ampyra

May Warrior Check In

Posted on by tresswann

Back for MAY :

How do I feel today – Nice day.  Attended a tea.  I actually did a table.  I was all tizzed about it but think it went well.  However, mixed feelings.  This is my fourth one.  I walked in first time four years ago  in a dress, today with a cane and pants.  But I am walking better than I have due to the drug.

What did you do for yourself today?

See above.  I went to a tea, very girly.  My husband was wonderful and helped set up and breakdown.  There’s a jewelry boutique so I got to shop!  And then went to Odd Job afterwards for this and that.  I didn’t work.  It’s a real break.

What did I eat today and how did it make me feel – BAD.  It was tea!  I did do a smoothy before I went but scones, salmon tea sandwiches, chocolate.  Then Chinese food.  I have been seriously sliding and need to recommit to proper eating.  I need to max the opportunity the Ampyra has given me.

Did I exercise? What did I do? How did it feel – Still not going to the gym or Zumba. But I am walking more.  I will get to gym.  This was the least I have walked all week.

For whom or what are you grateful? What matters most in life?   Grateful for friends and the possibilities of new ones.  Grateful for the people I am meeting through the blog.  Ampyra.  New possibilities.

Do I have a higher purpose or driving force in my life?   Make a mission statement – Higher purpose still not defined.  Beginning to dream again.  Uh, maybe some sort of sharing

How long have I been treated with conventional medicine Ampyra,  two weeks.  And it is working.  I was able to walk longer and stronger.

The first time I had a symptom – June 2004 walking on the beach boardwalk

What symptoms are most troublesome – being off balance and not walking well, wearing ugly shoes and consequently ugly clothes

Do I blame myself for things –  Yes, I am still blaming myself for not being aggressive against this. Still!  And I think always.  It’s funny how we don’t take things seriously

How is stress level? It’s high.  Trying to tone it down.

What can I do tomorrow to make it better than today?   Start over.  It’s a new month. Have a different day.  And yes, I am thinking about things other than disease and death. I am thinking about art and new jobs and possibilities, flowers and spring.

Until next month.

Ampyra Plus

Posted on by tresswann

Well, I started the Ampyra a week ago.  I had fought against taking drugs for ages.  When I finally gave in,  my insurance wouldn’t pay for it.  New insurance pays.  And it’s reasonable.  So, I started it last Saturday.  Yes,   I was/am worried about side effects.  Uh, seizure is one?  Much trepidation.  So far, so good,  no side effects.  And I am walking better!  It’s amazing.  Thursday, I walked 11,000 steps and was not stumbling and half dead, that night or the next day!  I can’t believe it.  I am fearfully optimistic.  On the one hand, I have read the literature.  This is not a cure.  I can continue to deteriorate.  I do not want to think about this.  Here’s where I am going.  I am taking this as a second chance.  I can go back to Zumba.  I need to find my way back to the gym and build those muscles.

This morning,  I went for MRIs.  I have been getting them from a research study.  It was de-funded and the doctor pointed out that it had been two years and since my left side seemed to be having trouble….  This time the insurance is good.  I didn’t want to go.  What is the point?  I know things have changed.  There’s nothing they can do, so why?  Of course, I had to take the spectral leg off for the MRI and the tech wanted to wheel me into to the room in a wheelchair.  NOOOOO!  I stumbled and gimped on it.  Puhleez!

And I am on a roll,  yesterday I went to get a new spectral leg.  I was shown one that had two thin metal strips in the back but my ankle is too wobbly.  However, there is a graphite one with a thinner back and slimmer sole.  I may be able to wear  nicer shoes. I hate, hate looking disabled.  I am like a newscaster behind a desk – everything looks good until I stand and walk!  I am very vain and ugly shoes impact me.  And I don’t buy what some of my friends tell me about being older and not wearing heels.  Okay, I wouldn’t want to wear stilettos anyway but I see no reason why I can’t with practice and determination get back to kitten heels.   Let’s not even consider crutches or wheelchairs.

My goal is to go back to wearing spectral leg only to and from work and to ditch the cane.  Build those muscles.  So, I need to amp the clean eating.  I am on my way.

Aftermath of the Doctor’s Visit

Posted on by tresswann

What can I say?  I never like going to the neurologist as I find it a very draining experience. I hate seeing people worse off  than  me.   She is always telling me how I am not doing badly. Last time she said I was more spiritual.  Don’t get me wrong.  She is nice and listens to me.  Not sure, if she really hears me.  When we first started, she said everything wasn’t all about the disease/condition.  She was for me and my kitten heels.  The last few years the exams have been cursory.  My husband thought that once I wasn’t participating in research drugs she wasn’t really interested in me.

I have had a bad few weeks. Not enough walking or exercise due to bad winter.    I am never in pain except for when I fall.  My knee has been hurting me and it’s not a “fall” hurt.  I have been barely able to walk.  Well, I did turn a corner last Thursday, even though I did fall but I walked 11,500 steps.  Still, it’s been a real struggle.  I hate the way I am walking and looking.  I knew this time wasn’t going to be good.

I had the very sympathetic look – so sorry you are falling more often with the unspoken words what do you expect?

Bad news – we expect your symptoms to worsen in your already effected area but it appears things have changed and we need to look.  Yup, my left leg and my fingers are going.  And did I know that I have arthritis in my spine?  No, I didn’t and it looks like it might be getting worse?

Oh and the falling?  You may not want to hear this but maybe bilateral support?  As I was asking, can you say it in English?  My husband was saying, she’s not going for it.  Crutches!!!  Is she f’ing kidding??

And drugs?  She wants me to take the Bac more regularly.  I needed bloods for the Ampyra.  I hate needles.  Once a doctor told me he needed blood and I said needles?  He said, well I am not a vampire.  I thought this visit was going to be about other drugs.  Nope, she wants MRIs.  Luckily, with my change in insurance, they are only $75.  Last time, it took me almost two years to pay them off. Glutathione?  Complementary treatment.  I did get scrips for a new spectral leg though.

I also feel out of balance, literally and figuratively.  I thought I was finally getting to a place where I didn’t have to stress about buying “stuff”.  As I approach my milestone year, I wanted to stop settling.  I like being able to buy the Hourglass blush and highlighter.  I wanted to upgrade my car.  Material, superficial stuff I know.  And I know walking is more important.  I guess I just want to live as if this isn’t happening.

Oh, and the neurologist is not covered under my new insurance.  She wants to see me in about a month.  Look at it this way, I’ll be getting a larger tax refund next year.

So, what do I want to do about all this?  Fight back.  Restart and commit to the physical therapy, get in more walking (read lurching) and be more aggressive foodwise. Neuro says one of her patients gets good results but it’s not a good idea, just be moderate.  I am going with my plan and let’s see if I can have improvements by next time.  I am betting on me.  I hope to blog about it daily.  We’ll see.