CFS is not rare. Four millions Americans have it (says CFIDS.org),
yet over 80 per cent remain undiagnosed and untreated.
Here's the heartwarming story of one young sufferer...
and what she did to finally gain her life back!
Beating Chronic Fatigue Syndrome: Heather's CFS Story
CFS is sometimes known as post-viral
syndrome, yuppie flu, ME , CFIDS or CEBV.
But whatever you call it, it's a life-changing experience!
A very personal story of how one family did battle with
CFS, in a time when most doctors doubted it even existed.
Yet there was no denying that something had knocked the
stuffing out of this ambitious, lovable 12-year old.
When we needed it, there was no help available like this.
So we write to let you know...
what CFS felt like -- the fatigue, the emotions and
the heartache
how Chronic Fatigue Syndrome manifested itself in
our daughter's life and body
what we learned during those awful years (and the
immense good that came from it all), and...
how you can help if someone you love is in the depths
of the CFS pit.
Our hope in sharing this is that we might encourage
CFS sufferers and their families with what we learned,
what helped us most, what to avoid, and much more. But
especially we think you'll find it encouraging to know
that Heather has since graduated from University (that
was in February 2003) and has now completed her Honours
degree.
"This feels like a lifetime away from theseemingly-endless days of pyjamas and tears of
those dreadful CFS years" says Heather.
We share the photos and we share the facts (as well as
some opinions, fashioned from our 8+ years of day-in,
day-out experience with CFS). And we pray that our family's
story will provide encouragement
and hope for CFS / ME sufferers and their families.
So may I introduce you to our family... the Harvey family.
Gary: the writer of this story, who's also privileged
to be Heather's father.
Pam: my wife, the devoted mother of our two
children, and very definitely the co-star of this whole
saga... despite her own frequent migraines.
Paul: our son, now a 28 year old computer programmer.
A tall, compassionate young man with a thirst for life.
Heather: now 24, married, loving life and teaching
in a range of business and marketing subjects at university
while she works towards her Ph.D. Heather has kindly
consented to sharing the inspiring story of her battle
with this strange debilitating illness.
At 13, the world was her oyster
Five doctors in one month: The medical runaround
How we knew it was CFS
Alternative treatments, potions and other whiz-bangery
Effective CFS therapies: What actually helped Heather
get better
The medical specialist's letter
Medical information about CFS: More of what we learned
from our research
Dealing with social isolation
Dealing with depression
Was there a risk of suicide?
Is chronic fatigue "all in your head"?
Schooling: Here's what worked for us
What to avoid
The impact of CFS on Heather's career and marriage
15 lessons learned: Heartfelt advice to the CFS sufferer
(and your family)
Other CFS success stories: Restore your hope by meeting
these winners
Websites and books you might find helpful
Available
for immediate download
This
is the full 45 page PDF which can be
read on ANY computer, including Macs.
IMPORTANT:
After your payment is completed, please be sure
to click the 'Return to Merchant' button
so you can get immediate access to the PDF report. When it appears on your screen, please save it to your computer.
"Beating CFS: Heather's Story"
comes with a money back guarantee.
If for any reason you are not satisfied, simply ask me for a refund within 30 days.
*
If you would prefer to download the free 'lite'
version first, please click here.
This can be read on any IBM-compatible computer.
Sorry, Mac users.
(Click here for the zipped
version. Needs WinZip
to open it.)
Alphabet soup anyone?
CEBV
Chronic Epstein-Barr Virus
CFIDS
Chronic Fatigue and Immune Dysfunction
Syndrome
CFS
Chronic Fatigue Syndrome, though the
term is "inadequate and demeaning, given the
breadth and seriousness of the symptoms", says
the CFIDS Association of America. Some day medical
officials may come up with a more accurate name.
ME
Myalgic Encephalomyelitis
PWC
People with CFS
YPWC
Young people with CFS
Yuppie flu
Another demeaning and misleading term
because it affects all socioeconomic groups ...and
it's not influenza.
Disclaimer: The information
presented here is for informational and educational purposes
only. It is not intended as medical advice, nor has it
been reviewed by any medical authority. Please consult
with your health care professional. We assume no liability
for any medical treatment or other activity undertaken
by readers. The content of this document, for legal purposes, should be read or viewed for entertainment purposes only, and as a work of fiction.