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Dizzyland

cavernous malformations

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Dizzyland | erinsdizzyland.blogspot.com Reviews
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cavernous malformations
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2 pages
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Dizzyland | erinsdizzyland.blogspot.com Reviews

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cavernous malformations

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1

Dizzyland: September 2014

http://www.erinsdizzyland.blogspot.com/2014_09_01_archive.html

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Sunday, September 14, 2014. I can’t believe it’s been six months since I had Damian removed. He is gone – hopefully forever. The week before my anniversary I learned, again, the hard lesson that it is not always forever as a Facebook friend found out hers is back. And so, Lord, where do I put my hope? My only hope is in you. You can imagine how much this helps; you got it, NOT one bit! I have to remind myself ...

2

Dizzyland: January 2014

http://www.erinsdizzyland.blogspot.com/2014_01_01_archive.html

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Wednesday, January 29, 2014. What can you do? Over the past year I have been dizzy, staggered around like a drunken Jack Sparrow – including the arms flapping around, been nauseous and on and on it goes. I could use this as an excuse to sit around and watch TV all day and do absolutely nothing, or I can get creative. I replied yeah I am fine, why? I have also started using those electric buggies’s at Wal...

3

Dizzyland: 6 months!!

http://www.erinsdizzyland.blogspot.com/2014/09/6-months.html

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Sunday, September 14, 2014. I can’t believe it’s been six months since I had Damian removed. He is gone – hopefully forever. The week before my anniversary I learned, again, the hard lesson that it is not always forever as a Facebook friend found out hers is back. And so, Lord, where do I put my hope? My only hope is in you. You can imagine how much this helps; you got it, NOT one bit! I have to remind myself ...

4

Dizzyland: What you don’t see

http://www.erinsdizzyland.blogspot.com/2014/06/what-you-dont-see.html

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Monday, June 23, 2014. What you don’t see. I have been told numerous times how good I look. I walk without my cane; for the most part, so I must be much better. My speech has improved so I must be awesome! 1 Peter 2:24 (NIV). 8220;He himself bore our sins” in his body on the cross, so that we might die to sins and live for righteousness; “by his wounds you have been healed.”. Pressure headaches – these a...

5

Dizzyland: My one year brainnniversary!!

http://www.erinsdizzyland.blogspot.com/2015/03/my-one-year-brainnniversary_13.html

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Friday, March 13, 2015. My one year brainnniversary! One year ago I had Damian removed! Here is a video showing the past year! Subscribe to: Post Comments (Atom). My one year brainnniversary! Slow and steady wins the race. Symptomatic multiple Cavernous Malformations. View my complete profile. Awesome Inc. template. Template images by molotovcoketail.

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windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: Pray for Nick

http://windlessdandelionwishes.blogspot.com/2015/06/pray-for-nick.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Monday, June 15, 2015. I just received this message tonight:. Nick has a rare tumor in the pons area of the brainstem. These were the only physicians that gave us any hope. My son is a healthy soccer player and they feel like they can get him back to how he is today. Hearing your story makes me feel like that is true.". It makes me so happy that these people have hope again! Subscribe to: Post Comments (Atom).

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: September 2012

http://windlessdandelionwishes.blogspot.com/2012_09_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Tuesday, September 25, 2012. Central nervous system cavernous hemangioma. The incidence in the general population is roughly 0.5%, and clinical symptoms typically appear between 20 to 30 years of age.[2] Once thought to be strictly congenital, these vascular lesions have been found to occur de novo. It may appear either sporadically or exhibit autosomal dominant inheritance. CCMs and venous angiomas. Raises the...

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: May 2013

http://windlessdandelionwishes.blogspot.com/2013_05_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Friday, May 31, 2013. How it all started. Hello my loves :). People often ask me "How did you find out? Or "How did you know? How it all started,. It felt like I had zillions of bugs eating me inside the head but I remember telling myself how much worse it can be in life. Yea I thought "ok is this really getting worse? Is that really all because of ONE loss eardrum, come on! He told me we had to rule out MS&#46...

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: ~SUCCESS STORIES~

http://windlessdandelionwishes.blogspot.com/p/success-stories.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. After Dr.Spetzler offered the surgery, what made my decision to have the surgery so agonizing, is the fact that I could not find anybody who had a successful Brainstem Surgery after being told Inoperable over and over again! So dear friends, here are very inspiring, amazing, successful "inoperable" surgeries stories for you! From Texas, USA. NeuroSurgeon: Dr. Robert Spetzler. From London, UK. From NY, USA.

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: My Neuro Psychological Evaluation

http://windlessdandelionwishes.blogspot.com/2015/03/brain-fog-cognitive-dysfunction.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Monday, March 16, 2015. My Neuro Psychological Evaluation. My Neuro-psychological testing is done. I was incredibly challenging for me. My brain was completely shot the first time from focusing so hard. I got 14 hours sleep that night and 10 hours , 2 nights in a row after that. It's life, you know! Or I am not crazy! Subscribe to: Post Comments (Atom). One day at a time: No pity allowed. I love my Followers.

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: July 2012

http://windlessdandelionwishes.blogspot.com/2012_07_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Tuesday, July 17, 2012. Its almost like playing God. Wait, it IS like playing God! I was told yesterday that this is permanent. It does feel better when i have little to no seizures. They come and go and are so unpredictable! This video inspired me to try:. Thursday, July 12, 2012. That is what I have been told. very coldly, blunt. "go enjoy your family". God Help me. Monday, July 2, 2012. Ready, Set, Go! I hav...

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: February 2013

http://windlessdandelionwishes.blogspot.com/2013_02_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Wednesday, February 27, 2013. And one thing leading to another for a really sick person. I finally got some sleep without their help, and with every 10 mins of sleep (mind you, i didnt sleep in 4 days then) I got better. However, one did admit "i am not a neurosurgeon, I am a neurologist. I respect that so much more. Now, if it was a bleed 2 weeks ago, I will most likely find out thru Dr.Spetzler! Friends have ...

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: June 2012

http://windlessdandelionwishes.blogspot.com/2012_06_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Monday, June 18, 2012. 8221; and he would think the same on his end, but funny enough, our love for each other was a caring one, wanting the best for the other, and we didn’t have any romantic plan. My husband is my best friend, my soul mate. He knows me better than I know myself. We will never take each others presence for granted. Being apart for so long was so hard, yet, I am thankful for it....In 2008, I wa...

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Windless Dandelion Wishes: ~About Cavernous Malformation~

http://windlessdandelionwishes.blogspot.com/p/according-to-mayo-clinic-this-is.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. According to The Mayo Clinic, this is the definition for "Cavernoma":. 8220;Cavernous malformations are abnormally formed blood vessels that have the appearance of a small mulberry in the brain or spinal cord. These malformations may be hereditary or they may occur on their own. First, a Cavernous Malformation goes by different terms:. CM (Short for Cavernous Malformation). When I was first diagnosed, I found i...

windlessdandelionwishes.blogspot.com windlessdandelionwishes.blogspot.com

Windless Dandelion Wishes: December 2012

http://windlessdandelionwishes.blogspot.com/2012_12_01_archive.html

Life after "inoperable" Brainstem Cavernous Malformation Surgery. Donate Life. Organ Donation. Sunday, December 2, 2012. Its been about 6 months since i was diagnosed with the thang. That’s what i like to call it. The thang. Go ahead… tell me “oh its ok, i’ve never been active, you’ll be ok”. haha. You’ll be ok. Christmas is almost here! I have been good this year. As I should of been all these years, but i took it for granted! I lost 20 pounds. I am proud of that too. WOOT I have more energy too since t...

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Dizzyland

My journey with Cavernous Malformations . . . Please donate to help raise money for my surgery. Friday, March 13, 2015. My one year brainnniversary! One year ago I had Damian removed! Here is a video showing the past year! Links to this post. Sunday, January 11, 2015. I’m so worthless! My clothes aren’t in style! I’m so ugly! My teeth aren’t white! I have big feet! Well, I have news for you –. GOD DON’T MAKE NO JUNK! I don’t have many friends! 8220;Before I formed you in the womb I knew. For God so loved.

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