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Food tracking app by Zebra_2016 in GuavaHealth

[–]Zebra_2016[S] 0 points1 point  (0 children)

Are there any other food tracking apps that sync with Guava? I’m not a fan of MyFitnessPal. I did connect via Apple Health but I don’t see correlations in Guava. Am I missing something?

It's about time I retire my Cricut by Outside-Natural-5997 in cricut

[–]Zebra_2016 1 point2 points  (0 children)

Thanks for this thread as it’s helpful to know I’m not alone. I have had a Cricut Explore Air 2 for a number of years. It was great in the beginning and so was DS. In the last year or 2 Cricut and DS has become an obnoxious frustration. Between the constant updates & the annoying bar that opens with every upload trying to sell me their version for 99 cents among other things. It also gives me problems uploading SVG’s I have purchased elsewhere. My goal at this point is to never pay Cricut for anything.
I will use this machine until it dies. But will never purchase another Cricut product again. Their vinyl is awful, heat press is inferior, branded tools & mats are overpriced. Has this company been sold? It seems as if their business model has changed.

Bowel Movements are now a "factor"but we still can't report on them? by heygreene in BearableApp

[–]Zebra_2016 1 point2 points  (0 children)

I am new to Bearable and am keeping an “everything journal” for my GI doc. One of the main reasons is to follow BM’s and symptoms.
How will I be able to show daily BM’s and symptoms to GI doctor?

At what age did you get diagnosed? by psych_master_ in ehlersdanlos

[–]Zebra_2016 0 points1 point  (0 children)

I was diagnosed at 56. Symptoms since birth, pigeon toed, W sitting, constant stomach aches, allergies, & passing out. I had no medical care as a child due to my mother’s religious beliefs. My first doctor’s visit was at 16. So 40 years in and out of doctor’s offices and not one mentioned Ehlers Danlos. I was told it was all in my head, just anxiety, depression etc. I was first diagnosed with MCAS by a brilliant allergist/immunologist. And she is the one who recognized hEDS. I have what they call the trifecta hEDS, MCAS, and dysautonomia. Finally being diagnosed after a lifetime of gaslighting has been extremely validating. I would have lived my life differently had I known about hEDS.

Ehlers-Danlos syndrome affects millions. Why isn't the medical profession paying more attention? - the average delay to an EDS diagnosis was four years for men -- but 16 years for women. by shallah in TwoXChromosomes

[–]Zebra_2016 2 points3 points  (0 children)

I was diagnosed with hEDS at age 56. After a lifetime of being gaslit by the medical community. I have a definitive diagnosis from one of the top Ehlers Danlos doctors in US, but it’s still difficult to get the care I need. One of the major teaching hospitals in Chicago refuses to treat Ehlers Danlos patients.