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Adventures in Multiple Sclerosis

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Tingly Feeling | tinglyfeeling.com Reviews

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Adventures in Multiple Sclerosis

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1

Stability and Multiple Sclerosis Symptoms | Tingly Feeling

http://www.tinglyfeeling.com/symptoms/stability

Adventures in Multiple Sclerosis. April 20, 2011. Multiple Sclerosis obviously throws a huge wrench in my plans. It goes without saying, really, but you can’t plan for MS. So, even though I know all this, why do I let it bother me so much when my symptoms suddenly act up, like they have this week? Deal with it.). You’ve got WHAT now? I thought that new medication fixed all that! Blah blah blah …” I have to explain over and over that it never ends with this disease and the sooner they stop mak...That soun...

2

drug vacation | Tingly Feeling

http://www.tinglyfeeling.com/ms-drugs/drug-vacation

Adventures in Multiple Sclerosis. May 29, 2010. Hi Hello. Been awhile. I’m still here, it’s just that the rest of my life–the non-MS part–has sort of taken over. But that’s good, right? Also, could the packaging Aetna sends the 1-month supply of Avonex in be any less discreet? Seriously. Why not put a bright orange sticker next to the green one that says “DRUGS INSIDE.” Plus, you can’t recycle these containers in WA state. Boo-urns. Previous post: “Try on MS” at Pacific Place. Carnival of MS Bloggers.

3

Activism | Tingly Feeling

http://www.tinglyfeeling.com/activism

Adventures in Multiple Sclerosis. 8220;Try on MS” at Pacific Place. April 22, 2010. Slip into our skin. February 25, 2010. Health insurance reform rant. September 8, 2009. The faces of MS. May 27, 2009. We’ve got spirit! April 8, 2009. Well, most of us are walking. April 1, 2009. February 11, 2009. Aboutcom Multiple Sclerosis Blog. Carnival of MS Bloggers. Carolyne’s MS Odyssey. My Journey with Multiple Sclerosis. No Time for MS. All the Top MS News. National Multiple Sclerosis Society.

4

Holistic Medicine | Tingly Feeling

http://www.tinglyfeeling.com/holistic

Adventures in Multiple Sclerosis. More balanced, more bendy. February 16, 2009. Aboutcom Multiple Sclerosis Blog. Carnival of MS Bloggers. Carolyne’s MS Odyssey. My Journey with Multiple Sclerosis. No Time for MS. All the Top MS News. National Multiple Sclerosis Society. PatientsLikeMe – MS Community. Follow me on Twitter. Get smart with the Thesis WordPress Theme.

5

meeting and greeting | Tingly Feeling

http://www.tinglyfeeling.com/ms-support/meeting-and-greeting

Adventures in Multiple Sclerosis. August 29, 2010. So what’s been going on in the last two months? Well, other than the usual sunshine-feeding frenzy that is a Seattle summer (blink and you’ll miss it), I’ve made some new connections with other MSer-types. In July, I met a vibrant, athletic woman who’s currently dedicating herself to spreading the word about CCSVI. But I haven’t seen any updates yet. I hope she’s still doing well. I went with my sister. So I’m happy to have found these people. They welco...

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talesoflifewithmultiplesclerosis.blogspot.com talesoflifewithmultiplesclerosis.blogspot.com

Tales of Life with Multiple Sclerosis: Swimming and new goals!

http://talesoflifewithmultiplesclerosis.blogspot.com/2014/10/swimming-and-new-goals.html

Tales of Life with Multiple Sclerosis. Thursday, 23 October 2014. Swimming and new goals! Last year my best friend and I organised a sponsored swim for us both to do. We had both started swimming.we have a friend with a pool.and I had discovered that I could still swim just with my arms, even though my legs don't work! I was loving being in the pool, the sense of freedom it gives me and I finally felt that I was doing some exercise, however small that may be! We worked out a proper training plan. We ...

talesoflifewithmultiplesclerosis.blogspot.com talesoflifewithmultiplesclerosis.blogspot.com

Tales of Life with Multiple Sclerosis: May 2014

http://talesoflifewithmultiplesclerosis.blogspot.com/2014_05_01_archive.html

Tales of Life with Multiple Sclerosis. Saturday, 31 May 2014. Our London trip - May 27th to 31st 2014! If you've read my post called London Bound you will know the background to mine and Martin's trip to London to see some West End shows. This is a follow up post about our trip.which was amazing! We stayed in three different Premier Inns! We struck gold though! Normally the rooms just have a shower over a bath which is useless to me as I can't get into a bath! So being offered a wet room was fantastic!

mgafox.wordpress.com mgafox.wordpress.com

April | 2011 | mgafox's space

https://mgafox.wordpress.com/2011/04

Me and My 'Monster'(MS)……………. Archive for April, 2011. April 22, 2011 at 9:13 AM · Filed under Day by Day. I am taking this opportunity to wish all my family and friends a Happy Easter.🙂🙂🙂. April 15, 2011 at 4:08 PM · Filed under Day by Day. I’m feeling good! Late Nights…………. April 10, 2011 at 2:41 PM · Filed under Day by Day. Had fun @ my friend’s 50’th B-Day party last night, but the late night has me feeling like I’m the one turning 50. The combination of a. I think the world would be a. Nea 3 year...

mgafox.wordpress.com mgafox.wordpress.com

February | 2011 | mgafox's space

https://mgafox.wordpress.com/2011/02

Me and My 'Monster'(MS)……………. Archive for February, 2011. Dr’s Appointment………. February 26, 2011 at 12:14 PM · Filed under Day by Day. 8230;… that little blue pill works real well; had my first good night’s sleep in month’s :):):) May start taking this long-term, if the results are good and long-lasting; and the side affects are minimal. New Zealand Earthquake Spurs Giant Glacier Collapse. February 24, 2011 at 4:10 PM · Filed under Stuff. New Zealand Earthquake Spurs Giant Glacier Collapse. February 22, ...

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 ...

talesoflifewithmultiplesclerosis.blogspot.com talesoflifewithmultiplesclerosis.blogspot.com

Tales of Life with Multiple Sclerosis: February 2014

http://talesoflifewithmultiplesclerosis.blogspot.com/2014_02_01_archive.html

Tales of Life with Multiple Sclerosis. Wednesday, 5 February 2014. The generosity of people, it puts your faith back in human nature! 2014 is going to be a good year! I still wasn't sure that we really deserved anything like this but she got cross with me and said that nobody deserved to go through everything that Martin and I have been through over the past couple of years. I told her my Paris idea and that to begin with I wanted to do it as a surprise for Martin but I then decided that if we were going...

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