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Shaw

ChattyCushie
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Posts posted by Shaw


  1. That's fantastic! Getting a doctor who will thoroughly test you is one of the hardest parts of the disease. Nobody wants to be sick of have Cushing's but with a lot of us it's gets to a stage where you just know in your gut what's going on and then you have to fight with doctors to get them to listen. I hope testing is quick and the proof comes back right away so you can get back to feeling like a human again.

    • Like 1

  2. It's not nearly as rare as some doctors think. Honestly, most of us have bad experiences with at least one endo so that's a possibility but fingers crossed you get one that's willing to listen and will let you do some testing; push for testing. Do your research, read as much as you can before the appointment - bring pictures of your physical changes if you have them and write down your symptoms. I never saw Dr. F for diagnosis but his website and the boards were the best thing ever for me. His site has lots of good articles so I would read everything there http://www.goodhormonehealth.com/cushings-patients/ and read old postings from these boards.

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  3. I never had a hump but still had Cushing's. Unfortunately your symptoms (and most Cushing's symptoms) can also be caused by other medical conditions so it's important to test everything and if you're concerned about Cushing's I would do some cortisol testing if you haven't already. Have you done any 24 hour urinary free cortisol tests? or had your ACTH checked?

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  4. Oh boy me too. I was paranoid for the first few years and anxious because I always thought Cushing's was coming back. Luckily I had family and a doctor who understood where I was coming from so I could test anytime I wanted to.  It took a long time for me to remember things like women have PMS at times and that has nothing to do with Cushing's. I will say I only worried when I wasn't feeling great, when I feel good it never crosses my mind and these days I'm much better at not worrying or feeling anxiety about it.

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  5. So saliva is not reliable in your eyes because serum results may or may not be symmetrical to your standards? Well there goes about half the diagnoses on this board then.

     

    My thoughts exactly! Saliva was useless for me during diagnosis but that's just me, I know of many others who owe their diagnosis to spit! I'm thrilled with this cortisol meter because I know it will help SOME people and it just might serve as a building block for a future blood cortisol meter. At least someone out there recognizing the need for immediate cortisol testing.


  6. For me it was like watching a car accident, I couldn't stop reading.

     

    The short version is after 5 failed pit surgeries this 64 year old woman was totally dismissed by the Ontario Medical Board. The Drs were given a slap on the wrist for discharging her with menningitis

     

    Not to sure how I feel about Dr. G now. He was the only one who could have spoken up for the women. In Ontario you are judged by your peers and it's their opinion that the Board heavily relies on in making their decision. To win, they would have needed another neurosurgeon that agreed with the patient, clearly Dr. G didn't. Unreal, it is more than obvious she shouldn't have been discharged. Poor family!

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