Share/Bookmark

Topics

Did you forget something…

Dementia is something that is usually associated with older people. However, children, teenagers and young adults can experience dementia as a result of a number of rare diseases and conditions. Niemann-Pick Disease Type C (NPC) is an example of one of these diseases, and one of its main symptoms is dementia. (Hinton et al, 2005)
AccessDNA community leader badge graphic

Meet Brisan & Parker

Bath Time

Put in Perspective

What is NP-C?

Dr. Marc Patterson on NP-C

Blogroll

Brisan & Parker

RSS Addi & Cassi Hempel

  • Rare Disease Day Logo and Ribbons – Patient Advocates Join The RARE Team!
    Here are the Rare Disease Day logos for 2012 from the Global Genes Project, the leading rare disease advocacy organization for the rare disease community. Since Rare Disease Day 2012 falls at the end of February each year, the date for 2012 is Feb. 29 (leap year). Wear jeans or demin on Rare Disease Day […]
  • Is Your Disease on the RARE List™ – If So, More Bad News!
    I wonder if people truly understand what it means if their rare disease or disorder is on the RARE List™? Last week, the R.A.R.E. Project and Global Genes Project, leading patient advocacy organizations representing the rare disease community, issued the RARE List™, a stunning 65 page alphabetical listing of roughly 7,000 known rare diseases and disorders. [ […]

Archives

  • 12Apr

    We wanted to say thank you to Market Leverage!

    Thank You Newsletter

    The winning Team!!!!  To view all the Thank You’s for this event, please visit: BriParDun

    pieroguys-winning-team-market-leverage

  • 03Apr

    Tim Jones is a great guy who was one of many that participated in the Bowl-A-Thon!  You can visit his website to learn more about who he is and what he does for the online community:  The Real Tim Jones

    This is from his blog:

    On Tuesday, I was down in Orlando to captain the Affiliate Summit bowling team for Market Leverage’s Bowl-A-Thon to raise money for the Niemann-Pick Children’s Fund.  One of Market Leverage’s publishers has two children with this rare, terminal illness.  The drugs to help with the effects of the disease are currently very expensive and the Fund aims to offset many of the medical costs associated with Nieman Pick and fund research for a cure.

    The Affiliate Summit team came in second place among five teams and took home a small trophy.  We also had the second highest score from our teamate, Richard, from Market Leverage, who scored a 169.  I personally scored a 108 in the first round and a 113 in the second round.

    First, take a look at some pictures from the event and then I’ve included a video to watch.

    DSCN0345

    @Missy Ward and I

    DSCN0340

    Ben Spark and IZEA’s Door Prizes

    DSCN0342

    Round 1 Final Scores for Team Affiliate Summit

  • 03Apr

    This is a news story that me and Jennifer have anticipated hitting the media. We are waiting for the Wall Street Journal to publish a story relating to this.

    This seems very exciting and might provide as a manageable treatment for Brisan and Parker. The Hempel family are good people and are blessed to be able to use their talents and resources to make this a possibility.

    It is amazing how something that we eat, drink, and use are in very common products like toot paste, butter, and etc yet it has taken this long to get to this point?

    [youtube=http://www.youtube.com/watch?v=lnc_bQCNoOw]

    At Children’s Hospital in Oakland, researchers searching for the cure to a rare disease afflicting a pair of twin girls have discovered a startling ray of hope that may lead to a breakthrough treatment for AIDS.

    Five-year-old Addison Hempel and her twin sister Cassidy are both stricken with Niemann Pick Type C Disorder, a rare and deadly disease that disrupts the metabolization of cholesterol.The brain cells die because of it. They can’t process cholesterol, explained the twin girls’ mother Chris Hempel. They end up in wheelchairs. They can’t swallow. It’s fatal and there’s no treatment.The first symptom was a swelling of their spleens. It was a cancer specialist who first noticed signs of Niemann Pick Disorder.

    The girls also started having symptoms of weakness and clumsiness similar to very early onset Alzheimers’. Niemann Pick is often referred to as “childhood Alzheimer’s” because of these similarities.The lack of available treatment for the disease led the Hempels to search for a cure on their own. They went on the Internet and found a study that said it cured mice that were genetically modified to have Niemann Pick Disorder.

    The treatment was a simple inexpensive sugary compound made from starch called Cyclodextrin.The Hempel family took that research to their Doctor Caroline Hastings of Children’s Hospital in Oakland. With the twins’ condition rapidly getting worse, the Hempels knew there was no time to lose.”We wanted to take the risk now, because our kids are deteriorating,” said Chris Hempel. “We don’t know what will happen. But I know it’s not going to hurt them, and we know in our mice that have the disease, it provides a big benefit. So why not?”

    After receiving a special FDA exemption, Addi and Cassie are set to become the first humans to take Cyclodextrin therapeutically. Surgeons recently implanted intravenous infusion devices under the skin of each girl.

    The hope for an even bigger benefit from Cyclodextrin treatment brought Nashville Doctor James Hildreth to Oakland. He studies HIV/AIDS. The connection between the two diseases?”We made the discovery that cholesterol is required for HIV to be infectious,” explained Dr.HildrethThe same compound that will hopefully drain cholesterol from the children’s brain cells – Dr. Hildreth has discovered – also drains cholesterol from the AIDS virus, killing it.Collaborating with the Hempels, Dr. Hildreth is now working on an AIDS prevention based on Cyclodextrin.”What’s really, really remarkable and got me so excited is here’s a substance that’s used by humans,” said Dr. Hildreth. “Millions are exposed to it every day. It’s exceedingly safe, but it can kill HIV. What more can you ask?”The one-of-a-kind cholesterol trial for the twins will commence with a very low dose that doctors hope to increase steadily.”What we don’t know about the drug is if it works,” said Dr. Hastings. “How much do we give and how frequently? We’re just starting with the protocol.”The twins will get intravenous Cyclodextrin every week or so. Ultimately, doctors hope to develop a sort of portable pump that can deliver it directly, twenty four hours a day.The twins’ are thrilled that the treatment might give their girls a fighting chance at surviving their battle with Niemann Pick Disorder.”I feel such a relief to even have something to try that’s even a glimmer of hope,” said Chris Hempel.

    The AIDS preventive, instead of being intravenous, could be a cream as cheap as ten cents a dose, that people worldwide could use.”We hope to be doing trials in humans very soon,” said Dr. Hildreth.Doctors say this collaboration could be a remarkable example of how smart use of basic research can save lives.

  • 18Mar

    This is a follow up on the post earlier about Cyclodextrin.  Addi & Cassi are twin girls that live in Reno, NV and their parents Chris & Hugh Hempel are great people doing a lot of great things with the abilities they have been given.

    The research is early and the talented people working on this don’t exactly know how it is working or how it might ultimately turn out in children with NPC but it is a good risk to take from their perspective.

    The girls will have mediports installed so they can inject Cyclodextrin right into their bloodstreams.  Of course they will be heavily monitored for any progress or digression.  This is great news.  Our prayers and wishes are with them.

    Here is the blog post on Addi & Cassi website:

    Continue reading »

« Previous Entries   Next Entries »

Recent Comments

  • Gary, Thank you for posting a comment! With Niemann-Pick Typ...
  • My mother has picks - age about 65, showed first signs aroun...
  • Hey Chris. Yes he is chewing on everything. If is not his sh...
  • I noticed that Brisan is chewing in the video on a rubber wr...
  • hey guys. can't wait to see you tomorrow . happy bday dunc...