thepitterpatterboutique.blogspot.com
The Pitter Patter Boutique: December 2009
http://thepitterpatterboutique.blogspot.com/2009_12_01_archive.html
Wednesday, December 30, 2009. Or maybe not so much. I received a few gift cards for Christmas. After traveling the busy streets of Cali in search of Cute Shoes to spend them on, I decided I'd take to the internet. Surely that won't let me down. After searching the typical sites like Steve Madden, Aldo, DSW, Zappos, and a few others, I decided I'd hop into Fredericks and see what they had to offer. And yes, I can walk in 5' heels. And I will continue to wear them until the day I die. LOL! Another lesson l...
stocktonmsgroup.org.uk
Useful Links
http://stocktonmsgroup.org.uk/7.html
Stockton MS Group take no responsibility for the content of external web sites, nor can they endorse or recommend any of the companies mentioned therein. Web site or contact. Offering an unbiased, unaffiliated site dedicated to eradicating Multiple Sclerosis. They offer an open-minded approach to *all* potentially viable treatments, ranging from the FDA-approved disease-modifying drugs such as Copaxone to alternative treatments such as Low Dose Naltrexone. Http:/ www.ms-uk.org/. The Trust recognises and ...
sofija.wordpress.com
Personal diary – MS Spasms abruptly disturb a quiet night’s sleep | Multiple Sclerosis & Life
https://sofija.wordpress.com/2014/01/07/personal-diary-ms-spasms-abruptly-disturb-a-quiet-nights-sleep
Multiple Sclerosis and Life. Multiple Sclerosis – new findings. Personal diary – MS Spasms abruptly disturb a quiet night’s sleep. In Multiple Sclerosis (MS). Hi, it has been a while. and this is an unusual post from me… but… Im scared. :/. I had after my first interferon/avonex injection (as expected, being a side effect), but I haven’t had it since then.and that was ages ago (2005! So what does my mind start wondering about? I am thinking of death.is it nearby? Although he really truly does love me, an...
sofija.wordpress.com
EBV-specific adoptive immunotherapy | Multiple Sclerosis & Life
https://sofija.wordpress.com/2014/03/08/ebv-specific-adoptive-immunotherapy
Multiple Sclerosis and Life. Multiple Sclerosis – new findings. In Multiple Sclerosis (MS). It feels like most of the time news are centred around discoveries that seem to be focused on the RRMS types… I have just read this article and it seems to shed light also for SPMSers too! Personal diary – MS Spasms abruptly disturb a quiet night’s sleep. Leave a Reply Cancel reply. Enter your comment here. Please log in using one of these methods to post your comment:. Address never made public). JEM – EBV. Multi...
ccsvisunlounger.blogspot.com
CCSVI sunlounger: CCSVI treatment and current symptoms
http://ccsvisunlounger.blogspot.com/2010/05/last-treatment-and-current-symptoms.html
Recovery from secondary progressive multiple sclerosis. Wednesday, 26 May 2010. CCSVI treatment and current symptoms. I first went to Poland on the 13th Jan 2010 where I had balloon angioplasty on my left jugular,unfortunately after having no improvements from this I returned in March for a doppler with Dr Simka,It was found that I had re-stenosis. On the 7th May I had my second procedure where my left jugular was ballooned first then implanted with 2 stents and also my right jugular was ballooned. IR...
guyinacube.wordpress.com
Just a guy in a cube | Life with MS and having fun with my family! | Page 2
https://guyinacube.wordpress.com/page/2
Just a guy in a cube. Life with MS and having fun with my family! Skip to primary content. Skip to secondary content. Newer posts →. Eye issues and UT Southwestern. February 17, 2014. On Sunday, it felt like it did on Wednesday and Today it really hasn’t surfaced too much. Sigh Needless to say I’m not overly happy with this doctor. The Results… or not…. February 12, 2014. The answer was yes. She had recommended getting a second opinion at an academic institution with an MS specialist. Which is in Dallas&...
guyinacube.wordpress.com
February | 2014 | Just a guy in a cube
https://guyinacube.wordpress.com/2014/02
Just a guy in a cube. Life with MS and having fun with my family! Skip to primary content. Skip to secondary content. Monthly Archives: February 2014. Eye Update and what’s next…. February 24, 2014. The pain I was feeling appears to have subsided. Last Saturday was the last day I recall feeling it. So, that is good at least. Still leaves a? I also got a call from the MS Clinic at UT Southwestern this morning. They are going to get me an appointment! Eye issues and UT Southwestern. February 17, 2014.
myliberationadventure.blogspot.com
My Liberation Adventure: Five month anniversary!
http://myliberationadventure.blogspot.com/2011/10/five-month-anniversary.html
This blog is for all of my family and friends who want to join me on my adventure of a lifetime: Liberation. Want to learn more about CCSVI? Check out www.ccsvi.org! Wednesday, October 5, 2011. It has officially been 5 months since my last venoplasty. That is exactly one month more than my longest run of good health after treatment. I hope it continues! How quickly things can change. Sigh. I had a lot to tell him. I am very lucky to have such a supportive and open-minded doctor. I wasn't worried that...
pwms-v.org.au
Letter from the President
http://pwms-v.org.au/index.php/websites
People with Multiple Sclerosis - Victoria Incorporated. Click image below to watch a recording of this event. NDIS Road to Readiness. MS Research Australia awarded 2015 Charity of the Year. Lemtrada treatment for active RRMS now available on PBS. Walter and Eliza Hall Institute of Medical Research. Progressive MS Webinar by the MS International Federation - November 2014. Barts and The London Neuroimmunology Group Research Updates. People with MS Victoria. Letter from the President. NDIS Two Years On.
pwms-v.org.au
Letter from the President
http://pwms-v.org.au/index.php/continence-aids-payment-scheme-suppliers
People with Multiple Sclerosis - Victoria Incorporated. Click image below to watch a recording of this event. NDIS Road to Readiness. MS Research Australia awarded 2015 Charity of the Year. Lemtrada treatment for active RRMS now available on PBS. Walter and Eliza Hall Institute of Medical Research. Progressive MS Webinar by the MS International Federation - November 2014. Barts and The London Neuroimmunology Group Research Updates. People with MS Victoria. Letter from the President. NDIS Two Years On.
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