IleneK
07-30-2002, 11:38 PM
I was hoping to be able to get some
information.
I have a rare connective tissue disease called Ehlers-Danlos
Syndrome (type III, or as they called it now, Hypermobility type).
Because I have this type of EDS, a lot of times local anesthesia will not work on me. (That is how I became very phobic. Dentists will tell me I don't feel pain I
feel pressure. I think we all know the difference between pressure and pain.) So because of it I stopped going.
I did find a dentist who worked with me very nicely but he retired. I am now with a new dentist who knows all about EDS and does iv conscious sedation.
I would like to get other people's comments about it as I am very nervous. In fact I am terrified.
Sorry this post is so long. I kept hesistating sending this because of the length.
Thank you for reading this.
------------------
Ilene
You have one life to live, live it to the fullness.
information.
I have a rare connective tissue disease called Ehlers-Danlos
Syndrome (type III, or as they called it now, Hypermobility type).
Because I have this type of EDS, a lot of times local anesthesia will not work on me. (That is how I became very phobic. Dentists will tell me I don't feel pain I
feel pressure. I think we all know the difference between pressure and pain.) So because of it I stopped going.
I did find a dentist who worked with me very nicely but he retired. I am now with a new dentist who knows all about EDS and does iv conscious sedation.
I would like to get other people's comments about it as I am very nervous. In fact I am terrified.
Sorry this post is so long. I kept hesistating sending this because of the length.
Thank you for reading this.
------------------
Ilene
You have one life to live, live it to the fullness.

