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« on: March 18, 2009, 09:46:44 am » |
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 CONGRATS to LupusMCTD.com for expanding our vision further by using radio to reach many more Lupus MCTD families.
UPCOMING GUEST LIST: Tyler Malcolm author in the 1980's of the SLE/TissueCatabolism theory. Watch for it on www.BlogTalkRadio.com/LupusMCTD2Mr. Geoff Thomas from Australia who in 2008 rode a bicycle from NYC to California and back to raise awareness and funds for this most often overlooked disease. Watch for it on www.BlogTalkRadio.com/LupusMCTDDates and times will be listed as soon as we can confirm a solid schedule!  
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« Last Edit: April 01, 2009, 11:41:50 am by Adminஐﻬ »
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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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Adminஐﻬ
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« Reply #1 on: March 25, 2009, 09:16:21 am » |
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« Last Edit: March 25, 2009, 12:13:31 pm by Adminஐﻬ »
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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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Adminஐﻬ
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« Reply #2 on: March 25, 2009, 05:10:37 pm » |
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Tuesday March 31, 2009
3:00 PM Pacific Time
6:00 PM Eastern Interview with cyclist, Lupus patient and advocate, and author Mr. Geoff Thomas 
This is a show you won't want to miss!
30 minutes.
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« Last Edit: March 25, 2009, 05:11:06 pm by Adminஐﻬ »
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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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lupusjoy
GOD`S GIFT
Full Seeker of Support
 Offline
Gender: 
Posts: 712
I AM BLESSED AND SO ARE YOU!!
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« Reply #3 on: March 28, 2009, 06:57:52 pm » |
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I AM GOING TO MAKE SURE I CATCH YOU ALL THIS TIME BECAUSE IT WAS ALSOME YOU HERE ME IF ANY ONE HAS TIME PLEASE FILL FREE TO CHECK IT OUT OK MUCH LOVE TO YOU ALL STAY BLESSEDAND PLEASE SUPORT US PLEASE IT IF FOR THE BEST AND LOVE FOR OUR SITE SO PLEASE SUPORT US STAY BLESSED LOVE YOU ALL ((TESA))  |
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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 .....
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lupusjoy
GOD`S GIFT
Full Seeker of Support
Offline
Gender:
Posts: 712
I AM BLESSED AND SO ARE YOU!!
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« Reply #4 on: March 28, 2009, 06:58:28 pm » |
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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 .....
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Adminஐﻬ
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« Reply #5 on: April 01, 2009, 01:14:23 pm » |
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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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« Reply #6 on: April 08, 2009, 05:15:35 pm » |
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WANTED:Fibromyalgia patients who would like to join us on a special radio show.
We want to hear from YOU!
Let the public hear your Fibro Voice on what it's like for your everyday life living with an Invisable Illness.
Our radio address is www.BlogTalkRadio.com/LupusMCTD
If you are intrested please post here what day next week and hour would be good for you to be interviewed. The more the merrier as we have our Userplane chat room with audio & video.
If you are too shy to call in, post a question in the chat room while we are live on the air.
Once date & time is established for the Fibro Show the date & Time will be posted here.
Email me too LupusWebsite@aol.com
THANKS!
Kathy
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« Last Edit: April 08, 2009, 06:29:00 pm by Adminஐﻬ »
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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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Adminஐﻬ
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« Reply #7 on: October 14, 2009, 01:32:15 pm » |
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Is anyone up for a new guest?
If yourself would like to be a call in guest, send me a note to LupusWebsite@aol.com
put BTR guest on subject line .
Tell me a bit about your story you would like to share with others.
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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Adminஐﻬ
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« Reply #8 on: August 14, 2010, 01:44:53 pm » |
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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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Adminஐﻬ
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« Reply #9 on: November 02, 2010, 08:34:12 am » |
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 REMINDER !! Nov 9 sale of LOVE SIMPLE will be released! 10% of the sales going to Lupus Research Institute http://lupusresearchinstitute.org/
COMING SOON! My interview with the movie Writer/Director & Producer on Blog Talk Radio!!
Date to be announced ASAP!!
Join us to call in! |
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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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Lupus & MCTD Q & A
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