Cookies help us deliver our services. By using our services, you agree to our use of cookies. Learn more

Candida Glabrata

What is Candida Glabrata?

Candida Glabrata is a rare strain of yeast infection of the vaginal area.

 

Candida Glabrata is a rare strain of yeast infection of the vaginal area.
Acknowledgement of Candida Glabrata has not been added yet.
Prevalence Information of Candida Glabrata has not been added yet.
Synonyms for Candida Glabrata has not been added yet.
Cause of Candida Glabrata has not been added yet.
Symptoms for Candida Glabrata has not been added yet.
Diagnosis of Candida Glabrata has not been added yet.
Diagnostic tests of Candida Glabrata has not been added yet
Treatments of Candida Glabrata has not been added yet.
Prognosis of Candida Glabrata has not been added yet.
Tips or Suggestions of Candida Glabrata has not been added yet.
References of Candida Glabrata has not been added yet.
candida glabrata Created by Loretta
Last updated 16 Sep 2010, 02:39 PM

Posted by Loretta
16 Sep 2010, 02:39 PM

I have been diagnosed with Candida Glabrata, and am currently on IV Caspofungin. Diflucan won't even touch it. I did a 14 day round of Caspofungin IV in July of this year, one month later it's back again, this time my doc is putting me on a 6 week dose 50ml once a day, I also have Lichen scelroses. Has anyone else out there been treated for Glabrata? I'm 63, menopause for 5 years now. It started out a candida 2 years ago and I was always given Diflucan, after awhile even that wouldn't get rid of it. I'm also on oral and vaginal hormones. Any feed back would be appreciated.

Community Resources
Title Description Date Link

Clinical Trials


Cords registry

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.

Community Leaders

 

Expert Questions

Ask a question

Community User List

Master's degree in human Nutrition

 

Master's degree in education

 

PhD candidate in health science

Start a Community


Don't See Your Condition On Rareshare?

Start your own! With a worldwide network of 8,000 users, you won't be the only member of your community for long.

FAQ


Have questions about rareshare?

Visit our Frequently Asked Questions page to find the answers to some of the most commonly asked questions.

Discussion Forum

candida glabrata

Created by Loretta | Last updated 16 Sep 2010, 02:39 PM


Communities

Our Communities

Join Rareshare to meet other people that have been touched by rare diseases. Learn, engage, and grow with our communities.

FIND YOUR COMMUNITY
Physicians

Our Resources

Our rare disease resources include e-books and podcasts

VIEW OUR EBOOKS

LISTEN TO OUR PODCASTS

VIEW OUR GUIDES

Leaders

Our Community Leaders

Community leaders are active users that have been touched by the rare disease that they are a part of. Not only are they there to help facilitate conversations and provide new information that is relevant for the group, but they are there for you and to let you know you have a support system on Rareshare.