There is a Utah Lyme Support Group that meets the first Saturday of every month at Alta View Hospital, classroom A from 3-5 p.m. in Salt Lake City. The next meeting is Saturday Feb. 6th from 3-5 p.m. One can also join the Utah Online Lyme Support at http://******.******.*****.com/group/UtahLyme.
I am trying to bring an awareness to Utah Dr.s that Lyme patients need help! I have a great naturpathic Dr. In Provo at "Integrated Healing Arts" they will know who you are looking for if you ask for the naturpathic Dr.Tell her Jenny... The Lyme patient sent you. If you want to join a support group for Utah Lyme patients and families I am starting a website and working with the LDA ( national Orgnization) to bring assistance to Utah. e mail me @ ***@****.
The more people from Utah that respond the easier it will be to make a difference!
Try googling things like "Utah Lyme MD". The first hit I got on that search was UtahLyme [dot] org. It's not a huge website, but it is where I would start looking.
Also look at ILADS [dot] org, and generally google things like "LLMD Utah" or if you are close to another state, add that one to the search too."
LymeDiseaseAssociation [dot] org I think may have a referral link. Googling is the way to go. Good luck.
Find a support group for Lyme in your area and contact the leader. Email or call the leader and ask them for names of LLMD's in your area.
I am in Utah also did you find anyone?
Thank you so much! I appreciate it.
The only way i found one in pittsburgh is by going to lymenet . org and hitting flash dicsussion then wrote seeking a doctor in pittsburgh. Then they sent me a list of names. You have to reguster first too! Hope this helps theres a few others but i forget there websites