flick to watch instead of whatever “boy movie” Dad was watching in the living room.  I found a show on ABC Family called Lucky Seven . We like these silly girly movies. They have been our thing for as long as I can remember.  Growing up in a family of girls, a chick flick usually wins out over an action film.  Plus Patrick Dempsy, aka Dr. McDreamy and Kimberly Williams from Father of the Bride, it’s the perfect combination for us! 

I turned on the movie and sat on the bench at the end of my parents bed with Mom. We were watching the movie, just sitting there.  No words spoken.  Happiness being felt.  Mom took my hand and said “Will you please just love me and be patient with me.”  I don’t remember what I responded but it doesn’t matter.  In that one sentence Mom summed up how she felt and continues to feel.  It was a sweet moment and made me wish I could freeze time so we could stay there forever.  Sitting on the bench, watching a movie, Mom not in pain or stressed, me not worrying or stressed.  I don’t remember what had exactly happened earlier in the day but I am guessing I let my lack of patience with Mom get the best of me.  I have a tendency to do that…   

I want to remember that moment because it was a gift.  It was simple.  There weren’t a lot of words and there was not even a lot of activity.  Many people would say there wasn’t even a good movie on tv, but I would have to disagree since we love girly ABC Family movies.  The point is that as MS has come into our lives our time together has changed and the activities we share are different.  We don’t run around as much as we used to but I find I cherish our simple moments more.  They cause me to pause more and really focus on them.  Today I don’t remember the shopping trip we may have had that weekend, even where we went for dinner but I do remember this evening spent holding Mom’s hand while we shared a movie.  I need to focus more on our sweet moments and less on big picture stress. 

In moments like this MS isn’t the focus but the love of a mother and daughter is and I have an ABC Family movie to thank for that.

Dad. Husband. Caregiver.

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I can’t put into words the love and respect I feel for my Dad. I believe deep down he is the reason our family is surviving Mom’s battle with MS.  I have watched and continue to watch a transition as my father has become a caretaker.  It brings back unsettling memories because I just watched my Grandpa go throught he same thing with my Grandmother as she battled Alzheimer’s.  I watched as he became a caregiver to her and feel now I am watching Dad go through the same transition.  And it is hard to watch. 

Since this transition began I have felt my mind sharpened to the reality of marriage.  My family is not large and up until I got married these two men, were the biggest male influences in my life.  They still continue to be large influences as well.  As I got married in 2010 and said my marriage vows, they really meant something very personal to me because I felt I was watchingthe tough parts of those vows lived out everyday.  I understood the meanings behind the powerful words “for better of worse, in sickness and in health.”  I understood the meaning of a committment and what it can mean through the tough times. 

But I struggle with Dad’s transition in becoming a caretaker.  He basically is one but I prefer to believe he is transitioning because it is difficult to think of Dad and Mom’s relationship that way.  It is something I never gave much thought and if I did think about it, they were thoughts that this would not occur for many years from now.  I also struggle because this level of responsibility and constant caretaking can take a toll on anyone.  Dad will talk to me sometimes about what is going on and I don’t know what to say.  I don’t know how to offer support.  What I want to do is pack up and move back home.  I want to find a way to be there for my parents all the time.  I want to help him with Mom, be an extra set of hands for him and just provide extra help.  But this hasn’t been in the cards for me up until this point and I don’t think it is. 

So what can I do.  I feel helpless again.  I continue to feel helpless.  I feel helpless because the best way to offer assistance in this situation is to be there. I also feel helpless because there is no way for me to be there except for brief visits home on the weekends.  In the past year my husband began graduate school for his MBA so we moved about an hour and a half away closer to my hometown.  We were 4 hours away before.  This was a step.  But without physically being there, how do you offer assistance.  How do you help someone who is doing everything and you are doing nothing.  And he does it all- he takes care of Mom full-time day/night and works full-time.  He balances both of those responsibilities and he never complains.  So I complain for him because I know he must be exhausted.  I know he must struggle.  How does he do it I wonder.  How. 

I think it’s love that makes him do it.  It’s love that keeps him going, keeps him supporting Mom. Love is powerful but is it enough?  I still struggle with how I can help him.  How can I be there for him.  Going home more weekends, calling to give him a sounding board to talk to, reassuring him that what he is doing is so important and we are all here for him.  The struggle continues and it’s something I think I will struggle with for a long time.  But it’s a struggle because of the love I have for my family.  It’s a struggle because I want to be there for them as much as possible.  So while it is a struggle, it is a struggle worth having and one I should feel fortunate to feel at all.

One Day At A Time

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I feel overwhelmed.  Overwhelmed by Mom’s MS.  Overwhelmed by my thoughts about Mom’s MS.  Overwhelmed with my inability to focus on one particular thought and come up with a way to fix it.  So I think I am going to rattle.  Rattle my thoughts off and see if I can come to some sort of plan for myself.  A plan to mentally deal with this because it’s becoming a lot. 

I wish there were a more direct path with solutions to fighting MS.  I feel like everyone has tried something different.  You could try this but this worked for me.  Maybe you should try this.  Lately Dad is talking a lot about considering stem cell research for Mom.  He is researching it, talking to people about it but Mom doesn’t want to talk about it.  I understand both points of view.  But I think we will try anything because we all feel helpless.  I feel helpless as I live my life and watch Mom get worse.  I think the MS is not only impacting her physically but it’s changing who she is, how she sees the world, how she lives her life.  It’s changing all of our lives.  It is putting an added stress on our family and on each of us.  What is the best treatment, how do we continue living our daily lives trying to keep them as normal as possible, how do we encourage her, how do we live with a disease where we take 1 step forward as a family and shortly after are forced 2 steps back.  And we continue this dance as we continue our lives. 

I guess I need need to start taking things day by day.  Everyone says to just live life day by day, take it one day at a time, and I agree with them but I never believe it in my heart.  That’s where the life of a planner comes into play.  I like plans.  I like to make them.  I struggle with taking things one day at a time.  But what if I didn’t.  What if I could just not think too far into the future but just into my day’s future.  What if Mom’s good days and bad days were just that…a good day was reason to smile and a bad day was not a reason to panic that things are getting worse.  They were simply just a good day and a bad day.  Because I tend to not enjoy the good days as much as I wish I could could because I am focused on the bad day that recently passed or worried for the next bad day to come.   

So how do I do it? How do I train myself to take things one day at a time? To not jump to the worst conclusion in a bad moment and to celebrate the good moments more.

Lights, Camera, Action?

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Seeing old friends. Fear of the unknown. What kind of challenges await me there? Will I be able to get inside? Will my legs be stiff? They know I have MS but will I be able to hide it well enough so they don’t know how bad it has gotten? These are only a few of the thoughts I can imagine go through Mom’s head as we go into a new situation.  A new situation where you can’t visualize what the future holds.  You can’t visualize how it will all go down.  Life is a big unknown but when MS is involved, it makes the unknown always scary.  Never exciting.  Not anymore. 

Driving up to visit us last Friday I imagine all of these thoughts were in Mom’s head, plus some others.  If it had just been a visit to see Sister K and me it would have been relaxed.  There would not have been nerves but excitement.  Instead though we were meeting with one of Mom’s college friends and her family for dinner.  It brought an entirely new set of cards to play with Friday night.  Mom got so anxious in anticipation of the visit that she psyched herself out.  She let the evil weasels get the best of her.  The problem is once the weasels begin to attack, if you cannot get a handle on the first one the others quickly pop up, taking over.  They can take over fast too.

I was not there as they took over, but Dad and my Grandpa were.  They were there as the weasels took over Mom’s mind.  Took over her thoughts and they brought on stress which when mixed with MS is never good.  Sister K had made some phone calls because they were running late.  We were putting our stories together to determine what had happened.  Then Mom called me crying.  She called me crying like I call her crying.  There was a panic in her voice, a please help me tone and helplessness.  As I listened I almost felt like I was in a dream.  Is this really happening.  What do I say.  What do I say to my Mom when she is always the one who provides this comfort.  She is better at this than me.  This isn’t my strength.  I wish she’d called Sister K.  Sister K always knows the right thing to say and I am a gamble.  Sometimes I get it right and sometimes I get it terribly wrong.  So I thought of Sister K and what she would say.  I came up with a new plan for the evening with the delay, that’s the easy part for me.  I comforted Mom and assured her it’d be fine, that was the hard part for me.  I felt a different sadness though in this situation.  I felt sad becuase this was happening.  Because this was a nightmare.  Becuase no one else I know has to deal with this besides Mom.  Because Mom wants nothing more than to get in a car for a little trip and have it be smooth sailing.  Because it isn’t fair.  It isn’t fair.  It isn’t fair.  I wanted to scream when I got off the phone with her like a little child and throw a tantrum with legs kicking and arms wailing it’s not fair.  Because it’s not. 

I also thought about how lucky so many people have it and they don’t even realize it.  How simple their lives are in comparison to mine.  How they have never watched a disease this horrible take over their Mom.  How they have never seen their Mom feel so helpless and felt helpless themselves too.  It was a tough tough afternoon.  It got resolved as it always does.  My family stepped up and we did our thing.  Sometimes in situations like this where other people are involved I feel as though we are performing on a stage and some nights are easier than others.  But somewhere in the middle of our “performance” the problem that was once there is lost.  The happiness we felt we were faking takes over.  We begin to laugh again genuinely, not forced.  Our minds stop wandering from what just happened to the present.  We stop saying in our heads “it’s all going to be okay” to calm ourselves down and instead we are comforted becase we begin to feel like it is all okay.  We survived another battle with MS.  We didn’t let it bring us down again.  Maybe it’s okay to perform, to focus on the stage because by forcing ourselves on stage there is no time to be sad.  No time to dwell on solutions to a problem that can’t be fixed.  It is on that stage where somehow life becomes okay again.

Fashionably Late x 2

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My family has always been late for things.  For as long as I can remember punctuality was not a characteristic that people would use to describe us.  It was never done in a rude fashion, but just about 5 to 10 minutes behind schedule.  I say typically because it was selective.  We were on time when it really mattered for things like school, dance class, weddings, etc.  Things where punctuality was important and necessary.  Now that my mom has MS our tendency to run late for things has taken on a new life of its own.  We operate on a completely different time schedule, usually running very behind. 

It’s not all my mom’s fault, I can’t completely blame her at all.  Let’s take Christmas 2010 for example.  I have always had a bad habit of biting my nails but I finally grew them out for my wedding…and so I could wear dark nail polish for Christmas.  As we were running around trying to get out the door for Christmas Eve mass I realized I had forgotten to paint my nails.  At this point my dad was running around looking for the checkbook, mom was making sure everything was in her purse and my newlywed husband just stood there in awe of this.  This is because his family runs 10 minutes early to everything, but I digress. We had about 3 minutes before we were walking out the door.  My sister looked at me and said we’re going to paint them, grabbed her nail polish and we did it.  We put my hands on the kitchen counter and with 3 minutes to walking out the door she painted my nails.  They were drying as we arrived at church. 

I bring this up because it makes me laugh but also because my family is having to learn to be a little more organized to get out the door now.  I also have to learn to be okay with the fact that we do run a little later now.  I have a slight Type A personality when it comes to these things.  I don’t mind running a little late but I have a point when I decide it’s too late.  It’s a basic formula for my meltdown: Getting out the door drags on for various reasons that don’t relate to my mom (forgetting keys, forgetting garage openers, forgetting sunglasses) + my mom needs extra time = me putting stress and pressure on my mom in the situation.   

The reality of the sitaution is the world is not going to end if we are late.  We will get there when we get there.  We are not going to be in trouble if we are late.  One of my college best friends used to say “what are they going to do?” and that’s the attitude I need to have.  I need to repeat these statements over and over.  Over and over.  I need to have them screaming in my head in these moments, drowning out whispers of stress as I begin to pass the whispers on to everyone else.  Instead I need to take a mental step back in these moments.  I need to help where I can but I also need to treasure the chaos, treasure these moments.  Treasure that we are all together piling into our car to go somewhere the same way we have done all my life.  We are all together in these moments.  I need to focus on the moment and enjoy being fashionably late x 2.

My mom has MS: 101

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My mom has MS.  Words that have become part of my identity.  They are now an element of my family and an element of my life.  When I processed these words in my head for the first time I didn’t know the perfect way to react.  I still don’t know the perfect way to react. 
 
No one writes an instruction manual to help you deal with the words.  I wish they did.  Instead I am making it up as I go along, trying to do give myself lessons day by day, trying to deal with this day by day.  Some days I do really good, some days I do really bad, some days I give myself an A+ and some days I give myself an F.  I was a good student when I was in school.  I studied hard and I made good grades.  But this test I am now being given everyday, this class I am now enrolled in everyday, I didn’t register for it.  I didn’t get a syllabus for it.  I don’t know how to study for it, how to prepare for it or how to get an A+ in it and that frustrates me to no end. 
 
Everyday my world is the classroom and everyday I am the student.  My hope is that through this blog I can become a better student.  I can collect my thoughts so when I return to the classroom I am better prepared.  I can take a break from this class and enjoy recess.