Posts Tagged ‘Kiss My ALS Fundraiser’

A Big Beautiful Shout out! Malachi Leopold Saves the Event!

Monday, February 15th, 2010 by annemarie
Malachi Leopold & LBRB Productions

Malachi Leopold & LBRB Productions

I have to GUSH for a minute…with all the last minute details and business of the Kiss My ALS Fundraiser there are NUMEROUS people to thank. But one man is responsible for saving the event from visual obscurity: Malachi Leopold of Left Brain/ Right Brain Productions. We’d never met, but as fate would have it he contacted me from an event flyer at the Mark Carter’s Networking for a Cause event on Feb 4th at Fado Irish Pub. Malachi generously offered to video the event for posterity, and it’s a good thing he did as our 2 photographers DID NOT SHOW! HE SAVED MY ALS! Seriously.

If not for him and his generosity there would be no professional photographs or visual record of the event. I don’t know what happened to my other 2 photographers, but shame on them! And shame on us for not thoroughly inspecting their commitment to document the event.

Thank you from the bottom of my heart Malachi!
With out you no one would have captured the joy, celebration and spirit of the evening.
I am forever grateful.
Your new BIGGEST fan,
Anne Marie

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Left Brain/Right Brain Productions is a values-driven production company with a triple-bottom-line mission of “People. Planet. Profit.” We strive to run a profitable company while making the world a better place at the same time.

We work with both for-profit and non-profit organizations in the Chicagoland area, providing advertising, marketing and promotional video content for television and web distribution.

The economy has taken a toll on the non-profit sector, and Malachi Leopold, President & Executive Producer of Left Brain/Right Brain Productions, has doubled its efforts to provide ways for Chicago’s non-profits to creatively and effectively tell their stories and continue raising the funds upon which their missions depend.

To lean more about Left Brain/Right Brain Productions please visit www.LBRBProductions.com

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Telling the truth…

Monday, February 8th, 2010 by annemarie

I did not realize how much time and energy I spent on hiding the impact of ALS on me, from others in my life, until my last post. I have realized in the last few days just how often I will supress my communication so I do not worry others, or I will manage myself to look good for events/ meetings/ occassions and then come home and crash…I have let go of some of that urge to keep it on the down low this past week. It’s time to start telling the truth and letting people in on what’s actually happening.

I need more rest now. That’s just how it is, and I’m struggling to be with that’s just how it is…which is odd for me. Usually I am more than eager to grasp what’s so about any given situation, because I know if I can get down to what’s accurate I will always have power around a situation. I guess it started when the emotions were beginning to interfere with me being with my clients. You see as long as the spotlight isn’t on me, I’m good. No worries. I’m present and focused and right in the conversation. However, the moment I am asked about myself, I get teary eyed and sad and my jaw is paralyzed into a 2 yr old’s pout complete with protruding lower lip!
I feel like a Dr. Jekyl, Mr. Hyde situation….powerfully coaching and making a difference one moment/ an inconsolable crying emotional wave rider the next. So I’ve kept the focus on others during my days as much as possible, however as my energy has flagged I see the need to be more forth coming about slowing down my pace.

I’ve created a disconnect for people I think, because the person they see isn’t what they hear when I speak … and the person they interact with isn’t the person who needs 2 naps a day and 2-3 days of rest on the weekends. Or maybe it is…and I just need to communicate what I need and tell the truth. I now see that I’ve been distancing myself by not communicating what’s accurate about my condition and what I now need and will soon need to keep moving, being productive and living powerfully with ALS. I don’t feel like I’ve been in denial, more like I’ve been acting or hiding what’s really going on. And that’s just ridiculous! I started this blog so I could have a venue for expressing what was really happening, so it’s time to tell the truth and ask for what I need!

Only – I suck at asking for what I need – this event has taught me that! My identity is still wrapped up in the “strong like Bull” vision of myself even though I’m half way into a wheel chair…and back to sleeping 12+ hours on my time off, which is 3 days a week. If I don’t completely shut down for 2-3 days a week I’m useless the other 4. UGH. I intend to emulate the woman who I helped across the street last week…primal scream therapy is for me!

Here’s a few things I need that you may be able to assist me with:
You may not know someone, but you may know someone who know’s someone….ya know?? At any rate…

I need a PR person to assist me with my business, next years fundraising campaign ( which I intend to take national ) and getting my story out.

I need sales people to market and sell my executive coaching programs in the Chicago, Denver and Los Angeles areas. I have program leaders being trained, but what makes a good program leaders may or may not make a good sales person!

I need a good internet marketing person who can produce results…I know my program is effective – amazingly so…and I realize in this market it’s 10% quality of content and 90% marketing… this person needs to be able to convey the authentic value of the Master Plan and actually give a poo about altering the way people are managed…and how they manage themselves.

I need a biography writing partner…I have enough books in the works – I need assistance on this one.

I need 400 smiling happy faces at my fundraiser Weds eve…2-10-2010…500 N Lasalle…7-11pm…

then I need a vacation!

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tick tock tick tock…

Monday, February 1st, 2010 by annemarie

What’s that quote by Gandalf in the “Tale of the Two Towers”? Something of the order of…”Years and Years of waiting for people to get it together and suddenly I don’t have enough time!” This is a gross extrapolation on my part, and it’s exactly how I feel right now!

It could be because my event – the 1st annual Kiss My ALS Party/ Fundraiser begins in 10 days, or it could be that my surgery to install a feeding tube is now being pushed with the vigor of a broke used car salesman, or perhaps it’s because my energy has been lower and I’m behind on writing the workbook for the Master Plan program…AND we launch our 1st teleseminar February 18th! visit www.masterplanseminar.com for more information…either way all I can think about it there’s not enough time and the pressure is on!

I am not yet in full panic about the event – even though I can see I have tried to do too much and I haven’t delegated well, and I under-estimated both the expense of the event and the tendency of folks to wait til the last minute to purchase their tickets…FYI it would be a BIG FAT SUPPORT if ya’ll could buy your tickets SOONER aka NOW rather than later…so I can get a bead on the attendance. Please go to the event page on this site or to www.als.net and visit their event page to register…every dime we take in goes to ALS-TDI and the research they are doing there.

If I tell the truth, I’ve been living inside the conversation of ” There’s not enough time” since my diagnosis in March. Before then I had no lable or context for my condition – I only had symptoms and actions to correct the symptoms. I didn’t have a community or a type of disease or any expectation of what was to come. This is both good and bad. Good in that it’s brought me a laser focus to my work and to my speaking…I simply don’t waste my breathe if what I’m about to say is trivial or not critical to move the conversation forward. Good in that I’ve devoted this year to completing projects ( always an achillies heel for me~ I’m the QUEEN of leaving it 95% done) and fulfilling on my promises. Bad in so far as I’m fighting the mind set that there is no cure or process of healing for ALS. I refuse to believe this. There must be a way. It must be out there and I will do what there is to do in the meantime to keep myself in optimal health regarless of my condition.

My “condition” is slowing me down and it’s pissing me off! Just in the last 2 months, typing has become more of a struggle, both for accuracy and for my ability to write for long periods of time. I need to take frequent breaks…in my next post I’ll blog about some tricks to conserve my energy I have recieved from my genius Speech pathologist, Harvey Ostriecher. My forearms ache, as does my back from just above my waist to my shoulder blades. The muscle twitching has gone into overdrive feeling like hundreds of fireants are busy under my skin eating my connective tissue alive along the outside of my thighs, ribcage and across my tummy.

I am being a complete and total WUSS about my by-pap machine, which makes me feel as though I am suffocating under water, and turns me into an audible blubbering drooling fish face. Pretty. I am crystal clear this is just the beginning of my surrender to machines to support my every bodily function. Lovely. What a pain in my fat ass. Honestly. I finally have the vision and purpose and life’s work question sorted out for my self and now it’s a goddamn race. Really? Too bad I don’t have the Wizard’s staff and the White stallion to ride away into the sunset with, it’s so much more picturesque.

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