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myfamilyandmsa | Living with Multiple System Atrophy. A life limiting, neurological brain disease.

Living with Multiple System Atrophy. A life limiting, neurological brain disease.

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myfamilyandmsa | Living with Multiple System Atrophy. A life limiting, neurological brain disease. | myfamilyandmsa.wordpress.com Reviews

https://myfamilyandmsa.wordpress.com

Living with Multiple System Atrophy. A life limiting, neurological brain disease.

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myfamilyandmsa.wordpress.com myfamilyandmsa.wordpress.com
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Holidays, exam results, appointments and catching up. | myfamilyandmsa

https://myfamilyandmsa.wordpress.com/2013/08/07/holidays-exam-results-appointments-and-catching-up

Living with Multiple System Atrophy. A life limiting, neurological brain disease. Laquo; I wished on a star. MSA, carers, and auctions. Holidays, exam results, appointments and catching up. On August 7, 2013. I would love to tell you that since my birthday I’ve been wonderfully well but that would be wishful thinking, I’m only awake now for very short periods of the days and fall asleep as though like hypnosis! I’m in the process of building a website (says 5 minutes) on it DON’T BELIEVE IT lol! It’s for...

2

Three little letters – MSA | myfamilyandmsa

https://myfamilyandmsa.wordpress.com/2013/09/21/three-little-letters-msa

Living with Multiple System Atrophy. A life limiting, neurological brain disease. Laquo; Make you feel my love. Light a candle for MSA Awareness Day. Three little letters – MSA. On September 21, 2013. Well I did it, I went through with the Botox for my bladder, I’m very glad I didn’t realise what it involved beforehand or I’m not sure I would have been going! I know I haven’t posted on the blog as often but I am so very tired a lot of the time now and fall asleep at the drop of a hat. An amazing family t...

3

Growing up with MSA | myfamilyandmsa

https://myfamilyandmsa.wordpress.com/2013/09/03/growing-up-with-msa

Living with Multiple System Atrophy. A life limiting, neurological brain disease. Laquo; MSA, carers, and auctions. Make you feel my love. Growing up with MSA. On September 3, 2013. So enough depressing news…We were extremely lucky to be offered a trip of a lifetime by The Willow Foundation who organise trips for people like us, well I couldn’t think of anything I really wanted so we let Rhanna choose and she chose Harry Potter Studios just outside London! We all LOVED it, honestly it was great! So now i...

4

MSA, carers, and auctions | myfamilyandmsa

https://myfamilyandmsa.wordpress.com/2013/08/22/msa-carers-and-auctions

Living with Multiple System Atrophy. A life limiting, neurological brain disease. Laquo; Holidays, exam results, appointments and catching up. Growing up with MSA. MSA, carers, and auctions. On August 22, 2013. I sleep mostly leaving Andy kind of alone in the sense of the word, you know what I mean, I’m there but I’m not? He makes me smile when he walks in the room and I love him more than I can explain. Rhanna who is without a doubt my reason for fighting this horrible disease has taken to coming in to ...

5

myfamilyandmsa | Living with Multiple System Atrophy. A life limiting, neurological brain disease. | Page 2

https://myfamilyandmsa.wordpress.com/page/2

Living with Multiple System Atrophy. A life limiting, neurological brain disease. I wished on a star. I wished on a. That all my dreams would come true and on this one day they did. 131 birthday cards with the most beautiful messages of hope, inspiration, joy and laughter. Gifts from people I have never met but will treasure always and my family and friends along with card, gifts, a cuddle and a kiss that meant I can carry them with me forever. There wasn’t one person on the barge that shouldn&#821...

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msaonedayatatime.blogspot.com msaonedayatatime.blogspot.com

One Day at a Time ~ Brenda's Journey with MSA: Friends ~Their Journey

http://msaonedayatatime.blogspot.com/p/friends-their-journey.html

One Day at a Time Brenda's Journey with MSA. Multiple System Atrophy (MSA) - My journey and interesting tidbits. Helping Hands Where To Get It. Http:/ myfamilyandmsa.wordpress.com. Http:/ www.karenolsonblog.com/. Http:/ sonjasegriffels.blogspot.com/. MSA in South Africa. Http:/ msainsouthafricawithsonja.blogspot.com/. Http:/ findingprettyagain.blogspot.com/. Https:/ www.facebook.com/profile.php? Denns and Lori Jankeway. Https:/ www.facebook.com/ljakeway. Simon Roodhouse and his new companion-MSA. Awesome...

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Living with Multiple System Atrophy. A life limiting, neurological brain disease. MSA – pulling us apart. So since my last blog I received over 91 emails about the subject matter I wrote about really lovely, really sad and definitely mostly agreeable. We finally got the chance to meet Paul Bellars and his lovely kids Rachel and Andrew! The memories made in just a few days will last forever and a friendship definitely set in stone! A – shouting at me. B – whispering back? I’m not sure if I will be a...

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