Welcome:

Welcome:

StopCAIDnow, Inc. is a non-profit organization recognized globally. We are a 501c3 accredited non-profit. The foundation is focused on treatments, awareness, diverse genetic testing, genomics.
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Help StopCAIDnow by giving generously. Transactions are secure through PayPal and all major credit cards are welcome.
Contact Us:

Contact Us:

C.A.I.D Foundation
Lisa Moreno-Dickinson, President

P.O. Box 992
Chadds Ford, PA 19317
| c: 1.877.CAID.644
| f: 1.877.CAID.640
| e: stopcaidnow@aol.com
Currently viewing the category: "Family Stories"

This is why I coined CAID. We are focused on the mechanism to shut off the process in all auto inflammatory diseases~bigger picture!!

On January 11, 2013 By

MEFV gene (FMF) codes for the protein pyrin. Pyrin mutations were found in the MS patients. Pyrin is implicated in the maturation and secretion of the proinflammatory cytokine IL-1β. (IL-1β is a major mediator of fever and systemic inflammation).

(see table with frequency of common MEFV mutations among MS patients)
http://www.ariel.ac.il/research/brain/PDF/Shin03.pdf

Familial Mediterranean [...]

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StopCAIDnow Fundraising GALA 2013

On December 18, 2012 By

Epic Chic & Red Hot Sleek

2nd Annual StopCAIDnow Gala

Featuring New York Fashion Week Designer, Von Alexandria
Honoring Our Real-Life Superheros

LIVE Performances by L’Renee & Bread, A-List Celebrities, Red Carpet Hosts
Local Media Coverage, Televised on Chance, Maxx Spititual Coaching, Martini Luge

Click here to buy tickets online

[...]

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StopRareDiseaseBullyingNow/StopCAIDnow

On November 1, 2012 By

Protecting our children from Bullying who have a Rare Disease~ LET US DO MORE THAN SIGN A PETITION TO STOP RDB LETS JOIN A MOVEMENT
Mission
To provide awareness and education to schools and the community about Rare Diseases. To educate the community by visiting schools and talking about Rare Diseases. The more [...]

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OK CAID families post one thing here YOU want all to know about your child the exp with having a CAID..this is YOUR TIME TO VOICE!!

On September 24, 2012 By

Sherian Kaneaster McCoy I want others to know that just because he plays, works or socialized “normally” doesn’t mean he’s not in pain or sick.
August 31 at 10:54pm via mobile · Unlike · 8

April Fraser We are their voice. They look to us for answers and we can’t give them one. But [...]

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The VOICE from one “our” children with CAID by :Miss Julia Drummond

On September 24, 2012 By

Written by a Child with CAID ♥

Did You Know……….??
Did you know that I am one in a million? Now you are probably thinking has she won the lotto or did she win the Nobel peace prize? Has she discovered the solution to world peace? Unfortunately my being one in a million is [...]

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COME TOGETHER WITH OTHER FAMILIES WITH INSPIRE

On July 27, 2012 By


The Stop CAID Now Support Community connects patients, families, friends and caregivers for support and inspiration. This community is sponsored by Stop CAID Now, an Inspire trusted partner.

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FIRST NATIONAL CLINIC 4 CAID AT THE CLEVELAND CLINIC giving.ccf.org/stopcaidnow

On July 24, 2012 By

StopCAIDnow is focused on providing tools which build awareness of all childhood auto-inflammatory diseases (CAID), a group of rare hereditary recurrent unprovoked inflammation disorders. It is the voice for the children suffering and the physicians who are dedicated to helping the cause.
Your donation will help to fund the first national evaluation [...]

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La Fin du CAID ~ Absolutely a beautiful fragrance and 100% of proceeds goes to help our children with CAID~ A Wonderful Mother’s Day Gift

On April 22, 2012 By

 

Thank you for your support
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WE ARE LIVE…COME JOIN US ON INSPIRE.COM

On April 17, 2012 By

WE ARE LIVE

You can view it here:
http://www.inspire.com/groups/stop-caid-now/
or here:
http://stopcaidnow.inspire.com/

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On March 4, 2012 By

“A truly touching speech,my husband and I had tears the whole time. The whole night was surreal and a blessing that gave our children Jarin and Gianna a voice for the pain and constant battle they fight everyday”.

 

 

 

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