10 replies to this topic

[susanpb50@yahoo.com]

Could anyone tell me of any support groups in Michigan!! I am having no luck getting resonses from any email addresses I have been provided with thus far. I live in Bay Cituy and am willing to travel to an extent. I am recently diagnosed and hear such great comments about support groups and the importance to join one. Please...anyone out there with any info?
Susan

[khyricat]

Glad you posted this- hope its still accurate... not positive yet, but I am starting gluten free now... I think it will be positive when I get the results from the blood test back on Monday- I had never considered Celiac, but the more I learn the more it sounds like this is what I have! I never thought I'd be hoping for a medical test to be positive, but if this is true- it sounds like it will solve/explain about 90% of my medical issues!

I am in ann arbor.. will look into lansing, flint or Rochester- all are an hour plus away... physically rochester is closest, but unless its at an odd time of day or a weekend, traffic may make that take the longest to get to. Also- I work weekends, so looking into all 3 may give me the best chance of finding a group I can actually attend. I am surprised there isn't one closer to home- Ann Arbor.. I'll have to ask the doc on Monday when I get my test results from her.

Amie in MI..

[Kim]

There is actually a gluten free vendors' fair (food fair) this Saturday in Farmington Hills Michigan. 11 am -2 pm First Presbyterian Church, 26165 Farmington Road (corner of 11 Mile Road). It's a good way to try gluten-free foods before you buy them and also you may be able to find people who live near you. Good luck. Kim.

[khyricat]

I wish I could go, but I'll be at work this Saturday from 5 Am to 2 PM.. one of the last weeks on that shift, but I still won't have weekends off under the new schedule..

[joemoe003]

hey im from michigan it would be really nice to talk to someone from michigan with celiac disease i know this doesnt really have ta do with a support group but the only people i talk to that have celiac disease are from canada (which there is nothing wrong with that) but it would be kinda nice to know there is someone that may live near you that is "like you" know what i mean? it would be really cool if some of us michigan people could swap email addresses or somethin! mines pippigirl32@hotmail.com email me when ever ya wanna i would love to hear from ya!

Julianne

[dianne]

There is a Detroit area support group. It's the Tri-County Celiac Support Group. They meet once a month, on Mondays, in Farmington Hills. Their website is http://www.tccsg.com.
Dianne

[sweetie101282]

Speaking of Michigan Support Groups... is anyone else from the mid-michigan CSA on here that could let me know when the September meeting is?? Thanks!
Amy

[valeriemates]

I am surprised there isn't one closer to home- Ann Arbor..

<{POST_SNAPBACK}>

In case it's useful: I've started a small celiac support group here in Ann Arbor. You can find it at
http://health.groups...enFreeAnnArbor/

-Valerie

[LeahBanicki]

Live in SW lower Michigan and also not finding anything close.

[valeriemates]

Live in SW lower Michigan and also not finding anything close.

Leah, have you found the Michigan Capital Celiac Support Group? They are awesome! Here's their website:
http://micapitalceliacs.atspace.com/
I don't know if you are near Lansing, but if you are anywhere near there, they are a good group to get in touch with. They run an annual food fair, a summer camp for kids, meetings throughout the year that are sometimes potlucks or sometimes with a speaker, and they have an excellent newsletter that they will e-mail to you.

-Valerie
(momma to the Gluten-Free Ann Arbor group - currently at 726 people!)