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Parkinson’s Disease Treatment for Walking and Balance – Video

Posted: Published on October 29th, 2012

Parkinson's Disease Treatment for Walking and Balance This patient was in between diagnoses of Parkinson's Disease and Spino Cerebellar ataxia. The medication for Parkinson's disease was not helping her. Within twenty minutes I diagnosed the directional balance problems with Balance-Based Torso-Weighting and strategically weighted her. She received a BalanceWear OW200 orthotic. I will be discussing our current research in Parkinson's Disease.From:motiontherapeuticsViews:1600 2ratingsTime:01:59More inScience Technology Read the original here: Parkinson's Disease Treatment for Walking and Balance - Video … Continue reading

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Ataxia treatment – Video

Posted: Published on October 29th, 2012

Ataxia treatment From:motiontherapeuticsViews:1904 3ratingsTime:03:55More inScience Technology View post: Ataxia treatment - Video … Continue reading

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ViroPharma Incorporated Reports Third Quarter 2012 Financial Results

Posted: Published on October 29th, 2012

EXTON, Pa., Oct. 25, 2012 /PRNewswire/ --ViroPharma Incorporated (VPHM) reported today its financial results for the third quarter ended September 30, 2012. Since June 30, 2012, we: Net sales were $91 million for the third quarter ended September 30, 2012, as compared to $143 million in the same three months of 2011. The decrease was the direct result of the impact of generic oral vancomycin entries into the market. Regarding Cinryze, during the quarter the U.S. channel inventory increased by approximately $2 million. Net sales were $321 million for the nine months ended September 30, 2012, as compared to $399 million in the comparative period of 2011. "The third quarter of 2012 was a period of tremendous fundamental execution for ViroPharma," stated Vincent Milano, ViroPharma's chief executive officer. "Despite several early challenges in 2012, the progress and achievements that have been made across our entire organization in the first nine months have rapidly shifted the focus towards the promise of what ViroPharma can deliver for both our patients and our shareholders alike in the years ahead. We are seeing remarkable growth with Cinryze here in the United States, our product launches in Europe are beginning to gain ground and the … Continue reading

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Health Canada Approves New Drug Submission for Cinryze™ (C1 inhibitor [human])

Posted: Published on October 29th, 2012

EXTON, Pa., Oct. 22, 2012 /PRNewswire/ --ViroPharma Incorporated (VPHM) today announced that Health Canada has granted a Notice of Compliance (NOC) and approved a New Drug Submission (NDS) for Cinryze (C1 inhibitor [human]). Approval of Cinryze was granted for routine prevention of angioedema attacks in adult and adolescents with hereditary angioedema (HAE). Until now, there have been no approved plasma derived C1 inhibitor therapies for routine prevention of HAE attacks in Canada. ViroPharma's Canadian headquarters are located in Oakville, Ontario. We anticipate Cinryze to be commercially available in Canada as early as the second quarter of 2013. "Hereditary angioedema is a complex and life threatening disease that must be managed carefully by physicians," said Dr. Tom Bowen, clinical professor of medicine and pediatrics at the University of Calgary. "The approval of Cinryze to help prevent HAE attacks provides an essential addition to the patient care arsenal of physicians across Canada. Disease management options that provide choices for patients for both treatment and prevention of hereditary angioedema can help patients reach their own personal health and wellness goals." "It is important to have a number of disease management options available for those living with hereditary angioedema," said Della Cogar, founder, HAE … Continue reading

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Epilepsy Drug Fycompa Receives FDA Approval

Posted: Published on October 29th, 2012

Featured Article Main Category: Epilepsy Also Included In: Regulatory Affairs / Drug Approvals;Neurology / Neuroscience Article Date: 24 Oct 2012 - 3:00 PDT Current ratings for: Epilepsy Drug Fycompa Receives FDA Approval 3 (2 votes) 3 (1 votes) The drug, made by Eisai Inc, the US arm of the Japanese global pharma company, is already approved for use in Iceland, Norway and the European Commission on behalf of its 27 sovereign member states. Epilepsy is a spectrum of brain disorders, ranging from severe, life-threatening and disabling, to more benign. It arises because of abnormal or excessive activity of nerve cells in the brain, which can cause seizures that give rise to symptoms ranging from strange sensations, unusual behavior, repetitive limb movements (spasms), to generalized convulsions with loss of consciousness. Partial seizures are the most common type of seizure, affecting some 60% of people with the condition. They affect only a limited or localized part of the brain, but can spread to other parts. Russell Katz, director of the FDA's Division of Neurology Products in the agency's Center for Drug Evaluation and Research, emphasizes this point in a press statement, adding: "It is important to have a variety of treatment options … Continue reading

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Patient Advocates Tell of Struggles in Getting Drugs Developed for Rare Diseases

Posted: Published on October 29th, 2012

HORSHAM, Pa., Oct. 18, 2012 /PRNewswire/ --A panel of parents who became patient advocates after their children were diagnosed with rare diseases will discuss their struggles and successes in navigating the drug development process on Monday at a Washington, D.C., conference sponsored by DIA and the National Organization for Rare Disorders (NORD). The work carried out by these parents through rare disease associations can be one of the most important factors in getting lifesaving help for their children. For many parents, the news that their child has a rare disease has changed the course of their lives, including their leaving other careers to work full time to advance the development of therapies to treat severe illnesses that may affect as few as 500 people in the United States. Five of these parents and one patient will speak at the 2012 U.S. Conference on Rare Diseases and Orphan Products. "People are going along living their lives and then learn their child has a rare disease. These parents are diving into a world unknown to them to navigate the complicated path to find a treatment," said Peter L. Saltonstall, NORD president and CEO. "We see it over and over again. The result … Continue reading

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To Your Good Health: Keloid is scar that won't stop growing

Posted: Published on October 29th, 2012

Question: I am a 26-year-old black woman. All through high school, I begged my mother to let me get my ears pierced. She said to wait until I graduated from college and was on my own. I did. On each ear, the piercing left a huge scar. The doctor called it a keloid. What are keloids and what is their treatment? Answer: Keloids are scars that form far too much scar tissue. The result is an unsightly, overgrown and sometimes disfiguring scar. Scars from surgery, from an inadvertent cut and from procedures as innocuous as ear piercing can become keloids. People of Asian and African descent are particularly vulnerable to developing such scars. I don't want to discourage you, but keloid treatment often involves a recurrence of a keloid scar. Plastic surgeons and dermatologists are the doctors to consult for possible correction. I'll give you some examples of how keloids are treated: One way is injecting them with potent cortisone drugs, such as triamcinolone. A good response occurs in 70 percent of patients, but the recurrence rate is also high. Excision of the scar followed by triamcinolone injections into the newly healing tissues is another method. Silicone gel sheeting can … Continue reading

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I’m Depressed, Anxious, Depersonalized WHAT DO I DO? WILL I EVER BE OK? – Video

Posted: Published on October 29th, 2012

I'm Depressed, Anxious, Depersonalized WHAT DO I DO? WILL I EVER BE OK? Please SHARE THIS VIDEO if you found it useful or if you know somebody who is suffering and scared. Thank you. GREAT WEBCITE: healingfromdepression.com MY STORY My name is Noah and on May 18 2011, I had a rare reaction to a vaccine called VIVITROL and consequently spiraled into a major, agitated, suicidal depression with depersonalization. I lost 25 lbs in 4 weeks and was in full panic or near panic for 8 weeks straight mixed with the darkest most painful depression I cold have ever imagined. I immediately could not work and had to move in with my parents who along with many siblings and friends had to watch me 24/7 as I was so suicidal. I was eventually hospitalized. Getting through each day seemed truly unbearable and I knew I would surely die. I have been put on many many different SSRI's SNRI's Tricyclics, Mood stabilizers, anti psychotics, holistic meds, acupuncture and even a form of shock therapy called RTMS. I barely saw any improvement in my condition for a full year. It was decided I had treatment resistant depression and I … Continue reading

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30 percent lower risk

Posted: Published on October 29th, 2012

Hormone therapy may cut Alzheimers risk in menopausal women (Reuters) / 25 October 2012 CHICAGO - The latest data from a long-running study of hormone therapy suggests women who started taking hormone replacements within five years of menopause were 30 percent less likely to develop Alzheimers disease than women who started years later. The findings, reported in the journal Neurology, add to evidence suggesting that taking hormone treatments around the time of menopause may be doing more than just helping women cope with hot flashes and night sweats. Our results suggest that there may be a critical window near menopause where hormone therapy may possibly be beneficial, Peter Zandi of Johns Hopkins University in Baltimore, one of the study leaders, said in a statement. The findings come as menopausal women and their doctors continue to parse out the risks and benefits of hormone replacement therapy. Most researchers agree that hormone replacements do not protect women from diseases of aging, and taking these drugs for long periods of time are associated with significant risks, including breast cancer, heart disease and gall bladder disease. Earlier this week, the U.S. Preventive Services Task Force reaffirmed its 2005 guidelines recommending against the treatment as … Continue reading

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Early HRT 'may cut Alzheimer risk'

Posted: Published on October 29th, 2012

Women who begin taking hormone replacement therapy (HRT) within five years of the menopause may reduce their risk of developing Alzheimer's disease, a study suggests. Scientists monitored 1,768 women aged 65 and over for 11 years, taking note of their history of HRT use. During the study, 176 women developed Alzheimer's disease. The researchers found that women who started HRT within five years of the menopause had a 30% lower risk of Alzheimer's than those who had not used hormone therapy. The risk was unchanged among HRT users who began the treatment more than five years after the menopause. A higher risk of dementia was seen in women who started combined oestrogen and progestin therapy when they were at least 65 years old. "This has been an area of debate because observational studies have shown a reduced risk of Alzheimer's disease with hormone therapy use, while a randomised controlled trial showed an increased risk," said study leader Dr Peter Zandi, from Johns Hopkins University in Baltimore, US. "Our results suggest that there may be a critical window near menopause where hormone therapy may possibly be beneficial. On the other hand, if started later in life, hormone therapy could be associated … Continue reading

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