Management of Mast Cell Activation Syndrome (MCAS) by Dr David Saperstein

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  • เผยแพร่เมื่อ 15 ก.ย. 2024
  • Management of Mast Cell Activation Syndrome (MCAS) by Dr David Saperstein
    (MCAS) Mast cell activation syndrome is a condition where the allergic system goes haywire. This occurs in many patients with EDS, POTS, or Dysautonomias. Individuals with MCAS are prone to unpredictable rashes, hives, or skin sensitivities.

    MCAS can be hard to diagnose. There are blood and urine tests, but these are frequently normal. Through the use of antihistamines, mast cell stabilizers, and other medications, the symptoms of MCAS can often be brought under control.
    Dr. Saperstein worked with a group of mast cell activation specialists, an effort led by Dr. Lawrence Afrin to propose new diagnostic criteria to update a Diagnosis Journal that was first published on January 22, 2014. This journal is called Diagnosis of Mast Cell Activation Syndrome: a Global "Consensus-2". It is a must-read for all neurologists.
    We are now accepting new patients from Arizona and from out of state. Click here to learn more about our Center. bit.ly/LearnMo...

ความคิดเห็น • 9

  • @ChronicExcessiveManliness
    @ChronicExcessiveManliness 8 หลายเดือนก่อน +16

    Many MCAS patients can't tolerate OTC meds due to excipients, dyes etc. So when they try them and get worse, most doctors brand them as a "difficult patient" but in reality, they're getting worse from the meds themselves. It's most unfortunate.

    • @pandoratalks
      @pandoratalks 3 หลายเดือนก่อน

      There is now a treatment for MAST CELL ACTIVATION SYNDROME. Please contact Jen Donovan a pioneer in the successful treatment and remission of MCAS. It has been in my family for generations and I am the first one not to perish of it.

    • @ChronicExcessiveManliness
      @ChronicExcessiveManliness 3 หลายเดือนก่อน

      @@pandoratalks It sucks when half baked, non scientific, snake oil salesmen spam people online to try to exploit sick people with made up fictional "remedies" just to make a few dollars. Which is what "Jen" is doing...and beyond anaphylaxis, no one "perishes" from MCAS. Go away....

    • @sharlene4mylife
      @sharlene4mylife หลายเดือนก่อน

      @@pandoratalksdo you want to give any info on how to contact this person?

  • @writerscorp
    @writerscorp 2 หลายเดือนก่อน +1

    This is one of the most helpful videos I've seen on this subject. If I lived in Arizona I would most definitely come see you. Thank you!

  • @colleenlysen2969
    @colleenlysen2969 หลายเดือนก่อน +1

    Great mcas resources for mcas on the turn to app

  • @sarahhamdan4695
    @sarahhamdan4695 7 หลายเดือนก่อน +2

    I live I Texas. Do I need to travel to ur state ?

    • @centerforcomplexneurology
      @centerforcomplexneurology  7 หลายเดือนก่อน +4

      Yes. Due to state medical board regulations, we are required to see patients in the office once before we can do telemedicine and once annually for ongoing care. We often see patients from other states and have a hotel partnership for suites with set lower rates.