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National Sarcoidosis Friends

WELCOME TO NATIONAL SARCOIDOSIS SOCIETY, NFP (NSS). National Sarcoidosis Society was established by Ms Glenda Fulton, a. 33 year old survivor of the disease known as Sarcoidosis, in 1995. Because a lack of educational awareness information on this. Disease.We provide services, educational awareness, advocacy,. Referals and research initiatives. Founder and Nat'l Chairperson of NSS.

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National Sarcoidosis Friends | nationalsarcoidosisfriends.org.tripod.com Reviews
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WELCOME TO NATIONAL SARCOIDOSIS SOCIETY, NFP (NSS). National Sarcoidosis Society was established by Ms Glenda Fulton, a. 33 year old survivor of the disease known as Sarcoidosis, in 1995. Because a lack of educational awareness information on this. Disease.We provide services, educational awareness, advocacy,. Referals and research initiatives. Founder and Nat'l Chairperson of NSS.
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1 nationalsarcoidosisfriends org
2 welcome
3 organization history
4 our mission
5 what is sarcoidosis
6 calender of events
7 research/survey
8 support groups
9 resources
10 to make donations
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National Sarcoidosis Friends | nationalsarcoidosisfriends.org.tripod.com Reviews

https://nationalsarcoidosisfriends.org.tripod.com

WELCOME TO NATIONAL SARCOIDOSIS SOCIETY, NFP (NSS). National Sarcoidosis Society was established by Ms Glenda Fulton, a. 33 year old survivor of the disease known as Sarcoidosis, in 1995. Because a lack of educational awareness information on this. Disease.We provide services, educational awareness, advocacy,. Referals and research initiatives. Founder and Nat'l Chairperson of NSS.

INTERNAL PAGES

nationalsarcoidosisfriends.org.tripod.com nationalsarcoidosisfriends.org.tripod.com
1

H. RES.1149

http://nationalsarcoidosisfriends.org.tripod.com/id14.html

Hello from the National Sarcoidosis Society, NFP (NSS). Thanks to Glenda Fulton and NSS partners an important House Resolution will be voted on Wednesday, April 30th regarding Sarcoidosis. 150 congressional co-sponsors are. Required. Take a moment to email your Congressman to ask them to co-sponsor House Resolution # 1149. Attached is a file that has more information regarding House Resolution # 1149. This resolution contains lots of hope and potential for those affected by Sarcoidosis. This letter is to...

2

Resources

http://nationalsarcoidosisfriends.org.tripod.com/id6.html

Enter subhead content here. Illinois State NAACP Health Committee. National Jewish Medical and Research Center. Sarcoidosis Foundation for Research. Karen Barwick - online support group. Loyala University Medical Education Network. OP Sharma, MD. The Sarcoidosis Center of Excellence at the Cleveland Clinic Foundation. Enter supporting content here.

3

SARCOIDOSIS SURVEY

http://nationalsarcoidosisfriends.org.tripod.com/id13.html

Sarcoidosis: What is it? Join the National Sarcoidosis Society in conjunction with the Illinois Department of Health (IDPH) is conducting a Sarcoidosis Research Survey. If you, a family member, friend or someone you know has Sarcoidosis you can help by partici-pating in this Research Survey. Remember your OPINION counts and it is important. For more information contact Ms Glenda Fulton @ 312-567-6626 out of state toll-free number 1-877-762-4389 or e-mail:. GET INVOLVE - - - - MAKE A DIFFERENCE.

4

Calender of Events

http://nationalsarcoidosisfriends.org.tripod.com/id4.html

National Sarcoidosis Society Chicago Chapter. March 1st - May 30th - - Sarcoidosis Membership Drive. Please support us by purchasing a membership). March 1st - April 30th - - Sarcoidosis Research Survey Initiative. It's important that you participate). March 15th, Saturday - - "Sarcoidosis Let's talk about it". 1:30 - 3:00 (est) at Mercy Hospital Rm. 204. 2525 S. Prairie Ave. Chicago, IL. March 15th and 16th (Saturday and Sunday) at 10 am (est). Chicago Navy Pier Health Fair at Ford City Mall , Chicago.

5

Our Mission

http://nationalsarcoidosisfriends.org.tripod.com/id1.html

To provide information and assistance to patients and. Professionals on a wide-range of health related educational. Issues that will result in enhanced and empowerment methods of. Diagnosis and treatment of this disease and to improve and. Empower the overall health of individuals, families, and. Communities throughout the United States and engage in. Research initiatives that will result in a cure for the debilitating. Enter supporting content here.

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sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: July 2011

http://sarcoidunited.blogspot.com/2011_07_01_archive.html

Wednesday, July 13, 2011. RIP Gene P. I. Duffy. I know you suffered a lot Gene now it's time to rest in peace. Prayers go out to the family. Sarcoid free 2 years now. Just thought I'd check in. Subscribe to: Posts (Atom). RIP Gene P. I. Duffy. Sarcoid free 2 years now. RIP Steve L. Jefferson. Click on the picture to see is tribute page on Facebook. The Bernie Mac Foundation. A UK based site with some really great people. Mount Sinai Hospital New York. Mount Sinai Sarcoidosis Support Group.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: RIP Gene P. I. Duffy

http://sarcoidunited.blogspot.com/2011/07/rip-gene-p-i-duffy.html

Wednesday, July 13, 2011. RIP Gene P. I. Duffy. I know you suffered a lot Gene now it's time to rest in peace. Prayers go out to the family. Subscribe to: Post Comments (Atom). RIP Gene P. I. Duffy. Sarcoid free 2 years now. RIP Steve L. Jefferson. Click on the picture to see is tribute page on Facebook. The Bernie Mac Foundation. A UK based site with some really great people. Mount Sinai Hospital New York. Mount Sinai Sarcoidosis Support Group. Foundation for Sarcoidosis Research.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: July 2009

http://sarcoidunited.blogspot.com/2009_07_01_archive.html

Friday, July 31, 2009. Fox 5 news Interview with Kim Grant Sarcoidosis Patient. Kim Grant, sarcoidosis patient on the news with her Doctor explaining the disease to the Washington DC, Metro area and now on facebook! It's a huge step in the right direction for sarcoidosis awareness. Fox did the right thing and Kim thanks for spreading the word. . Subscribe to: Posts (Atom). Fox 5 news Interview with Kim Grant Sarcoidosis Pa. RIP Steve L. Jefferson. Click on the picture to see is tribute page on Facebook.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: The Bernie Mac Foundation

http://sarcoidunited.blogspot.com/2011/08/bernie-mac-foundation.html

Sunday, August 14, 2011. The Bernie Mac Foundation. I haven't been on the site for awhile but noticed they revamp and it looks great. Love the video and the About Bernie section. Please check it out and donate if you can. Subscribe to: Post Comments (Atom). The Bernie Mac Foundation. Get your TeeGee sarcoidosis awareness shirts here! RIP Steve L. Jefferson. Click on the picture to see is tribute page on Facebook. The Bernie Mac Foundation. A UK based site with some really great people.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: August 2009

http://sarcoidunited.blogspot.com/2009_08_01_archive.html

Monday, August 31, 2009. A fellow sarkie passed away today. Rest in Peace Steve. Subscribe to: Posts (Atom). A fellow sarkie passed away today. RIP Steve L. Jefferson. Click on the picture to see is tribute page on Facebook. The Bernie Mac Foundation. A UK based site with some really great people. Mount Sinai Hospital New York. Mount Sinai Sarcoidosis Support Group. Foundation for Sarcoidosis Research. Foundation for Sarcoidosis Research, Big Daddy of all forums. American Auto Immune Association.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: April is National Sarcoidosis Awareness Month

http://sarcoidunited.blogspot.com/2012/04/april-is-national-sarcoidosis-awareness.html

Tuesday, April 17, 2012. April is National Sarcoidosis Awareness Month. The month of April was declared National Sarcoidosis Awareness Month by US Congress in 2008. Many organizations are observing this and it's a great month t participate in walks, garage sales and many other ways to raise funds for research. Also please read this really great article on the Huffington Post. Making a Difference: The World of Giving - Sarcoidosis Awareness Month. Subscribe to: Post Comments (Atom). Sila The Sarcoidosis C...

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: September 2010

http://sarcoidunited.blogspot.com/2010_09_01_archive.html

Wednesday, September 22, 2010. Jazz for a Cure. JAZZ FOR A CURE. I would love to hear from anyone who attends! Tuesday, September 7, 2010. John Hopkins finds new lead that may bring us closer to a cure. Or at least an official diagnosis. I didn't see this article until TeeGee posted it on his Facebook I gotta say I have been out of the loop, my job has been keeping me real busy. It makes me feel good though, like someone "is on it". Here is the article's link. Great find TG thanks! Jazz for a Cure. The B...

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: Autoimmune Walk for a Cure

http://sarcoidunited.blogspot.com/2012/04/autoimmune-walk-for-cure.html

Monday, April 16, 2012. Autoimmune Walk for a Cure. I just received a pamphlet in the mail on the annual Autoimmune Walk for a Cure. There is one in NYC for those of us in the metro area. I'm wondering if anyone is interested putting together a team to walk this thing and raise money for this cause. Although I no longer suffer from sarcoidosis I am forever linked to autoimmune diseases where ever I happen to look. Http:/ www.autoimmunewalk.org/. Http:/ www.facebook.com/AutoimmuneWalk. Have a look at my h...

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: September 2012

http://sarcoidunited.blogspot.com/2012_09_01_archive.html

Monday, September 24, 2012. Bernie Mac Speaking about Sarcoidosis in a Radio Interview 2009. I never came across this till now but though I would share an article on Bernie speaking of sarcoidosis. Bernie Mac Speaks Candidly About Sarcoidosis. What do Floyd Mayweather Sr.,. Tisha Campbell-Martin, Evander Holyfield, Bill Russell and Angie Stone have in common? They are all victims of Sarcoidosis. Subscribe to: Posts (Atom). Bernie Mac Speaking about Sarcoidosis in a Radio I. RIP Steve L. Jefferson.

sarcoidunited.blogspot.com sarcoidunited.blogspot.com

Sarcoidosis United: Sarcoid free 2 years now

http://sarcoidunited.blogspot.com/2011/07/sarcoid-free-2-years-now.html

Wednesday, July 13, 2011. Sarcoid free 2 years now. Just thought I'd check in. I just found your blog. You are so lucky to be in remission. I was diagnosed 17 years ago with lupus. Only one problem with that; I never had lupus, I have sarcoidosis. It has affected my right eye, lungs, heart, nervous system, parotid lymph node, and adrenal glands.Thanks for your blog it is very helpful. January 4, 2012 at 10:18 PM. Havent these doctors ever watched house? March 18, 2012 at 10:02 AM. Sarcoid free 2 years now.

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National Sarcoidosis Friends

WELCOME TO NATIONAL SARCOIDOSIS SOCIETY, NFP (NSS). National Sarcoidosis Society was established by Ms Glenda Fulton, a. 33 year old survivor of the disease known as Sarcoidosis, in 1995. Because a lack of educational awareness information on this. Disease.We provide services, educational awareness, advocacy,. Referals and research initiatives. Founder and Nat'l Chairperson of NSS.

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