• Family Conference 2023
  • DecNewsletter
  • First Legacy Guardian Peggy Davis


OUR MISSION

In our drive to find a cure for NBIA,
we provide support to families, educate the public and accelerate research with collaborators from around the world.


 

News

NBIAcure prepares to submit for FDA
approval of CoA-Z compound

 

Educational Resources

​Posters, flyers and
other educational handouts

 

Our Networking Program

The Networking Program is for one-on-one contact with other NBIA families. Participating families provide addresses, ages of affected individuals and the NBIA disorder they have. This is important information if you want to reach out to someone living nearby or with a similar diagnosis.

Our organization keeps names and addresses confidential unless a person (or parent) provides written permission for NBIA to send their name to other people (or families) affected by NBIA. Those indicating they want to be part of the Networking Program understand their information can be shared with others in the program.

 

Note: We will not add the names of third parties (i.e., teachers, social workers, etc.) to the NBIA Networking Program.

 

Networking Program
Networking Program
Networking Program

Please read all information on this page before joining.
Important links and problem solving tips are provided.

The NBIA Disorders Group Forum is open to NBIA individuals, their families and caregivers. Once you subscribe to the forum, every email sent to the group will automatically go out to you.  It comes into your email inbox so you don’t have to hunt elsewhere for postings. You can also go to the group site online if you wish to view, post or respond to messages. You may just want to learn by reading what’s there.

This group is very useful to families who want to share information, ask questions or exchange news about therapies they’ve heard about or tried. It’s also a way for families or affected individuals to give and receive emotional support. Because we are so spread out geographically, this is an opportunity for families to network quickly and easily.

The organization also uses this forum, powered by Google, to post announcements and other important news for NBIA families.

DISCLAIMER: The views expressed in the NBIA Disorders Group Forum do not necessarily represent the views of the Board of Trustees or the Scientific & Medical Advisory Board of NBIA Disorders Association. Consult with your doctor before trying anything new.

INSTRUCTIONS

If you do not yet have a Google account, you will be instructed on how to set one up. It is free. You may use your current email address for the group and do not need to create a gmail address. You will be sent a link to verify your email address if it is not gmail, and once you do this, you will have a Google account.

You will then be able to request to join our group. This is a closed group and not open to the general public. Only members of the group can see and post messages. Once you are approved for membership by the group administrator, you will be sent an email indicating that you have access to the group and may begin posting and receiving messages from others subscribers. You can also see all past postings which can be a valuable source of information.  They are searchable by keywords to make it easy to find topics of interest.

The NBIA Disorders group email address is NBIAdisorders@googlegroups.com. Please be sure to put this address in your address book as a safe sender so your invitation to join and other messages don’t go to spam.  This is also the address that you will use to send messages to the group after joining.

To "unsubscribe" from the group, simply click the "unsubscribe" link at the bottom of the message list from the group. You will be sent a message from the group indicating that you have been "unsubscribed".

Please Note

Many people use filters to control unwanted email or spam. If you are using filters, then be sure that they are set so you can receive email from the group and also from Patty Wood, NBIA Disorders Association president and group administrator. Her address is pwood@NBIAdisorders.org.

If you choose not to do this, then you may not be able to receive postings from the group or email from Patty Wood. This may also affect our ability to approve your subscription email. The group administrator may need to contact you through email before approving your subscription requesting further information before adding you to the group.

If you have been approved as a member, you may also want to check the group site to see if there are postings you have not received. If you are missing messages, you may have to contact your Internet service provider. The problem could be with the provider blocking messages for some reason.

If you have any questions, please email them to: info@NBIAdisorders.org.

 

Click the "Join Our Group Forum" button near the top-right of this page to join us!

 

 

Our Mission

In our drive to find a cure for NBIA, we provide support to families, educate the public and accelerate research with collaborators from around the world.

If you or a loved one has an NBIA Disorder, we can help!

If your loved one is newly diagnosed with some form of NBIA, your family is no longer alone in coping with this disorder. If you have been living with a diagnosis but never reached out before, welcome to the NBIA Disorders Association. We are here to help you.

We provide emotional support to families through our Networking Program, Facebook group and Zoom Meet Ups. These programs put you in touch with other families and enable you to ask questions about treatments and other matters. You can learn from others how they cope with a rare disorder and care for their loved one.

We have Family Conferences every two years that bring together families from around the world. NBIA researchers and other experts attend and share their knowledge with us. We have clinical sessions with the leading NBIA experts where you can hear the latest updates on how to best care for your loved one with NBIA.

Check out the family conferences link with recorded sessions from previous conferences that you might find helpful.

We hope you will join our NBIA community and be a part of our efforts to support families, educate the public about NBIA and spread awareness in our search for a cure for all NBIA disorders. Everyone can make a difference in his or her own way.

Partners

nbia alliance logo1NBIA Cure logoRare Disease Day PartnerTIRCON

Genetic Alliance logoNORDEURORDISGlobal Genes


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