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brainfingers

Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: " That self-indulgent, egocentric ass! We do that by researching, l...

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brainfingers | brainfingers-ron.blogspot.com Reviews
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Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: That self-indulgent, egocentric ass! We do that by researching, l...
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1 brainfingers
2 introduction and involvement
3 life changing adaptations
4 thats my introduction
5 posted by
6 brainfinger
7 8 comments
8 followers
9 blog archive
10 about me
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brainfingers | brainfingers-ron.blogspot.com Reviews

https://brainfingers-ron.blogspot.com

Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: " That self-indulgent, egocentric ass! We do that by researching, l...

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brainfingers: Introduction and Involvement

http://brainfingers-ron.blogspot.com/2009/05/introduction-and-involvement.html

Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: " That self-indulgent, egocentric ass! We do that by researching, l...

2

brainfingers: May 2009

http://brainfingers-ron.blogspot.com/2009_05_01_archive.html

Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: " That self-indulgent, egocentric ass! We do that by researching, l...

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kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: The Dreaded Phone Call

http://kelleysmsblog.blogspot.com/2008/12/dreaded-phone-call.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Friday, December 5, 2008. The Dreaded Phone Call. Missed the first parts of the story? Go to So it begins. I guess I should explain. I don't drive. I learned how to drive in the event of an extreme emergnecy, but I do not have a driver's license. I am, shall we say, visually challenged. I have a condition known as optic nerve hypoplasia. That night. As we were ...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: So it begins...

http://kelleysmsblog.blogspot.com/2008/11/so-it-begins.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Monday, November 10, 2008. Although Mom didn't have the outward appearance of MS, she displayed many of the invisible symptoms that the general public are not aware. After her diagnosis, Mom started on Copaxone, a disease-modifying drug, and has not had a relapse since. Next, Fast Forward to May 2008. Or have you been? Again, welcome to the ms blogger club. I write...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: June 2010

http://kelleysmsblog.blogspot.com/2010_06_01_archive.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Friday, June 18, 2010. Today is my second anniversary on Copaxone. I have not missed a dose in these two years and I have been so fortunate to not have any relapses. Woohoo! While everyone else is getting very excited about the approval of oral disease-modifying drugs, I am sticking with what works for me. As we say in Oklahoma, "If it ain't broke, don't fix it!

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: May 2009

http://kelleysmsblog.blogspot.com/2009_05_01_archive.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Thursday, May 28, 2009. One year ago today I received my "official" diagnosis of MS from a neurologist. What a year it's been! When I reminded GH about it today, he said, "Un-gratulations! What a thoughtful GH! What have I learned from my first year of living with MS? I have learned that there are comfortable, stable and cute. The main thing I have learned is just ...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: Six month followup

http://kelleysmsblog.blogspot.com/2008/12/six-month-followup.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Tuesday, December 2, 2008. How did I get here? Start at So it begins. So, I'm skipping ahead to the present. I'll fill in the gaps later. I saw my neurologist yesterday and learned that I have NO active lesions and no new lesions! So, I don't see the neurologist again for six months, unless I have a problem. Hopefully, I won't! Hey Kelley-congrats on the good news!

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: Another Semester Ended

http://kelleysmsblog.blogspot.com/2009/05/another-semester-ended.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Friday, May 15, 2009. The glitch is that the university for which I work requires that transfer students complete 45 hours at this university. So I was like, "What? I have to take 15 more hours before I get a degree? I waited until I received my grade for the Mark Twain course this semester (an A! Until I discussed this with GH. For some odd reason, I thought h...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: It's Official!

http://kelleysmsblog.blogspot.com/2008/12/its-official.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Monday, December 8, 2008. Missed the first parts of the story? Start at So it begins. The doctor enters the examination room, introduces himself and then asks me, "What did your doctor tell you? So, there it was. I had my official diagnosis. Wow. Actually, I should say we. Of course, we had an obligation that night. GH was in rehearsal for The Chosen. You left such...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: December 2009

http://kelleysmsblog.blogspot.com/2009_12_01_archive.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Thursday, December 24, 2009. Merry Christmas, everyone! Just a quick post to wish everyone who reads this blog, all of you in the MS online community and anyone else a Merry Christmas. May you have a blessed Christmas and a healthy and Happy New Year! Only one of the many reasons I love him dearly. May you all have a blessed holiday season, from Casa F in Oklahoma!

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: It's Walk MS Time!

http://kelleysmsblog.blogspot.com/2010/04/its-walk-ms-time.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Saturday, April 17, 2010. It's Walk MS Time! Sorry for my lengthy absence, but things have been incredibly busy. I had to conserve my compromised myelin for other things, so the blog suffered. For those of you in the MS community, I hope your walks are successful and put us closer to our goal of ending MS. Thanks for your support. April 19, 2010 at 5:41 PM. I am a ...

kelleysmsblog.blogspot.com kelleysmsblog.blogspot.com

Sisterhood (and Brotherhood) of The Compromised Myelin: April 2010

http://kelleysmsblog.blogspot.com/2010_04_01_archive.html

Sisterhood (and Brotherhood) of The Compromised Myelin. This blog is to journal my triumphs and challenges of living with multiple sclerosis. Saturday, April 17, 2010. It's Walk MS Time! Sorry for my lengthy absence, but things have been incredibly busy. I had to conserve my compromised myelin for other things, so the blog suffered. For those of you in the MS community, I hope your walks are successful and put us closer to our goal of ending MS. Subscribe to: Posts (Atom). Someone else's brain on MS.

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Tuesday, May 5, 2009. After being a bystander, and reading the blogs from my wife's fellow MS bloggers (and online friends) I now feel comfortable to offer my thoughts and supportive efforts to those of you who share your first-hand MS experiences, but more so, to those who share their lives with, and support their mates as only true loving, caring, and optimistic partners in life can. Before some of you yell out loud to that empty room: " That self-indulgent, egocentric ass! We do that by researching, l...

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