Retirement

So Friday was my last day of work.  I didn't consider the weekend official retirement days because it was the weekend.

Today, Monday, 12/22 is my first official day of retirement.

It's this wide-open, vast feeling.  I look to the future and it stretches out ahead of me.  Which really is another way of telling myself I can clean the bathroom tomorrow...

I'm not a super structured, disciplined gal.  I tend to let the day direct me -- I don't really plan much.  As much as I like to think this is going with the flow, it's really more not being comfortable in a planning, leadership role.  At work it was different -- I was good at figuring out what needed to get done and doing it. I could juggle 12 things and maybe drop one plate.  At home, I don't even pick up the plates.

It's going to be an adventure for sure planning out each day.  I feel like a clip board might be in order.

Being with someone a lot feels, ummmmm, interesting.  I think I need to set aside this feeling that I'm Julie from the Love Boat.  Entertainment Director.  On the flip side, I have to remember to go be with him.  We aren't on the same level (my 3 level townhouse).  Sometimes I get to doing something and two hours go by and I realize I've left him downstairs.  Being responsible for someone's activity is weird.  Do you have an itch?  Do you need to eat?  Glass of water?

It will be great when we move to be on one level.  And have the wheelchair inside the house so he can move around on his own.

Well - off to go do retirements stuff.

Disclaimer:  This probably isn't 100% retirement.  More a family medical leave.  As is the norm these days, my work future is in limbo.  My work's been great in terms of allowing me to change positions, go to different stores, take time off when needed.

On my last day, I kind of expected a parade or confetti.  I've worked at Turn Style for 18 years!!  My boss did show up with flowers and a hug but he said he wasn't planning on doing anything because he figured I'd be back.

Who knows?!  I might be...

In the meantime, I'm going to go make a plan!

on the upswing

Life seems relatively sane lately.

Luther's coughing has decreased quite a bit because of his new meds.

His new meds make him feel good, less pain.

His mobility isn't the greatest; in fact it's gotten worse.  For me,that's ok.  I can lug him around any time.  I'm just so happy to have him lucid and still eating and talking and swallowing.

There was a time in our relationship I wasn't sure if Luther was the guy.  The one.  I hate that he's sick, I hate that he's in pain and has to go through this.  But in so many ways, this stupid sad disease has made me fall in love with Luther so much more.

I get mad at him like regular couples get mad at each other.  It's not like the ALS has created this fairytale.

Quite the opposite - it's a nightmare at times.   But struggling through all this together creates an amazing bond.  He's so patient with me, he's so kind and generous and he's the one who holds me together most of the time.

I just wanted to write a post to tell everyone we do have fun, we do enjoy each other and it's not always such heavy, sad stuff all the time!!

I let a friend down tonight

What a weird feeling.  I'd made plans with a friend tonight and I completely forgot about it.

There are a million things I want to say:  why didn't you call when I didn't show up?  why didn't we connect from the time we made the plans to today to reconfirm?

But there really is no excuse other than I forgot.  It's a really lame reason.  I know it.

I know I made her feel not important.  I feel selfish and wrapped up in this.  I can try to defend myself and say I have a right to feel selfish.  This is an extraordinary time.  And yet, my friends are my friends.  In this extraordinary time, they are my lifeline.  My support system.

It's a two-fold thing:  life in it's most ordinary of ways, marches on and I have to march with it.  I still have to make dates, go to appointments, remember to show up.  I still have to be a friend.

The second part of it is I'm in a situation I've never faced.  Maybe in this time, I need to be more aware, more diligent. An even better friend.

I owe it to her but I also owe it to me to make sure I'm keeping connected. I need her friendship, more now than ever.  But she needs mine, too.  It makes me feel good to be a good friend and tonight, I wasn't.

This feeling is reminiscent from several months ago when I was forgetting a ton of stuff.  I think I forgot a plan with this friend back then, too.

I was forgetting times, dates, appointments.  When I started using a calendar, I was putting the wrong time/date in to the calendar.

I don't know why I'm in this mode? I mean, I guess I can put it all on Luther's illness.  But it's not that. That's too easy.  It's got to be more.

Thank goodness I have therapy tomorrow.  This goes to the top of the list.

Guilt. Grief. Just another day.

Today, I'm giving up my cat.  I've retyped that sentence about five times.  Giving her away. Surrendering.  Giving up on her.

I've had her 14 years.  She's a good girl.  A lot like me, I guess.  She doesn't like a lot of attention. She hangs out by herself a lot.  When she wants something, she'll let you know without too much drama.

When I come home from work, she'll run down the stairs and come sit wherever I am.  She doesn't really like Luther too much.

If you've read my previous posts, you know Luther is pretty much always downstairs. When I spend time with Luther, once in a great while, she'll come down and sit a few feet away from us. Generally, though, she hangs out on the stairs so she's near us but not in the same room with him.

When I first got her, I didn't see her for about 3 months.  She hid.  I knew she was alive because she was eating and pooping.  Eventually she came out and we became friends.  I am her only friend because she is unwilling to come out and meet anyone else.  Most of my friends and family don't believe I have a cat; they've never seen her.

Now that we're heading south for a few months, now that we're moving and don't want cat hair and allergies at anyone else's home, it's time to surrender my cat.

I've been thinking about this for a long time.  I'm off to let her go right now.  More later.

Later:

Well -- I guess I don't need to write Baby's (that's her name) obituary.  She's not dead.  She's finding a new home (hopefully).  They said they have a couple different programs for older, shy cats - well, probably for cats that don't get adopted right away because they aren't super cat-cute... one of the programs is called "Hidden Gems" - which made me smile.  My hidden gem of a cat.

I think this whole thing isn't about the cat.  Well -- it is.  I'm sad.  I'm sad right now that she isn't here. I wonder if she's scared or lonely.

But it's more about the changes, these changes we're all going through... the feelings we all get to feel.

I'm pissed off that I gave up my career, that I gave up my cat, that I'm giving up my home.  Pissed off in a general, shake-my-fist at the sky kind of mad.   I'm not mad at Luther.  Far from it.  Just pissed at ALS.

It's difficult to explain to most folks.  We're so so so fortunate that I can afford to stop working.  How lucky is it that I can move in with my parents?  They live close.  They said YES.  We're going south for the winter.

At the same time, I'm feeling scared.

Ok.  Enough, I guess.  I can "wrassle" with these feelings forever.

I talked to my therapist about letting go of these feelings and he said you'll never let go of the feelings.  They aren't things to let go of.  The stuff that makes you feel is what you let go of, not the feeling.  Makes sense in many situations but... in this case, it's a terminal illness that makes me feel this stuff.  How do I let go of that?

Rollercoaster back on the way up...

Well, it's one in the morning - Sunday night.  The typical can't sleep. But I have tomorrow off and have nothing but a relaxing day planned.

It's been a couple weeks since Luther and I had a whole day off - no appointments, no work, no engagements.

I had a moment of melancholy tonight.  A two minute cry resolved that issue.

Now, I feel a little lighter and am looking forward to hanging out with my guy tomorrow.

The goal tomorrow is to just enjoy the day.  No worrying about the next day.  No thoughts about what happens next.

I might even cook something.  It feels like a meatloaf kind of a day.

Things too sad to read

I belong to many ALS support groups online.  It helps to be connected.  I've talked about the side effects of being that connected before.  Do I want to look in to our future?  It's very very difficult to hear what's going to happen.  

Sure, I know everyone's ALS path is different and yet, eventually, the end will be somewhat the same. The decisions we face, the guilt, frustration and exhaustion we feel, the extreme sense of duty and love that grows each day - these are the same although might be expressed in different ways.

Do I stay subscribed to these groups?  Do I continue attending support groups?  I think yes.  As hard as it is to read, to hear, it's good to know there are folks out there who've been through this.  That helps.

Here is an excerpt of just one of the messages posted on just one of the groups I subscribe to.  

Original post from a woman who took care of her dad:

It's been two weeks since my dad passed away from ALS. I stopped working to be his caregiver for the last two years. I feel completely lost. Has anyone out there had to take their loved one off of the ventilator? The guilt has become overwhelming but he no longer wanted the trach or life support.


--------------------------------------------------------------

Each ** paragraph is just one person's reply:

**  We are at one year today since losing my brother. My sister in law was at his side. They had made decisions and she stuck to his wishes. She's one of the strongest people I know.

**  So sorry for ur loss, I lost my mother in 2011 after her battle with ALS, as the child/caregiver to my mother when she passed I too was full of guilt, wondering what I could have done more of, or how could I have supported her more, especially since she passed away just half hour after I left her, I focus on the fact that she is no longer suffering, and that she is at peace now... Time doesn't heal the wounds any, however learning to live again does... My mother choose not to have any life sustaining measures taken, so we honored her wish, which is what u done as well. My prayers are with u!! Hugs from ur ALS family!

**  What I have learned doing hospice work, is abide by the patients wishes and never doubt yourself or your actions. I now have to do this with my husband who is 49 and has a hard time talking, swallowing and at times chokes.

**  Yes my dad was on the vent. The last week was so horrible. We were suctioning nothing but blood from his lungs. He was starting to become out of it mentally. That Friday he was completely gone mentally. He would go through all of the facial emotions but would never focus on us. It was like he was seeing right through us. When we would walk by and the lighting in the room would change it would somewhat get his attention but he still wasn't there. He was grinding his meet so bad. That evening we called his doctor to come over. He asked my dad a fee questions to which he answered yes to even though he should have answered no to one or 2. We went out of the room and decided to give him pain meds to make him comfy. Then added in high doses of Ativan to calm him and slow his breathing. Once he was calm and pretty much sleeping with his eyes open, they began to turn off his oxygen and turn down the vent. The entire time this was happening it took all I had not to yell stop. But I knew it my heart that he would pass very soon and would suffer. Once the vent got to a certain point it was switched to automatic mode and within a certain amount of time, I don't remember exactly, it slowed his breathing until it shut off. He was no long able to breathe on his own, the vent was keeping him alive. He passed away peacefully with his family surrounding him may 10, 2014 at the age of 51.

**  You gave him peace, my sister had to do it for my mom and sister. 
She feels like you, I feel like she was an angel. I hope that she would do it for me as well. 
Hugs

**  Hi, I'm so sorry got your loss. I was my mom's caregiver and it is very natural to feel guilty. My mom didn't want any medical assistance so not being able to help with a ventilator was excruciating but I wanted to honor her wishes. I also left my job to take care of my mom. I spent 2 years after mom left us to write and write and write. It helped my mourn and heal.

**  My husband was not trached but I have guilt for other things...the 'sins' of a caregiver are overwhelming... Trying to keep your loved one comfortable as they die caused me enuf guilt to last 3 lifetimes... Why him and not me?!?! And endless other questions... 4+ years later all I can say is we do the best we can as caregivers and that is all there is...no right, no wrong, just our best...

**  My.husband refused artificial breathing. 
He died last January. 
Diagnosed 4 years ago.

**  I had to take my husband of 30 yrs off, it has been 3 yrs, and yes I still live with the guilt

**  I think as caregivers we always say why them and not me. I think that all the time she had more to offer this world then myself. My wife choose to not even get feeding tube. I feel guilt and thought she didnt want to stay alive cause she didnt want to be with me. Women are so much stronger then men are i believe when it comes to death but my wife had so much faith. Had hospice nurse and tell me i should go tell her its okay to leave. I feel guilty cause i couldn't do that i felt like i was giving up on her. This ALS is so nasty to watch it suck the life out of someone like it does. When they told my wife i didnt believe it thought something like cancer we could fight it together i kept looking for it to be something else i was in denial the home time. been over ten years and holidays seem to get worse every year. I pray all the time for my wife to come to me in dreams and nothing. Really stinks just hope i meet her in heaven someday.

**  My father was wide awake during the night in which he yelled and cried begging for someone to lift him out of bed to walk. Just sad.

**  Sorry for your loss, my mother on law refused any invasive procedures to extend her life. She was complaining of shortness of breath 2 days prior to her death and i gave her the choice that either I would drive her to the hospital sans oxygen, or the ambulance would take her. She went via ambulance and never left the hospital remaining steadfast that we complied with her directives. My wife and I spent 8 months caring for her as well as my father in law and our 4 children. The point it, do not feel guilty, it wasnt your choice and you dedicated 2 years, we did 8 months and that was stressful, but it is out of love that we sacrificed and no matter how hard it feels, i cant envision what they went through!

**   My husband died July 15-13. We were married July 15-1999 and had 3 beautiful daughters. My girls told me the day if his funeral, mommy we are sad and sorry that daddy died on your wedding day. I told them and I believe this to be true, God brought us together this day and separated us this day. Mommy is happy that your dad is no longer suffering and home with God. Take the days one by one. The pain is the same but the days do get easier.

My mom and dad

My mom and dad are awesome.  I know I've said this before.  But they deserve extra special mention.

This whole ALS thing is an extraordinary situation.  It's put us all in places we'd never thought we'd be.  Emotionally, financially, where we live, how we live!

If I back up a little, pre ALS, even pre Luther, my parents have always been pretty great.  They're all about family.  They lead their life by example.  They are true and honest, hard working and moral.  They are thoughtful, funny, patient and really really kind.

They are there for all us kids, usually no questions asked.  Maybe a few!  But generally no judgement.  For me, I've made some questionable choices and always, my parents have always been there to support me... not necessarily the choice, but to support moving me forward.

Fast forward to now.  To this terminal diagnosis.  It's created all kinds of situations we weren't prepared for.

We will be moving in with my mom and dad at some point in time.   It should've been by now.  We have a VA grant to get their house wheelchair accessible but moving through the grant process has been super snail like.  Part of it has been mis-communication between me and Luther, us and our grant advisor, my parents and the contractor, us not signing something correctly, etc etc etc   The grant process started in June.  Maybe earlier.  6 months later, the work hasn't even started.

My parents have ripped up their carpet, moved furniture, peeled wallpaper in order to get the process rolling.  And it's still not rolling...

Did I mention my parents are patient??  This was supposed to be interim housing.  Done by now, we'd go south for the winter, come back and live with mom and dad while we re-group, have the time to look for a new place, figure out what to do with my old place.  We're all adjusting.  I can only imagine their frustration and yet, we're all learning to accept the idea that this is what it is... we can only deal with and control what's in front of us.

Luther owns a mile-long RV.  It's still in Virginia.  A part of his past.  Sadly, a part of our future since there are payments still to be made.  My mom, in her zest for thinking outside the box, wondered if she contacted Ellen about our story, if Ellen would take the RV off our hands and use it to pass on to someone else?  Or as a celebrity dressing room??

Which got me to thinking about the Ellen show and how she honors every day people who do extraordinary things.

I sent in the following to the Ellen show, hoping I could get my parents in the audience or something like that.  You only have 1500 words to convince someone at the Ellen show they need to recognize someone!!   To date, I haven't heard anything.   So here's my own little tribute to my mom and dad.  I want to recognize how much I appreciate their support.  How much I love them.  How proud I am they are my parents.

Hi!  I'm Lynn.Thank you for highlighting the faces of ALS.  Your spotlight on this terrible illness is great!  

My guy, Luther, was diagnosed last November. We met a little over 2 years ago and jumped in feet first, thinking we'd have the rest of our lives to keep falling in love. A year after meeting, Luther got sick. It took almost 9 more months of testing to finally get the diagnoses. The "rest of our lives" took on a whole new meaning. 

But this isn't my story. Or Luther's. Instead, I'm writing about my mom and dad. Married 53 years, they are amazing. Every day, they show us what strength of character and unconditional love means. 

Luther and I can't stay in our house; it isn't feasible to make it accessible. So, at 53, I am moving back in with my parents. They are tearing up their home and my dad is giving up his man cave so we have an accessible place to live.

My mom loves your show!  She called with this zany idea I should contact you to see if you wanted this monstrous RV I inherited via marriage. Her words: "Ellen could use it for a blood drive or a celebrity dressing room!"  

That's not why I'm writing, but it got me to thinking...is there a cool Ellen kind of way to acknowledge my parents? 

I've told them a million times how lucky I am, how grateful we are. This illness is devastating and sad but time after time, my parents step up and keep us moving forward. It would mean the world to be able tell the world about my quiet heroes who expect nothing and deserve so much.