Ollier's Disease anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Ollier's Disease. You're not alone.
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Members Sharing the Experience "I Have Ollier's Disease"
5 Members
This Experience at a Glance
Story highlights
These snippets show some of the most common themes mentioned in this experience's stories:
These snippets show some of the most common themes mentioned in this experience's stories:
- "after the x rays i started really seeing whats actually happening, and it is spreading in my body..."
- "anyone with information on it or would like to put in their thought, feelings, ideas or knowledge it would be appreciated thanks a bunch Just remember live it up and rally on life's life live it Forrest..."
- "i was diagnosed in 05 having visible problems with my bones i was lucky at first the doctor thought it was just a calcium deposit, and was going to smash it haha good that he didn't..."
Statistics:
60% of people who have this experience are in their thirties, 20% are in their forties, and 20% are in their teens.
You may cite any I Have Ollier's Disease statistics, provided you link back to this page
Check out this group's What Is It Like To Have Olliers Disease guide, where people with this experience share their tips and hints.
Members said this page is also related to:
Do You Have Ollier's Disease? , What is it like to Have Ollier's Disease? ,Have Ollier's Disease personal stories, Have Ollier's Disease personal experiences
Other experience groups that have been combined into this group include: None yet.
Other experience groups that have been combined into this group include: None yet.
This is an experience group where everyone says: I Have Ollier's Disease. It features support, personal stories and experiences, advice, chat, talk, forums, videos, pictures and resources from real people, just like you.
It's free to join, and the people in this group would love to meet you! If you've had this experience, or plan on having it in the future, simply click 'Me Too' or 'Plan To' and add it to your experiences. As you add more experiences, we're better able to
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