The Multiple System Atrophy Coalition
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MSA Coalition to Raise Awareness for Multiple System Atrophy Disease 

MSA Coalition to Raise Awareness for Multiple System Atrophy Disease  | The Multiple System Atrophy Coalition | Scoop.it
The MSA Coalition is encouraging to finance MSA research fund so as to identify the cause, treatment & cure for the MSA disease. Help Multiple System Atrophy in doing research. CALL Now @866-737-5999
 
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MSA-Multiple System Atrophy Disease - All about its History

MSA-Multiple System Atrophy Disease - All about its History | The Multiple System Atrophy Coalition | Scoop.it
History of MSA-Multiple System Atrophy is very rarely known to people. MSA was discovered by Dr. Milton Shy and Dr. Glen Drager and thus named as Shy Drager Syndrome. For Support call us at 866-737-4999.
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Starting the MSA Fundraising for MSA Research Fund 

Starting the MSA Fundraising for MSA Research Fund  | The Multiple System Atrophy Coalition | Scoop.it
To help starting in MSA fundraising, Multiple System Atrophy Coalition has partnered with FirstGiving & CrowdRise. Donate MSA research fund as much as you can so as to know cause & treat MSA patient. Call MSA Coalition @ (866)737-5999 for details.
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The Multiple System Atrophy Coalition - Read the Story of Patients affected by it 

The Multiple System Atrophy Coalition - Read the Story of Patients affected by it  | The Multiple System Atrophy Coalition | Scoop.it
MSA diseaseThe only way to defeat Multiple System Atrophy disease is to create awareness & contribute in MSA fundraising. Individual donations are very important, along with asking family & friends for contribution can be more beneficial. To read the full story visit our blog.
 
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Symptoms, Causes & Diagnosis of MSA Multiple System Atrophy

As Multiple System Atrophy is a rare neurodegenerative disorder, the cause for MSA is still unknown. MSA Symptoms include- Parkinsonism disorders, slurred speech, rigid muscles,etc. Researchers are finding the way to diagnose MSA.
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The Multiple System Atrophy Coalition partnered with The Mighty to cover stories of MSA Diseased people

The Multiple System Atrophy Coalition partnered with The Mighty to cover stories of MSA Diseased people | The Multiple System Atrophy Coalition | Scoop.it
The Multiple System Atrophy Coalition is now partnered with The Mighty, a story-based health community focused on improving the lives of people facing MSA disease. Now you can watch many stories on the home page of the mighty.
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What is MSA Shy Drager Syndrome? What are its Cause & Symptoms, Diagnosis, Treatment, Prognosis?

A lot number of people from America are suffered from Shy Drager Syndrome or MSA. It causes progressive damages to the autonomic nervous system. Know about causes, symptoms, diagnosis, treatment & prognosis of this rare disease.
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Why to Support MSA Coalition & make Fundraising? Read the Updates on MSA Blog

Why to Support MSA Coalition & make Fundraising? Read the Updates on MSA Blog | The Multiple System Atrophy Coalition | Scoop.it
The Multiple System Atrophy Coalition is leading the fight to cure MSA disease. It also helps to provide support & informative resources to researchers. Fundraising begins on Giving Tuesday, just click on "Fundraise For This Campaign" to join the Team & support MSA Coalition.
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Know about Multiple System Atrophy Symptoms & its Types

Know about Multiple System Atrophy Symptoms & its Types | The Multiple System Atrophy Coalition | Scoop.it
Many people are not aware about Multiple System Atrophy symptoms, disease & its types. MSA is a neurological disease which occurs due to degeneration of certain nerve cells & it is of 2 types- MSA-P & MSA-C. To Know more Read File Now.
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What is Shy Drager Syndrome- Know its Symptoms

Shy Drager disease or MSA is a rare disease named after 2 physicians- Dr. Milton Shy & Dr. Glen Drager who noticed the symptoms of Shy Drager Syndrome in two patients. Symptoms are dizziness, constipation, momentary blackouts & movement disorders in their body. Read More
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MSA Coalition Patient and Caregiver Conference - 7 Days Remaining!!!

MSA Coalition Patient and Caregiver Conference - 7 Days Remaining!!! | The Multiple System Atrophy Coalition | Scoop.it
Hurry up to attend the MSA Coalition Patient and Caregiver Conference which is going to be held on 14 & 15 October 2016. Limited seats available, Book now or reach us @ (866)737-4999.
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Know the History of MSA - Multiple System Atrophy Coalition

The history of MSA or Multiple System Atrophy is not known to most of us. Go through it and get in detailed about what actually MSA disease is, what are its symptoms, causes, etc? For more information call (866) 737-4999.
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An Update on MSA Coalition Research Grant Program 2016

An Update on MSA Coalition Research Grant Program 2016 The Multiple System Atrophy Coalition provides updates on the status of its MSA Research Grant Program. 36 grant pre proposals were submitted for review. Call (866)737-5999 for support.
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Read about Neurogenic Orthostatic Hypotension & its Symptoms 

NOH or Neurogenic Orthostatic Hypotension is caused due to the failure of autonomic nervous system and seen in people with an existing neurologic disease like MSA, Parkinson’s disease, etc. Read Here for the Symptoms.
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Is MSA Fundraising Time Consuming? Just copy paste, and send

Is MSA Fundraising Time Consuming? Just copy paste, and send | The Multiple System Atrophy Coalition | Scoop.it
MSA Donation/ Fundraising- now you don’t have to set up anything to help us fundraise, all you need to do is copy, paste and send the prewritten asks through email ,social pages or MSA blogs etc. Read more to see why your help is so important.
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Support The MSA Coalition - Attend Support Meeting on 12th Feb

Support The MSA Coalition - Attend Support Meeting on 12th Feb | The Multiple System Atrophy Coalition | Scoop.it
On 12 Feb'17, The Multiple System Atrophy is organizing MSA support meeting to defeat MSA disease. Help the MSA research by making donations in finding the cause for it. Call our Hotline Support at (866)737-5999.
 
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Are you a Patient with MSA Disease? Donate Brain-Read the facts about it 

Researchers are still unknown about the Multiple System Atrophy Causes. To help researchers in finding more about MSA disease, donate the brain of the patient. Call Support Hotline: (866)737-5999
 
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Look at the list of doctors world wide for MSA Diagnosis & Treatment

Multiple System Atrophy is considered as a type of Parkinsonism that affects both men and women. View the list of doctors diagnosing & treating MSA . Call MSA Coalition @ (866)737-5999 for details.
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Support The Multiple System Atrophy Coalition by Donating in Crowdrise Holiday Charity Challenge

Support The Multiple System Atrophy Coalition by Donating in Crowdrise Holiday Charity Challenge | The Multiple System Atrophy Coalition | Scoop.it
The Multiple System Atrophy Coalition is leading the fight to cure this disease by participating in the Crowdrise Holiday Charity Challenge. Till now $200,616 money has been raised. Our goal is to raise $500,000 and finish in 1st place to claim the $100,000 prize. Come on, We Can Do It!!
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Support MSA Coalition to raise Funds via Holiday CrowdRise Challenge for Research

Support MSA Coalition to raise Funds via Holiday CrowdRise Challenge for Research | The Multiple System Atrophy Coalition | Scoop.it
Help MSA in fundraising through the Holiday CrowdRise Challenge. The motto behind this is to help affected families. You can contribute to MSA donation by which will be used for research, advocacy, education.
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The MSA Coaliation to Raise Research Funds Through Crowdrise Challenge on 29th November for MSA Research- #Giving #Tuesday

The MSA Coaliation to Raise Research Funds Through Crowdrise Challenge on 29th November for MSA Research- #Giving #Tuesday | The Multiple System Atrophy Coalition | Scoop.it
Multiple System Atrophy Coaliation is raising funds through "Giving Tuesday" via crowdrise challenge. We are leading the fight to cure MSA patients by providing compassionate support & informative resources. All donations made will go 100% to the MSA Coalition Global Research Grant Fund.
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MSA Coalition Surpasses $1 Million Milestone in Research Funding

MSA Coalition Surpasses $1 Million Milestone in Research Funding | The Multiple System Atrophy Coalition | Scoop.it
With the global efforts to achieve a greater understanding of MSA Coalition, it have been enhanced by ten research projects that received awards in 2016. We have been awarded over $1 million in MSA research grants. From 2014, MSA started awarding funds & has funded 27 projects till now around the world.
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2016 MSA Patient & Caregiver Conference- Watch Live or On Demand

2016 MSA Patient & Caregiver Conference- Watch Live or On Demand | The Multiple System Atrophy Coalition | Scoop.it
Now view live or on demand recordings of 2016 MSA Patient & Caregiver Conference held on October 14 & 15. If you missed live session, don't worry recordings are available for these sessions. Stay updated with us @ (866)737-5999.
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Attend MSA Coalition Conference - 17 Days Remaining!!!

Attend the MSA Coalition Patient and Caregiver Conference which is going to be held on 14 & 15 Oct'16. Only 17 days are remaining for the conference and space is limited. Hurry up and book your seats now. Reach us at (866)737-4999.
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Multiple System Atrophy encourages to raise fund by Gift of Hope

Multiple System Atrophy encourages to raise fund by Gift of Hope | The Multiple System Atrophy Coalition | Scoop.it
MSA Research Fund by campaign "gift of hope" encourages people to raise fund for research which is used to know its causes, treatment and cure. For Donation, contact us @ (866)737-5999
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