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Madison, Mommy's Angel in Heaven

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Thank you for coming to Madison's site. This is my way of honoring her memory and keeping her alive in some small way. This site is NOT intended to make you cry but to make you smile and cherish her memory as much as I do. Also, it is a site to promote awareness for Mitochondrial Diseases/Disorders! Madison died 5 days after her 2nd birthday. I got to have her for 2 years and 5 days! That was a blessing to me. She suffered a LOT in her short life, but she also taught me many lessons and she showed me what real unconditional love is! I hope that by browsing this site you smile and realize all the families out there living with this disease/disorder love their children very much, wether they are here on earth or angels watching over us! Enjoy reading our babies stories! Donate if you can!
Mitochondrial Disease is, at heart, a disease of energy deficiency. The mitochondria, tiny organelles living inside our cells, are responsible for converting food and oxygen into energy. When the cells can’t get enough energy, due to malfunctioning mitochondria, the cells begin to die, and the organs in which these cells live—the liver and kidneys and eyes and digestive system: the brain, the heart—begin to fail. Miotchondrial disease is no single disease, in other words. It can affect any organ, appear as any disease, it is progressive, and it has no cure. Yet!
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In loving Memory of Madison Morgan Grantham, may she never be forgotten!
July 29, 2004 thru August 3, 2006
Support Stem Cell Research
HEAVEN'S VERY SPECIAL CHILDA meeting was held quite far from earth. "It's time again for another birth," said the angels to the Lord above, this special child will need love. Her progress may seem very slow, accomplishments she may not show, and she'll require extra care, from the folks she meets way down there. She may not run, or laugh or play, her thoughts may seem quiet far away, in many ways she Won't adapt, she'll be known as handicapped, so let's be careful where she's sent, we want her life to be content, please Lord, find parents who will do a special job for you. They will not realize right away, the leading role they're asked to play, but with this child sent from above, comes stronger faith and richer love, and soon they'll know the priviledge given, caring for this gift from Heaven. Their precious child, so meek and mild, It's HEAVEN'S VERY SPECIAL CHILD
This is something another Mom wrote, she also lost her child through an "Undiagnosed" Mitochondrial disorder. This TRULY explains what a parent who has ever lost a child goes through and how they feel! Thanks Jennifer!
You start out with the best of intentions. Their nursery is going to be the best ever. It's going to have Butterflies everywhere and a is going to be pink and purples. They have every possible childhood toy and gadget. And the clothes and shoes are just so much fun.They have the most beautiful smiles. All they want is to be loved and protected. Why don't we get the option to protect them? We do everything humanly possible and it's not nearly enough. There are no answers and there's a good chance there never will be. The best minds in the world are baffled. All you can do is tell them every day that you love them, are proud of them, and will be with them every step of the way. You also have to tell them if it's too much you understand and it's okay because you don't want them to be scared.Their spirit amazes you every day. They have such strength. Each day they teach you that you have so much more strength then you ever knew you had. They teach you things about the human spirit and experience that you would never have known existed if everything was okay. They teach you to sweat the small stuff because each one of those little things is so priceless.No matter how bad it is you still hold out hope for a miracle. Maybe one day they will get to spend some time in their nursery playing with all of their toys, watching their train, and naming all of the puppies. Sometimes these miracle do happen, but it's very rare. You take them to regular doctors, witch doctors, and anything else in between just for a chance to change the inevitable outcome. You try hippie products, every vitamin known to human kind, healing meditations, and even crystal tones.Then you have to say goodbye. How do you ever say goodbye? You've had your heart and soul torn out over and over again. How is that ever repaired? They look so beautiful - being sent off to play. You keep expecting them to just wake up and say something, anything or give you that look - and we all know that look. It never happens.Now you have to rebuild your life. Do you go back to the way it was before like nothing ever happened? How can you because you will never be the same person again? Where is that strength to put one foot in front of the other and conquer all obstacles that was here not that long ago? How do you tap back into that? How do you respond to others? There are just so many questions and still no answers.

My Interests

I'd like to meet:

Michael J. Fox (got to see him, but not meet him), Christopher Reeve (if he was alive). Nelly!

Click on a line below to go to that link!

Ways to support stem cell research

Ways to support United Mitochondrial Foundation

Michael J. Fox Foundation

Christopher Reeve Foundation

Times Article on Mito Disorders

Alpers_Summary_for_Families_2007.pdf
A Beginners summary of Alper's Syndrome (this is a GREAT article by Dr. Robert Naviaux, the leading expert on Alper's Syndrome. He has graciously allowed me to post this on this site.)

tagfantasy.com

Did you know that 1 in 4,000 Americans has a MITOCHONDRIAL DISORDER?

Did you know that AUTISM, ALZHEIMER'S, DIABETES, PARKINSON'S, RETT'S SYNDROME, SIDS, and other disorders are actually a result of a "Mitochondrial Disorder" or a "Mitochondrial Dysfunction"?

Did you know that MITOCHONDRIAL DISEASE affects both sexes, all ages, all races, all IQ and educational levels, and all socioeconomic backgrounds?

Did you know that this disease is what my daughter died from? Did you know that there are at least 17 families in the milwaukee area that I know of that have children with this disease? (there may be more I don't know of)

My precious angel was only 2 years old when she died.

Did you know you could help? By giving donations to the UMDF (www.umdf.org)! You could give donations in honor of someone you know who has the disease or just because you just want to help researchers find a cure!

My Blog

Madison's Story - May 19 is the last time I saw my baby happy and healthy..........

Madison's StoryMadison Morgan Grantham was born on July 29, 2004. She weighed 5lbs. 6oz., and was 19 long. She was a perfect & beautiful baby. Madison progressed normally as the months went on. At 6 ...
Posted by on Tue, 19 May 2009 11:36:00 GMT

Mitochondrial Disease Awareness week

The candle burning on my page today is in memory of those lost to or suffering from Mitochondrial Disorders!  My daughter, Madison, was lost at 2 years and 5 days old to a rare Mitochondrial Depl...
Posted by on Wed, 24 Sep 2008 12:42:00 GMT

She Is Gone

 POEM BY DAVID  HARKINS   She is gone     You can shed tears that she is gone or you can smile because she has lived.   You can close your eyes and pray that she'...
Posted by on Tue, 23 Sep 2008 19:13:00 GMT

August 4th!

Yesterday was the 2nd anniversary of Madison's death.  Today brings on a whole new set of pain because of that.  Today marks the day that she's been gone longer than I had her.  It's li...
Posted by on Mon, 04 Aug 2008 13:01:00 GMT

Mother’s Day!

My Mother's day dilemma.  Do you celebrate mothers day if you ARE a mother, but you don't have the child on earth any longer?  My cousin called me 2 days ago, she had 2 miscarriages over the...
Posted by on Fri, 09 May 2008 08:11:00 GMT

May!

As most of you know, May, July and August are hard months for me.  May 20th 2005 Madison had her first seizure and was forever changed.  July 29th is her birthday and August 3rd is her Angel...
Posted by on Thu, 01 May 2008 09:08:00 GMT

Volunteering for Mito!

I am volunteering for a fundraiser for Mitochondrial disease happening in May!  I’ve been trying so hard to get motivated to do things that will help raise money to find a cure and I finall...
Posted by on Tue, 01 Apr 2008 19:52:00 GMT

Today was a tough day filled with tears!

When I moved last august I put most of Madison’s stuff at my mom’s.  Well I decided to put it in storage with the rest of my stuff today.  So we get all the boxes out and decide ...
Posted by on Sun, 16 Mar 2008 17:34:00 GMT

Madisons Story

Madison Morgan Grantham was born on July 29, 2004.  She weighed 5lbs. 6oz., and was 19" long.  She was a perfect & beautiful baby. Madison progressed normally as the months went on....
Posted by on Mon, 10 Mar 2008 13:11:00 GMT

CNN Today, RE: Autism/Mito Disorders!

THE EVE OF BATTLE: VACCINE INJURED CHILD LARRY KING TO INTERVIEW FAMILY OF VACCINE INJURED CHILD The Eve of Battle By Kent Heckenlively The war has begun. On Thursday March 6, 2008 at 11:30 a.m. at...
Posted by on Thu, 06 Mar 2008 06:35:00 GMT