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Emma's World

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Friday, February 25, 2011. Overdue updates about my sweet Emma. Emma, Thanksgiving 2010. First big thing to let you know about: Emma's post-surgery recovery continues, and she's doing well! She doesn't talk to them so much anymore, but still refers to them by their names, so I will...

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Emma's World | planetemmaclarissa.blogspot.com Reviews
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This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Friday, February 25, 2011. Overdue updates about my sweet Emma. Emma, Thanksgiving 2010. First big thing to let you know about: Emma's post-surgery recovery continues, and she's doing well! She doesn't talk to them so much anymore, but still refers to them by their names, so I will...
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1 emma's world
2 customized splint
3 kenesio tape
4 handy before surgery
5 handy after surgery
6 posted by
7 joann
8 5 comments
9 post surgery report
10 no comments
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emma's world,customized splint,kenesio tape,handy before surgery,handy after surgery,posted by,joann,5 comments,post surgery report,no comments,she walks,4 comments,wah hoo,emma isms,sometimes,recent examples,more soon,i promise,3 comments,got her,posts
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Emma's World | planetemmaclarissa.blogspot.com Reviews

https://planetemmaclarissa.blogspot.com

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Friday, February 25, 2011. Overdue updates about my sweet Emma. Emma, Thanksgiving 2010. First big thing to let you know about: Emma's post-surgery recovery continues, and she's doing well! She doesn't talk to them so much anymore, but still refers to them by their names, so I will...

INTERNAL PAGES

planetemmaclarissa.blogspot.com planetemmaclarissa.blogspot.com
1

Emma's World: May 2009

http://planetemmaclarissa.blogspot.com/2009_05_01_archive.html

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Sunday, May 31, 2009. After Dr. Paley received Emma's x-rays via email, he responded very quickly:. I see the spike you are referring to. Do you feel it is painful to her? He added in another email that this is usually not painful, and I have to admit that Emma is not. Maybe I'm wr...

2

Emma's World: She WALKS!!

http://planetemmaclarissa.blogspot.com/2010/08/she-walks.html

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Monday, August 9, 2010. Even one step is exciting.and she knows it's an event! Check out the expression on her face! August 9, 2010 at 6:32 PM. Thanks so much Kristen.we are absolutely thrilled with Emmas progress! August 9, 2010 at 8:06 PM. JoAnn, this is awesome! A cerebellar mal...

3

Emma's World: February 2009

http://planetemmaclarissa.blogspot.com/2009_02_01_archive.html

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Sunday, February 22, 2009. Emma has her Rifton walker! We did buy a used Rifton walker a while back but it turned out to be much too big for her. Well, she'll grow into it eventually. This walker is on loan from California Children's Services. As you can see, she LOVES it! But I ha...

4

Emma's World: August 2009

http://planetemmaclarissa.blogspot.com/2009_08_01_archive.html

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Saturday, August 8, 2009. Something WONDERFUL to report! Emma is standing up! With support, yes, but she has learned to get up from a prone position all the way to standing in her Pack-n-Play! Links to this post. Subscribe to: Posts (Atom). Purpose of this blog. In addition to thes...

5

Emma's World: Post-surgery report

http://planetemmaclarissa.blogspot.com/2010/09/post-surgery-report.html

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Saturday, September 4, 2010. Emma is home from the hospital, with a hot pink cast and a straight right wrist! I've rigged a sling for her with a cut-up dishcloth, since the sling sent home from the hospital has not been very successful.Emma wiggles out of it very quickly! This blog...

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heavensdeclaretheglory.blogspot.com heavensdeclaretheglory.blogspot.com

The Heavens Declare: May 2009

http://heavensdeclaretheglory.blogspot.com/2009_05_01_archive.html

The heavens declare the glory of God; the skies proclaim the work of his hands. Day after day they pour forth speech; night after night they display knowledge. There is no speech or language where their voice is not heard. Their voice goes out into all the earth, their words to the ends of the world. Psalm 19: 1-4. Thursday, May 21, 2009. They were frightened at first, thinking He was some sort of ghost. Then He spoke to them, identifying Himself, "It is I; be not afraid.". Links to this post. While at w...

rhombencephalosynapsis.blogspot.com rhombencephalosynapsis.blogspot.com

Life with Rhombencephalosynapsis: A Unique Guest Post

http://rhombencephalosynapsis.blogspot.com/2015/03/a-unique-guest-post.html

Friday, March 27, 2015. A Unique Guest Post. I Am hoping to incorporate a new "series" on this blog which will include blog posts from individuals living with RS. If you or someone you know would like to contribute please let me know via the contact information in the right column. The first blog post in the "Life With Rhombencephalosynapsis" Series comes from my girl, Abby. Written By Abigail Fescoe:. Posted by Kristen Fescoe, March 2015. That which does not kill us makes us stronger. Abby was born with...

rhombencephalosynapsis.blogspot.com rhombencephalosynapsis.blogspot.com

Life with Rhombencephalosynapsis: Alopecia?

http://rhombencephalosynapsis.blogspot.com/2013/10/alopecia.html

Sunday, October 13, 2013. One of the more odd hallmarks of Rhombencephalosynapsis is alopecia. Whether male of female, most people with RS have some degree of baldness, typically patches. I was asked by researchers conducting a study on RS to send pictures of her patches and her ears (kids with RS typically have low set forward slanted ears also) and I thought I would share. When she was first diagnosed I remember thinking "how awful. on top of everything else my kid is going to have bald patches". I mar...

rhombencephalosynapsis.blogspot.com rhombencephalosynapsis.blogspot.com

Life with Rhombencephalosynapsis: Slowly But Surely

http://rhombencephalosynapsis.blogspot.com/2015/07/slowly-but-surely.html

Saturday, July 25, 2015. The girls had their 8 year well check this past week. Both girls are the picture of health and both girls grew very nicely. Miss Abigail is now a whopping 42 pounds and 47 inches. That puts her in the 3rd percentile for weight and the 5th for height. It doesn't sound like much but it's on the chart! Subscribe to: Post Comments (Atom). She also has structural malformations in her. Follow us on Instagram. Our words to live by. I married my high school sweetheart and our life has be...

lymetwistontherocks.blogspot.com lymetwistontherocks.blogspot.com

Life...with a Twist of Lyme: You know you have Lyme when....

http://lymetwistontherocks.blogspot.com/2011/07/you-know-you-have-lyme-when.html

Lifewith a Twist of Lyme. My Life with Multiple Chronic Illnesses, Including Lyme Disease. Saturday, July 9, 2011. You know you have Lyme when. Retrieved from the "Truth About Lyme Disease Forums" on 5/6/2011. YOU KNOW YOU HAVE LYME WHEN:. 1) You don't care where your spouse goes, just as long as you don't have to go along. 2) You are cautioned to slow down by the doctor instead of by the police. 3) "Getting lucky" means finding your car in the parking lot. 7) You get exhausted from just waking up. 17) Y...

lymetwistontherocks.blogspot.com lymetwistontherocks.blogspot.com

Life...with a Twist of Lyme: August 2011

http://lymetwistontherocks.blogspot.com/2011_08_01_archive.html

Lifewith a Twist of Lyme. My Life with Multiple Chronic Illnesses, Including Lyme Disease. Sunday, August 21, 2011. You can now watch the entire documentary film about Lyme disease, Under Our Skin. This film is a MUST-SEE for anyone who has (or suspects they have) Lyme disease! PS Yes, there are commercials, just be patient! Tuesday, August 16, 2011. Lots and lots of important info! I want to catch you up on miscellaneous exciting news in the world of Lyme research, so this is a bit of a hodgepodge post.

lymetwistontherocks.blogspot.com lymetwistontherocks.blogspot.com

Life...with a Twist of Lyme: January 2011

http://lymetwistontherocks.blogspot.com/2011_01_01_archive.html

Lifewith a Twist of Lyme. My Life with Multiple Chronic Illnesses, Including Lyme Disease. Monday, January 17, 2011. Go Directly to Jail, Do Not Pass "Go". It's so hard to explain this to people who are not chronically ill.but it's just like being in prison. I can't go out, I have Lyme and lupus and twenty other diagnoses, and I'm extremely. He doesn't feel like going anywhere, so even if I wanted. To go somewhere (which doesn't happen very often), I can't because he won't take me. I suppose this is comi...

lymetwistontherocks.blogspot.com lymetwistontherocks.blogspot.com

Life...with a Twist of Lyme: February 2011

http://lymetwistontherocks.blogspot.com/2011_02_01_archive.html

Lifewith a Twist of Lyme. My Life with Multiple Chronic Illnesses, Including Lyme Disease. Thursday, February 24, 2011. A Lyme Obituary - and a Message to the Living. I received this obituary in email and felt I had to share it with you. No, I didn't know the gentleman in question. Unfortunately, this is what can happen if you have Lyme disease and you're forced to rely on conventional medicine and doctors who follow the IDSA guidelines. Vernon Dale Kyle, 55, Kansas. Vernon’s illness was bacterial ...

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Emma's World

This blog is dedicated to differently-abled children, particularly those diagnosed with a radial ray defect, hematological issues, Failure to Thrive, developmental delays, microcephaly, cerebellar dysgenesis or cerebral palsy. Friday, February 25, 2011. Overdue updates about my sweet Emma. Emma, Thanksgiving 2010. First big thing to let you know about: Emma's post-surgery recovery continues, and she's doing well! She doesn't talk to them so much anymore, but still refers to them by their names, so I will...

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