Schwannomatosis
What is Schwannomatosis?
Schwannomatosis is a rare disorder affecting the peripheral nervous system where benign tumors called schwannomas grow on perippheral nerves.
Last updated 6 Oct 2010, 10:09 AM
6 Oct 2010, 10:09 AM
I have recently been diagnosed with schwannomatosis and I am interested in talking to other people with experience of this condition. I am in England and so far I have found the condition is not well known. Fortunately we have two expert centres here, one in Manchester and the other at Guy's Hospital in London. I have an appointment at Guy's in 2 weeks, to meet Dr Ros Ferner. I am scheduled to have surgery to remove a sciatic schwannoma at the Royal National Orthopaedic Hospital at Stanmore. I am interested in talking to anyone else with this condition, especially their experience of monitoring of their condition and prognosis.
Clinical Trials
CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access.
Enrolling is easy.
- Complete the screening form.
- Review the informed consent.
- Answer the permission and data sharing questions.
After these steps, the enrollment process is complete. All other questions are voluntary. However, these questions are important to patients and their families to create awareness as well as to researchers to study rare diseases. This is why we ask our participants to update their information annually or anytime changes to their information occur.
Researchers can contact CoRDS to determine if the registry contains participants with the rare disease they are researching. If the researcher determines there is a sufficient number of participants or data on the rare disease of interest within the registry, the researcher can apply for access. Upon approval from the CoRDS Scientific Advisory Board, CoRDS staff will reach out to participants on behalf of the researcher. It is then up to the participant to determine if they would like to join the study.
Visit sanfordresearch.org/CoRDS to enroll.
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schwannomatosis
Created by jollyjane | Last updated 6 Oct 2010, 10:09 AM
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