Posts Tagged ‘ALS’

It’s a big fat hairy deal…

Wednesday, July 28th, 2010 by annemarie

I hope you find this funny!
I’m annoyed. One of the not so lovely side affects of ALS is a shift in hormones apparently, and while I enjoy not being as “regular” with the monthly “curse” I am sure as hell not liking the new forrest that has blossomed on my face! EW!

I didn’t have as big of a problem with it until recently but in the last 6 months the hair growth on my upper lip and around my mouth has gotten completely out of hand! Given my hands are weaker now I can no longer shave it effectively~ I can’t belive I’m even admitting that I have to “shave” . BLECH.
Free hair removal for all! Now there is a slogan I can get behind!

I know it’s not earth-shaking or tragic, it’s just one more annoying aspect of this condition AND I’ve written about other more embarrassing things like Powerful Pooping and the trouble with sex in the missionary position when you have a weaker diaphram~( you can hyperventilate! It happened to me.)
however I find this topic to be particularly embarrassing. I have plenty of italian, armenian and african american friends who will be laughing their ass off at my discomfort with my newly found facial hair issues…as a blonde austrian nordic mix it’s all new to me!

Just another moment when you go, REALLY? This TOO? BLECH.

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I’m not Dead Yet! (God Bless Monty Python)

Sunday, April 25th, 2010 by annemarie

So why is it that every time I meet a doctor -even socially they are shocked! SHOCKED I TELL YOU! To find out I actually have a schedule to keep and I’m not available at all times for their appointments? How about we try treating people who are alive as LIVING.

I’m not Dead YET!

Jeez oh peez! People act like just because you have a terminal diagnosis you’re suddenly handicapped or catatonic or some such nonsense! WTH?
It’s ridiculous. The opposite of what I would expect. When Life got short, I got busy being focused: what am I doing here, what am I saying? what’s the lesson or message of my life? What difference can I make? Who do I need to be in communication with before I go? What’s the legacy I’m leaving?
I mean the truth is I feel fortunate to have had a yellow light on the road of life. At least I got a warning, slow down smell a rose and prepare your people…

Seriously. I mean this victimology mindset is complete Bull shit. That’s a technical term…Bullshit. The expectation that I would have any interest in being a victim or being at the effect of the circumstance I am facing is intolerable. Perhaps if we started treating people with a serious health challenge as if they had something to say to the rest of humanity that would make a difference, we could get somewhere! How about having a conversation for OPTIMAL WELLNESS IN THE FACE OF ANYTHING… instead of a support group indulging in the abuse of kleenex.

It’s almost as shocking to them as the fact that I am not on ANY MEDICATION. None nada nothin. I’m taking some supplements and a higher dose of Vit D…which I’ll share about when I have more research…but NO meds.

Look, I did have a dark time…the 4 weeks in 2009 between hearing the words NMD and “average 14 months to live after diagnosis” from 1/14/09 to the day in February when I found out my brother was diagnosed with testicular cancer. That was the straw that woke me up out of the confusion and Slapped me right back to my attitude of “KISS MY ASS THIS IS GOING MY WAY!” which has been my motto for years. I had been confused because the doctors were telling me I was dying but I didn’t feel like that at all! I had been doing fine – adjusting to my new limited speech which was 10x’s better than it is right now after that damn peg tube surgery! So I had about a month of “woe is me I’m so sad” before I got to my RAGE against the Machine: “Fuck you I won’t do what you tell Me!” ( Relax folks it’s a song title) Anger isn’t bad – it’s what you do with it. To me anger is energy and fuel, I don’t look for it but I don’t avoid it either.

People are always telling me – “You’re so brave!” or “I don’t have your courage!” …and again I call BULLSHIT. I’m doing what there is to do – LIVE. And so would you. Each and every one of you would do the same thing given the choice between quitting and dying or LIVING and appreciating the moments of your life. Human beings are by nature endlessly adaptable, infinitely creative and powerful. To pretend other wise is a LIE. You may not know yourself to be that way yet, but Believe you me… you’ll undoubtedly get an opportunity to find that out so you might as well practice now! Act as IF you are…and see how that alters your reality. You might have to fake it til you make it, but so what?

What the hell else are you going to do with your life? Lay down and DIE?

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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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I wish I had a chemo…

Tuesday, January 26th, 2010 by annemarie

Yes I KNOW Chemo sucks and it’s poison and it’s dreadful and nauseating and all that Jazz, my brother went through 4 rounds of the stuff last year in his battle with the big C…but hey at least it’s a treatment! I was suprised too find myself mildly jealous of the opportunity Chemotherapy was for him as I watched him care for his 6 month old triplets over the holidays. So, more accurately said, while I wouldn’t wish the process on my worst enemy, I am jealous of the OPPORTUNITY that chemotherapy is for people with cancer, not the method or the concept of poisoning oneself in order to survive.

The opportunity allows for one to focus one’s mind more readily on being well, and getting rid of the dis-ease in the body. I am amazed at the array of resources for folks with cancer, oddly it feels like I’m a kid outside the candy store looking in through the frosted glass, “Oh what I wouldn’t give for a chance…” I cannot be alone in this if truth were told. Anyone with any condition that has no treatment must experience the same thing at sometime or another. The opportunity to DO SOMETHING! To put your idea into action in a way that can be measured, tested for it’s efficacy…to feel one can make some progress, priceless!

This is why research is so important. This is why I turn to alternative health practices to bolster my mindset against the foe I am facing. I HAVE TO DO SOMETHING! I get a massage every week to preserve my muscle tone and release the tension/pain in my back and shoulders. I do occasional rawfood cleanses to detox my body from heavy metals and all that our modern enviroment brings. I keep lots of plants and life around me in my home. I watch funny movies. I do the work to clear and complete any emotional/mental barrier that may be in the way of my self healing. This is why I dig up the rocks of the past and own up to my own severe case of ass-hole-ism and apologize for it to people who no longer know me. I will dig and look and transform and turn myself inside out to create a pathway for healing. So when I put my spinach,carrot,ginger,garlic,celery juice in a wine glass, next to my green tea, don’t laugh! It’s my Chemo.

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How I set the stage for my own illness…I dare researchers to prove me wrong!

Tuesday, January 19th, 2010 by annemarie

Here is my pet theory on the development of my ALS: I believe that continually placing my self in a work enviroment that had a high stress factor- one that constantly reacted my biological fight or flight mechanism and that had a rigorous schedule of 12-14 hour days/6 days a week, combined with playing hard rather than taking care of myself, depleted my adrenal system over time and damaged my immune system. I also had a diet that caused alot of inflamation in my body: lots of caffiene,diet soda, nicotine,dairy, soy and meat and one that was for the most part low in nutrients while high in calories. The key I think was inadequate recovery time between periods of intense activity and regular sleep deprivation. I pushed too fast too far for too long and with out the proper care and attention my body broke down. I believe that this triggered the gene that is present in people who have familial ALS as my uncle died from ALS, or it triggered ALS in me spontaneously.

When I look at the groups of people who have been identified as having a higher occurance of ALS in their population I see some common cultural threads. We have Combat veterans from the Gulf war, Professional football and soccer players and Type A personality executives who, research tells us, are more likely than the general population to develope ALS. Now 2/100,000 versus 1/100,000 cases doubles the occurance but doesnot emcompass a large population as there are only about 30,000 people with ALS at any given time. That number stays fairly steady due to attrition, read death. However, if we can extrapolate the common enviromental threads and eliminate them perhaps we can diminish the occurance of ALS in these groups and the general population as well. Given only 10% of ALS is familial and 90% of ALS is spontaneous this deserves a conversation about prevention. I would not wish my symptoms upon my worst enemy. The experience of disintegrating before your own eyes isn’t pretty and the discipline it takes to maintain a positive mindset in a world with no cure is relentless.

So what do we know about these professions that makes them a breeding ground for this particular dis-ease? Well, they have a common language… the language of war permeates the cultures. Appropriately so in the case of combat military, however the same language exists in professional football in the US and Professional soccer overseas. I found it very telling that this year the Cincinatti Bengals brought in a Navy Seal to talk to the team about “fighting in honor of” their fallen comrad after the tragic death of a young player. It has been said that language creates our experience of the world around us. If people really believe they are in a fight for their job or survival, based on performance, the “life” or death of that “life” which comes from their job can be excruciatingly real. Professional athletes are always fighting to keep their position on the team. While this struggle may not be a literal matter of life and death, it is very much a battle to remain in the world of professional athletics, which could be the only dream that person ever had. This is when “It’s not like anyone has a gun to your head…” feels very much like someone has a gun to your head.
Many corporate cultures also promote the thinking that they are “at war” with the competition, fostering a state of emergency in their work enviroment. My work enviroment was like that…there was a delibrate concerted effort by the upper managment to foster an ethos of emergency…CONSTANTLY, and regardless of what ever results had been achieved. I actually spent 5 quarters living in the experience of failing when the truth was I was the only bonus-able performer on my region’s staff for those 5 quarters. When I found out I was actually performing well I felt completely duped, and cheated of any sense of accomplishment, even though they gave me a raise. I believe working in an enviroment of perpetual emergency is harmful to the business by virtue of it’s unsustainability and equally harmful to the health and wellness of the staff. It’s simply not accurate and has no integrity. Unless you are in an emergency room OR you are in a war zone- Where that would be accurate, though if the people are in there too long we know it has long term effects on their mental, emotional and physical well being.

There is something about the cycle of cortisol combined with the continual rush of adrelaline that is a nasty, dis-ease producing super-combo. It’s time to start telling the truth about what makes us sick. It may not manifest the same way in all people, however setting the stage for destruction and setting ourselves up to win are two totally different things.

I don’t know if I would have changed my behavior had I known about the destructive effects of my enviroment, but at least I would have been informed and had the opportunity. I had a vaugue feeling that this atmosphere of continual PRESS can’t be good for me over the long haul, but it wasn’t until I was on the outside that I saw clearly just how destrucutive it was. You’d think that gaining 70 lbs over 6.5 years would have been the wake up call all by itself, but I’m a stubborn one! I urge you not to be as hardheaded as I was and to manage your sleep and your stress levels in such a way that you are set up to win over the long haul ~ not solely driven for the immediate results, no matter what.

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Sticky Situation: Dating with ALS

Thursday, January 14th, 2010 by annemarie

Exactly how does one go about dating when one has a chronic illness and/or a terminal diagnosis? Anyone?

I am reminded of the line in Spamalot, ” I’m Not Dead Yet!” So I am trying to navigate this issue and I find myself with out a rudder or a sail. I gravitate to those who knew me before my symptoms began, finding comfort in the knowledge that they have seen me at the top of my game. It makes up for me feeling somehow lesser now, as in fact my capacities have diminished. I no longer sing, or even speak all the time ( I am well aware this may make me more attractive to some!). I try to have 2-3 days of not speaking per week to save up my speech for the 4 days I’m working.

I remember telling the boyfriend I was with as my symptoms became more pronounced that I felt like I was loosing my ability to kiss. He dismissed this as ridiculous, when in fact it was completely accurate. I have found myself recycling former relationships, and lets face it, while those men are fabulous, there is a reason that it didn’t workout the 1st time. So here I am, wondering is it even fair to prospect for a relationship given my expected life span and all the complications involved with the progression of ALS? Or am I just being a chicken shit?

Suggestions anyone? Other than prayer I’m fresh out of new ideas…

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I’m a spectator internally and externally to the progression…

Sunday, January 10th, 2010 by annemarie

It all feels so strange. When I am alone and I’m quiet I almost forget I have ALS. I’m not talking so I’m not reminded, at least that’s how it was until this last month. This Christmas it became difficult to stand up from a squat or get up from a chair. My left leg is fading fast….the majority of the twitching muscle activity had been in the left leg for the past 6 months. my doctor says not everyone feels the twitching 1st, but I sure do…it’s my harbringer of decay.

Last May when I did a rigorous raw food cleanse the twitching stopped for 2.5 whole months….it just went away, then returned when I added caffiene and more cooked foods into my diet again. It returned with a vengence. So next Monday I will begin a raw food regime again and see if it has the same impact. Cutting out caffiene is going to suck but so what!?! If I can delay the twitching perhaps I will extended my time and preserve my stregnth.

I believe I may have taken my last independent trip. Fairwell privacy, fairwell. Things have gotten so damn awkward! I can’t open water bottles and once opened I invariably spill or drop them. In fact the dropsies have become a daily occurance, it used to be occasional however now it’s consistent: I’m always dropping something. I know I should be gratefull that I’m still walking around but for someone who used to spin around in pointe shoes this is a pain in my AAA. For those PALS who were athletes with a high level of kinesthetic awareness, this process is a damn nightmare! As if all your cellular memory was robbed from you one night or better yet blocked- you still have the memory of how to execute a move, step or motion flawlessly but the message is picked up and spirited away before it can hit the muscle that’s just aching to perform. ANNOYING.

My meat is hanging off the bone. It’s as if the connective tissue that binds the muscle to the tendons and bones is missing and the only thing holding that muscle near the bone is the skin. The same with the skin that now hangs from the muscle as though it’s no longer interested in being associated with it. At almost any angle I can feel bone 1st not muscle -I am not skinny and I have alot of muscle. I was strong like bull! I actually think all the weight training I did in college and gradschool is the only reason I have been walking this long. I used to have traps like a man…now my neck muscles are so weak I can’t read laying on my stomach for more than 2-3 minutes at a time. I am constantly concerned about herky jerky cab drivers and possibly injuring my neck in the cab so I push my spine back into the seat to support myself.

I had intended to write for most of the day today, however I rested instead. The tremors had returned to my face while I was in California, nasty little bastards that they are. They were gone for 2 years but now they’re BACK. On my face mind you! My once so pretty face…my mouth is now pulled into a perpetual frown by the twitches on the right side of my smile like a fish hook pulling my lips down toward my jawbone. Then there is the one that feels like a piercing through my left eyebrow creating a V in the browline from time to time. But my favorite has to be the slight mobile tingle from the inside of my left eye socket running over the bridge of my nose and trailing off in my right cheek. Lovely. So I rested today, hoping that it was fatigue from traveling that spurred the facial twinges. So far it eems to be working…I’ll keep you posted.

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My Mission or why I get up in the morning

Thursday, January 7th, 2010 by annemarie

My mission is to transform the way people are managed in corporate America, such that management by threat is extinct and managing for the wellness of the whole person is the norm. I believe it behooves any company to do this and it will positively impact their bottom line. The Master Plan is a clear pathway to managing for sustainable high performance and the health of one’s employees and oneself, without being invasive or awkward. This program fosters accountability and trains people to manage their mental, emotional and physical space for sustainable excellence and wellbeing.

In 2006 I left a job which demanded more than my failing speech could deliver. Over 6.5 years I had managed, coached and trained thousands of individuals, by the last few years I was accountable for training an average of 300 leaders and managing their results in 30-60 events/wk. I had loved my job,and it was one of those cause/jobs, except for a few things: I hated the hours, the results at any cost mentality and the “press” of it or what I would now call the manufactured state of emergency that was ever present regardless of one’s actual performance.

I believe this enviroment had a direct impact on my wellbeing over time and in this way I contributed to the development of my condition. The hours 75-80 hours /wk combined with the PRESS and the continual activation of the body’s fight or flight system from 2-3 times a day to once every hour PLUS an eat on the run diet coke filled empty nutrition habit formed a perfect storm which pummeled my immune system. There was no recovery time, no release of tension; I was strung like a violin and it took me hours and more than 1 drink to wind down most days. My work dominated my life, my dreams, my friendships and when I was on vacation I would most likely be collapsed on a couch with a twice annual sinus infection.

It took me 6 months to feel normal and hear myself think after I left. I went parttime in June and within 2 weeks my headaches/jaw pain went away. The first 2 months I slept 18 hrs/day, then 14hrs/day for 2 more months…I lost 25 lbs of the 70 I had gained in my 6.5 years there. During this time I contemplated what didn’t work for having sustainable results in that enviroment and why that company had such horrific turnover despite it’s committment to high performance. I came to believe that sustainable high performance is a function of a high level of self care, and in fact self care can be a primary access to sustainable excellence. I combined this with the structure of thorough planning ( trust me it took some mega watt planning to manage 300ppl by phone!) and began to develope the Master Plan program.

“The age of the proudly sleep deprived diet coke infused executive is over. The time for treating our human resources as precious and renewable has come.”~ ME

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Kissing 2009 Goodbye!

Sunday, January 3rd, 2010 by annemarie

I have a whole process I do to put a year to bed, and powerfully create a new year: you can find my step by step instructions on my Facebook group -Care and Feeding of a High Powered Professional. I’ve noticed most people don’t take the time to powerfully complete the past year such that the “new” year can be truly newly created. Part of that process is to write out a year in review:

2009 Year in Review:
My brother Tom and his wife Danni announce they are expecting triplets
January 3rd~ I have a breathing incident while “tango-ing” with my boyfriend which sends me back to the Doc for a redux of tests
Doc says a Neuro Muscular Disorder, may have 14 m’s life expectancy
I finally get depressed vs upset; realize being in Limbo for 5.5 yrs of symptoms wasn’t such a bad thing
For the 15th time a Dr recommends anti-depressant to deal with symptom of Emotional Lability…I finally acquiese
Mid January I begin filming the Master Plan Program in executive coaching
I begin to recreate my business so the value will live beyond me
Mid February, my brother is diagnosed with testicular cancer and goes in for surgery
I immediately stop taking anti-depressants as they make me have to fight to get out of bed which has never before been a problem!
March 9th I am diagnosed with ALS after 5th MRI and 3rd EMG, life expectancy gets moved to 3-5 years with a 10% chance at 10-15, as I have always been an exception I choose to focus on 15yrs and beyond…it just feels right!
There is no medicine or treatment so I get back to a rigorous nutrition and supplement program which makes me feel like I am doing SOMETHING!
May- I do a Raw Food cleanse- and drop 20 lbs of needed fat- my constant muscle tremors STOP.
I meet Viktoras Kulvinskas during the cleanse and he recommends a 70-80% raw food diet, dietary enzymes and plenty of protien…most importantly he gives me hope and a pathway to prolong life and improve my wellbeing: I am now an Empowered patient
June 1, the triplets are born: Beau, Brody and Mylee
My brother Tom finishes 4th round of Chemo
I take a spa-cation to Vegas and LA and return feeling better than I have in years
I have an immense surge in creativity – outlining 3 new programs to write.
One day in July I loose 50% of the function in my right hand
I make plans for turning over my business and begin training others
September- My 1st fully trained Seminar leader takes on his 1st program and is superb
Participation in my programs 2x’s
In October I attend a research symposium at ALS-TDI via the web and begin to plan my fundraiser
I begin to blog
I make plans for in home care in mid 2010
By November I have dropped 40 lbs this yr due to 60-75% raw food…I needed that!
The eve before Thanksgiving Dawn Trice contacts me for an interview in the Chicago Tribune
My family has an early Christmas in Denver with the 6 month old triplets Ty who is 2.5 and the teens Taylor and Brock
I close out the year with what may be the last independent trip I take to Vegas and LA again.
As I write this I am at the Terranea resort and spa, in Rancho Palos Verdes for the weekend to create my year.

I need to acknowledge my sainted mother for whom this year was a crisis of faith given both of her children face their mortality. I also acknowledge my clients who deal with my ALS accent: with out you my life would be all about me and that would just suck. You are the pathway to me fulfilling on my mission and the reason I get out of bed in the morning, Thank you for your work! I acknowledge Facebook, without which I would be disconnected from my community, friends and family as I cannot be understood on the phone. I thank all of you who read this blog and allow yourselves to be impacted by it, the support of the people I have met in the ALS community have given me another reason to be active and engaged versus supressed and inert.

Thank you for your time and consideration, please take a moment and make a difference for someone today!

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Alternative therapies that make a difference:

Saturday, December 26th, 2009 by annemarie

Disclaimer: I am not a doctor though I have seen one played on TV; which merely qualifies me to hawk an over the counter painkiller… (and Pharma Co’s if you are listening~can we get a liquid aspirin/ ibuprofen etc? with out having to take cold meds? Thanks for getting right on that.)

I am relating what I have heard from other patients and experienced myself.

Damon Storm wrote me recently regarding the effectiveness of Qi Gong in managing his sarcoidosis…which has some symptoms very similar to ALS including occasionally slurred speech and difficulty breathing. He is completely without medication and thriving. I also was told about the wonders of Qi Gong through the remarkable film by Ben Byer, “Indestructible”. I highly recommend this exceptional film for all people, not just those of us touched by ALS. You can get more information at www.indestructiblefilm.com

Certainly, I am buying the book Damon requested I pick up “Qi Gong for Beginners” by Stanley Wilson.

In an earlier post I referred to the success I have personally experienced with adding lots of raw foods to my diet. Not only has the increase in fiber assisted in the smooth move department, but the increase in my energy level has been unprecedented and immediate. Even though I can no longer chew most salads I have been delighted by the variety on foods and recipes in the world of raw food. I usually stick with fresh fruit shakes in the mornings supplemented with hemp protein powder, ground flax seeds, liquid vitamins and greens( as in Perfect Food Greens) and spirulina. I also make several types of juices from fresh veggies. The Chicago Diner, Karyn’s Raw Cafe and Karyn’s Cooked ( www.karynraw.com) are 3 of my favorite local Chicago resources/ restaurants for vegan and raw food delights.
I will add a list of cook books or uncook books as the case maybe, in the future.

When it turns colder in Chicago, I have difficulty sticking to the raw food and I am drawn to more warm veggie dishes. Keep in mind I am not a vegetarian, in fact I have been an avowed carnivore much of my life, and I am a committed foodie as well as a certificate level Semollier since 1998. This is one of the reasons being reduced to a feeding tube is borderline unacceptable for me. However, regardless of my love of a great steak, venison roast or Lamb chop the difference in my overall energy level is undeniable when I focus on uncooked fruits and vegetables. Eating closer to the sun, I call it. 2-3 times a year I also participate in a raw food cleanse, for a month I will only have raw foods and I will do a 7-10 day veggie juice fast.

Interestingly enough my doctor had no dietary advice other than eat well, until I mentioned my intention to do a cleanse and to thereafter stick to a 70-80% raw food diet. Then we had nutritionists and concerns form my weight loss coming out of the woodwork. And I needed to drop a few lbs. I could actually lose 20 more and not be unhappy. I am conscious of keeping up my protein with nuts, protein powder, beans and the occasional eggs, fish and meat.

I have to attribute the fact that I am still walking and moving around so well due to a weekly massage. Every week for the past 3 years I have had a massage for 75 minutes at least. My muscle tone and overall strength is still pretty good, though I can no longer walk long distances along my beloved lake front, and the last 6 months has seen a marked weakening of my neck muscles.

I also highly recommend chiropractic care, upper cervical chiropractor Dr. Dan Fedelli, actually restored my smile after the right side of my face fell… it was lopsided for almost a year. I definitely notice the difference in my overall well being when I see him regularly and when I don’t, and he’s great about telling you when enough is enough.

I almost forgot my FAVORITE discovery: Bach Flower Remedies. For the first 4.5 years of my symptoms I had no diagnosis and was constantly dealing with the upset and uncertainty of the unknown. Little did I know I would yearn for the “unknown” in the months directly after my diagnosis! The result was emotionally I was ok as long as I wasn’t focused upon myself and my situation. The moment I had to speak of it with others I would tear up, especially at Doctor’s appointments out of shear frustration. Every single physician and specialist I saw recommended anti-depressants. It made me sick! I wasn’t depressed I was UPSET! Big difference. Anyway; the best thing that came out of my diagnosis was finding out emotional lability is a SYMPTOM. I wasn’t crazy and hyper emotional it was a freakin SYMPTOM! In retrospect it was perhaps the 1st symptom I recalled. Instead of dealing with anti-depressants, which in the 3 weeks I broke down and tried them had only made me more depressed and lethargic…I turned to Bach Flower remedies at my local Whole Foods Store. They are amazing and effective. I only take them when I want to or feel the need for support. There are no side effects. Only a mood stabilizing effect that allows me to get on with the business at hand.

So far we have Qi Gong, Raw food diet, Massage, Chiropractic care, Bach Flower Remedies and a must see movie. I have had some fantastic energy healing experiences, and dabbled in acupuncture though not enough to attribute any specific results.

I’d love to hear from you as to what you have experienced and had success with in reality.

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