The Multiple System Atrophy Coalition
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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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Countdown Begins for MSA Coalition Patient and Family Conference

Countdown Begins for MSA Coalition Patient and Family Conference | The Multiple System Atrophy Coalition | Scoop.it
Countdown begins for MSA Coalition Pateient and Family Conference which is going to be held on October 14 & 15 in New Orleans, LA. For more information and to register visit: https://www.multiplesystematrophy.org/newsroom/annual-conference
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Get updates about Multiple System Atrophy via MSA blog

Get updates about Multiple System Atrophy via MSA blog | The Multiple System Atrophy Coalition | Scoop.it
Get the know-how about MSA - Multiple System Atrophy by visiting this official “MSA Coalition blog”. Read the most recent blog posts and make yourself updated about this rare neurological disorder. Help people and spread MSA Awareness around them. For Toll Free Support: (866)-737-5999.
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Do You Know History of MSA-Multiple System Atrophy?

History of MSA-Multiple System Atrophy is very rarely known to people. MSA was discovered by by Dr. Milton Shy and Dr. Glen Drager and thus named as Shy Drager Syndrome. MSA disease is a neurological disease occurs due to degeneration of certain nerve cells in the brain and spinal cord. For Support call us at 866-737-4999.
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Neurogenic Orthostatic Hypotension & its Symptoms

Neurogenic orthostatic hypotension (NOH) is a very rare syndrome where low blood pressure occurs upon standing. The Multiple System Atrophy Coalition® is an inclusive U.S. based 501(c)3 charity dedicated to funding MSA research that in turn leads to cure of such diseases. Call now @ (866)737-5999 to donate to the MSA Coalition.

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MSA Conference: October 14 & 15 This Year | Follow Us On Slideshare

Get registered for upcoming MSA conference! Read file to know the venue and dates. If you need more information visit- www.multiplesystematrophy.org for more details. Follow us on Slideshare. Call 866-737-4999.

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Attend 2016 MSA Coalition Patient & Family Conference on 14 & 15 October

Register early! Space is limited for 2016 MSA Coalition patient and family conference. Follow us on Weebly and read the complete steps to register. Call 866-737-4999.

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Start Fundraising With MSA Memorial Envelopes

Start Fundraising With MSA Memorial Envelopes | The Multiple System Atrophy Coalition | Scoop.it

How useful are multiple system atrophy memorial envelopes? Read about the fundraising in details to understand the donation procedure. Call 866-737-4999 for more details.

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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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MSA Coalition Conference-51 days remaining!!!

MSA Coalition Conference-51 days remaining!!! | The Multiple System Atrophy Coalition | Scoop.it
Countdown begins and only 51 days are remaining for the conference. Hurry Up and register for the 2016 MSA Coalition Patient and Caregiver Conference which is going to be held on Fri, October 14 & 15 at New Orleans, US. You can reach MSA Coalition at (866)737-4999 or mail at conference@msacoalition.org.
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Getting Northera for Neurogenic Orthostatic Hypotension patient

Read the steps involved in getting Northera drug for nOH (neurogenic orthostatic hypotension) patient with the help of licensed doctor. Know what is required and contact our Support Hotline at (866) 737-4999 for any with an MSA diagnosis and prognosis.
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Why is nOH so common in Multiple System Atrophy patients?

Neurogenic Orthostatic Hypotension i.e. nOH is known to be caused by Multiple System Atrophy – MSA a rare disease that occurs when the autonomic nervous system is damaged. Visit https://goo.gl/dyraac for more info.
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Join GoodShop & help find a cure for Multiple Systems Atrophy

Join GoodShop & help find a cure for Multiple Systems Atrophy | The Multiple System Atrophy Coalition | Scoop.it

Help find a cure for Multiple Systems Atrophy just by just shopping online. Multiple Systems Atrophy Coalition provides patient support and educational resources. Use Goodshop portal every time you shop online. Call (866)737-5999 for details.

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Register for 2016 MSA Conference | Follow Us On Slideshare

2016 MSA Coalition Patient & Family Conference is to be held at New Orleans on 14 and 15 October. Follow us on slideshare and know the complete details and about tentative schedule. Call 866-737-4999.

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Join With The Multiple Systems Atrophy Rare Disease Awareness Program

Join With The Multiple Systems Atrophy Rare Disease Awareness Program | The Multiple System Atrophy Coalition | Scoop.it

How Orioles and Gorman family were impacted by MSA (Multiple System Atrophy) rare disease? Read blog to know in detail. Call 866-737-4999 to raise money to research MSA treatments.

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