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II
Week Speaker
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Guest
Blogger
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Lisa
Copen
Lisa
Copen is the founder and executive director of Rest Ministries,
Inc., an organization for people who live with chronic illness
or pain which was incorporated in 1998. She is editor of hopekeepers
Magazine which she began in 2004. Rest Ministries is the sponsor
of National Invisible Chronic Illness Awareness Week. She was
diagnosed with rheumatoid arthritis is 1993 at the age of 24,
She eagerly anticipates how God will continue to use it, by reaching
out to others who are hurting, as well as providing tools for
churches who want to increase their awareness of chronic illness.
Send
Lisa and Christine your questions in advance.
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Kick off the Week with Lisa &
Christine Miserandino
Monday, Sept 8, 9 a.m. Pacific
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Attorney
Scott E. Davis
Mr.
Davis is regarded as one of our nation's legal specialists in
representing clients who are disabled due to fibromyalgia or chronic
fatigue immune dysfunction syndrome. Mr. Davis has successfully
represented Social Security disability clients of all ages throughout
the United States. Mr. Davis has won Social Security disability
cases in every region of the United States and in approximately
40 states. And Mr. Davis' extensive experience is evident in the
fact that his firm wins chronic pain and fatigue Social Security
disability cases over 90% of the time. This success rate is significantly
higher than the average disability attorney and more than double
the success rate of Social Security claimants who are not represented.
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Wednesday,
Sept 10, 3:00 p.m.
What
You Need to Know
About Applying for Disability
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Shelley
Echtle
Shelley
Echtle, 48, is the director of the North Texas Fibromyalgia Support
Group. With 218 members enjoying weekly socials and monthly lectures,
she seeks diversity in presentations and shares information from
many sources she pulls from the internet and printed publication.
She writes part time and believes healthy boundaries in a healthy
life are important and even more so when you are chronically ill!
Shelley suffers with Fibromyalgia, Spinal Stenosis, Hypothyroidism
and Arthritis.Her mission in life is to be an encouraging thaumaturgies.
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Tuesday,
Sept 9, 5:30 p.m.
Healthy
Boundaries with a
Chronic Illness
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Laurie
Edwards
Laurie
Edwards is author of Life Disrupted: Getting Real About Chronic
Illness in Your Twenties and Thirties (Walker) and founder
of AChronicDose.com. She also teaches writing for the health professions
at Northeastern University in Boston, MA.
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posting
9/8
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Friday,
Sept 12, 3 p.m.
Friendships, Dating and Marriage: Can it All Come Together
When You are Young and Chronically Ill
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Jo
Franz
Jo
Franz is a conference/retreat speaker whose memoir Soar Unafraid:
Learning to Trust No Matter What is the inspiring topic on frequent
radio and TV programs. Though she has lived with multiple sclerosis
since 1977 her life has been full of adventure. Her never-give-up
attitude is a source of encouragement and blessing to those living
with chronic illness as well as those who do not.
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Tuesday,
Sept 9, 3 p.m.
How You Can Help Those Who Help You!
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Julie-Allyson Ieron
Julie-Allyson
Ieron (pronounced: I-RUN) is a conference speaker and author.
Her newest book is The Overwhelmed Womans Guide to
Caring for Aging Parentsa project she not only wrote,
but lives on a daily basis. Her other books include: Praying
Like Jesus, Staying True in a World of Lies, Conquering the Time
Factor, and the Sisters in Faith Bible Study Series.
Julie is passionate about coming alongside others to encourage
them to pursue an ever-deepening relationship with Christ. She
is a frequent guest on national radio and TV broadcasts.
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Thursday,
Sept 11, 9 a.m.
The Overwhelmed Woman's
(and Men's!) Guide to Caring for
Aging Parents
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Jennifer
C. Jaff
Jennifer C. Jaff, Esq. is Founder and Executive Director of Advocacy
for Patients with Chronic Illness. She also has Crohn's disease.
A 1984 graduate of Georgetown University Law Center, when her
disease disabled her and she turned her skills towards the internet
and found a community of chronically ill patients in desperate
need of legal advice and help. She started Advocacy for Patients
then, when she was too ill to leave her home. Now, she serves
patients full-time. She is the author of Know Your Rights:
A Handbook for Patients with Chronic Illness, and Friday
Tired: A Feminist Rant on Healthcare in America in the 21st Century,
and she is the Chronic Illness Advocate on RevolutionHealth.com.
Handout
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[get
handout]
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Wednesday,
Sept 10, 9 a.m. Pacific
The Civil Rights of Patients with
Invisible Chronic Illnesses
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Rosalind
Joffe
Rosalind
is career coach for people who live with chronic illness and her
business, cicoach.com, is devoted to giving people the tools and
resources they need to thrive in their work while living with
chronic illness. In addition to over 30 years of personal experience
living with auto immune chronic illnesses, including multiple
sclerosis and ulcerative colitis, Rosalind has 30 years of experience
working and has held management positions in small businesses
and Fortune 500 companies. Ten years ago, she founded her own,
very successful executive coaching business. She is the author
of Women Work and Autoimmmune Disease: Keep Working, Girlfriend!
Handout
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Tuesday,
Sept 9, 9 a.m. Pacific
Assess Yourself: Find the Job You Desire and Can Do Despite
Illness Limitations
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Jacqueline
L. Jones
Stricken
with disabling pain and fatigue, which interrupted a promising
career as a journalist, Jacqueline L. Jones spent more than 20
years searching for the answers she needed to survive. This determination
led her to more than 15 years of extensive research and to improved
health.
Jones
has developed a practical system, based on her experiences, that
will teach you how to save time and money in seeking help for
a chronic illness. She is author of Unmasking a Diagnosis:
How to Find Help for a Confusing Illness Without Filing for Bankruptcy.
Download
her handout here to help you follow along with the workshop
easier. She has TONS of great information.
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Monday,
Sept 8, 5:30 p.m. Pacific
Secrets of Paying for Medical Care
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Jeff
Kenyon
Jeff
Kenyon was born and raised in the Bay Area, CA. He is married
his lovely wife Isabel of 13 years and they have an amazing, almost-4-year-old
daughter named Adie. He was a top athlete in many sports throughout
his life, healthy as a bull, but he became ill on April 18th,
2004 and then God blessed them with his baby girl on December
9th, 2004. He says, "It was all God's grace, love, church
family and faithfulness that got us through it all. Through all
the surgeries, emotional and physical pain, only God has been
able to bring me to a place where I am totally dependent on Him
and my goal is 'dying to self' everyday."
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Friday,
Sept 12, 2008
Join Jeff with Host, Lisa Copen for closing seminar of the
week where Jeff will also share some illness issues from a man's
perspective.
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Linda
Lundy
Linda
says her very best motivation experience was being a gymnastic
coach with Marta and Bela Karoyli. "The kids come first-no
matter how you feel-you put a smile on your face, out your best
foot forward, never sit down in the gym, and always have energy
and enthusiasm to share." She is a cancer survivor and has
a pituitary adenoma; which brings with it fibromyalgia, a non-functioning
thyroid, migraines, etc. She says, "I know how to put one
foot in front of the other and keep going!"
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CANCELLED
- Due to evacuation in TX
Get
out of Bed!
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Christine
Miserandino
Christine
Miserandino is a writer, speaker, patient advocate, wife and mother
living in Massapequa Park, NY. Her writing which has won various
awards has been featured in numerous newspapers, magazines, medical
newsletters and television media. Christine is the founder of
www.butyoudontlooksick.com, a website that provides resources
and useful tips for living life to the fullest with a chronic
illness. Through her website, Christine has created an online
community that brings people together from all over the world
to share their experiences, seek support, offer tips and advice,
and create friendships. She has been living with lupus for over
15 years, and has been volunteering for the Lupus Alliance, Long
Island/ Queens Affiliate for 12 years.
Send
Lisa and Christine your questions in advance.
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Kick
off the Week with
Christine & Lisa Copen
Monday, Sept 8, 9 a.m. Pacific
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Maureen
Pratt
For
more than 10 years, Maureen has written and spoken about health,
prayer, faith, and living with chronic illness and pain. She has
also lived most of her life"in the trenches" as a patient
who has lupus, cardiovascular disease, vasculitis, scoliosis,
fibromyalgia, thrombocytopenia, and chronic asthma and allergies
(to name a few)! Through it all, God is great -- and she is eager
to share practical, positive ways to increase our faith, hope,
and joy.
You
can email
her questions in advance.
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RESCHEDULED:
Friday, 9 a.m. pacific
Stress-Busters that Work: Faithful and Fun Ways to Lessen Stress
and Encourage Hope and Health
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Jenni
Prokopy
As
Founder and Editrix of ChronicBabe.com, I reach thousands of women
every day with messages of hope - and teach them how to maintain
their sense of self despite health-related limitations. Almost
2,000 people read my enewsletter every other week, and approximately
1,000 visitors come to the site every day. I love helping others
and I know I have a commanding message of hope and inspiration
to share.
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posting
9/10
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Wednesday,
Sept 10, 12 p.m. Pacific
Overcoming Self-Defeating Behaviors
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Trish
Robichaud
"AFTER
THE DIAGNOSIS:
THE JOURNEY BEYOND"
Have
you recently been diagnosed with a chronic illness? Do you feel
lonely and confused?
Trish
& Jeff have both been where you are today and can guide and
empower you to emerge on the other side of the journey with the
strength and determination to make the best of your life.
Trish
Robichaud is a Disability Awareness Coach, Maximum Life &
Business Coach & Motivational Speaker. She lives with major
depression and multiple sclerosis. To learn more about Trish and
Changing Paces, and to download her free 30-minute motivational
audio, visit http://www.ChangingPaces.com
Jeff
Cadwell
Jeff
is a Professionally Certified Life Coach, Radio Show Host, Speaker
and Author. Jeff lives with multiple sclerosis as well. For more
information about his products, programs and other services, please
visit his website at http://www.JeffCadwell.com
Handouts
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Thursday,
Sept 11, 5:30 p.m.
After
the Diagnosis: The Journey Beyond
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Connie
Roberts
Connie
has multiple chronic illnesses and has been blogging since April,
'07. She now writes 3 of her own blogs, co-authors 2 other blogs,
and works for various companies as a sub-contractor doing paid
reviews. By writing she uses her creative energy, is able to be
an advocate for people with disabilities of all types including
those of us with invisible chronic illnesses and earn extra money.
It is not only personally fulfilling but helps her to feel that
she can contribute to her family's income again. She says, "I
have taught people how to get into the world of blogging. They
now earn money and reap the benefits that I do too."
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Thursday,
Sept 11, 12 p.m.
How to Get Paid to Blog
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Lynn
Royster
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Paula
Kravitz
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Lynn
Royster, joined with Paula Kravitz
Lynn
is the Director of the Chronic Illness Initiative at DePaul University's
School for New Learning, a unique program designed to help chronically
ill students obtain a college education. In addition, she designs
and teaches courses in conflict management, adult psychology,
and writing. Dr. Royster also serves as Vice Chair of the CFIDS
Association of America, Inc. and as Board Secretary of the Chronic
Fatigue Syndrome, Fibromyalgia, and Chemical Sensitivity Coalition
of Chicago. She received her B.A. from the University of Michigan,
her M.A. from Prescott College, her J.D. from George Washington
University, and her Ph.D. from the Union Institute and University.
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Tuesday,
Sept 9, 3 p.m. Pacific
College with Chronic Illness: How to
Get Help and Respect from
Administrators and Faculty
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Jennifer
Saake
Jennifer
has lived 18 years of illness, with infertility for 10 of those
years. Balancing both conditions includes: medication side effects
(illness meds on fertility and fertility meds on illness), questioning
sanity of wanting desperately to have children yet fearing how
she would care for them when she can hardly care for herself,
facing the frustration of attempting adoption when her health
makes her less "marketable." She has written a book
on infertility and loss and is praying about someday writing a
book on living with chronic illness.
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Tuesday,
Sept 9, 12 p.m. Pacific
Medications, Illness, Fertility and
the Desire for Motherhood
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Leslie
Vernick
Leslie is a a Christian counselor, doing most of her work with
relationship problems. She focuses on improving our relationships
with others, God and self, teaching people how to address conflict,
speak the truth in love, handle adversity in a God-centered way
and negotiate through difficult and destructive relationships
with biblical principles.
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Monday,
Sept 8, 12 p.m.
TBA
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Christina
J. Werdebaugh
Christina
J. Werdebaugh is the Director and Support Group Leader of the
West Virginia IC Resource Center. She is an alumnus of West Virginia
University, and enjoyed many years of working nine-to-five before
her failing health forced her to leave the daily grind due to
severe Interstitial Cystitis (IC). Her health is further complicated
by lyme disease, which depleted her immune system and caused vast
systemic damage. After becoming disabled and homebound, Christina
felt God's calling on her life to create a local support network
for IC patients, and the West Virginia IC Resource Center was
born.
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Wednesday,
Sept 10, 5:30 p.m. Pacific
Support
Groups: The Changes and Challenges They Will Bring to Your Life
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Michele Williams
Michele has lived with chronic illness for over 23 years. Unfortunately,
she knows first hand how it effects the family. Being in the ministry
for over 34 years, she has ministered to many people with some
form of chronic illness and even death. She has a daughter recently
diagnosed with autoimmune hives and fibromyalgia. Her daughter
also suffers from bipolar along with her 13-year-old son. Michele
has had first hand experience on how illness can effect one's
faith. She says, "But most importantly, I do not know how
I would have been able to go through any of this without my faith.
My faith has brought me through some very difficult times."
You can
email her questions in advance.
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Friday,
Sept 12, 12 p.m.
Illness and Faith: Does Faith
Make a Difference?
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