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TEAM JOVIE - Raising Awareness and Fundraising for Rett Syndrome Research in Australia

RETT SYNDROME AWARENESS and FUNDRAISING IN AUSTRALIA. RETT SYNDROME AWARENESS AUSTRALIA. SHOW YOUR SUPPORT AS WE RAISE AWARENESS AND FUNDS FOR RETT SYNDROME RESEARCH IN AUSTRALIA. Every little bit counts. A little bit about me. Saturday 2 November 2014. In 2009, our daughter Jovie was born in Sydney Australia, and our lives were changed forever. Little did we know the very different path we were about to embark on. For the first 6-8 months, there were no signs of any issues heading our way. Team Jovie wa...

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RETT SYNDROME AWARENESS and FUNDRAISING IN AUSTRALIA. RETT SYNDROME AWARENESS AUSTRALIA. SHOW YOUR SUPPORT AS WE RAISE AWARENESS AND FUNDS FOR RETT SYNDROME RESEARCH IN AUSTRALIA. Every little bit counts. A little bit about me. Saturday 2 November 2014. In 2009, our daughter Jovie was born in Sydney Australia, and our lives were changed forever. Little did we know the very different path we were about to embark on. For the first 6-8 months, there were no signs of any issues heading our way. Team Jovie wa...
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TEAM JOVIE - Raising Awareness and Fundraising for Rett Syndrome Research in Australia | teamjovie.com Reviews

https://teamjovie.com

RETT SYNDROME AWARENESS and FUNDRAISING IN AUSTRALIA. RETT SYNDROME AWARENESS AUSTRALIA. SHOW YOUR SUPPORT AS WE RAISE AWARENESS AND FUNDS FOR RETT SYNDROME RESEARCH IN AUSTRALIA. Every little bit counts. A little bit about me. Saturday 2 November 2014. In 2009, our daughter Jovie was born in Sydney Australia, and our lives were changed forever. Little did we know the very different path we were about to embark on. For the first 6-8 months, there were no signs of any issues heading our way. Team Jovie wa...

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sh1ft.org sh1ft.org

_sh1ft.org

http://sh1ft.org/shutterbug

Our Rett Syndrome Story. It’s been a huge year. One of the best, though. I think after having gone through so much in the last 5 years, then not dealing with it properly and just learning along the way, and then actually settling in and addressing my personal issues with anxiety and panic attacks and boredom and being a carer and trying to find out who I am inbetween all of this stuff — I think I’ve come out a bit stronger and I like it. Which way is up? Look here, only a month between blog posts 😉.

rettaustralia.com rettaustralia.com

Rett Syndrome Association of Australia | Jovie

http://www.rettaustralia.com/portfolio_page/jovie

What is Rett Syndrome? What are the stages of Rett syndrome? What causes Rett syndrome? Is Rett syndrome hereditary? Who gets Rett syndrome? How is Rett syndrome treated? How is Rett syndrome diagnosed? What is the outlook for persons with Rett syndrome? Dr Andreas Rett and Rett syndrome An Insight. History of Rett syndrome in Australia. Selected resources specific to Rett syndrome. Do your own research. Rett Syndrome Association of Australia Jovie. A segment on The View. For Jovie, Rett syndrome has tak...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

On reading Keeping Katherine by Susan Zimmermann – charlottetwenty09

https://charlottetwenty09.wordpress.com/2014/07/15/on-reading-keeping-katherine-by-susan-zimmermann

Our lives with rett syndrome GRRR. On reading Keeping Katherine by Susan Zimmermann. It will be almost 2 years in a few weeks, since I received the call from my paediatrician , of a positive result for Rett Syndrome for our Charlotte. I didn’t think I would still be feeling so devastated about it all, 2years later. Isn’t 2 years long enough? She is a strong spirit like her sister, her Da and Mama. We are strong individually but together we are stronger. 8220;Sometimes we are deserted by those we’ve...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

Big Sister’s Snow Candy World – charlottetwenty09

https://charlottetwenty09.wordpress.com/2015/02/22/big-sisters-snow-candy-world

Our lives with rett syndrome GRRR. Big Sister’s Snow Candy World. Where honey is water and you bring it to school. With your slushies as water too. And everyone would learn iceskating everyday at school. And there were no vegetables as your vegetables were mint leaves. And there were candy sticks for door knockers. Slushies would be the bath water. And milk would be your shower. White chocolate would be soap. Pillows and sheets would be marshmallows. A wish would come true when you wanted it too. Address...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

you + me – charlottetwenty09

https://charlottetwenty09.wordpress.com/2015/03/09/you-me

Our lives with rett syndrome GRRR. Life, Love and Lyricality. We are more alike, my friends, than we are unalike. Maya Angelou. Yesterday was Rare Disease Day. I watched on social media as friends and family shared pictures and facts. I watched [and joined in] as the various organisations representing Rett syndrome [and many many other rare diseases] shared information. I was humbled by the similarities, by the kinship we share. You and me were always with each other. You and me we belong together. You k...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

Busy Gaps – charlottetwenty09

https://charlottetwenty09.wordpress.com/2015/01/21/busy-gaps

Our lives with rett syndrome GRRR. We means a group of local CE families for school and Rett families we have befriended for research.That was 2014. Because sometimes there are no words , just some of my fave spots and moments for 2014-. I have to add I only really covered a few months of faves. There are too many! What I do like is they show what we are trying to do , which is to include Charlotte, despite Rett Syndrome into our lives and for Charlotte to include us in her life. January 21, 2015. Baby E...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

You know, you’re a mom – charlottetwenty09

https://charlottetwenty09.wordpress.com/2015/03/09/you-know-youre-a-mom

Our lives with rett syndrome GRRR. You know, you’re a mom. Woman, Daughter, Sister, MAMA to 2 beautiful girls, our youngest being diagnosed with RS in August 2012. My life and our lives since. View all posts by cdfitz73. March 9, 2015. Day to Day RS. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. Notify me of new comments via email. When she is fed up o...

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

a voice – charlottetwenty09

https://charlottetwenty09.wordpress.com/2012/09/12/a-voice

Our lives with rett syndrome GRRR. Im starting this blog to process this journey I have started and we have started and Charlotte has started, since our youngest daughter’s Severe Global Developmental Delay (named in May 2011) became more specifically Rett Syndrome at 1230 on Monday 6th August. We are, Mama Caroline and Da Mark to Charlotte, 3 in November and oldest daughter Georgia, 6 in May this year. September 12, 2012. September 12, 2012. 3 thoughts on “a voice”. Pingback: a voice charlottetwenty09.

charlottetwenty09.wordpress.com charlottetwenty09.wordpress.com

cdfitz73 – charlottetwenty09

https://charlottetwenty09.wordpress.com/author/cdfitz73

Our lives with rett syndrome GRRR. This slideshow requires JavaScript. Just some pictures from the last few 6 months showing Charlotte winning and earning a special achievement award at the end of her school year in 2015, beach times with big sis, wearing her horseriding helmet, Christmas beach breakfast with The Dempsters, helping me make a cake, dressups after school, catching up with Grandma Gloria and Communication Award winner a few weeks ago. March 5, 2016. March 5, 2016. Day to Day RS. One of Char...

sh1ft.org sh1ft.org

_sh1ft.org

http://sh1ft.org/blog

Our Rett Syndrome Story. It’s been a huge year. One of the best, though. I think after having gone through so much in the last 5 years, then not dealing with it properly and just learning along the way, and then actually settling in and addressing my personal issues with anxiety and panic attacks and boredom and being a carer and trying to find out who I am inbetween all of this stuff — I think I’ve come out a bit stronger and I like it. Which way is up? Look here, only a month between blog posts 😉.

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TEAM JOVIE - Raising Awareness and Fundraising for Rett Syndrome Research in Australia

RETT SYNDROME AWARENESS and FUNDRAISING IN AUSTRALIA. RETT SYNDROME AWARENESS AUSTRALIA. SHOW YOUR SUPPORT AS WE RAISE AWARENESS AND FUNDS FOR RETT SYNDROME RESEARCH IN AUSTRALIA. Every little bit counts. A little bit about me. Saturday 2 November 2014. In 2009, our daughter Jovie was born in Sydney Australia, and our lives were changed forever. Little did we know the very different path we were about to embark on. For the first 6-8 months, there were no signs of any issues heading our way. Team Jovie wa...

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