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Author Topic: "A Gift of Life"...Tesa's Story  (Read 5006 times)
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« on: April 12, 2009, 06:50:09 pm »

SHOW LINK:http://www.blogtalkradio.com/LupusMCTD/2009/04/16/A-Gift-of-LifeTesas-Story


Call-in Number: (347) 326-9503
Upcoming Show: 4/15/2009 3:00 PM Pacific 6:00 PM Eastern

Host Name: LupusMCTD    
Show Name:"A Gift of Life"...Tesa's Story
Length:    30 min
Description:

Seizures caused her to code blue and was on life support. In 1990 she had her ovaries removed, in 2005 she has her right knee replaced. By 2007 she had her left knee replaced. Her hip was destroyed twice by Osteoarthritis.

But it was 9 years ago today that Tesa had a kidney donated. All because of LUPUS. Come join us on Tesa's journey to "Keep The Light Going" and to "Stay Blessed". You will be inspired by this young woman's story of faith, courage and love for others.

Tesa resides in Washington DC and is planning to walk down Pennsylvania Avenue on May 18 to raise money for a cure for Lupus.
 


Join us as we learn more about how serious Lupus can be and what it did to Tesa. How she over came the odds and is a survivor!
Kathy
« Last Edit: April 14, 2009, 09:26:14 pm by Adminஐﻬ » Logged


I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
Adminஐﻬ
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Gender: Female
Posts: 10407


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« Reply #1 on: April 14, 2009, 09:29:22 pm »

REMINDER!!!

"A Gift of Life"...Tesa's Story

by LupusMCTD

Date / Time: 4/15/2009 3:00 PM

Call-in Number: (347) 326-9503

Chat room with Audio, Video & Microphone is available during the recording of the live show.

Please join us give Tesa your salutations during this wonderful time of celebration!
She is a 9 year kidney transplant survivor!!!  LUAW  CandleSmilie
Logged


I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
lupusjoy
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I AM BLESSED AND SO ARE YOU!!


« Reply #2 on: April 16, 2009, 09:47:04 pm »

I JUST WANT TO THANK YOU ALL FOR GIVING ME A CHANCE TO TALK AND SHARE MY STORY
I HOPE THIS WILL HELP SOME ONE OR MAYBE EVEN SAVE A LIFE ,BECAUSE LUPUS WILL HAVE YOU DEPRESSED AND IT CAN GET YOU DO BUT NO THIS GOD IS THE ONE WHO MADE IT POSSIBLE FOR ME TO BE HERE AND SHARE MY STORY ,SO I NO THIS IS MY CALLING TO SHARE MY STORY AND HELP OTHER THAT FILL DOWN ,KEP THE FAITH AND THE LIGHT WILL STAY BRIGHT(((TESA)))    STAY BLESSED:)
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I JUST WANT TO SAY TO YOU ,WHEN YOU FEEL SAD JUST LOOK UP, AND ASK GOD TO GIVE YOU JOY ,AND HE WILL GIVE YOU THAT...STAY BLESSED,And be not afraid;go tell my brethren that they go in to Galilee,and there shall they see me .....
Adminஐﻬ
"Pay It Forward" ஐﻬ
Site Owner
******
Offline Offline

Gender: Female
Posts: 10407


LupusMCTD Founder ஐﻬ


WWW
« Reply #3 on: April 17, 2009, 03:39:12 pm »

I JUST WANT TO THANK YOU ALL FOR GIVING ME A CHANCE TO TALK AND SHARE MY STORY
I HOPE THIS WILL HELP SOME ONE OR MAYBE EVEN SAVE A LIFE ,BECAUSE LUPUS WILL HAVE YOU DEPRESSED AND IT CAN GET YOU DO BUT NO THIS GOD IS THE ONE WHO MADE IT POSSIBLE FOR ME TO BE HERE AND SHARE MY STORY ,SO I NO THIS IS MY CALLING TO SHARE MY STORY AND HELP OTHER THAT FILL DOWN ,KEP THE FAITH AND THE LIGHT WILL STAY BRIGHT(((TESA)))    STAY BLESSED:)
Tesa
Your story did reach out and touch others. I recieved a PM from my Blog Talk Radio account a lady named Grace. She has Fibro and her close relative has had Lupus for over 30 years.

My next show will be on Fibromyalgia. I am working on it and will announce the date & time soon.
Thank you Tesa for sharing your story with us, your story is an inspiration to many!
Kathy

   
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I look normal, as I have an "Invisible Illness". You can not catch it, you can not see it. It's called Lupus.My body is attacking itself on the inside.
www.LupusMCTD.com Represents:
1) We are patients helping researchers build a future for the lives of others...
2) Where HOPE is a WORK In Progress
3) Pay It Forward~Giving Back To The Future Lupus/MCTD Patients
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LupusMCTD Founder & Patient
Former Domestic Violence SURVIVOR
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Author of the Upcoming Memoir Book:
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A lupus patient fights the beast within her immune system and the beast at home....

e-Booklet filled with photos and videos of what abuse was, signs to look for,
where to turn to for help, and much more to help others like me...


For more information
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