When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way.
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Mike & Sarcoidosis | mikebl0g.blogspot.com Reviews
https://mikebl0g.blogspot.com
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way.
mikebl0g.blogspot.com
Mike & Sarcoidosis: February 2009
http://mikebl0g.blogspot.com/2009_02_01_archive.html
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Saturday, February 28, 2009. Dizzy, a Spot in the Eye and Yet. On the upside the pain has gone down a bit, even though I did a lot of walking during the day. This is GREAT news!
Mike & Sarcoidosis: January 2009
http://mikebl0g.blogspot.com/2009_01_01_archive.html
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Tuesday, January 27, 2009. The Shakes and Ice Cream. Also, I have noticed ice cream appears to increase the likelihood of me getting cramps in my feet and legs. Doah! I am very excit...
Mike & Sarcoidosis: December 2008
http://mikebl0g.blogspot.com/2008_12_01_archive.html
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Monday, December 22, 2008. Sudden and Painful Leg and Foot Craps. It's hard to know if the leg and foot cramps are coming from the Sarcoidosis, the medicine, the overweight effects o...
Mike & Sarcoidosis: April 2009
http://mikebl0g.blogspot.com/2009_04_01_archive.html
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Sunday, April 26, 2009. Imuran, Cancer and Messing with DNA. Sarcoid is bad, but cancer is MUCH WORSE! Especially with the increased risks of cancer). Have to figure this one out.
Mike & Sarcoidosis: The calm after the storm
http://mikebl0g.blogspot.com/2013/11/the-calm-after-storm.html
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Sunday, November 24, 2013. The calm after the storm. I just got back from a vacation with my lovely wife celebrating our 20. Medrol (Methylprednisolone) 4mg twice per day (Much, Much...
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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.
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.
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.
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.
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.
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...
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...
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...
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.
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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Mike & Sarcoidosis
When I was diagnosed with Sarcoidosis I had no idea what to expect or how it would impact my life. I created this blog to potentially help others in this same situation. Hopefully you can find some insights as to what life might be like, what some of the challenges might be and hopefully laugh a little with me along the way. Sunday, November 24, 2013. The calm after the storm. I just got back from a vacation with my lovely wife celebrating our 20. Medrol (Methylprednisolone) 4mg twice per day (Much, Much...
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Dept of Biomedical Sciences. TEL: 850 644 3361. FAX: 850 644 9399. Email: michael.blaber@med.fsu.edu. Welcome to mikeblaber.org. This site is produced and maintained by Dr. Michael Blaber. Feel free to browse around! This web site is intended to provide access to information and resouces associated with, or produced by, Dr. Michael Blaber, and was previously located at http:/ wine1.sb.fsu.edu. Dr Blaber decided to register the domain name "mikeblaber.org" and transfer the material to this site. Drs Micha...
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