Jump to content

lindsay.sparkles

Members
  • Posts

    5
  • Joined

  • Last visited

Country

  • Interests
    music (country especially), songwriting, politics, the outdoors, spirituality

Recent Profile Visitors

The recent visitors block is disabled and is not being shown to other users.

lindsay.sparkles's Achievements

Newbie

Newbie (1/14)

0

Reputation

  1. I was referred to a geneticist by my GP for the initial diagnosis, then I saw a rheumatologist and a physiotherapy practitioner at the EDS Clinic at Toronto General Hospital. Not on my period (I don't get periods because I have a hormonal IUD).
  2. My original diagnosis was EDS, but I saw a specialized clinic and basically the criteria for hEDS is super specific now (they just changed it) and I fall a bit short. Basically you need 5 of 12 listed signs of a generalized connective tissue disorder. I basically have 3.5 - soft skin, stretch marks, and atrophic scarring - and piezogenic papules on one heel but not the other (you need both for it to officially count). So what I have is VERY close to EDS, even though they're not calling it exactly that.
  3. I have orthostatic intolerance (not quite full-blown POTS but something of that sort) and I'm convinced it's what's making me feel terrible right now, for the last week or so. I'm exhausted, light-headed, occasionally nauseous, little-to-no appetite, occasional headaches...I just have no energy to do things because everything drains me. I work full-time and manage that but just don't feel good. I also have Hypermobility Spectrum Disorder. I'm not depressed at all or anything, I don't think this is psychological. Does anyone have any idea of what's happening? Can you relate? What do you do about it?
  4. Yup, I bruise super easily. From what I've been told it's probably related to my Hypermobility Spectrum Disorder.
  5. Hi everyone, I'm a 25-year-old woman. I have hypermobility syndrome/hypermobility spectrum disorder and was evaluated by an EDS/HSD clinic in my city. I have a lot of issues with lightheadedness and palpitations when standing up and especially if I've been bending down and stand up, or even with mild exercise, such as climbing a few stairs. I've had an echo (normal) and a holter (no arrhythmia). During the appointment at the EDS clinic, they did a "poor man's tilt table test" (got me to lie down and stand up) and said that while I definitely have orthostatic intolerance, and my heart rate goes up, I don't quite have the 30 bpm increase associated with POTS. I don't have orthostatic hypotension either, my blood pressure runs kind of low in general but does not drop significantly when I stand up. My biggest issue is intense tachycardia (sometimes up to 160 BPM) with mild exercise like climbing stairs or walking up a hill. I can't possibly be that out of shape - I walk a ton. Does anyone else have orthostatic intolerance without technically having POTS? Is this another form of dysautonomia?
×
×
  • Create New...