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Hypoparathyroidism

What is Hypoparathyroidism?

Hypoparathyroidism is a rare disorder in which your body secretes abnormally low levels of parathyroid hormone which plays a key role in regulating and maintaining a balance of your body's levels of calcium and phosphorus.

 

Hypoparathyroidism is a rare disorder in which your body secretes abnormally low levels of parathyroid hormone which plays a key role in regulating and maintaining a balance of your body's levels of calcium and phosphorus.
Acknowledgement of Hypoparathyroidism has not been added yet.
Prevalence Information of Hypoparathyroidism has not been added yet.
Synonyms for Hypoparathyroidism has not been added yet.
Cause of Hypoparathyroidism has not been added yet.
Symptoms for Hypoparathyroidism has not been added yet.
Diagnosis of Hypoparathyroidism has not been added yet.
Diagnostic tests of Hypoparathyroidism has not been added yet
Treatments of Hypoparathyroidism has not been added yet.
Prognosis of Hypoparathyroidism has not been added yet.
Tips or Suggestions of Hypoparathyroidism has not been added yet.
References of Hypoparathyroidism has not been added yet.
So frustrated Created by racheldh
Last updated 28 Oct 2013, 02:23 AM

Posted by racheldh
28 Oct 2013, 02:23 AM

I am so frustrated with this disease. My husband’s calcium and magnesium is not controlled. He takes 22 pills just for this diagnosis and his levels are still not normal. The doctors just don’t seem to understand what he is going through. I feel no one understands what I am going through watching the love of my life not have the capability to have 1 normal day without symptoms of hypoparathyroidism.

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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.

  1. Complete the screening form.
  2. Review the informed consent.
  3. 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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I suffer from Thyroid Nodules and I've recently discovered that I have hyperparathyroidism as well. Need to find support group/community.
My husband has non-surgical hypoparathyroidism and Bartter syndrome. Either one is controlled.

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So frustrated

Created by racheldh | Last updated 28 Oct 2013, 02:23 AM


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