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Lucinda Dalton
- Female
- Lancashire
- United Kingdom
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Lucinda Dalton's Page
Latest Activity
Sylwia Antkowiak left a comment for Lucinda Dalton"Hi Lucinda,
Welcome to the site. We live in London and my daughter is a patient of Great Ormond Hospital. You will find a wealth of info here and people who are always willing to help.
All the best"
Linda Burke left a comment for Lucinda Dalton"Hi Lucinda,
Perhaps our new UK member would be a interesting person to contact?"
Cheryl Biermann left a comment for Lucinda Dalton"Hi, welcome to our site! Hopefully you will find our site and the informational site some help as you deal with the complexities of the disease. Feel free to join in discussions and add your questions and comments, all are welcome!"
Linda Burke left a comment for Lucinda Dalton"Hi Lucinda,
Welcome to the interactive website of The Foundation for Children with Atypical HUS, a place to share information, inspiration, and insights about this rare disease. Please do let us know of your special interest topics, or questions…"
Profile Information
- Birthday
- August 30
- Do you have a friend or family member diagnosed with aHUS?
- Yes
- Are you medical personnel or an aHUS researcher with an interest in aHUS issues?
- No
- My child ( or myself as a patient) is best described as:
- Tested but Results are Inconclusive
Comment Wall (4 comments)
- At 7:18pm on May 5, 2010, Sylwia Antkowiak said…
- Hi Lucinda,
Welcome to the site. We live in London and my daughter is a patient of Great Ormond Hospital. You will find a wealth of info here and people who are always willing to help.
All the best
- At 10:39pm on April 29, 2010, Linda Burke said…
- Hi Lucinda,
Perhaps our new UK member would be a interesting person to contact?
- At 9:04am on April 8, 2010, Cheryl Biermann said…
- Hi, welcome to our site! Hopefully you will find our site and the informational site some help as you deal with the complexities of the disease. Feel free to join in discussions and add your questions and comments, all are welcome!
- At 1:38pm on April 7, 2010, Linda Burke said…
- Hi Lucinda,
Welcome to the interactive website of The Foundation for Children with Atypical HUS, a place to share information, inspiration, and insights about this rare disease. Please do let us know of your special interest topics, or questions about aHUS, and we'll all pitch into the conversation. If you haven't checked the top tab "A Parent's Perspective", it gives a brief overview of aHUS. We look forward to your participation on this site.
WELCOME - Friends, Family Members, Patients, and Researchers - JOIN US!
The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this rare complement disorder. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome.
Sharing information, inspiration and support for one another, we seek to gather together people and knowledge as we strive to improve the lives of patients and families dealing with a diagnosis of aHUS.
NEW DIAGNOSIS OF aHUS?
Be proactive! Get the medical basics of aHUS, what lab values to monitor, and areas of concern...check out the "aHUS Bootcamp" and "About aHUS" tabs at the top of this page!
If your doctor has never treated a case of aHUS, please print out our 'Doc to Doc Registry' and ask him/her to contact a physician versed in the complexities of aHUS and new options for 2011 genetic testing and treatment.
************************
NOTE: Our 'Send a Message" function on each Member's page allows for private discussion of personal content. As with any social network, be cautious about giving personal contact information (home email info, phone number) until you have an established relationship with another person, organization, or associated website.
Did you know...
CFH (Serum Complement Factor H) is a regulatory protein. The secreted protein product of CFH consists of 20 repetitive units named "short consensus repeats" or SCRs (each approximately 60 amino acids). In patients with aHUS the last 5 "pearls" in the twenty pearl strand protein, SCR16 - SCR20, should bind to protect cells but do not- they are defective in one or more of the last 5 SCR locations. If they cannot bind or stick to the kidney to protect that tissue, the platelets clump into clots that affect the glomeruli of the kidney -potentially causing acute renal failure.
• • • • • • • • • • • •
It is estimated that there are about 300 cases of aHUS in the U.S., and it is most common with young children. The condition is life threatening and either can be chronic or can recur at intervals.
more factoids...
• • • • • • • • • • • •
It is estimated that there are about 300 cases of aHUS in the U.S., and it is most common with young children. The condition is life threatening and either can be chronic or can recur at intervals.
more factoids...
Help us fight the battle
Your tax-deductible purchase of one or more bracelets will directly fund research to help end the tragedy and heartbreak that aHUS families live with every day. Each bracelet has an appraised value of $825, but your purchase price is only $295.
Or you can donate a specific dollar amount-every dollar will help the Foundation for Children with atypical HUS atypicalHUS.50megs.com
Donations may be made via credit card or Paypal. If you prefer, checks made payable to The Foundation for Children with Atypical HUS may be mailed to:
Atypical aHUS Foundation
19 Olde Colony Lane
Cape Elizabeth, ME 04107
For pearl bracelet orders, please allow extra time for processing checks.
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