I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome.
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The Pain & The Glory: Living With Congenital Myasthenia Syndrome. | thecongenic.blogspot.com Reviews
https://thecongenic.blogspot.com
I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome.
thecongenic.blogspot.com
The Pain & The Glory: Living With Congenital Myasthenia Syndrome.
http://thecongenic.blogspot.com/2008/11/wow-has-it-really-been-that-long.html
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Sunday, 2 November 2008. WOW has it really been that long. Actually not too much has happened however saying that I have been sitting here for the last few weeks bracing myself for any illness coming my way. I'll explain:.
The Pain & The Glory: Living With Congenital Myasthenia Syndrome.: Life On Pause...
http://thecongenic.blogspot.com/2009/01/life-on-pause.html
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Monday, 19 January 2009. Now usually my Myasthenia doesn't get in the way of my life, yet today of all days it knocks me for six. I haven't made the appointment and I guess I have lost out on that property. However there m...Hello...
The Pain & The Glory: Living With Congenital Myasthenia Syndrome.: Friday, 20 June 2008
http://thecongenic.blogspot.com/2008_06_20_archive.html
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Friday, 20 June 2008. The FAT Facts About Me. Posted by The Congenic. Subscribe to: Posts (Atom). AfterHours.FM - Free Internet Trance Radio. The FAT Facts About Me.
The Pain & The Glory: Living With Congenital Myasthenia Syndrome.: Wednesday, 6 May 2009
http://thecongenic.blogspot.com/2009_05_06_archive.html
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Wednesday, 6 May 2009. Onto The Sword Of Fear. (About overcoming my problem with Anxiety). I wrote the following on a forum and I thought I would leave it here to share. Onto The Sword Of Fear. Fri Sep 26, 2008 11:58 am. Once upon...
The Pain & The Glory: Living With Congenital Myasthenia Syndrome.: Fat Laces
http://thecongenic.blogspot.com/2008/06/whats-that-all-about.html
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Tuesday, 17 June 2008. So Run if you are ever reading this. Thanks Man you helped me become the person I am today. You made life a little easier to travel. Repsect. . Oh and . . Hit It Run! Where it all began:.
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Myaware Kids – UK & Ireland » In the Media
http://myasthenickids.org/index.php/ventilation/in-the-media
Committee & AGM. 8216;myaware kids’. Myaware, the Charity. Committee & AGM – Archived. Paris to Florence – Tom’s Epic Bike Ride. Radio Newcastle – Raising Awareness. Physiotherapy for childhood myasthenia. Speech & Language, and Feeding Therapy. Toby, Acetylcholine Receptor Deficiency. Ellen, unknown gene fault. Charlie, unknown gene fault. Living without a diagnosed condition…. Naomi’s Story – On the inside of a Myasthenic Crisis. Raquo; In the Media. 3,4 DAP / Firdapse Orphan Drugs and cost to the NHS.
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Jeremy, Kimberly, and Roxy
Jeremy, Kimberly, and Roxy. Friday, January 21, 2011. News for the New Year! It's a new year and I'm here for my 4 month check-in. Okay, I vow to do better as always. So we are expecting the end of August and are very excited! The Sunday before we found out I was craving what else but pickles:) I sat down and ate an entire jar of baby dill pickles and they were so good! Posted by Kimberly Congdon. Wednesday, September 1, 2010. The view from my tractor. Nearly 1000 pounds of apples in each bin! We went on...
The Congenial Hour
Dennis Rodman checked into an alcohol-rehabilitation center to re-evaluate his life, not give up drinking. Ldquo;I needed to decompress from all the things I was going through,” Rodman said Friday by phone from Miami. Rodman said he will return to the rehab center every six months “to see where I’m at.”. The 52-year-old Rodman…denied he is an alcoholic. He said he could curb his drinking and that he does not have a problem because he doesn’t drink every day. Craft cocktail = craft cocktail. Craft coc...
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The Pain & The Glory: Living With Congenital Myasthenia Syndrome.
The Pain and The Glory: Living With Congenital Myasthenia Syndrome. I wish to share an insight into the life of Adam, in the hope that someone maybe able to find some sort of help, hope or comfort from it. Adam was born with the very rare illness Congenital Myasthenia Syndrome. Wednesday, 6 May 2009. Onto The Sword Of Fear. (About overcoming my problem with Anxiety). I wrote the following on a forum and I thought I would leave it here to share. Onto The Sword Of Fear. Fri Sep 26, 2008 11:58 am. Once upon...
The Conger Chronicles
Our crazy little world as a party of five. Thursday, August 13, 2015. These two just melt me. Having a great time together on this last week of summer! Soaking up the family time! Labels: Grant 3 years old. Jack 5 years old. Wednesday, August 12, 2015. Jack's love for the horse is as strong as ever! Here he is (on the left) on his very first pony ride. And today we went back to the same stable in Hilton Head! I'm fairly certain he is on the same horse too! Crazy how fast time is moving! Jack 5 years old.
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THE CONGERS
OUR LIFE, OUR LOVE, and THE LOVE OF OUR LIFE. Sunday, November 9, 2008. Our friend Heather and her precious little girl, Emma. Anyways, tonight we put her on it before her bath and she went #1! She was rewarded with a dum dum lollipop.kind of funny since she's a little smarty! Links to this post. Monday, November 3, 2008. A Halloween Filled with Pand-a-monium! Just a few pictures from our busy day on Halloween. We started our day by heading to Luke and Hudson's Halloween Bash! Some fun memories included ...
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