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Maddie's Marathon – Our amazing daughter's battle with leukemia and intractable epilepsyOur amazing daughter's battle with leukemia and intractable epilepsy
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Our amazing daughter's battle with leukemia and intractable epilepsy
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Maddie's Marathon – Our amazing daughter's battle with leukemia and intractable epilepsy | maddiegorman.wordpress.com Reviews
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Our amazing daughter's battle with leukemia and intractable epilepsy
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May 2009 Photos – Maddie's Marathon
https://maddiegorman.wordpress.com/photos/may-2009-photos
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. May 7 – Playing in the yard. Running away from mama. It was breezy, so I’m sporting the layered look. I’m not sure how I feel about all this sand. May 13 – Figure 8. Look how pretty the ocean was…. May 20 – Playing in my playroom. Am I beautiful or what?
MileStones Walk 2008 Photos – Maddie's Marathon
https://maddiegorman.wordpress.com/photos/milestones-walk-photos
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. MileStones Walk 2008 Photos. We look cool in bandanas…. To see the news story about the walk Click Here. You can also watch a clip of the walk, where Maddie, Brandon and I make a few quick appearances. Share on Facebook (Opens in new window). Follow “M...
December 2008 Photos – Maddie's Marathon
https://maddiegorman.wordpress.com/photos/december-photos
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. Wearing my new Christmas PJs. Share on Facebook (Opens in new window). Click to email (Opens in new window). Click to print (Opens in new window). Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:.
End of ’08 – April ’09 Photos – Maddie's Marathon
https://maddiegorman.wordpress.com/photos/new-years-2008-april-12-2009-photos
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. End of ’08 – April ’09 Photos. New Years Eve 2008. Bathtime January 1 2009. I love my DaDa - Feb 8. The new face I make when Mama tells me to smile. Playing in the yard in my jammies - Feb 8. I am sooo big - Feb 8. Throwing balls, my favorite game - Feb 10.
Photos June 8, 2009 – Maddie's Marathon
https://maddiegorman.wordpress.com/photos/photos-june-8-2009
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. Photos June 8, 2009. Share on Facebook (Opens in new window). Click to email (Opens in new window). Click to print (Opens in new window). 2 thoughts on “ Photos June 8, 2009. Bec-Andrew's Mom from IS forum. June 11, 2009 at 5:50 pm. Hope all is well with you!
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noahsweitzersarchives.blogspot.com
Noah's Archives: Ahhh....Colorado
http://noahsweitzersarchives.blogspot.com/2010/07/ahhhcolorado.html
Life has meaning only in the struggle. Triumph or defeat is in the hands of the Gods. So let us celebrate the struggle! Thursday, July 15, 2010. Noah is great. I'm great. Life is great. Subscribe to: Post Comments (Atom). Live in an incubator, grow, get blood transfusions, have multiple IVs, and so many other things you just never want your child to endure. He fought every step of the way like a champ (he is much stronger than I) and finally we were discharged! After 2 months of Prednisone. Dr R : ENT.
noahsweitzersarchives.blogspot.com
Noah's Archives
http://noahsweitzersarchives.blogspot.com/2010/06/i-know-its-been-too-long-since-update.html
Life has meaning only in the struggle. Triumph or defeat is in the hands of the Gods. So let us celebrate the struggle! Tuesday, June 22, 2010. I know it's been too long since an update when my friend Amy texts me to get the latest on my little man. : smile:. I keep thinking about what to say but when I get to my keyboard I get stuck. Noah is being Noah. Which means he's healed from the pneumonia (Thank God) and he's back to his usual self when it comes to feeds and then some. Such a Bad Bad. Dr R : ENT.
The Extreme Parenting Video Project | Beautiful Chaos
http://beautiful-chaos.org/the-extreme-parenting-video-project
Living life, one deep breath at a time. The Beginning and Beyond. The Extreme Parenting Video Project. The Extreme Parenting Video Project. Leave a Reply Cancel reply. Your email address will not be published. Required fields are marked *. You may use these. A href= title= abbr title= acronym title= b blockquote cite= cite code del datetime= em i q cite= strike strong. Back at it. Can you believe it? I must have problems. Bluebelle on Reality checks. Angi Grasso on About Us. My Name is Sarah.
Austin's IS Journey: July 2011
http://love4austin.blogspot.com/2011_07_01_archive.html
This blog tracks our family's day to day life while battling our son's diagnosis of Infantile Spasms. Feel free to follow us as we continue to fight against the seizures and devastating effects of this terrifying form of epilepsy. You may also read Austin's full story at the bottom of the page. Friday, July 22, 2011. I'm going to copy and paste this one to my fb because I still haven't had the patience to figure out how to link to my feed. That and I don't want to write it twice. lol). Why he thinks this?
Austin's IS Journey: Three little words
http://love4austin.blogspot.com/2011/07/three-little-words.html
This blog tracks our family's day to day life while battling our son's diagnosis of Infantile Spasms. Feel free to follow us as we continue to fight against the seizures and devastating effects of this terrifying form of epilepsy. You may also read Austin's full story at the bottom of the page. Friday, July 22, 2011. I'm going to copy and paste this one to my fb because I still haven't had the patience to figure out how to link to my feed. That and I don't want to write it twice. lol). Why he thinks this?
Austin's IS Journey: In Detroit
http://love4austin.blogspot.com/2011/07/in-detroit.html
This blog tracks our family's day to day life while battling our son's diagnosis of Infantile Spasms. Feel free to follow us as we continue to fight against the seizures and devastating effects of this terrifying form of epilepsy. You may also read Austin's full story at the bottom of the page. Wednesday, July 13, 2011. Also, unlike at TCH, there must be one parent awake at all times to watch for seizure activity. THE biggest downside! I think I'm also spoiled to the private rooms at TCH too. ;). So, the...
noahsweitzersarchives.blogspot.com
Noah's Archives: Happy Birthday Noah!
http://noahsweitzersarchives.blogspot.com/2010/08/happy-birthday-noah.html
Life has meaning only in the struggle. Triumph or defeat is in the hands of the Gods. So let us celebrate the struggle! Sunday, August 29, 2010. May this year be better than the last! August 30, 2010 at 7:13 AM. A big Happy Birthday to Noah! August 30, 2010 at 8:25 AM. I believe in all my heart it will. August 30, 2010 at 10:11 AM. Happy Birthday Little Man! August 30, 2010 at 12:31 PM. I hope you have a wonderful year because you deserve it! August 31, 2010 at 9:40 AM. Subscribe to: Post Comments (Atom).
noahsweitzersarchives.blogspot.com
Noah's Archives: July 2010
http://noahsweitzersarchives.blogspot.com/2010_07_01_archive.html
Life has meaning only in the struggle. Triumph or defeat is in the hands of the Gods. So let us celebrate the struggle! Thursday, July 15, 2010. Noah is great. I'm great. Life is great. Links to this post. Subscribe to: Posts (Atom). Live in an incubator, grow, get blood transfusions, have multiple IVs, and so many other things you just never want your child to endure. He fought every step of the way like a champ (he is much stronger than I) and finally we were discharged! After 2 months of Prednisone.
noahsweitzersarchives.blogspot.com
Noah's Archives: ReDo
http://noahsweitzersarchives.blogspot.com/2010/06/redo.html
Life has meaning only in the struggle. Triumph or defeat is in the hands of the Gods. So let us celebrate the struggle! Tuesday, June 22, 2010. After reflecting about my last blog (and I am tempted to delete it but I won't because the emotions I expressed are real), I'm bothered. I hate putting negative blogs out there although honestly it's way easier to list the negative aspects of the day when I think about what my kid does NOT do than to reach deep down and find the positive. June 23, 2010 at 7:45 AM.
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Maddie's Marathon – Our amazing daughter's battle with leukemia and intractable epilepsy
Our amazing daughter's battle with leukemia and intractable epilepsy. Photos Taken by Angela Shea. Sept 14, 2008 B/W Photos. Sept 14, 2008 Photos. MileStones Walk 2008 Photos. End of ’08 – April ’09 Photos. Photos June 8, 2009. Liz’s Random Thoughts. August 23, 2015. RoC Golf Tourney 2015. Nicole Smith, CEO of Mary’s Medicinals, gives a wave just prior to the start. Beautiful day for golf. Former Broncos (including Tarheel Ebenezer Ekuban) joined us. Blythe (Head of RoC Fundraising). The entire day was a...
MaddieGotSchwag
Reblogged 4 years ago from causeweliketopartaaaay ( Originally from viridiannightmares. You don’t get to say, “Mom, I can’t get grounded, I’m Justin Bieber”. Laughs* She will slap me in the face. Reblogged 4 years ago from causeweliketopartaaaay ( Originally from dashingslore. If I were Justin, every time I saw my crazy fans act like they’re about to eat me, I’d probably make this face:. Posted 4 years ago. One less lonely girl 3. Posted 4 years ago. Posted 4 years ago. She grew up good. She grew up slow.
MaddieGra | Fine Gifts & More!
Zwilling J.A. Henckles. Aprons & Potholders by Lynne’s Whim. Original Artwork by Monica Kelly. Hand blown vases & serving pieces. Original Stoneware by VanDyke Pottery. Arevada Herbal soaps, oils & body butter. Olivina soaps & lotions. BigLick Barkery Dog Treats. Zwilling J.A. Henckles stainless steel flatware. Gift & Bridal Registry. We hope to see you soon! Zwilling J.A. Henckles. Polish Stoneware & Kitchen Accessories. Monday 10am - 6pm. Tuesday 10am - 6pm. Wednesday 10am - 6pm. Thursday 10am - 6pm.
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Madelyn Grace | our 23 week micro miracle
Our 23 week micro miracle. The end of summer is nearing. August 19, 2014. August is already halfway through and the summer has gone by too quickly! Our summer has been really nice. We’ve been kept fairly busy, so that’s probably why time just seems to be slipping away. Maddie handled the trip really well (being in the car for 14 hours). She actually has been my best baby-road-tripper so far! Ready for our big drive on the “really long road” (as the girls like to call it). I love these babies! They liked ...
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Si les souhettes sont des chevaux...
Si les souhettes sont des chevaux. Whats the quickest way to say I dont know? View my complete profile. Thursday, March 19, 2009. The pony games were AWESOME! And by the way in the treasure hunt we came in 2nd! I was super happy! Maddie two time "champion" hehehehehehe. Saturday, March 7, 2009. Ok, I am SO sorry! I keep forgetting to post! I've been doing alright. I'm so happy next week I'm going to pony games at my stable! She may look like a horse but she is actually a treasure hunting machine! Sorry I...
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