Showing posts with label Amy. Show all posts
Showing posts with label Amy. Show all posts

Wednesday, 12 October 2011

BBC2, Human League and oh no, I'm falling in love

As they say on Chan4 tl;dr

If you don't understand that, then don't worry. Read ahead!

Look at this gem Trish Dainton of Curse in Verse & Much More Worse found! Its only a video I've wanted to see since I was 13 years old.  I'm so excited to share this with you. Its one of the Human League's second television appearances and their first after signing with Virgin Records. They performed two songs, including Empire State Human, shown here on BBC2's Mainstream.


Just for this, I'm going to push your book again tonight Trish.  Again, Curse in Verse & Much More Worse is a book of poetry by a woman who was the carer of her husband Steve who died of Huntington's Disease earlier this year. The book is a combination of prose as well as her poems in which she places herself in both the roles of a person with HD as well as a Carer. It is a very good book for anyone who is either taking care of a person who suffers from a terminal illness or their carer. I can't recommend it highly enough. You can buy it in the UK at Amazon as well as in the US by clicking the title above.

Please forgive the first part of this blog as the internet is down so I'm posting on my mobile.

Last night was crazy and I felt violated.


Yesterday I did too much and got stressed out. It can happen to the best of us. I also took Naprosin for my back which ate through my gut and codeine which made me dizzy. No fun. So I get sick in the bathroom and J decides it must be some Huntington's thing. As if I can't get normal sick,right? Its one of those times when I think she sees the disease and not the person, you know?



This is the kicker and what royally pissed me off. She f'cking posted on my Twitter account! WTF? So here I am in the bathroom, willing to take the Visteril for my naseau which I never do and she's on MY Twitter account asking for help. Yeah, she doesn't want me to take the Vistaril because it can cause random movements but that's her issue. Yeah I normally don't like those drugs but last night I didn't have a choice.

So here I am, on my hands and knees over the porcelain king and I blew up. I haven't been this upset in years.

My blog and Twitter are my personal space and just because I wasn't able to lock my computer down doesn't mean I should be worried about someone in my house using it.

I know she has feelings for me and is worried but that gives her zero right to go into my space. That's a whole other issue. Still, unless she passed away I'd NEVER EVER go through  her address book, Twitter,  or Facebook. Its just wrong.



Let me tell you if I wasn't sick I'd have taken my laptop and Droid to a hotel for a couple days. Instead, when she relaxes after class I'll explain that for me its a private thing. As mad as I was then, now I realize she's not a mind-reader.

I went to see my shrink this morning and told him everything that has happened the last week.  The last previous weeks'  my mood swings were severe enough I went on a mood stabilizer, which feels like its starting to work. Still I felt it was important to make sure that isn't the underlying cause so I ran everything I could remember from the week to him. There was a lot of stuff. Sometimes we don't realize it while we're in the midst of it.

In fact, I finally told him about this blog (and he promised all on his own not to look for or read it). It even came up that I am more open here than anywhere else. He asked if I would give him an example and I told him about yesterday's post about my mum. His mouth nearly dropped open as its not something I've been able to really talk about with him, even after two years. He asked who reads it and I told him as far as I know no one I've met personally, maybe one person I know as she's on my Twitter and I post entries there.

Doc said its okay and I'm not weird to want to keep it that way. I only know one person in real life on my Twitter account and they're the reason for my Twitter addiction. So I blocked J.
Its not personal but as I told my doc I want to be open here, not worrying what X person is going to say about Y statement. I also don't want it used against me.

I needed to go out soon to fill my anti-depressant and make copies of my Living Will and posters about Amy Ahearn. I was going to distribute them today with my friend but all these psychiatric drugs (Xanax, Tofranil and Lyrica) are making me so very tired on top of the Vistaril last night. I have fallen asleep three times today. Then again I slept like crap the  whole week. The police & sheriff stations will have to wait until tomorrow. Of all people to understand the importance of medicating the psychiatric side of Huntington's it is Amy's sister. Sadly, Amy is like me in terms of suffering from those types symptoms, only worse. I will get the copies made today.




Sometimes at home I feel like three people. And I've heard all these quotes with my own ears. There's Paul the normal guy who J and most of society wants to be around. He's a normal guy looking for a normal job. "Poor boy hasn't found the right woman yet to settle down with and have kids but give him time...in fact I have just the woman in mind..." 




Second, there's the guy who's mom was "cookoo" and even though we don't say anything to his face we are careful around him. We all hope he doesn't end up like her. 

Then there's the HD Paul (note the HD comes before the name). Its this third one they're all worried about right now. His personality is a bit different to those close to him and people don't want to see the HD part of it. They don't like it when he goes out to show posters to strangers of a missing woman just because she has Huntington's Disease and he realizes it could have been him that went off missing. Come on folks! He's giving money to help find a cure for HD, and how do we really know his mother had it at all anyway? Or his other relatives before her? He "only has large involuntary movements right now, not fine ones."

"I know," someone else said , "I saw the large tremors so it can't be HD, Paul. And while I have you here, we all know the mumbling is just being lazy. I hate how you've been doing that lately. Don't you care enough about me to even talk clearly all the time? I think it could be all those meds, do you have to take them all?"



I want to scream "If I could go without all these meds don't you think I would? This isn't exactly fun!" but I just keep quiet. I know its not the meds causing the mumbling and that my mother never had minor tremors nor  dancing. I also know that she died early on in progression and had already fallen often enough she was in a wheelchair most of the time. I know that she suffered from extreme depression and anxiety like I do and those along with dementia were her primary symptoms. I know the results of her brain scan look just like the ones of HD patients in the  documentaries. I know that's what the radiologist in his report said without using the words "HD". I know that generations before all died of things such as pneumonia, suicide or dementia. It doesn't take a genius to figure out what was going on.

I hope that if I disappeared my older brother back in the UK would make sure there was a police officer in charge of my missing persons case and that the officer understood why a person with HD might run away due to false thinking. I hope the HD community would come together to help him, as they are Amy's sister Margie.  

You know what else I hope? I hope someone will bother to be troubled, just a little, and make sure I'm okay and comfortable. We did that for Mum and without those memories I don't want to think of how I'd feel now. I'm not asking for the world on a plate here, just someone making sure I have medical insurance and I'm in a bed that is comfortable.




What I don't hope for is someone to be tending to my every need. Look, only once have I had a relationship that was serious enough I would even consider marriage. My shrink says that I push people away before they can become that close. Perhaps he's right. I don't know.  I do know that it would make sense after seeing what happened to my father once my mother died from her own hand due to her HD. I know I don't want to put anyone through that.

Its as the couple sang at the end of La Vie Boheme (Third video down at the link) "No one's perfect, I've got baggage."  "Life's too short babe, time is flying, I'm looking for baggage that goes with mine."  Well, I haven't found anyone who's baggage goes with mine yet. I haven't ever led anyone to believe that their's does because chances are there isn't anyone who's baggage will match mine. In fact I've always gone the other way as I've said above. Sorta like Neil in this song.



I'm playing this next song because my anti-D and mood stabilizers are starting to work tonight putting me in a better mood. I took some time to explain to J how I felt about the Twitter thing and she had no idea. "They call it the WORLD Wide Web for a reason, Honey" is actually how she worded it. In fact she apologized and is sitting here on her side of the bed reading her book while I finish this on my laptop. The book is one of my late friend Penny's: Mark Bowden of Black Hawk Down's newer book Guests of the Ayatollah: The Iran Hostage Crisis: The First Battle in America's War with Militant Islam. I'm going to curl up in a few minutes myself.


First I want to end with a few words from my Doc today. He asked me if I didn't have any feelings for J why the hell was I so wrapped up around her and cared what she though and said. Why was she able to influence my attitude so much? So I did I lot of thinking between the lines here in this entry today.



I know it sounds weird after all my ramblings but I really had some things I needed to think about today. You see, I think I might be falling in love. This isn't supposed to happen. Not to me, not now.


Is love so fragile...
And the heart so hollow
Shatter with words...
Impossible to follow
You're saying I'm fragile... I try not to be
I search only... for something I can't see

I have my own life... and I am stronger
Than you know
But I carry this feeling
When you walked into my house
That you won't be walking out the door
Still I carry this feeling
When you walked into my house
That you won't be walking out the door

Lovers forever... face to face
My city or mountains
Stay with me stay
I need you to love me
I need you today
Give to me your leather...
Take from me... my lace

You in the moonlight
With your sleepy eyes
Could you ever love a man like me
And you were right
When I walked into your house
I knew I'd never want to leave
Sometimes I'm a strong man
Sometimes cold and scared
And sometimes I cry
But that time I saw you
I knew with you to light my nights
Somehow I'd get by
First time I saw you
I knew with you to light my nights
Somehow I would get by

Lovers forever... face to face
My city or mountains
Stay with me stay
I need you to love me
I need you today
Give to me your leather...
Take from me... my lace

Lovers forever... face to face
My city or mountains
Stay with me stay
I need you to love me
I need you to stay
Give to me your leather
Take from me... my lace
Take from me... my lace
Take from me... my lace


Catch Paul Ware on Facebook or Twitter

Friday, 7 October 2011

Ahearn story, More Depression,poetry and other news

First up, a new article on Amy Ahearn is here with more details. Please read, share and the closer you live to Norwalk or Cerritos (auto square!) the better. I'm an hour north but will have a few copies made up to post in high traffic areas. 


Next up, I'm exhausted. I'm beyond exhausted. I'm sick to my gut and was only able to keep soup down last night. I felt terrible as my girlfriend (as Facebook nicely says "It's Complicated") had made a nice dinner. I felt just awful. Then today before the plumber came back I made it to my dad's and to the bank to get my current living will notarized. Now I need to xerox it and mail it to the California Secretary of State. I recently discovered in California  you don't need to be a citizen to take advantage of this service. For ten dollars I'll have an Advance Directive that "moves around the state" with me, that is peace of mind. 


This is the Future, a band made up of Martyn Ware and Ian Curtis Marsh of Heaven 17 before they added a vocalist to become The Human League. Ware and Marsh left several years later, when Philip Oakey took the The League's name, large debts to Virgin Records and added Sue Anne Sulley and Joanne Catherall to cover for the now lack of Ware's higher tone backing vocals. I really like The Future's sound. 

I went down for my nap after the plumber left and woke up early, it was 5 p.m. but felt like I'd slept so late I missed dinner. What scared the crap out of me was before I'd even opened my eyes I was thinking to myself "Enough of this, I give up." Its times like this I am so very thankful I'm not living alone. I immediately told her what I was thinking and she's brushing it up to the remnants of my old carb heavy diet combined with lack of nutrition the last two days. I hope she's right, but I know who to call if I need professional help which is half the battle. 




Then I drank some Gatorade to be safe until I ate dinner. I've been in a bit, okay a lot, of pain the last few days as well and the pain meds I take upset my stomach. I wasn't the brightest bulb on the block when I refused to take my anti-nausea pill. Its in the family of anti-psychotics as most of them are, and make me uncomfortable. Tales of things which may come in the future so-to-speak have a tendency to spook me. As a consequence my anti-depressant and mood-stabilizers came up at night. Next time I'm taking Naproxen instead of the narcotic. This is a second time since January I've had trouble with a narcotic pain killer. 





For all I know the depression could be a blood sugar issue or med withdrawal. Just in case I  need to make an appointment Monday to see the doctor about blood work.



. Berlin- The Metro

While waiting for the bus (I didn't feel safe to drive today) I was reading an interesting piece in Trish Dainton's book Curse in Verse & Much More Worse (pg 92) today that really struck home. According to a prominent HD researcher the unknown part of the brain that enjoys and appreciates music does not turn off in the degeneration of Huntington's Disease.

 I think the premise of this blog is proof of this!

Catch Paul Ware on Facebook or Twitter

Monday, 26 September 2011

Survived the DMV, Amy Ahearn and more.

Please take a good look. This is Amy Ahearn. She's been missing for a few weeks now. She is suffering from psychiatric symptoms related to her Huntington's disease. Last seen in Norwalk & Cerritos in Southern California. 


If you live in these areas, would you please distribute this flyer on your facebook or any other way to help Amy's sister be reunited with her? 

Thank you.



I've been Facebooking and tweeting her flyer daily. Amy lives about a hundred miles South from me. I'm really concerned for her.

I survived the DMV today, yes I did. It wasn't very bad at all, and I was in and out of there. There were only three people ahead of me so I got my duplicate license right away.



If you aren't in a decent enough mood you may want to skip this next song. Its the Cars song drive, sung by their late guitarist Benjamin Orr. These guys had the guts to bring a full Fairlight CMI onstage with them at Live Aid. Talk about being insured, those synthesizers cost 20,000 pounds sterling new.



From the Cars to Paul Oakenfold performing some Trace.





I was asked on Twitter earlier if the back pain I alluded to in my last blog is related to my HD. Its actually an old sport injury from my pre-HD days.

I hope to find you well rested tomorrow.

Catch Paul Ware on Facebook or Twitter