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TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS
June 18, 2013 6:57 AM
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Committee Approves $7.5 Million for the ALSRP The House Appropriations Committee approved legislation to provide an additional $7.5 million in continued funding for the ALS Research Program (ALSRP) at the Department of Defense. If enacted, it would bring total funding for the program to nearly $50 million. Thank you to everyone who made the trip to Washington last month for National ALS Advocacy Day and also to those who participated in our online virtual Advocacy Day. Your outreach to Members of Congress in support of
From
boston
Argeo Paul Cellucci, a Hudson native who rose from a smalltown selectman to become governor of Massachusetts and later US ambassador to Canada, died at home this afternoon after a five-year battle with Lou Gehrig’s disease.
From
www
Increased iron levels may be causally associated with a decreased risk of developing Parkinson's disease, researchers in Italy say.
From the familiar steps of "West Side Story" to as-yet unseen professional dance choreography, a group of enthusiastic dancers joined professional dancers David Leventhal and Lesley Garrison today for a dance for Parkinson's disease.
From
q13fox
SEATTLE - Former University of Washington women’s basketball player Melissa Erickson died Wednesday after a long battle with ALS, also known as Lou Gehrig’s disease. Erickson was 34.
To honor and recognize wonderful caregivers who care for their friends and family in need, Chanda Brigance, co-founder of the Brigance Brigade Foundation, pr...
MADISON, Wis. — Transplantation of human stem cells in an experiment conducted at the University of Wisconsin-Madison improved survival and muscle function in rats used to model ALS, a nerve disease that destroys nerve control of muscles, causing death by respiratory failure. ALS (amyotrophic lateral sclerosis) is sometimes called “Lou Gehrig’s disease." According to the ALS Association, the condition strikes about 5,600 Americans each year. Only about half of patients are alive three years after diagnosis. In work recently completed at the UW School of Veterinary Medicine, Masatoshi Suzuki, an assistant professor of ..........................
Exposure to pesticides and other chemicals is linked to an increased risk of developing Parkinson’s disease, according to a fresh look at some past research. Dr. James Bower, a neurologist from the Mayo Clinic in Rochester, Minn., said the finding is consistent with previous research, but the........
It was September 1997. I had hoped the weakness in my leg would be treatable, but my doctor shook his head. The intravenous immunoglobulin treatments he'd been giving me for a possible motor neuropathy weren't working, leading him to conclude I had "probable ALS."
From
tbo
Parkinson’s compresses you, Bruce Wright says of the disease he’s lived with since 2005. It makes your life smaller, slower and more careful.
Of all the medical diagnoses a physician can make, the diagnosis of ALS--amyotrophic lateral sclerosis--is one of the most devastating. Commonly known as |
Organic food advocate, Colle Farmers Market, responds to a Medical Daily article outlining how patients with Parkinson’s disease may benefit from eating food grown without pesticides.
Prof. Molly Shoichet (photo courtesy of Shoichet Lab) One of the challenges facing stem cell researchers is how to ensure that cells delivered to patients don't die after transplantation to the point of care.
Wayne Channon's curator insight,
June 18, 2013 12:16 PM
A possible way of keeping stem cells at the point of insertion or even keeping them alive following transplant.
He’s back. Last autumn, Hisashi Moriguchi stunned the world of stem-cell science by claiming he had become the first person to transfer induced pluripotent stem cells into patients. In a now-infamous front-page spread in the Yomiuri Shimbun — which has the largest number of subscribers of any newspaper in the world — Moriguchi said he created a type of iPS cells, differentiated.....
The ALS Association Greater Chicago Chapter’s Run to Defeat ALS
I am running in the 2013 Chicago Marathon in memory of my mother, Donna McNeice, my friend John Keator, and a family friend Bob O'Neil who all recently lost their battles to ALS. I am also running in memory of Michael Lopez (Team Cure ALS), who lead an inspirational battle with ALS and in the process has raised ALS awareness and was a source of hope to so many people. I want to help all those who are currently battling ALS. It is my goal to raise ALS Awareness and help find a cure for this dreaded disease.
If you would like to make a donation and help David "Stay Commited to a CURE for ALS please visit this link:
T.E.A.M.-Together Everyone Accomplishes More!
TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS's comment,
May 24, 2013 8:33 PM
David- We are beyond grateful and honored to have you running in Memory of Micheal Lopez Jr. & TEAM Cure ALS. We would like you to know that friends and support from individuals like you continues to bring our family extreme comfort and peace with our healing and loss of Michael after his battle with this horrendous disease ALS the last 17 years. We are family, brought together by such a horrendous disease, but yet for so many valuable and important reasons in our lives. The loss never leaves, the hurt never ceases but we have each other in our continued fight for our loved ones, friends and and all others that continue to FIGHT and hold HOPE for a Cure! Michael is so PROUD to have you represent him! Thank You will never be enough!
Rock Steady Boxing, the first and only boxing program of its kind in the country, was founded in 2006 by former Marion County Prosecutor, Scott C. Newman, who is living with Parkinson’s.
The seed for what would eventually become Rock Steady Boxing was planted when Newman began intense, one-on-one, boxing training just a few years after he was diagnosed with early-onset Parkinson’s at the age of 40. Newman witnessed the dramatic improvement in his physical health, agility and daily functioning through the.........................
From
spie
A new home tracking system based on a Microsoft Kinect sensor will help patients with the symptom of ‘freezing of gait.’
Researchers based at the University of California, Los Angeles announced today that they’ve found an abundant, cheap, easy-to-obtain source of stem cells that could prove to be ideal for regenerating all the basic tissue types of the human body.
From
www
Medicare Coverage of Speech Generating Devices (SGD)Medicare will cover the cost of a SGD if you have Medicare Part B services.
1. You must live in your family home or an assisted living facility
2. Medicare will not cover the cost of a SGD if you are in a hospital, skilled nursing facility, or on hospice.
*Medicare will cover 80% of the allowable cost of the device. Secondary insurance should pay the remaining 20% but that is not always the case. If you do not have secondary insurance, you will be responsible for the 20% co-pay. There are funds available from charitable organizations that may help pay for any deductible or co-pay that insurance does not cover.
*Medicare classifies SGD’s as “durable medical equipment” (DME) and will cover the device under this classification.
*An assessment by a speech-language pathologist is required to document that this device is needed to meet your daily functional communication needs. 80% of the cost of the assessment is covered by Medicare. The remaining charge can be billed to secondary insurance (if applicable) or will be billed to the client.
*A doctors prescription is required.
*Once the assessment has been completed, appropriate paperwork will be submitted to the vendor of the device. This process usually takes approximately one to two months.
*If the vendor feels all the paperwork is in order, they will ship the device directly to you.
Training on your device can be provided by:
> Vendor—many vendors offer training sessions at no cost.
> Facility—the facility where you received your device can provide training. The cost of the training session is covered by Medicare.
> Chapter—the ALS Association may have resources available for training.
Howard Mason's curator insight,
July 17, 2013 10:53 PM
We just bought some medical equipment last week for my grandfather. It is very important to him since, he easily get sick. The good thing that I like about this home medical equipment is, they are easy to use.
TEAM Mike Lopez Memorial Foundation |Find us on Twitter:@TEAMCUREALS's comment,
August 5, 2013 6:34 PM
Thank you Howard for your input! What device did you purchase?
At the present, no cure exists for Parkinson's disease, although symptomatic intervention, including treatment with dopamine agonists, can alleviate patients' motor impairment.
A recent stem-cell breakthrough reported by Oregon researchers has sparked an anonymous critique questioning images used in the paper, and the authors plan to issue a correction, according to a scientific journal.The study published by Shoukhrat...
New insights into the cause of motor neurone disease have been uncovered with a study showing mutations in a specific gene lead to the death of the nerve cells responsible for powering our muscles.
Researchers at the Stanford University School of Medicine have identified mutations in several new genes that might be associated with the development of spontaneously occurring cases of the neurodegenerative disease known as amyotrophic lateral... |
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