“Wanted: Chronic Fatigue Syndrome Caregivers!

Act Today !
Battle The Thief That’s Stolen
Your Loved One’s Health And Your Freedom!

“Finally – Get the hope, help, and care that you want for your
CFS-CFIDS-M.E. loved one – and yourself!”

A CFS caregiver reveals how to get the support you want and need for this misunderstood and forgotten illness.

Dear Loving Caregiver;

As you know, for anyone dealing with this sickness, common experiences include being

• tired of feeling stuck and lonely as a CFS-CFIDS-M.E. caregiver – and that even your loved one doesn’t understand?
• In a constant struggle to explain the confusing CFS-CFIDS-M.E. symptoms

Frequently, a loved one’s symptoms of Chronic Fatigue Syndrome make Caregivers feel chronically overwhelmed, exhausted, lonely and frustrated from too little support.

If you can identify with any or all of these experiences or feelings, this could be the most important letter you ever read! Let me tell you why.

Hello - my name is Ann Corcoran, and I’ve been taking care of my older brother for 7 years. He has been severely disabled from the sickness of Chronic Fatigue Syndrome (CFS/CFIDS/ME) for 20 years.

I have devoted my life and career to helping the disadvantaged and disabled. During this time, while married to a wonderful, physically disabled man for 30 years, I earned a Masters of Science degree in Special Education, and trained others to teach and become advocates for physically and mentally disabled children.

I specialized in analyzing what it takes for a person to learn and accomplish something and in teaching them, step by step, how to learn and get something finished.

 And yet…

My brother’s Chronic Fatigue Syndrome
had me stumped!

Here’s why:

Many years ago, when I picked up my brother from the airport after not having seen him in years, I was shocked. This was not the smart, funny, high energy guy I remembered growing up with.

Sure, he’d tried to explain his illness – but I just didn’t understand what he had gone through until I began to live, face-to-face, with CFS every day, like you do.

I’d worked with disabled people, but Chronic Fatigue Syndrome was completely different!

Pretty soon I discovered that dealing with my own sibling’s chronic illness made me tired – and I felt resentful and guilty.

Does this sound familiar?

When some of my brother’s symptom’s weren’t so bad and he felt able to speak, he explained why Chronic Fatigue Syndrome was more than just chronic “fatigue”.

This was severe fatigue, worse than any “tired” I’d ever seen – and it lasted for weeks. Sometimes, for days and days, he couldn’t get out of bed at all. Because he was also suffering from chronic muscle pain, chronic headaches, chronic everything!!

He also had chronic cognitive skills impairment.

It was so sad.

In his 40s, he was a highly successful Sales and Marketing Executive who put together - and won - multi-million dollar sales.

Now he was destitute, homeless, and couldn’t think his way out of a paper bag.

And yet, sometimes we had so much fun, I forgot he was sick – until a few hours later when he was sick AGAIN!!

“How could that be?”

I couldn’t understand it…How could he be okay one day and then sick for a whole week!

My friends did not believe me and told me my brother was lazy and if he just stopped acting like a victim, he’d be okay!

I felt sick at heart and so alone …

Dealing with CFS was driving me crazy.

Yes, I knew my brother was sick, but still resented that he was in bed when I left and still in bed when I got home -- when I had to go to work all day.

His short term memory loss made him put things away in odd places and then he couldn’t remember where he had put them!

My house was a confusing mess. I felt angry…and then I felt guilty.

Our relatives lived far away and they didn’t understand anything about Chronic Fatigue Syndrome symptoms. As a sibling of CFS, I felt totally and utterly alone.

I learned that in families when one sibling is chronically impaired, this can be common.

Sibling support for chronic illness – any chronic illness - can be rare.

Nobody I knew had ever heard of this “chronic fatigue stuff”. Even my own doctor pooh-poohed the whole idea of CFS.

He told me, “Chronic Fatigue Syndrome is just an excuse!” He said that CFS “didn’t exist!“

Other doctors told me there was no cure for chronic fatigue - as if my brother wasn’t also suffering from so many other symptoms at the same time!

CFS was turning my life upside down!

The doctors couldn’t help - especially since the cause of chronic fatigue syndrome isn’t known. They didn’t know about chronic fatigue syndrome drugs, and their training led them away from recommending any alternative therapies for anything.

Stunned by my own strong emotions, I stayed up for hours late at night searching for information. What really was the name of this illness, anyhow?

Chronic Fatigue Syndrome?
Chronic Fatigue Immune Dysfunction Syndrome?

And why was it sometimes called Myalgic Encephalomyelitis – who could even SAY THAT?! And all those initials – M.E., CFIDS, CFS!

My head was spinning with so many confusing names – for ONE SICKNESS!

This Whole Thing Felt Like A
Big Fat Chronic Headache!

I couldn’t believe that my life had changed so much. I wanted to help my brother, but felt so burdened -- and guilty about how I felt!

I remember the jokes people used make about this “yuppie flu’ and “chronic fatigue syndrome”.

“I work so hard that I’ve always got “chronic fatigue!” they would joke…

Truth to tell, I had said those things myself.
I felt guilty, tortured, angry, and tired.

I had NO idea where to turn for help!

It took a lot of time and research, but FINALLY, I learned where to get support.

I learned the reasons that some people prefer one name over another – but that we were talking about the same sickness my brother has. I mostly use CFIDS and CFS, while people who live outside of the U.S. favor M.E.

I learned that even though there isn’t a Chronic Fatigue Syndrome cure, there are support groups and associations, there ARE alternative treatments for CFS-CFIDS-M.E.

I learned the right words to use -- how to be a good advocate for my brother -- and I took him to one of the USA’s top doctors for Chronic Fatigue and Immune Dysfunction Syndrome.

I got him help. He’s still got CFIDS, but now he has a happier life.

And so do I.

And, MOST IMPORTANTLY, I learned how to talk with my brother so we could both say – in a healthy way – how we felt.

Our family began to understand – unbelievable loving support!

Listen…I’m not saying life is now peaches and cream.

Sure, my brother’s CFIDS still doesn’t have a cure, and it still knocks him down. He and I still have all our feelings – and we both pray for CFIDS to go away forever.

And sure, my own life has changed, but it’s somehow even better, now that we’ve found coping skills for this chronic illness.

We’re closer – to each other and to our friends and family. My co-workers and boss understand when I’m tired or showing my feelings.

We have help, understanding, and support. It’s not always easy, but we’ve found ways to bring more joy, more love, and more hope to our lives.

Suddenly, I realized something…

It’s not right for me to keep this information about CFS to myself – because YOU deserve help for your loved one and hope and relief for yourself. YOU deserve to enjoy life, too!

Here’s the little story of what actually happened to change my circumstances:

After about two or three weeks of my brother’s feeling too sick to go out, he was finally feeling okay enough to get out of the house. We were slowly walking across a parking lot to hear some folk music.

Something you should know about my brother is that he is known to all as a bright, funny, articulate guy with a terrific interest in folk music and musicians. In fact, he’s a musician himself, who at one time had a very successful career in computer sales and marketing.

For me, someone who now understands his illness, his seeming to “fall off the face of the earth” for months at a time – for no apparent reason at all – makes sense. But, for many others, you can understand why it is mostly quite puzzling.

Well, on this day when we were out, we bumped into an old friend of his, who exclaimed, “Hey – I haven’t seen you in a while!” upon seeing my brother.

Who responded, “Yeah, haven’t been able to get out. I’ve been laid up with this sickness I have – chronic fatigue syndrome.”

Friend: “Yeah, fatigue – don’t I know it!”

Me (muttering under my breath to brother): “No, he doesn’t know, he doesn’t know.”

My brother, to me, under his breath: “No, he doesn’t know. It’s CFIDS. How could he?”

I knew, of course. And my brother knew – and YOU know - But Peter, our friend, THOUGHT he knew. AND MOST people think they know – but most people still don’t!

And you want and need them to know.

Well, later I took his friend aside and told him what Chronic Fatigue Syndrome is like - really like.

That week, that same musician friend called my brother to ask how he was. My brother could barely lift the phone, but boy, did his spirits rise! Someone actually CARED!

Now, my brother feels understood, KNOWN – and this friend greets him extra warmly, helps him get a chair when my brother can come to a standing-room-only event. Now, I’m not the only one looking out for my brother at concerts and get-togethers now. Now, when my brother can’t come to an event, other friends call or email him to see how he is. Life has gotten to be more fun for my brother and me now.

And I realized…. Maybe YOU want to know how to explain CFS better.

That’s when I decided I HAD to share what I’ve learned with you and with others who are dealing with these kinds of experiences….

Here’s a secret. I didn’t start out to write a book. I just knew I needed help to understand my brother’s CFS and to get help for him and myself. So I scoured the internet and bookstores. It was so confusing! Where should I start? Who could I trust? In fact, I was searching for a concise guide for CFS-CFIDS-ME caregivers – for me to use!

Because I Know What You’re Going Through!

CFS-CFIDS-ME closes you off from the very people you most need. So you can’t socialize the way you used to.

The nature and history of Chronic Fatigue Syndrome illness makes this happen.

Before you go any further, here’s what you must realize:

Socializing is a MUST if you want to become hopeful --- because hopefulness is the KEY to a Happier Life!

You want to help your loved one – and you need and deserve help, yourself, from people who understand what you’re going through.

But , when people don’t understand CFIDS…

It’s essential for you to quickly get the help you need, as a caregiver, so that YOU can keep caring for your loved one.

That’s why I developed my guidebook for CFS/CFIDS/ME caregivers, because I know you want to help your loved one.

“The CFS Caregiver’s Guide To Hope”

Let me tell you about this extraordinary book that can give you back your life.

How would you like to….

My friend, you take this illness very, very SERIOUSLY. As a caregiver, you want to help your loved one. Maybe now and then you wish you didn’t have to know so much about this illness….

You want to ease your loved one’s suffering - You want to shout out loud…

“CFIDS is a Thief! CFIDS steals Life!”

The very sad truth is …

Now let me ask you an awkward question. As a caregiver, do you sometimes feel “doomed” too? No wonder. You keep on giving and giving out of love. The amazing thing about you is even when you feel like giving up, you keep on giving.

The world doesn’t know this about you
or your loved one.

What’s also amazing is that

Most CFIDS Caregivers Also Want To Help End All CFIDS Suffering

You, your loved one, and every other CFIDS victim deserves respect and compassion as you cope with this affliction.

True story: Radio talk show host interviewed a famous American football player. Football player changed the subject, to talk about a cause that he and his wife support – help for persons with Multiple Sclerosis (MS). The football player said that his wife has a relatively mild case, not too many symptoms. He said, “But the fatigue! It’s AWFUL. With MS, your symptoms come, sometimes they go – and sometimes you wake up and each part of your body feels like it weighs 2,000 pounds. You just can’t move. It’s a disease of the central nervous system.”

This radio interviewer was completely respectful. He said, “Oh, Multiple Sclerosis sounds extremely difficult! MS is a terrible disease and you and your wife are doing a wonderful job to help raise funds to combat MS.”

This radio interviewer didn’t need to ask a zillion questions. He didn’t ask, “MS? What’s that?!” He never said, “Your wife has fatigue? Well, why doesn’t she sleep more or get more exercise?” He already knows that Multiple Sclerosis is serious. He treated Multiple Sclerosis seriously - with the respect any serious illness deserves. So he treated the football player very respectfully.

You deserve that SAME respect -
and SO does your loved one!

CFS-CFIDS-M.E. isn’t widely respected yet, because the world doesn’t know what you and I know:

1. CFS-CFIDS-M.E. is serious.

2. CFS-CFIDS-M.E.victims are being treated like second-class citizens.

3. And so are YOU, the caregiver.

 What If You could Help Get Rid of the Ignorance and Prejudice? And…

What if CFIDS/CFS/M.E.’s symptoms became well-recognized - no matter WHAT it was called:

Chronic Fatigue Syndrome
or
Chronic Fatigue and Immune Dysfunction Syndrome
or
Myalgic Encephalomyelitis!

Try to imagine how good you will feel….

Take a deep breath, sit back… let your mind drift …to the future…to a better place and time…

In your imagination…you feel so good because…

You hear a movie star or sports star being interviewed. The interviewer asks, “Tell us about this upcoming charitable event that you are running to raise money for CFS. Some people believe that it should be called ‘Myalgic Encephalomyelitis’. Can you tell us a little about that?”

Then, what if the movie or sports star says: “My friends and I are raising money for research to help the thousands and thousands of people all over the world who suffer from CFS – including children, teenagers, and people like my husband who are in the prime of life. Chronic Fatigue Syndrome is a terrible sickness and we want to find a cure.”

Now, in your mind’s eye, imagine that the interviewer asks: “Chronic Fatigue Syndrome – Myalgic Encephalomyelitis - is a great cause, and we should all be aware of how CFS ravages its victims’ lives. How can our listeners help and find out some more?”

Imagine how happy you’ll be when you don’t have to struggle to explain what CFS-CFIDS-M.E. is like!

Stay here in this future, and enjoy all the good things you are discovering….

You mention your loved one’s CFS at work. Later, your boss tells you, “I know what CFIDS is like. There’s no problem using your sick days to take a break for yourself; I can understand why you need it.”

Your club or church tells you that you don’t have to fix dinner on Wednesday nights anymore. They’re going to bring dinner over, enough for plenty of leftovers…

Your neighbor says, “I saw a TV show about Myalgic Encephalomyelitis. Isn’t that what your wife has? I didn’t understand what both of you have been going through! How can I help?”

You mention your daughter’s CFIDS and your work group holds a raffle to raise money for CFIDS research - with a good percentage going for YOUR daughter’s care.

Your town librarian goes online and prints out CFIDS information – and makes a display of books about CFIDS so the town can learn about CFIDS.

…Hospitals in your area hold a regional symposium on CFIDS.

…Healthy children sell lemonade to benefit CFS victims

...Every family doctor knows about CFIDS – and knows some top CFIDS specialists to recommend

…A TV telethon for Myalgic Encephalomyelitis is a regular occurance

…A Walk-a-thon for CFIDS/CFS/M.E. happens at least twice a year

…Every teenager who has CFIDS/CFS/M.E. has friends who think he’s cool - call his cell phone, “message” him, invite him out and visit him

…Every child with CFIDS gets diagnosed and immediately gets help,

…Every college age child with CFS has treatments that workso he can graduate from college

…Your loved one gets treatments that works so that she/he has the ability to go back to their job

…Your standard of living increases because of additional income

…Hospitals and care facilities offer respite programs for CFS caregivers.

…Billboards and other media display information about Myalgic Encephalomyelitis

…Your city government declares May as “CFIDS Awareness” month

 …Grocery stores run charitable, “give-a-dollar” campaigns for CFS/CFIDS/M.E., just as they do for other chronic illnesses

… You mention CFIDs and you don’t get a single blank stare

…Your loved one has a treatment that always works. Always.

…You receive enough help so you can relax

What if you could take just one simple step to make that world come closer to getting the help that you and your loved one needs and deserves?

If you can, stay in this possibility that’s so much easier…

Imagine how strong you feel as you…

Ø      …easily describe CFS/CFIDS/ME, so that relatives, friends and co-workers react with the same respect that they give to M.S., or Cancer, or AIDS victims and their caregivers

Ø      …easily break through ignorance and prejudice the way you want to!

Ø      State facts that are easy to say and easy to understand 

Ø      Paint vivid and unforgettable pictures in your listener’s mind

Ø      Take the mystery out of CFIDS symptoms with specific, real-life examples

Ø      List the mind-bending coping skills that you and your loved one use - every single day

Ø Confidently state in crystal clear words that

Chronic Fatigue and Immune Dysfunction Syndrome is not ordinary “fatigue”!

 CFIDS --- Myalgic Encephalomyelitis (M.E.) --- Chronic Fatigue Syndrome …. It’s all the same stuff - a physical ILLNESS!  

As a loving caregiver, you are determined to take action to help your loved one - and every CFIDS victim - to have a good life.

And yes, you deserve a happy, good life, too. To get there, you need help.

Taking one action step at a time will give you and your loved one the help you deserve.

You have a lot on your plate. I’ve been there, and I AM there. Some times all you can do is take one small step at a time.

That’s why I strongly urge you to take action today to invest $37.97 in your life and your loved one’s life and receive the valuable free bonus gifts.

Your Purchase Helps to make the “Dream World” we have created here - a Reality!

My commitment is to You – the person who lives every single day with the often miserable effects of CFS/CFIDS/ME – and to the education of all people, who have no idea what you and your loved one live with every single day.

You and I want everyone, all over the world, to learn more about what it takes to support and deal with the under-recognized CFIDS nightmare.  

And NOW, let me tell you more about the wonderful gifts I am going to include for you which will make this an even more extraordinary offer.

In addition to gaining the knowledge you need, AND having the satisfaction of knowing that you are contributing to the public education about CFS/CFIDS/ME, you will also receive the following – as a thank you for participating in this opportunity.

Bonus #1: Report on “The Seven Roadblocks to Self-Love”

Velma Gallant, founder and owner of Welcome Changes Abundance Coaching and Training, who coaches individuals and groups to create a life of joy, passion and freedom, now teaches you the secrets of simple ways of loving yourself so you can prosper in your business AND have greater peace and passion in your life – why wait to discover this!

Value: $19.97!

Bonus # 2: 30-Minute Professional Conditional Coaching Consultation

Velma Gallant will help you map your next step. Are you transitioning to a new business? Thinking about it? Whether you want more success in your business, or if you want to find a greater balance between your business and your life - Velma makes every minute count as she works with you on what matters most to you. Velma and you will arrange your individual phone consultation for a time that works for both of you. Velma is in great demand, so she can’t guarantee her generous offer will last forever – why not go for it now?

Value: $85.00!

photo of Author Tony Masiello

Bonus # 3: "5 Parables of Inspiration" by Tony Masiello Tony, author of Whispers from the Universe, takes experiences from his childhood and more recent events and turns them into parables so YOU can learn how to look at life in original and inventive ways. This loving and gentle book is essential for reducing stress and increasing happiness! Plus, inside this bonus is a link to another very special bonus - he's reducing his fee for his Intuitive Reading just for you! The information is on the last page of his bonus! Don't pass this up!" Value: $39.95!

Bonus #4: Bob Doyle’s Boundless Living Atmosphere Environmental Sound Software will allow you to enhance the atmosphere in your home!

Bob is the owner of “Wealth Beyond Reason,” and his business is helping people attract the kind of life they most desire! Choose the environmental sounds that bring the peace and excitement of real sounds from nature right into your home! For instance, R-E-L-A-X with the refreshing sounds of a shoreline beach – the wind, the shore birds, the lapping of the waves! Or choose soothing sounds of a nighttime meadow…. Click and choose which ever sounds fit your mood – or fit the mood you’d prefer to have! Keep this easy-to-use software right on your computer screen – and make your computer a more fun and helpful stress-reliever. Enjoy the almost infinite variety of combinations of soothing environmental sounds – immediately downloadable and ready to use! This is one of Bob’s Wealth Beyond Reason “members – only” gifts but he is letting me give it to YOU as a special gift!

AND

Bonus #5: Bob Doyle’s “Experiential Meditation” mp3!

Wishing you could reap the benefits of meditation – greater serenity, new ideas that seem to flow into your mind without so much effort?? Your brain loves to solve problems – but when your brain overworks you can’t really relax - until you train your brain to focus on something that’s NOT a problem!  Bob Doyle’s “Experiential Meditation” calms and directs your brain to re-focus, to “take a vacation”. This specially designed meditation has soothing music that will let your mind relax – no talking, no subliminal messages, just beautiful music that will keep you comfortable and relaxed, so you can re-enter the rest of your life revitalized and CALM. (This professionally designed meditation mp3 should not be used while driving) You can download it instantly and begin or renew your meditation practice immediately. This is another of Bob’s Wealth Beyond Reason “Members Only!” gifts – a special gift to YOU.

Value of both Bob’s bonuses: $70!

Bonus #6: “Healthy Snack Challenge Ebook and E-Course” by Cheryl Miller, M.S.

Cheryl, a professional Wellness Coach and Exercise Physiologist, guides you to healthy nutrition in her comprehensive, 4-week program designed to help you and your loved ones feel better. Cheryl sets up you for success with her 11-page ebook that will arrive in your inbox seven days before the ecourse starts. Cheryl’s complete package prepares you for success with specially designed “Worksheets & Posters Success Tracking Food Log”, Top 10 Snacks, Weekly Meal Planning, 200 Snacks under 100 Calories – and a Healthy Eating Quiz. After 7 days, inspirational and educational quick-read nuggets come straight to your inbox for 21 more days! Imagine delicious snack recipes, links to the best recipe web sites, a special feature for kids with information about junk food marketing. How reassuring to know for sure that your body will really benefit from high nutrition snacks that are quick and delicious!”

Value: $19.95!

Bonus # 7: “CFS-CFIDS-M.E. Caregiver Newsletter”by Ann Corcoran
Upon your purchase, I will automatically speed my newsletter to your inbox. Increase your knowledge and comfort with my weekly practical and inspirational Tips, Help, and Updates on CFS-CFIDS-M.E -- tailored to You, the Caregiver to make your own good choices for a better life for yourself and for your CFS loved one.

Value: $49.97!

Here is something else very important for you to know – I am SO sure that this book will have a highly positive impact on your life -- that I am giving you my personal, unqualified GUARANTEE that you will absolutely gain the knowledge I have promised or you will receive your money back – with no questions asked!

So, you see, you have NOTHING to lose – this is a 100% iron clad guarantee – AND, as a matter of fact, I am so committed to you receiving value from this offer and appreciating your own valuable time you have taken to read about it, that you will also get to KEEP the bonuses, AND the book!

That’s right –Through my no-risk, 100% no-questions asked, money back guarantee; your satisfaction is absolutely assured. If, for any reason, you aren’t thrilled and satisfied with my book, just contact me within a year and I’ll refund 100% of your purchase price. No questions asked. You’ll keep every single bonus. No questions asked. You won’t have to explain a thing.

There’s no way you can lose.

A guarantee on the product, AND you get to keep the book and ALL the bonuses.

What could be more beneficial?

Remember, these bonuses, worth a total of $284, are yours to keep, No Matter WHAT!

You just can’t lose!

If this book doesn’t do everything I say and more, if it doesn’t keep your interest, if it doesn’t give you ideas of where to get help or relief, if you don’t save frustration and time in getting the information you need, if this book is not inspiring, or give you enough facts and information you need to more easily convince people of CFIDS and its effect on your loved one, if the 11 pages of Coping Tactics are not helpful in any way, if the resources listed inside do not help you to become a stronger and more informed advocate for yourself and your loved one, if you do not feel more empowered to make your own good choices –

…you can get EVERY PENNY of your money back under my “no-loop-holes guarantee.”

You have everything to gain by giving it a try.

I want you to have the better quality of life that my brother and I have found in the past few years. I wrote this book to help you, the caregiver who works unfailingly and unselfishly to help your loved one. I know you want to help your loved one by taking every possible step that will benefit you, your loved one and other people who are sick with CFIDS.

Thank You for your partnership in this important cause, and

Warmest personal regards,

Sincerely,

P.S. Being a caretaker of any chronically ill person is a huge commitment of your time and love. Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS) has the extra demand of stigmatizing both victims – the person who’s ill and YOU, the CFS/CFIDS/ME caretaker.

You need all the resources you can get to help you receive the relief and hope you deserve – and to improve your life!

This book puts ALL the basic information – and more! - that you, the caregiver, need – into one book. You spend your hours taking care of your loved one’s needs – why spend hours trying to find out where to go to get the expert information you need? While my book is on your monitor, simply click your mouse on any highlighted link in this book – and you’re there. No more hunching over your computer for hours and hours to seek out what is quality and what’s not.

The bonuses alone, Velma Gallant's“The Seven Roadblocks to Self-Love”, Velma’s Professional Coaching Session, Tony Masiello’s “The Parables of Inspiration,” Bob Doyle’s Atmosphere Environmental Software, Bob’s “Experiential Meditation” downloadable mp3, Cheryl Miller’s report on "Healthy Snack Challenge Ebook and E-Course" and my weekly newsletter, “CFS-CFIDS-M.E. Hope “– all together the worth of these is more than $284! PLUS my ebook, “A CFS Caregiver’s Guide to Hope”. All these make this a value you just should NOT pass up!

P.P.S. Remember as well, my full one year, iron-clad, money-back guarantee!

P.P.P.S. I thought I had better mention another Big Benefit - Remember, your time and energy are probably stretched to their limits. Whenever you are too exhausted for explanations, you will be able to print out pages from this book, one by one if you want, and slide them across your desk or the kitchen table to your co-worker, boss, friend, relative – legislator, even – and say, “Here – You need to know this. This is my life with my CFIDS loved one.”

It’s true…I just have to say it one more time. This book is a one-stop shop full of all the basics – exactly what you need to get on your way to getting relief and a sense of hope for your own life as a caretaker of your loved one who suffers from CFS-CFIDS-ME.

I know, from my personal experience, you want to take the best care of your loved one.But you and I know that you have to get the help that YOU need. If the word-pictures, coping tips, explanations, and resources don’t inspire you or make you feel more hopeful – if for ANY REASON you do not find this helps you to take action to get some help – if for ANY REASON AT ALL you are not 100% satisfied, you have nothing to lose. No questions asked – just ask for your money to be returned, and you have my personal guarantee of a 100% refund – and the bonuses are still yours to keep.

So, you see, you have NOTHING to lose – this is a 100% iron clad guarantee – AND, as a matter of fact, I am so committed to you receiving value from this offer and appreciating your own valuable time you have taken to read about it,that you will also get to KEEP the bonuses, AND the book!

That’s right –Through my no-risk, 100% no-questions asked, money back guarantee; your satisfaction is absolutely assured. If, for any reason, you aren’t thrilled and satisfied with my book, just contact me within a year and I’ll refund 100% of your purchase price. No questions asked. You’ll keep every single bonus. No questions asked. You won’t have to explain a thing.

There’s no way you can lose.

A guarantee on the product, you get to contribute to a non-profit organization that informs and advocates for CFIDS victims and their loved ones, AND you get to keep the book and ALL the bonuses.

What could be more beneficial?

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