Butterfly Rewards - earn free credits and redeem for good causes -  learn more!
my care2
make a difference

community & fun

people

12 million members making a difference

 
 

Cheryl Sunshine Benson

"My Rights to Honest Neurological/Medical Treatment & Independent Assisted Living Care Housing"

Ontario, ONT, Canada
female
committed relationship
was Producer/Director&Prov.Gov. NOW- Ret/ill/Disabled
Speaks: English
Joined Mar 1, 2005


 
PUBLIC APPEAL FOR CHERYL'S RIGHT TO HONEST NEUROLGICAL MEDICAL CARE
My website isn't finished yet, it is very slow for me and hard to say the least as per below, so are the blogs, I have one blog open, and still needs editing.

 I have worsened so much and the myocolonic dystonia  convulsions are ongoing dailly since coming off the drugs in 2004 and  left  here with my whole body damaged, every muscle and liagemnt jjust prior, and spasmodic dystonia (cramping of groups of muscles) is spreading through my body now very rapidly, and paralizing increasingly I don;t know I will be able to finish the website, which isn't listed here right now.. I often can't type unless my mucles and ligaments ae softened enough, and some times type the way I speak, the wya my damaged brain chops off words. Often I can't even sit up. I am mostly bedconfined.

http://cherylspeaksout.blogspot.com/

http://www.youtube.com/cherylspeaksout

http://mobilebroadcastnews.com/MBN/blogs/CherylSpeaksOut














~ Introductions are needed, before friends link, and I my list is quite large as it is. See below, ABOUT ME, section for further details, wthank you.

~ Spirit soul in human body that used to work in high demanding Administrative positions in creative venues, freelance work, and a former Audio/Visual Producer and Director that had staff and freelancers working with me, working16- 18 hour day. In 1989 during the recession I competed for a job in the Ontario Provinical Government and won the position. Little did I know that the Long Term Disability I was paying for would be needed in 1994.. Now I often can’t put 2 words together, speak, read, concentrate, sit up, use my arms, legs, hands, or think straight. Often I can only copy/paste and click, often not even that, I am bed/houseconfined and have been since 1994 with alot of fluctuations until 2003, with the first brain body damage not on my records as in no diagnosis, and more damage was done and I was left here very damaged and convulsing everyday, I also endured several years of severe seizures coming off the drugs, I still have them, not that often, the myolconic dysotinia (would look like a seizure to many people, it is rapid or slow rhythmic movement of all the muscles in your body at the same time) which I wake up to daily is a nightmare, my arm sockets are badly damaged left like this and is the rest of my body and I continue to worsen.
 
 I am a survivor of many things,, However, Myalgic Encephalomyelitis
/Chronic Fatigue Syndrome (ME/CS) ended life as I knew it in 1991, a neurological illness defined by WHO and Ontario Medical Assoc. since 2005. Fibromyalgia (FM) and Multiplie Chemical Sensitivies (MCS) came with it and extensive discrimination. I also have HepC I found out in 1994. My ME/CFS was considered psychiatric or just a serotonin problem by many includng the pshycatric community, although I was diagnosied by 2 Infectious Disease Specialsts.

 In 1996 I was referred toa pshcyatrist for neruolgoical problems inherent with ME/CFS, which were at first focused on, however shortly after pshcyatric drugging started without proper informed consent. I endured 10 years of adverse reactions to SSRI's and other antidepressants, and drugs that were slipped to me with out telling me what they were, which were ignored as was my FM & the cause of much damage that continues to progress.




I belong to a group of ME/CFS survivors that are drug dose sensititive or intolerant. This is backdated in medical clinical journals to 1993 which mentioned antidepressants. However, all drugs were included some years later as thousands more were being documented.





At near 50 misdiagnosed bipolar and brain/body damaged repeatedly every muscle and ligament causing them to be shortened and stiff and greatly weakened in 6 days, I couldn't lift much more than a light book, prepare my own food, bath myself, or take care of myself., Acute dystonia with seziures March 2003, the dystonia and seizures lasted 2 weeks, I don't think it ever went away, I think the next round of drugs I was put on covered for it and did make it worse, every time I came off them, the dystonia nd seizures would come out again, until I came off the drugs, all of them in 2004 and the daily dystonia convulsions, and for some time seizures were non-stop.. . 

After the first brain/body damage of January 2003, I was verbally and phsycically abused in every hosptial to keep the damage off the records or as pshcyatric and me out of the hosptials and from suing for malpractice and negligence which I had started  later 2003 after getting no help from the medical community, just abused by them and no help from the government.

I dicontinued the bipolar medication after being damaged for life 2 times in 3 months, although I had 3 serious adverse reactions.
I was refused to be hospitalized by all those involved and was left to worsen and keep the extensive physical damage off my records.

 2003-2004 I was put on more drugs doing damage.  Psychiatric had been put on my medical files for repeated misdiagnosis, unethical medical practices, adverse side effects as well as purposely falsifying records, it's called collusion..

 In 2004 when I came off the remaining drugs, the left side of my body paralized and had started dragging behind me prior to coming of them and was more withered than my right side of my body, my speech was affected, and I couldn't hold my neck up.  My mom had to force the ER doctor to give me a catscan, he said what was written on my medical files no doctor or hosptial would want to give me one and could get in trouble for doing so. We were told there was a lesion or ambulism on the right side of my brain. Almost month later the written report came back negative, we were told the catscan film could not be found. The left side of my body remained weak and often drags around every day and is often a percouser to the dystonia convulsions or seizures coming on. I have several movement disorders from the drugs, mostly antidepressants, myoclonic dysotnia, and parkinsonium.

Diagnosis/damage is not on my medical records, nor have I received the diagnosis/care afforded to those with Acquired Brain Injuries (ABI) or my ME/CFS/FM, HepC and I was cut off doctors, and have increasingly worsened. Instead, systemic collusion and verbal and/or physical abuse followed encompassing 6 hospitals as well as homecare.  I was left severely and increasingly ill and badly damaged, with seizures, movement disorders/ convulsions, dystonia spreading through my body I endure every day.

 For several years I and my mom, and one friend who stuck by me “in real life”, fought for my rights to honest neurological medical care, human rights violations against me, and quality of life, even life itself. I have boxes full of letters for help to all levels of government, and we were told to get me out of the country, or find a Sponsor to no avail, the more we asked for help from “G”overnment, medical community etc., the more I was purposely isolated.  Several people behind the scenes tried to help me here, but I was just isloated more by those involved at the time.

Every document needed for government services, and much of my medical files have been falsified by the doctors, hospitals, Care Center involved leaving me with no medical care or supportive care, or government programs that help, or my personal insurance, as long as the damage is off the records. 
 


I have been an activist for various issues during my life, mostly Human Rights, and continue during my “net life”.






I have sponsored my 2nd family/community in Africa since 1993, and had to discontinue in later 2009, I barely holding on myself.




My disability forms for LTIP have to be signed yearly by a doctor or I can be cut off even though on since 1994.  I can’t get to one and still need to be hospitalized in an advanced neurological medical facility, for honest diagnosis treatment, and my falsified medical files cleaned up, and ensuring more damage isn’t done, as well as supportive care housing and a compassionate inhouse doctor that knows about ME/CFS and FM so the cycle of discrimination stops, as well my HepC has worsened, the extensive damage, everything worsened left like this. My records are so badly faslfied at this point which makes it harder, and I am a high maintenance case, I am also quite knowlegable about my illnesses and the damage done, the drugs involved and used, which is often a turn off to doctors.  I don't have all the answers that's for sure to the extensive damage. I have lost my faith in the medical community and so called healthcare professionals and the government for that matter. and have been bady tramatized by the damage, the collusion, the abuse in the hosptials, my own home. They have a lot of trust earning to do.

Since 2003 to 2008 there have been 15 attempts to have me hosptialized with honest tests and diagnosis at a pace I can handle including the former Minister of Health to no avail or abused and kicked out of the hosptials, including my mom who was assaulted.


  In 2008, using alternative health medications, I got some improvement for a short period of time, and took up my cause again, albeit less than snails pace, which I had mostly given up hope on for several years. It is an extremely slow go for me. Often I can not speak, type, or sit up; cognitive problems are extreme & I am mostly bed confined often left paralyzed in it and the daily convulsions. My arm sockets are very damaged fromt the dysotnia convusling daily.  It is beyond people’s comprehension, it has increasingly become beyond mine how I am still here.

website for help and more is being set up at a snails pace
.

















me_and_cfs_ribbon_large.jpg

cfsRobertEbertstatementAfterRemeberMeVideo.bmp

~ Like all illnesses, the severity of M.E./CFS varies from patient to patient.  Dr. Paul Cheney stated he had evaluated over 2,500 ME/CFS cases and it can be a nightmare of increasing disability with both physical and cognitive components. Severe cases can have both an MS-like and AIDS-like clinical appearance. Dr. Dan Peterson, found that, “ME/CFS patients experienced greater functional severity than the studied patients with heart disease, virtually all types of cancer and all other chronic illnesses”. 20 years after the epidemic, Dr. Peterson said he has never had a patient that recovered from ME/CFS. An unrelated study compared the quality of life of people with various illnesses, including patients undergoing chemotherapy, haemodialysis, as well as those with HIV (until the late terminal stage), liver transplants, coronary artery disease, and other ailments, and again found ME/CFS patients had the lowest quality of life. Dr. Leonard Jason stated in a radio interview that ME/CFS “is actually more debilitating than just about any other medical problem in the world
http://www.mefmaction.net/Caregivers/tabid/84/Default.aspx
















~ Here are some of the best on the web for ME/CFIDS/FM/MCS/HepC and Stopping Stopping Psychiatric Abuse :

http://www.immunesupport.com    Largest Research Library Worldwide, forums & natural supplements
http://www.mefmaction.net/   Canadian & Changing Canadian laws
http://www.cfids.org/   American CIFDS Org
http://www.ncf-net.org/index.html   National CFIDS Org. more directed to Research & funding
http://www.fibrohugs.com   Large support site & info
http://www.cfids-cab.org/MESA/index.html US, has CDN Definitions
http://www.co-cure.org/index.htm US & CDN, smaller site
http://www.care2.com/c2c/group/fm_cfs Care2 FM/CFS group
http://www.mindfreedom.org  Stopping Psychiatric Abuse
f I Can't Dance Is It Still My Revolution
http://www.lloydwright.com   NATURAL ALTERNATIVES FOR HEP C (and some for ME/CFS)
http://www.youtube.com/user/HeppersHelper











CANADIAN'S PLEASE WATCH

FIRST, DO NO HARM. 5th Estate/CBC Documentary, Please watch it SO YOU KNOW HOW OUR MEDICAL SYSTEM DOES NOT WORK IN FAVOUR OF PATIENTS.  PROTECTED BY POLITICIANS, DOCTORS, & SOME NURSES & HOSPTIAL STAFF FOR THE SECRET CODE OF SILENCE AND WHO ARE ABOVE THE RULE OF LAW
.

FIRST, DO NO HARM
Watch the
entire documentary online
(runs appox 41:30)

http://www.cbc.ca/fifth/donoharm.html

MORE:
The Story
The Interviews
Resources


CANADIANS DON'T BE COMPLACIENT: WAKE UP TO WHAT IS HAPPENING IN OUR OWN COUNTRY PLEASE
!
3 in 10 of Canadians report medical errors (November 2005) by the medical profession(the Tip of the Iceberg) & that is only what gets reported/makes it to court & does not include those damaged by prescription medications, which at present is only 10% as well that are reported by doctors that they know of There is now on Health Canada a site for Canadians to report adverse affects to medications. This is MILLIONS OF CANADIANS WE ARE TALKING ABOUT and the Canadian Medical Protective Assoc. has BILLIONS of $$ & MAKES THE LAWS HERE, are protected by the Politicians AND WE PAY THEM WITH OUR TAXES TO PROTECT THE DOCTORS & MAKE THEIR OWN LAWS & that keep us out of court! Even our government has a "hands off policy" because they have too much power and money. Don't wait until it happens to you or someone you love or know. We need or own Protective Medical Association FOR THE PEOPLE OF CANADA and which soon I hope you will be seeing a link to HERE! 

Tue. May. 31 2005 ,
A recent University of Toronto study showed that up to twenty four thousand Canadians are killed each year by mistakes in the medical system. This makes it the third largest cause of death on Canada. Only cancer and heart disease claim more lives and only three to four hundred Canadians are compensated each year for medical errors. ARTICLE LINK HERE

CMPA as a Defence Organisation

The Canadian Medical Protective Association (CMPA
) was founded in 1901 by a group of Canadian doctors for their mutual protection against legal actions based on allegations of malpractice or negligence.








Unlike insurance companies, the CMPA does not issue a malpractice policy to its members, nor is there a deductible. There is also no limit to coverage. While legal fees in medical malpractice cases can easily amount to hundreds of thousands of dollars, the doctor does not as a practical matter have to pay; the CMPA pays the legal fees to the doctor’s lawyers directly. If a doctor is ordered by the Court to pay money to a plaintiff, the CMPA pays, not the doctor. As an association of physicians, the CMPA feels strongly that the reputation of its members is paramount. For this reason, the CMPA will not settle a case solely because it is cheaper to pay the plaintiff than take the case to court

Continued: The Canadian Medical Association for DoctorPLEASEREAD:
http://www.hartelaw.com/artl_cmpa.htm 










BoycottIsrael.bmp

http://www.bdsmovement.net/

















http://www.abraham-hicks.com -free audio downloads, CD, as well as CD/Tape courses

http://www.centerpointe.com/holosync meditation Cd's - and Courses


A Course In Miracles

Bhagavad Gita As It Is

www.givegetnation.net

www.freecycle.org 

 
     Each time a man stands up for an ideal, or acts to improve the lot of others, or strikes out against injustice, he sends forth a tiny ripple of hope...

     And crossing each other from a million different centers of energy and daring, those ripples build a current that can sweep down the mightiest walls of oppression and resistance. 

                                                 ~Robert F. Kennedy














 
Personal Professional Contact Singles
Joined Mar 1, 2005
1° Network
zzzz_TEST
Activist Aspirations Rabid 
Here for Meeting Friends, Professional Connections, Support a Cause, Other 
Group Host of
CANADIANS PROACTIVE & GLOBAL CITIZENS (378) CHAT ROOM is OPEN 24/7 (348)
Groups 4 Writers from Writers and those who like to become writers, 9/11 CONSPIRACY ! ! !, ?Science?, A Flower Does Not Talk, A Forest in Brazil, A Mystical Realm, A Petition Posting & Grass Roots Activism Learning Center, A Picture Is Worth A Thousand Words, AHIMSA VEGAN DIVINE ~ CREATURES EARTH ~ RAINBOW LIGHT ~ PEACE LOVE !, ASSOCIATIONS AND COALITONS, Action Advocacy . . . is all about creating change!, Activists & Community Group Leaders, Activists & Damn Proud Of It!, Activists Against Factory Farming more »
Hometown Ontario, Canada 
Homepage http://cherylspeaksout.blogspot.com/  
Birthday Oct 17  
Languages English  
About Me REGARDING FRIENDS PLEASE INTRODUCE YOURSELF FIRST & WHY YOU WANT TO BE FRIENDS (SPECIAL INTEREST IN CANADIANS INTERESTED IN OUR COUNTRY'S MEDICAL/HEALTHCARE/PRIVACY HUMAN RIGHTS LAWS, and PALESTINE RIGHT OF RETURN) & TAKE TIME TO READ MY PROFILE AS I WILL YOURS WHEN ABLE. IF YOU ARE NOT GETTING A RESPONSE FROM ME IT IS EITHER BECAUSE YOU HAE NOT INTORDUCED YOURSELF/READ PROFILE OR BECCAUSE MY NETMESSAGES ARE VERY BACKLOGGED AND DIFFICULT FOR ME TO KEEP UP W.THANK YOU.

"Our ideal is not the spirituality that withdraws from life but the conquest of life by the power of the spirit." - Aurobindo.

UPDATED DEC.31/05: I was first directed here to Care2 to help find a Sponsor for a Neurological Hosptial hopefully outside of my country (which was the header on my Profile for along time & still neeeded by the way) & any means of finding alternatives & changes to my situation in my own country (which is not unique & affects millions of Canadians). At the time I could barley type, had been badly brain/body damaged & could not fend for my own rights anymore, and which continues to the present. I have a history of helping those in need and defending their rights. The cogntive/memory/brain problems were more severe and remain, although some aspects deminish during unpredicatable times. The current up date in on above on my profile.

i TRYING HERE & THERE COME HERE COPY & PASTE EASIEST FOR ME CAN'T DO IF your groups don't have HTTP TAGS, TOOL/icon BAR IN POSTS TURNED ON (Group Module)- God Bless thk you for your prayers

- REMEMBER MY OWN QUOTE "PEOPLE OVERCOMING OVERWHELMING ODDS"
-----------------------------------
----------------------------------
WE ARE NOT HUMAN BEINGS
HAVING A SPIRITUAL EXPERIENCE
WE ARE SPIRITUAL BEINGS
HAVING A HUMAN EXPERIENCE

"It is one of the most beautiful compensations of life, that no man can sincerely try to help another without helping himself." Once you make a decision, the universe conspires to make it happen.

-Ralph Waldo Emerson

To laugh often and love much; to win the respect of intelligent persons and the affection of children, to earn the approbation of honest critics; to appreciate beauty; to give of one's self, to leave the world a bit better, whether by a healthy child, a garden patch or a redeemed social condition; to have played and laughed with enthusiasm and sung with exultation; to know even one life has breathed easier because you have lived--that is to have succeeded.
Ralph Waldo Emerson


Our deepest fear is not that we are inadequate, Our deepest fear is that we are powerful beyond measure. It is our light, not our darkness,that most frightens us. We ask ourselves, Who am I to be brilliant, gorgeous, Talented, fabulous? Actually,who are you NOT to be? You are a child of God. Your playing small does not serve the world. There is nothing enlighteneng about shrinking so that other people will not feel insecure around you. We are all meant to shine, as children do. We are born to make manifest, on earth,the glory of God that is within us. It is not just in some of us. It is in everyone. And as we let our own light shine, we unconsciosly give other people permission to do the same. As we are liberated from our own fear, our presence automatically liberates other
MARTHA WILLIAMSON

"When the power of love overcomes the love of power the world will know peace." Jimi Hendrix, had original poster with that on my wall, silly me gave it away. I remember sitting in Rochdale College when I first heard he died.

""Still, if you will not fight for the right when you can easily win without bloodshed, if you will not fight when your victory will be sure and not too costly, you may come to the moment when you will have to fight with all the odds against you and only a precarious chance of survival. There may even be
a worse case. You may have to fight when there is no hope of victory,
because it is better to perish than live as slaves."
~Winston Churchill

Mourn not the dead that in the cool earth lie- But rather mourn the apathetic throng- The cowed and the meek- Who see the worlds' great anguish and its wrong And dare not speak.
RALPH CHAPLIN (1887-1961)

A human being is part of the whole, called by us "universe," a part limited in time and space. He/She experiences his/her thoughts and feeling as something separate from the rest -- a kind of optical delusion of his/her consciousness. This delusion is a kind of prison for us, restricting us to our personal decisions and to affection for a few persons nearest us. Our task must be to free ourselves from this prison by widening our circle of compassion to embrace all living creatures and the whole of nature in its beauty.

- - Albert Einstein

Courage and perseverance have a magical talisman, before which difficulties disappear and obstacles vanish into air.
-- John Quincy Adams
Heaven help us I pray so!
  Introduce yourself to Cheryl Sunshine
  Lifestyle
Pets not able  
Activist Aspirations Rabid
Political Leaning Very Liberal
Religions  
Eating Habits have added some protein for healing, Vegetarian  
Wild Fact About Me posted here! I think not, lol, not that blantant & would be too many to mention! lol, I see many mentioned on peoples profiles that to me are not wild at all.
My Philosophy truth enlightment love GOD = All That Is, FEAR is the worse 4 letter word, everything you need is within you except we have fotgotten how to access it, rights for ANY living thing/being/mother earth, Re-Member, keep on going through hell & highwater
What Gives Me Hope LOVE/BLISS,learning about All That Is, his Masters sent to earth to help us ex. Budda, Jesus Christ, Krisna. Meditation going within. This is 1 life of many before I excellerate & don't have to reincarnate here on plant earth anymore except my choice; LOVE, PEACE, CHANGE, PEOPLE, been very isolated 11 years now especially last 2; I get the medical treatment & deserve & am entitled to & being denied
If I were Mayor, I'd make the world a better place by
What/who changed my life and why Books: BE HERE NOW, Zen & the Art of Motorcycle Maintenance, Johnathan Livingston Seagull, Edgar Cayce Books; ONE, Celestine Prophecies, Course in Miracles (online course/tape,-book huge-too hard for me, lol) Conversations with God , Bhagavad-Gita, Cave In the Snow, Pure Bhakti, Everything you Know you learned in Kindergarten", A.C.Prabhupada Self REalization & Karma Free Diet & others, Paramahansa Yogananda's books, New Testament (what was allowed by the church to be printed),Complete Writings of Kahil Gibran. Louise Hay You Can Heal your Life, SETH Books, What The Bleep do YOU KNOW? ,Body Guard of Lies, Scottish/UK/Ireland/Euorpean History, History not in order as above.

PEOPLE: Ghandi, Winston Churchill, Gurudeva Narayana, Spartacus (was goin to name 1st son after him decades ago) have long list actually;of people still growing; ,A.C.Prabhupada;Mother Theresa, Jagadisa dasa, 17 friends who died from AIDS (4 best friends) Danny known since I was 16 died in my arms in a moving car from a ruptured lung tumor; Martha Williamson, Oprah, Kainda my sponsored child Kainda in Chad, Africa, Nelson Mandela, Terry Fox, Jim Hansen; Christoper & Danaa Reeve ANYONE OVERCOMING OVERWHELIMG ODDS.

EVENTS: Nature, the river, camp I went to when young. Africa! atrocities against humanity/any living thing including Sexual Assaults, peoples/ professions/ doctors TUNNEL VISION, BECOMING CHRONICALLY ILL with Invisable Illnesses & neurological CFS/FM/MCS mostly housebound for decade just with those. Prejudice/ignorance, not willing to learn from people, patients, government/aid people etc.; Brain/body damaged/disabled 2003-2004& 2004/2006 & continuing seizures coming off long term med was left on another year contributing to more body damage with Dr. knowing & too scared to call & tell me or new doc to get off as he had been giving it to me & braain/body damage x2, secondary myconolic dystonia with seizures (prescribed mes) & 1st equivlant of neuroleptic malginait syndrome (all muscles short & stiffened (prescribed meds ignoring my neurlogical illnesses saying they were physchatric), only reversed 1/2 way back and very much belately no one involved would hosptitalize me , not on neuroleptics, but because of neurological illness they chose to ignore & prior medical/prescription history - AND I took the damn medication, would BE SO VERY HELPFUL AND EXTENDING NOT ONLY MY LIFE BUT QUALITY OF SAME IF THEY WOULD STOP FROM FEAR AND HELP ME; ISLOATION; onwward, with no proper/on my medical redords!!!!!! diagnosis, treatment or care :Running Tenants Assoc. while sick getting Immigrants thousands of $ back back from landlord & who were to scared to go to court so I took him to court even after brain/body damage. Gave speech City Hall 2001 for tenant rights in City Council to thousands of tenants, after 9 years severely isloated, ill every day to some decgree &with severe cognitive/focus brain problems & wrote my own speech (used to do this and more for a living before CFS/FM/MCS! 18 HR days), difficult cognitibvley with neurologial illnesses. to bad off now getting worse since brain/body damage, as they are making sure I am not getting the help/support I need & cut off all gov. services had except 4 wee hours a week for bathing me shopping/laundry, no one to get me cash, buy clothes etc.. Medical Malpractice/ Negligence in Ont. Canada (2003-04 causing brain/body permanent damage not on hosptial records (or positive tests removed, changed,disappeared and phychiatric put in place TO KEEP LAWYERS AWAY, even my body injuries don't exist or seizures, was left on drug year after brain/body damage 1 doctor knowing still doing damage & not 1 phone caLL to stop it) or now starting to say I was always like this) due to extension collusion/ conspiracy-1 lawyer said worst case of collusion he has ever seen=cost of large law firm can't afford) how much power/money they have and what they get away with (CdnMedica lProtectionAssoc.)will pay quotes "Hartes Law Film a $100,000.00 to fight a persons little $5,000.00 case & extend the case long as they can to ensure the so called integrity of their doctors remains NO MATTER WHAT"- yes they wil let you die & Health Stats Canada keeps track of medical deaths & mutilations, only what gets reported or those who can afford a huge law firm) so only the tip of the iceberg. Not being able to care for myself & denied what others get because of lack of advocay & making court precedents & law firm. Being almost 99.99% bed/housebound now, will change with proper diagnosis & treatment. Not being able to READ BOOKS (bits at time), big blocks of type brain turns off, somethine can't even hold sentenance & never know when or can, lack of focus MISS MY MIND, computer lite sems to help but still not large blocks of ty0pe & still sometimees can't get past 1st/2nd sentance depending hour/day never know when how long unless I "crash" they sensory OVERLAD X 100 and almost did drive me crazy & put on wrong meds made me worse, eventulaly had soem cause in permananet brain/body damage head to toe.
What Bugs Me  
Passions helping others, music, but sound can hurt now, art, canoeing, camping miss very much nature, water especially rivers, Nature/Wildlife, reading, writing, photography, spirituality  
Inspirations human spirit, challenge, used to be dont know anymore, Water in nature, sunshine, spirituality, nature  
What Scares Me  
  Favorites
Role Models  
Quotation almost anything from Emerson :
"It is one of the most beautiful compensations of life, that no man can sincerely try to help another without helping himself." "He who has a thousand friends Has not a friend to spare,While he who has one enemy Shall meet him every- where." " What lies behind us and what lies before us are tiny matters compared to what lies with in us."
SOMEONE WROTE THIS TO ME ON MY QUIT SMOKING SITE: "To laugh often and much; to win the respect of intelligent people and the affection of children; to earn the appreciation of honest critics and endure the betrayal of false friends; to appreciate beauty, to find the best in others; to leave the world a little better; whether by a healthy child, a garden patch or a redeemed social condition; to know even one life has breathed easier because you have lived. This is the meaning of success." -Ralph Waldo Emerson "The only way to have a friend is to be one."
-Ralph Waldo Emerson

"When the power of love overcomes the love of power, the world will know peace. –Jimi Hendrix

MARTHA WILLIAMSON:
"We may have bad weather in Ireland, but the sun shines in the hearts of the people and that keeps us all warm.

Our deepest fear is not that we are inadequate. Our deepest fear is that we are powerful beyond measure. It is our Light, not our Darkness, that most frightens us.

Our deepest fear is not that we are inadequate, Our deepest fear is that we are powerful beyond measure. It is our light, not our darkness,that most frightens us. We ask ourselves, Who am I to be brilliant, gorgeous, Talented, fabulous? Actually,who are you NOT to be? You are a child of God. Your playing small does not serve the world. There is nothing enlighteneng about shrinking so that other people will not feel insecure around you. We are all meant to shine, as children do. We are born to make manifest, on earth,the glory of God that is within us. It is not just in some of us. It is in everyone. And as we let our own light shine, we unconsciosly give other people permission to do the same. As we are liberated from our own fear, our presence automatically liberates other

— Anaïs Nin
There came a time when the risk to remain tight in the bud was more painful than the risk it took to blossom


"Greatness is not measured by what a man or woman accomplishes, but by the opposition he or she has overcome to reach his goals." ~Dorothy Height
Interests nature, meditation, crystals, Spirituality/Philosophy, internet, Mythology / Folklore, Art/Design, Medicine / Health Care, history, reading, by on the water/river, spirituality, psychology, photography, Air Purification, Anatomy, Agriculture, Wildlife, Antiques/Collectible  
Books too many too mention  
Music sounds of nature, water and wildlife, sound of silence literally, classical, just about everything except heavy metal, Enya, Krsna Das, Madonna, Marvin Gay "What's Goin On", Blind Faith, Slow Train Coming-Bob Dylan, lots of 60/70/80's early 90's music, BLUES, sax, hi  
Movies Dangerous Beauty, Always, Rob Roy, Braveheart, The Princess Bride, Fried Green Tomatoes, Moulin Rouge, Brubaker, Shawshank Redemption, What the Bleep Do We Know?, Chariots of Fire, Altered States, Brainstorm, Ghandi, Amistad, Glory, Dancing with Wolves, Sitting Bull-Docum  
TV Shows no TV anymore, prior was, Nature of Things David Suziki, Oprah (sometimes used to be regular year, Nova, Dr. Phil (sometimes) Travel(Lonely Plane, Nature, History, Biographies, 60 minutes (sometimes), Movies, Nature Shows, documentaries, don't watch much TV  
Favorite Foods vegitarian  
Favorite Places rivers, woods, mother nature, by/on/in the water (canoeing miss it muc, especially in canoe or it parked by rock, almost private beach as well on island n, can't get to anymore but PLAN TO!  
Can't Live Without careprovider, GOD, fridge, microwave, While in this PHYSICAL BODY THIS LIFE TI, inner spiritual strength, money (unfortunately), &amp, amp, medical diagnosis treatment being deni, growing spiritually, oxygen, water, food, supporotive care, SUNSHINE, my wheelchairs-power  
  Introduce yourself to Cheryl Sunshine
 
Friends of Cheryl Sunshine

Alice K.

Christian B.

Gwendelyn P.

Cynthia V.

Harmonia A.

View all: 518 friends
Cheryl Sunshine's Sharebook
ME/CFS Chronic Fatigue Syndrome Advisory Committee Meeting (CFSAC) - Day 2 - 420 min Video
(Nov 4) Chronic Fatigue Syndrome Advisory Committee Meeting (CFSAC) - Day 2 Air date: Friday, October 30, 2009, 9:00:00 AM Time displayed is ... more »
ME/CFS Chronic Fatigue Syndrome Advisory Committee Meeting (CFSAC) - Day 1 - Video Link 480 minutes
(Nov 4) Chronic Fatigue Syndrome Advisory Committee Meeting (CFSAC) - Day 1 Air date: Thursday, October 29, 2009, 9:00:00 AM Time displayed is... more »
ME/CFS Fuctioning and Energy Index Tables take to your Doc
(Nov 4) For fuctioning charts, you can down load a PDF and take to your doctor,a nd keep one yourself, here is a link to one, I have seen othe... more »
More shares »
Cheryl Sunshine's Photos

MapsIsraelShadedRelief1988.jpg

palestine-boycott-Israel.gif

FairtyPurplePlus.bmp
1036 photos, 46 albums »
My Video    
Loading video...
My Butterfly Rewards
I’ve earned 756 Butterfly Credits
Kudos
7 New Green Stars, 5977 Total Send green star »
 


Karenlee H. (553)
Testimonial on Apr 12, 2006
Image hosting by Photobucket
Comment Board
Viewing 20 of 913: view all | add a comment »
Nov 19, 2009 11:58 AM

Pamylle G. (243)
BIg Hugs Wolves
Nov 15, 2009 10:09 PM

Mary P. (168)
Healing Comments
~Magickal Graphics~ Love and Blessings to you Cheryl I hope you find joy in each day in some special way
Nov 11, 2009 4:02 PM

Pamylle G. (243)
Wednesday 3
Nov 10, 2009 3:29 AM

Mary R. (814)
http://i323.photobucket.com/albums/nn441/DitziSis/HELLO/HelloForYouTeddy.gif?t=1257822715
Nov 2, 2009 10:51 AM

Mary P. (168)
MyspaceMagick-GypsyRose-BirthdayBle.gif
Dear Cheryl, I hope your day was very special and filled with joy
in so many different ways. Blessings

Nov 2, 2009 10:25 AM

Mary P. (168)
Friend Blessings dear Cheryl
Nov 2, 2009 12:37 AM

Mary R. (814)
http://i323.photobucket.com/albums/nn441/DitziSis/BIRTHDAY/HM2BBirthday--.gif?t=1257122167
Oct 17, 2009 11:20 PM

Gt P. (46)
Hi, Cheryl,

Happy Birthday, my dear friend! I hope you had a wonderful day today.


We'll write to you soon, we miss you so very much.


Hugs,
Gtp

Oct 17, 2009 4:10 PM

Sandra P. (116)
Dear Cheryl,


I wish you a Happy Birthday! May the sun shine brigth in this so very beatiful and special day!
cake

Love and hugs,

Sandra

Oct 15, 2009 9:40 PM

Gail C. (486)

Thank you very much for the green star, Cheryl


Oct 15, 2009 8:54 PM

Pamylle G. (243)
Hugs & Blessings Wolves
Oct 12, 2009 1:02 PM

Gail C. (486)



Oct 11, 2009 7:09 PM

Cheryl B. (155)
HAPPY THANKSGIVING, my friend
thanks
Love, Cheryl

Sep 28, 2009 3:24 PM

Pamylle G. (243)
Pamylle Happy Fall
Aug 27, 2009 2:02 AM

little w. (162)

Aug 23, 2009 5:25 PM

Gail C. (486)

Thank you very much, Cheryl, for letting me know about Mary.


Aug 23, 2009 4:01 AM

Cheryl B. (155)
Hi Cheryl - it's been quite a while since I visited you so I'm bringing some flowers, a river, and some beautiful mountains with me... for you! I hear you're getting some pretty rainy & windy weather there, so you might need these. Not bad weather here on West coast but forest fires are really terrible.
Lots of love,
Cheryl
beauty

Aug 9, 2009 5:43 PM

Pamylle G. (243)
Piggy Friends
Aug 4, 2009 10:14 AM

Gregory S. (261)
I hope you enjoy.
Jul 27, 2009 10:39 PM

Joycey B. (695)
cat tag.gif
Have A Great Week Sweet Friend
Thanks For The Green Star

Profile theme: "Animals: WTiger"   |    as your profile theme
Flag as Inappropriate
Copyright © 2009 Care2.com, inc. and its licensors. All rights reserved