GA VICTORY
The Loving Kind has entered the official UK charts at #10! OK, so I know that this may not be the best chart position the girls have ever received, and that the song definitely deserves a higher placing, but we have all reason to celebrate as this is now the girls' 20TH consecutive Top 10 single; a huge achievement which we and the girls should be very proud of! Well done everyone! We can now sleep safe in the knowledge that the single is in the Top 10. Keep buying your copies if you haven't though, as it's never too late! Well done girls!
TEAM CHIM
Reunited Bunnies
Viva LA LHOEhan
Salsa Dip anyone?
Susan Dowd Stone shares hopeful thoughts on the Melanie Blocker Stokes MOTHERS ACT
Susan Dowd Stone submitted the following article to EmpowHer yesterday and I want to help spread this info around because it's so crucial that this much-needed legislation gets passed. Please read below and click here to find out more about Susan and the tremendous work she is doing.
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Attention advocates of America’s mothers and the thousands of courageous women who are experiencing or who have survived a pregnancy or postpartum depression – you have not been forgotten. For among the significant challenges facing the 111th Congress, the issue of untreated maternal depression remains a top priority. One new Congressional focus is the rebuilding of national infrastructure. One might make the analogy that this should include enhancing the healthy infrastructure of our families by ending the preventable plague of maternal mood disorders which continues to ravage over 800,000 women – and their infants and families – every year. The long-term consequences of untreated maternal depression range from chronic illness, child learning disabilities, family stress and economic loss - to death.
Congressman Bobby L. Rush has reintroduced The Melanie Blocker Stokes MOTHERS Act to the 111th Congress. During the 110th Congress, the legislation had over 130 bi-partisan cosponsors and passed the United States House of Representatives on October 15th, 2007 by a vote of 382-3. I was so very proud to be sitting in the Congressional Gallery on that triumphant day as a unified Congress validated the suffering of millions of American women and families by promising more support to help end this public health crisis. Congressman Rush never forgot the Chicago constituent – Melanie Blocker Stokes – who lost her life to this illness and whose tragic death inspired his decades long devotion to end maternal suffering.
In the U.S. Senate, Sen. Robert Menendez has been similarly steadfast in his devotion and promotion of The MOTHERS Act. Initially based on New Jersey’s groundbreaking law inspired by PPD Survivor and former New Jersey First Lady Mary Jo Codey and spearheaded to passage by her husband N.J. State Senate President Richard Codey, the passage of this legislation has resulted in increased availability of services, public awareness campaigns and state-wide hot lines responsive to the crisis. While repeated attempts by Sen. Menendez and other senate leaders to pass the bill last fall narrowly missed, one pivotal result was that the national spotlight again became fixed on this incomprehensible Congressional stalemate.
The resulting new waves of national attention and support for this bill and its clear, purposeful mission have further galvanized public support and public outcry for its passage. The research, education, public awareness campaigns and grants for treatment and supportive services requested in The Melanie Blocker Stokes MOTHERS Act will help to end the untold agony that too often goes unrecognized, undiagnosed and untreated.
The countless women who walk through my practice door feeling shamed and marginalized for the medical illness they are trying to fight alone must know that these common disorders can afflict anyone - that these illness are treatable - that they did nothing to cause it - that they will be well again! That they are NOT ALONE!
As president-elect Barack Obama - one of the bill’s initial lead sponsors – takes the nation’s helm this week, we anticipate a timely convergence of forces which will lend impetus to the bill’s passage this year.
In addition to our legislative leaders, many thanks to all of you who have given voice and time and energy to turn this tide on the ignorance and suffering that has plagued American mothers and their families for decades – your moment is coming. With your renewed support and advocacy, we will pass The Melanie Blocker Stokes MOTHERS Act in 2009!
SUMMARY OF THE LEGISLATION Section 1: Short title of the bill- The Melanie Blocker Stokes MOTHERS Act.
TITLE I- Research
• Encourages HHS to coordinate and continue research to expand the understanding of the causes of, and find treatments for, postpartum conditions. Also, encourages a National Public Awareness Campaign, to be administered by HHS, to increase awareness and knowledge of postpartum depression and psychosis.
• Sense of Congress that the Director of the NIH may conduct a nationally representative longitudinal study of the relative mental health consequences for women of resolving a pregnancy (intended or unintended) in various ways, including carrying the pregnancy to term and parenting the child, carrying the pregnancy to term and placing the child for adoption, miscarriage, and having an abortion. This study may assess the incidence, timing, magnitude, and duration of the immediate and long-term mental health consequences (positive and negative) of these pregnancy outcomes.
TITLE II- Delivery of Services
• Encourages HHS to make grants available for projects for the establishment, operation, and coordination of systems for the delivery of essential services to individuals with postpartum depression. (Entities): Makes grants available to public or nonprofit private entity, which may include a State or local government, a public-private partnership, a recipient of a grant under the Healthy Start program, a public or nonprofit private hospital, community-based organization, hospice, ambulatory care facility, community health center, migrant health center, public housing primary care center, or homeless health center, or any other appropriate public or nonprofit private entity. o (Activities): Eligible activities include delivering or enhancing outpatient, inpatient and home-based health and support services, including case management and comprehensive treatment services for individuals with or at risk for postpartum conditions. Activities may also include providing education about postpartum conditions to new mothers and their families, including symptoms, methods of coping with the illness, and treatment resources, in order to promote earlier diagnosis and treatment.
TITLE III- General Provisions
• (Funding): Authorizes $3,000,000 for fiscal year 2008; and such sums as may be necessary for fiscal years 2009 and 2010.
• (HHS Report): Requires the Secretary of HHS to conduct a study on the benefits of screening for postpartum depression and postpartum psychosis.
• (Limitation): The Secretary may not utilize amounts made available under this Act to carry out activities or programs that are duplicative of activities or programs that are currently being carried out through the Dept of HHS.
SUPPORTERS: Postpartum Support International Association of Women's Health, Obstetric and Neonatal Nurses American Psychological Association American Psychiatric Association Children’s Defense Fund American College of Obstetricians and Gynecologists March of Dimes Mental Health America American College of Nurse Midwives National Council for Community Behavioral Healthcare Depression and Bipolar Support Alliance Suicide Prevention Action Network USA National Alliance on Mental Illness Association of Maternal and Child Health Programs National Partnership for Women & Families OWL- The Voice of Midlife and Older Women National Women’s Law Center
Playboy turns on the raunch!!!
Get ready to see a lot more of Aubrey O'Day!
The former Danity Kane singer will grace the cover of the March issue of Playboy she confirms exclusively to Usmagazine.com.
"I'm honored to be a part of the Playboy legacy and look forward to my March cover hitting newsstands on February 13,like we haven't seen her half naked any way.yawn yawn
Given the colorful, upbeat look (complete with little flash points) of the just-released cover art for her new album, All I Ever Wanted, due out March 17, Kelly Clarkson is obviously trying to break away from all the drama that surrounded her ill-fated 2007 disc, My December, and have a little fun.
In fact, American Idol's first viewer-created champ already hinted back on New Year's Day of a return to her more playful pop side when she unveiled the lollipop-loving cover for her first single, "My Life Would Suck Without You."Cant wait for the video here
Trouble Trouble!
The end Word
Hardcore Chick
Thanks to Tasha @ SarahHardingAddicts (one of our elite affilates go check it out!) has posted wonderful scans of Sarah Harding in today’s Fabulous magazine.Over in our fantasy world, Girls Aloud are our best friends, and Sarah Harding is the one we turn to for a party.
She’s the peroxide blonde, whippet-thin firecracker who’s always ready to hit the clubs. She sorts the guest list, orders the sambucas, and gets the chips and curry sauce in while we snog an unsuitable boy outside.
We can assume all of this because we feel we know her. But just five minutes in her company proves that there are many sides to Miss ‘Party’ Harding. If you think she’s just a good-time girl, you’d better wake up and smell the apple crumble (which she makes, by the way).
As we settle down on a battered leather sofa, before her transformation into a hard-edged va-va-vamp, Sarah’s thinking about what best sums her up.
2009 Update
2008 was defined as the year of new beginnings. In many ways it was. But beginnings are always something bright, shining and new. My year for beginnings meant revelation and resolution. 2009 will require reinvention. A beauty of a butterfly can only be realized after the transformative process of metamorphosis. Maturity and wisdom comes through learning, experience and revelation.
January, last year my expectations were high. But most of my perceptions were distorted by the euphoric high and mania caused by high doses of steroids as well as the neuropsychiatric component of my illness. That's the double edge sword of the current pharmaceutical treatment. Prednisone's suppression of the self inflicted immune attacks is life saving, but the havoc on the hormones intensifies many neuropsychiatric symptoms. It has been hard to determine the source of the devastation to my mind.
2007 was a year of tapering off the multitude of "anti-drugs"...antidepressants, anticonvulsants, antibiotics, etc. After 2008 was spent detoxifying, I began to feel like myself again. So I conclude that blind use of the pharmaceuticals led to a synergistic affect.
Unfamiliar with the extreme and strange symptoms uncommon in their usual lupus cases, my treatment was compartmentalized. Rheumatologists and Internist had referred me to other specialist to treat the unfamiliar "spells." The neurologist and neuropsychiatrist treated the "spells" according to the nearest diagnosis in their repertoire, "petit mal", "nonepileptic seizures." I eagerly consumed a daily cornicopia of brightly colored pills with every hope without any question. I became a zombie. I retained all of my knowledge but as a naive 6 year old. It took months of irrational behavior before I realized my mental status and began to suspected the drugs. That revelation led to the first steps of resolution, tapering my medications seeking non-pharmaceutical approach to managing my symptoms.
After being completely off of all the "anti-drugs", obsessive compulsive symptoms significantly improved. The overwhelming anxiety was no longer constant. I could recall the perceptions I had before. Beginning with detoxification, I began taking charge of my health I began asking questions. I began questioning, wikipediaing and googling every symptom, drug and doctor. The revelation was that many of my neuropsychiatric symptoms even certain strange idiosyncratic behavior that I'd developed were a part of a pattern consistant with frontal lobe problems. It didn't matter what the cause, traumatic brain injury of a car accident, ischemic lesion of stroke or something biochemically complex as Asperger Syndrome, their were defined set of symptoms that often occur together when specific areas of the brain are affected. No doctor had really defined what was causing my neurological problems. All they would do is tell me what it was not. I was not epileptic. Repeated MRI, EEG, etc that revealed nothing. They literally shrugged their shoulders. Yet I was prescribed antiepileptic drugs, because that's what they know. I was determined to have some concrete measurable evidence of the devastating neurological deficits that have turned my life upside down.
I read a poignant forum post about who could no longer work to support his family because he "couldn't think." The culprit APS. That was my next major revelation, the discovery that APS could be responsible for neuropsychiatric symptoms I was having impaired thinking, seizures, paralysis, etc. The APS website provided me with the first doctor, a hematologist, that had some familiarity with my strange symptoms. He recognized the foreign speech I'd aquired as a symptom not a West Indian accent its usually mistaken for. He'd witnessed a case of lupus with APS that aquired the same "accent". He warned that there's no cure or successful protocol for treatment. Comprehensive testing of blood and brain scans didn't reveal anymore. APS probably causes undetected tiny blood clots in brain capilaries coupled with the ubiquitous inflammation of lupus autoimmune activities to upset my brain chemistry, perhaps even causing TIAs or ministrokes. He could only offer continued maintenance of therapeutic blood thinners to reduce clotting and prevent the worse case scenario, stroke or pulmanary embolism. Having an expert acknowledge and clarify my symptoms within the context of SLE and APS was satisfying despite lack of new treatment He listened and didn't go straight to the prescription pad. I had made a decision not play guinea pig to anymore new fangled brain pharmaceuticals. He supported my decision. He also initiated the next major step of resolution. By suggesting neuropsychiatric testing for some measurable evidence of my symptoms and some help coping. I began very rewarding weekly sessions with a psychologist at the same cancer clinic trained for patient couseling. Not only have we dealt with the anger, grief, anxiety she has helped me find seek resources to solve the concrete problems such as a pro bono lawyer to help with child support or nonprofit organization help with home repairs I completed a battery neuropsychiatric tests in 8 intense sessions to produce a comprehensive detailed report on my brain. I finally had acknowledgment and evidence. My neurological
deficits have been defined.
2008 marked the beginning of taking charge of my symptoms. I had already began to regain my stamina through physical therapy. I began a diet that's therapeutic and preventative for my chronic secondary conditions, IBS and UTI.Participating in online groups led me to find therapy through blogging and sharing over the internet.
I established The Mission based on my new philosophy of thinking wholistic:
Surviving The Disease requires healing The Mind, The Body and The Spirit.
Now I've I'm reviewing my web development skills to establish a new social networking site to collaborate with fellow bloggers. Ardent Cerebrations: The Musings of Lupus Survivors! Last years revelations and resolutions broke me from a cocoon, my own metamorphosis into a new butterfly, this year I plan to fly.
January, last year my expectations were high. But most of my perceptions were distorted by the euphoric high and mania caused by high doses of steroids as well as the neuropsychiatric component of my illness. That's the double edge sword of the current pharmaceutical treatment. Prednisone's suppression of the self inflicted immune attacks is life saving, but the havoc on the hormones intensifies many neuropsychiatric symptoms. It has been hard to determine the source of the devastation to my mind.
2007 was a year of tapering off the multitude of "anti-drugs"...antidepressants, anticonvulsants, antibiotics, etc. After 2008 was spent detoxifying, I began to feel like myself again. So I conclude that blind use of the pharmaceuticals led to a synergistic affect.
Unfamiliar with the extreme and strange symptoms uncommon in their usual lupus cases, my treatment was compartmentalized. Rheumatologists and Internist had referred me to other specialist to treat the unfamiliar "spells." The neurologist and neuropsychiatrist treated the "spells" according to the nearest diagnosis in their repertoire, "petit mal", "nonepileptic seizures." I eagerly consumed a daily cornicopia of brightly colored pills with every hope without any question. I became a zombie. I retained all of my knowledge but as a naive 6 year old. It took months of irrational behavior before I realized my mental status and began to suspected the drugs. That revelation led to the first steps of resolution, tapering my medications seeking non-pharmaceutical approach to managing my symptoms.
After being completely off of all the "anti-drugs", obsessive compulsive symptoms significantly improved. The overwhelming anxiety was no longer constant. I could recall the perceptions I had before. Beginning with detoxification, I began taking charge of my health I began asking questions. I began questioning, wikipediaing and googling every symptom, drug and doctor. The revelation was that many of my neuropsychiatric symptoms even certain strange idiosyncratic behavior that I'd developed were a part of a pattern consistant with frontal lobe problems. It didn't matter what the cause, traumatic brain injury of a car accident, ischemic lesion of stroke or something biochemically complex as Asperger Syndrome, their were defined set of symptoms that often occur together when specific areas of the brain are affected. No doctor had really defined what was causing my neurological problems. All they would do is tell me what it was not. I was not epileptic. Repeated MRI, EEG, etc that revealed nothing. They literally shrugged their shoulders. Yet I was prescribed antiepileptic drugs, because that's what they know. I was determined to have some concrete measurable evidence of the devastating neurological deficits that have turned my life upside down.
I read a poignant forum post about who could no longer work to support his family because he "couldn't think." The culprit APS. That was my next major revelation, the discovery that APS could be responsible for neuropsychiatric symptoms I was having impaired thinking, seizures, paralysis, etc. The APS website provided me with the first doctor, a hematologist, that had some familiarity with my strange symptoms. He recognized the foreign speech I'd aquired as a symptom not a West Indian accent its usually mistaken for. He'd witnessed a case of lupus with APS that aquired the same "accent". He warned that there's no cure or successful protocol for treatment. Comprehensive testing of blood and brain scans didn't reveal anymore. APS probably causes undetected tiny blood clots in brain capilaries coupled with the ubiquitous inflammation of lupus autoimmune activities to upset my brain chemistry, perhaps even causing TIAs or ministrokes. He could only offer continued maintenance of therapeutic blood thinners to reduce clotting and prevent the worse case scenario, stroke or pulmanary embolism. Having an expert acknowledge and clarify my symptoms within the context of SLE and APS was satisfying despite lack of new treatment He listened and didn't go straight to the prescription pad. I had made a decision not play guinea pig to anymore new fangled brain pharmaceuticals. He supported my decision. He also initiated the next major step of resolution. By suggesting neuropsychiatric testing for some measurable evidence of my symptoms and some help coping. I began very rewarding weekly sessions with a psychologist at the same cancer clinic trained for patient couseling. Not only have we dealt with the anger, grief, anxiety she has helped me find seek resources to solve the concrete problems such as a pro bono lawyer to help with child support or nonprofit organization help with home repairs I completed a battery neuropsychiatric tests in 8 intense sessions to produce a comprehensive detailed report on my brain. I finally had acknowledgment and evidence. My neurological
deficits have been defined.
2008 marked the beginning of taking charge of my symptoms. I had already began to regain my stamina through physical therapy. I began a diet that's therapeutic and preventative for my chronic secondary conditions, IBS and UTI.Participating in online groups led me to find therapy through blogging and sharing over the internet.
I established The Mission based on my new philosophy of thinking wholistic:
Surviving The Disease requires healing The Mind, The Body and The Spirit.
Now I've I'm reviewing my web development skills to establish a new social networking site to collaborate with fellow bloggers. Ardent Cerebrations: The Musings of Lupus Survivors! Last years revelations and resolutions broke me from a cocoon, my own metamorphosis into a new butterfly, this year I plan to fly.
Cole Vouging
Heres a video from the Vogue website of Cheryl Cole posing for the cover.
Cheryl Cole has revealed how she struggles to control her weight - and how she felt about claims that her footballer husband Ashley had cheated on her.
‘It was horrendous,’ said the 25-year-old singer and X Factor judge.
‘But look, Ashley’s young and he’s got a young mentality - for his age anyway.’
Sparkling: Cheryl Cole poses in sequined trousers and jewelled belt for Vogue. She is the cover girl on the February edition
Cheryl Cole has revealed how she struggles to control her weight - and how she felt about claims that her footballer husband Ashley had cheated on her.
‘It was horrendous,’ said the 25-year-old singer and X Factor judge.
‘But look, Ashley’s young and he’s got a young mentality - for his age anyway.’
Sparkling: Cheryl Cole poses in sequined trousers and jewelled belt for Vogue. She is the cover girl on the February edition
Tisdale's shape
High School Musical starlet Ashley Tisdale shows off her fabulous figure on the January 2009 cover of Shape magazine. Here are some interview snippets from the 23-year-old actress:
On always being petite: “I was always super thin — too skinny, actually. I felt like someone could break me in half.”
On her big motivator, personal trainer Christopher Hebert: “He’s cute, which makes it fun, and he never lets our exercise session get boring.”
On her guilty pleasure foods: “I love carbs. Bread, corn bread, french fries—all that stuff.”
Shes Back
It’s 2009 and the original American Idol is elbowing her way back onto the music scene with the release of her still-untitled third studio album.
Keep your ears open for the “My Life Would Suck Without You,” the new single from Grammy Award winner Kelly Clarkson, debuting on radio stations nationwide Jan. 19.
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