accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: September 2014
http://accessdenied-livingwithms.blogspot.com/2014_09_01_archive.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Wednesday, September 17, 2014. Brilliant to be able to post again. Its enjoyable finally being. Back online thanks to the Lipstick mouse, what a wonderful invention from shannon electronics. Brilliant to be able to communicate again, nearly lost hope began to think i would never be able to use a computer ever again,.
accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: Trying to Seize The Moment.
http://accessdenied-livingwithms.blogspot.com/2015/05/trying-to-seize-moment.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Tuesday, May 12, 2015. Trying to Seize The Moment. It's more difficult than I thought to seize the moment and post again, but it is more difficult than I thought it would be. Realise now that I have to reinstate posting as a thing that I do everyday, today makes me think this ttime I will make it happen. A Cup of Jo.
accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: May 2015
http://accessdenied-livingwithms.blogspot.com/2015_05_01_archive.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Saturday, May 23, 2015. Links to this post. Friday, May 15, 2015. Links to this post. Thursday, May 14, 2015. Great To Post Again. Good to be writing something everyday, in that way hopely it will be possible to gently re-establish doing it daily, I have plenty to write about so my plan will surely work,. Tuesday, Ma...
accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: December 2014
http://accessdenied-livingwithms.blogspot.com/2014_12_01_archive.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Tuesday, December 30, 2014. Christmas 2014 has been great. Christmas has been very enjoyable with my darling Richie,. Even though I am a quadroplegic now, this ms has really fucked my body but not my mind, I am still cheerful and enjoy everything I can. In 2015 i shall post regularily,which. Which i look forward to.
accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: March 2015
http://accessdenied-livingwithms.blogspot.com/2015_03_01_archive.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Tuesday, March 24, 2015. The post I posted on 31st of December was meant to ttbe my first of many daily posts,sadly this did'nt happen and after that I had many more plans,good intentions towrite my blog dailysomething I miss. I am hoping that writing this will break my block and I can start writing again. A Cup of Jo.
accessdenied-livingwithms.blogspot.com
Access denied-living with multiple sclerosis: Good Intentions.
http://accessdenied-livingwithms.blogspot.com/2015/03/good-intentions.html
Access denied-living with multiple sclerosis. About trying to live with ms and discovering that suddenly most places are inaccessible and that life as a handicapped person is very different. Tuesday, March 24, 2015. The post I posted on 31st of December was meant to ttbe my first of many daily posts,sadly this did'nt happen and after that I had many more plans,good intentions towrite my blog dailysomething I miss. I am hoping that writing this will break my block and I can start writing again. A Cup of Jo.
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
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
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!