Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.


  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):
  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Any Celiacs From Gainesville, Florida?


eleep

Recommended Posts

eleep Enthusiast

There used to be a Gainesville celiac group, but it is apparently defunct. I'm a UF graduate student, so I'm thinking about starting one through UF (if there are a bunch of students) or just in Gainesville itself.

Let me know if anyone's interested -- I want to get a sense of how many people there might be before I take this on (otherwise, it's not a productive procrastination tool for me as I should be writing my dissertation).


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



samking72 Rookie

I'm in Orlando... kind of far :(

  • 4 weeks later...
Jace006 Newbie

I am a student at SFCC, is that good enough?

I have been looking for a local support group and have been unsuccessful so far, so I would be interested in starting one, or at least attending.

Let me know.

eleep Enthusiast

SFCC is definitely close enough -- and there's one other UF graduate student celiac on this listserv as well! I'm not in a great position for the next few weeks to get something started (turning in a major draft to my advisor soon), but perhaps sometime in September we could set something up?

beaglemania Rookie

I live in Sout Florida. :( far from Gainesville

*South*

floridanative Community Regular

I'm surprised they dont' have a group there. I go there to see DH's family every year and I'd always ask local groups where I should eat in their town. We almost always go to Hops and some place called Ashleys which is sort of a dive but I've been to neither since my dx. I think you can get help starting a group from www.csa.org (not sure of address). Best of luck to you!

  • 11 months later...
laurelfla Enthusiast

hi!

i'm very interested in getting together... you guys still up for it?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



beaglemania Rookie

I live in south florida. martin county. maybe in a couple of years I might be a gator though.

beaglemania Rookie

Florida is much to big of a state. everybody lives everywhere!! I just went on vacation and we drove from Ma to Connecticut and I was like, such a short ride to a completely different state!! We also had to drive through Rhode Island. You could drive for hours and never get out of Florida at the end of the day, depending on where you start from. boring, flat, swampland. That's where we live. Go FLORI-DUH. (I discovered from my cousins thats how they pronounce Florida in California.) Nice, huh? :lol:

  • 1 month later...
lj333 Newbie

hey,

I am currently a student at UF and was wondering about a support group. If you did start one, I would be more than interested! Let me know your progress!

Thanks!

  • 4 months later...
grantj Newbie

Hey, I'm a UF law student and I'd be interested in starting an SG-sponsored Celiac/gluten-free awareness group here at the university with you guys. Send me an e-mail if you are interested, or look me up on facebook.

-Grant Johnson

  • 1 month later...
Katherine Daly, Ph.D. Newbie

Hi,

I am a PhD student in psychology at UF. I was diagnosed with a pretty severe case of Celiac Disease in 2002 and still struggle to maintain a healthy weight. Besides the weight issue, I am finally feeling that I am able to stick to a 100% gluten free diet and exercise four times a week, which makes me feel very healthy. I also struggle with the skin condition associated with Celiac Disease when I am very ill and that has been pretty devastating. I would love to join a support group in Gainesville if one has been started. If not, I would also be willing to start a group.

Katie

p.s. try Pamela's pecan shortbread and chocolate chunk cookies...they are phenomenal!!

  • 1 month later...
laurelfla Enthusiast

Hi, Gainesville Celiacs!

Let's get together!! For our first meeting, we could go to dinner somewhere.... Outback? Carrabbas? or just meet at Starbucks or Maude's or somewhere and toss around ideas. I tried to find out about a group here when I was diagnosed Aug 2005, but the "contact person" said she was too busy. So then I went to Jacksonville for months after that to their support group, but it fell apart too! :( I would love to get together, please, please, please, let's do it! :D

  • 2 weeks later...
MJS Rookie

i don't have much time to work on getting a group together, but i would also love to attend a meeting. i live in gainesville as well.

  • 2 weeks later...
CarolAnne Apprentice

Hello! My name is Carolanne...and I've lived in Florida for over 20 years. I am a Celiac, and I've been Wheat-Free for 20 years, and Gluten-Free for over 3 years. I'm trying to locate people who live Gluten Free here in Florida...and it's not been easy. Most of the links I've found have been disconnected or discontinued...and I'm having a devil of time finding people to connect to. I'd really like to find others who are interested in getting together...and I understand that I am not alone. I've read several posts from people looking for help, Doctors, restaurants, support groups, meetups and such here in Florida.

GlutenFreeInFlorida-subscribe@yahoogroups.com

I've created a Yahoo Group in the hopes of connecting with other people here in the Sunshine State...and to help others connect as well. I'd like to know if anyone is interested in something that will enable you to contact others in your own local area. I'd like to make more information available to people who are living Gluten-Free in Florida.

  • 3 weeks later...
upearly-shelly Newbie
There used to be a Gainesville celiac group, but it is apparently defunct. I'm a UF graduate student, so I'm thinking about starting one through UF (if there are a bunch of students) or just in Gainesville itself.

Let me know if anyone's interested -- I want to get a sense of how many people there might be before I take this on (otherwise, it's not a productive procrastination tool for me as I should be writing my dissertation).

Hi there. My name is Michele. I believe I suffer from either an intolerance or sensitivity towards gluten. I live in G-ville as well. I attended SFCC several years ago, then I moved to go to a diff college (nothing personal towards UF) then I moved back. Anyhow, I am interested in getting together.

I was also hoping to find some info on a G-ville doc to test whether there's truth to my personal gluten theory, but I

  • 2 weeks later...
adoty Newbie

Michele,

I live in Gainesville also. Through diet elimination I have determined I have gluten intolerance. I searched through the Shands directory and all the doctors in Gainesville hoping to find one that was familiar with Celiacs; I did not. I ended up going to Digestive Disease Associates of America. Since it was at least 3 months until the next doctor was available, I ended up seeing an ARNP. She seemed to have an understanding of Celiacs. I have not been eating gluten for 1.5 years, so she will not do a blood test on me until I eaten gluten for 20 days. The thought of eating gluten for that amount of time makes me what to cry, so I am not sure if I will be returning. I wish I knew of a great doctor in Gainesville, but I can't say that I do. Nevertheless, I hope this information helps. Below is the link for Digestive Disease Associates. The website has the address, phone number, and a brief biography of all the doctors. Let me know if I can do anything else to help.

Open Original Shared Link

Best,

Andrea

laurelfla Enthusiast

I went to Digestive Disease and that is where I got my diagnosis. I just told them my symptoms and a PA ordered a bunch of blood tests, Celiac among them. They were not too helpful with the diet (I got the standard handout ordering me not to eat any gums and no vinegar -- so that was confusing for a while) but I am grateful to have been diagnosed so quickly. I can't remember the PA's name (Patricia, maybe?), but my Dr. is Leibach and I liked him all right.

Good luck!

As for the support group, I'm definitely open to getting together. I feel like a broken record when I say that ;) because I keep saying it but nothing ever happens! Andrea, Michele and Shelly -- if you want to get coffee sometime or something, let me know! :)

  • 1 year later...
murfsgirl Newbie

Hi Michele,

I know these posts are old, but in case you never found anyone (or for any other new people from Gainesville) I figured I'd post. I went to Dr. Dean Kramer. He's located near North Florida Hospital, and while he did want to diagnose me with IBS, he did agree to do the bloodwork for gluten for me when I asked him to. I haven't been back to him because he cost way too much with my bad insurance, but he did send me a letter stating my bloodwork results were postive for celiac and I've been gluten free for a few weeks now.

Also, did anything ever happen with a support group or meeting up? I'm interested, and I need help! :)

  • 1 year later...
JohnL Newbie

I was also wondering if a group ever got started up because I would definitely be interested in joining. I was diagnosed not too long ago. I'm a grad student at UF so I would be interested in one on campus or off.

Hi Michele,

I know these posts are old, but in case you never found anyone (or for any other new people from Gainesville) I figured I'd post. I went to Dr. Dean Kramer. He's located near North Florida Hospital, and while he did want to diagnose me with IBS, he did agree to do the bloodwork for gluten for me when I asked him to. I haven't been back to him because he cost way too much with my bad insurance, but he did send me a letter stating my bloodwork results were postive for celiac and I've been gluten free for a few weeks now.

Also, did anything ever happen with a support group or meeting up? I'm interested, and I need help! :)

  • 10 months later...
archaeo in FL Apprentice

Hello, I was just diagnosed and am in Gainesville. Would love to learn resources, pool local knowledge - did this group get off the ground? Any interest in getting one together, if not?

squirmingitch Veteran

This is all I was able to find:

Open Original Shared Link

Open Original Shared Link

Honestly, it doesn't look like much is going on.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,321
    • Most Online (within 30 mins)
      7,748

    Yvonne Thomas
    Newest Member
    Yvonne Thomas
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.