E36 - Symptoms and Diagnosis of Addison's Disease - What you need to know!

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  • เผยแพร่เมื่อ 22 พ.ย. 2022
  • If you are going through a possible diagnosis of Addison's Disease this short episode is for you.
    I go over the general symptoms of Addison's Disease, how it is diagnosed and the MUST-HAVE BLOOD TEST added to your blood requisition.
    I also share with you my personal symptoms that developed over 20 years before I was diagnosed and the symptoms my daughter is currently experiencing.
    Come and jump into the PICKLE JAR with me!
    Please help us build our community. Make this pickle happy and subscribe, review, and share THE PICKLE JAR PODCAST.
    If you would like to share your journey on THE PICKLE JAR please email me at thepicklejar@rogers.com
    Follow on Instagram @the_picklejar
    DISCLAIMER: The information from THE PICKLE JAR represents the experiences of the host Jill Battle and the individual experiences of each guest. No information is intended to provide or replace the medical advice of a medical professional. The host or guests are not liable for any negative consequences from any treatment, action, application or preparation, to any person following the information from the podcast.

ความคิดเห็น • 42

  • @sandrawheeler1521
    @sandrawheeler1521 3 หลายเดือนก่อน +2

    Unable to regulate heat body temperature. No body hair. Loosing head hair. Loosing wieght. Exhaustion. Low bp. I never had salt cravings. More sugar cravings. I had all the cardio issues too. Xx

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      cardio me too..still do...and yes sugar...I lived on marshmellows and chocolate frosting

  • @sandrawheeler1521
    @sandrawheeler1521 3 หลายเดือนก่อน

    I also had/ have nausea ,no appetite. Blurred vision. Fluid retention. And all the same symptoms you mentioned.xx

  • @sandrawheeler1521
    @sandrawheeler1521 3 หลายเดือนก่อน +1

    Oh yes terrible depression. Must have been so hard looking after twin girls Jill.❤❤❤

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      Yes a lot was going on...but my kids keep me motivated too...exhausted but motivated

  • @territn8871
    @territn8871 3 หลายเดือนก่อน

    I was just diagnosed with Addison's Disease. Only came home from hospital today. I'm 70 yrs old. I feel so much better being on my meds now. I had all the symptoms listed on the charts except no salt cravings. I think that's because my whole life I've been a heavy salter in my food. My family always fussed at me for using so much salt. My normal blood pressure is always low, it varies from 70/40, 80/50, sometimes it might even be 110/60. It's never the same. I freeze all the time. Have lost weight down to 95...normal used to be around 125-130. Hair is falling out. Brown pigmentation on my ankles and shins. Last Thurs my PCP asked if I'd been to a tanning bed. No, never been to one. She said my back and bottom was brown. All my blood work as been getting worse and worse. Before hosp admission last Thurs night, my potassium was 6.8. They told me at the hospital that was "widow maker territory". Scared me to death. They slapped EKGs and heart monitors on me too quick to talk about. Started pumping luquids of some sort in me thru IV. Had to drink a chalky drink twice that helps bring down potassium quickly. Once the hospitalist got my blood work back, he fully diagnosed me with Addison's disease. Started me on medications in the hospital. And sent me home today with Hydrocort and Fludrocort. Another symptom I've been having a lot was nausea/vomiting and loss of appetite. Lots of muscle weakness, low back aches, a dead sleep for 10-12 hours. There's times I've slept for 15 hrs. I'm a night owl so always contributed my long sleeping hours to that. Also I have occasional fainting spells. Since I've been getting my meds in the hospital, I feel better than I can't tell you how long. I have felt draggy and weak for years. Always figured it's because of my old age. I also have severe Hashimoto's thyroiditis that's near impossible to keep regulated. The hospitalist said that may be partly due to the Addison's as well. As far as I know, no one in my family has ever had this. My daddy died at 68 from a massive heart attack in his sleep. I remember he didn't have hair on his legs just like me. Thought mine was due to thyroid disease though. Maybe he had Addison's and just never diagnosed. Glad I found your channel! Thanks for your information on your journey with Addison's.

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  2 หลายเดือนก่อน

      Oh friend...I am so sorry bu thankful you have your answers and are feeling better. Wow...maybe your dad did too! Thank you for the comment and for watching my videos...I hope they are helpful!

  • @Grahamt978
    @Grahamt978 2 หลายเดือนก่อน

    I pickle jar, that juice sometimes is just what I need

  • @samanthathompson9199
    @samanthathompson9199 ปีที่แล้ว +1

    Thanks for this video! I am experiencing these symptoms and trying to figure out what’s going on. I don’t have hyperpigmentation though. Is there adrenal conditions that aren’t quite Addison’s or could this be early stages?

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  ปีที่แล้ว

      I hope you found the video helpful. If you haven't yet I would look into testing and discussing with a doctor. Personally, I had symptoms for years before I will 'sick' enough for a dx. I would educate yourself on how the disease progresses for symptoms and talk to your doctor about the possibility of testing. Anything else please message me

  • @AB-zq4fw
    @AB-zq4fw 4 หลายเดือนก่อน

    I have all of these symptoms. Pretty sure I have it. Please recap all the tests I should ask for that would completely rule out Addison's? Im going to ask my Doctor to test me. I've had severe, severe salt and sugar cravings since I was little and absolutely everything you stated. Thanks for sharing your story. ❤

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      Hey there...common is blood cortisol, potassium and sodium...I would also recommend a blood ACTH test and then a ACTH stimulation test. the ACTH test in important....this is for primary addison's...secondary adrenal insufficiency may require other tests. Please be safe and keep looking for answers

    • @sandrawheeler1521
      @sandrawheeler1521 3 หลายเดือนก่อน

      @@chronicallyfit_withjill Yes definately ask your Dr for morning cortisol blood test. And all the tests Jill said.
      I have no idea untill i see my Endo if had any abnormal pottasium or sodium blood tests. Or antibodies.?
      The short synacthen test. Will show clearly if your adrenals are working or not. ? Drs dont very often pick the symptoms up of Adrenal insufficiancy?. Or realize they are all connected? As Addisons is rare.? So stand your ground with your Dr. Tell them your symptoms. And ask to be refferred urgently to an Endocrinologist. And have a early morning cortisol blood level test. While you are waiting. If you Adrenals are not working. Your early morning cortisol will be low. ( proof) At least you will find out one way or the other. Good luck.x

  • @UKRinterpreters
    @UKRinterpreters หลายเดือนก่อน

    Do you have a quick cheat sheet on normal levels of acth/sodium/potassium etc.

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  หลายเดือนก่อน

      Sorry i dont. And depending on countries they may differ as well

  • @sandrawheeler1521
    @sandrawheeler1521 3 หลายเดือนก่อน

    I had painfull and weak joints too. And unable to cope with stress.x

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      my joints mainly my ankles were so bad in the mornigs!

    • @sandrawheeler1521
      @sandrawheeler1521 3 หลายเดือนก่อน

      @@chronicallyfit_withjill yes i used to wake up feeling 100. With all my joints aching...Better now I am on hydrocortisone...But still having symptoms? ..How long did it take you Jill to get your HC pills dosage right? I know you have the pump now.xx I am ok in morning 10mg. 5 hours later 10 mg. Then i just conk out about 4- 5pm.!! Get blurred vision. Cant bear to watch TV. Too much noise orsound. So go to bed between 6- 7pm...!! Maybe i need another half tab to keep me going through the evening??? I dont mind going to bed early in the cold dark winter. But i want to have energy in the light warm summer evenings?
      I will speak to my Endo. But i think its up to us to do whats best for our bodies wirh the meds? As we know how we feel. And when our bodies start to shut down...as run out of cortisol...? Its all a learning curve? Did you ever get your appetite back Jill? I never feel hungry. Just eat because i know i need too. ? I try and eat healthily. But those cravings. I just think. Oh let my body have what it wants.🤣🤣🤣. Then regret it...🤣🤣 one day all i eat is veg and fruit. The next choccy and bread.!!

  • @jermjermmason8710
    @jermjermmason8710 หลายเดือนก่อน

    How do you get on for people who have pre menopause and Addison

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  หลายเดือนก่อน

      That im not sure. Need medical professionals help. Very individual i would think. ❤️

  • @user-ut9zg4nr6i
    @user-ut9zg4nr6i 2 หลายเดือนก่อน

    I have recently had blood work and a cortisol level done and it was all pretty normal but I still feel horrible low blood pressure,extreme fatigue, brain fogand many other symptoms. Could I have addisons and the cortisol blood test just not measured it. It was not acth or what ever it is called

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  2 หลายเดือนก่อน

      My cortisol, sodium and potassium were all still normal on blood labs...did they test your blood ACTH...that is a good test to do...mine was very high. Then we did the ACTH stimulation test...don't rule it out if you feel it maybe Addisons!

    • @user-ut9zg4nr6i
      @user-ut9zg4nr6i 2 หลายเดือนก่อน

      @@chronicallyfit_withjill they did not test acth at all just cortisol

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  2 หลายเดือนก่อน

      @@user-ut9zg4nr6i I would request the blood ACTH test to start...my cortisol, sodium, potassium was normal but my ACTH from my pituitary was 30 times to high! My body was fighting so hard. After this we did the main ACTH stimulation test

  • @elizabethwright5650
    @elizabethwright5650 2 หลายเดือนก่อน

    I went and got my yearly physical. My cortisol came back a smidge below normal for 8 AM when it was taken. My sodium a potassium were fine. In the last couple months, I’ve been dealing with nausea and loss of appetite. My face has hyperpigmentation as well as the outlines of my lips. I’ve always loved salt. As a kid, I would pour it into my hand and lick it. I’m getting follow up blood work in the next few months because I was breastfeeding at the time. I’m curious to see what mg labs will say.

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  2 หลายเดือนก่อน

      You sound just like me ❤️. How are you doing? Keep fighting for answers ❤️

    • @elizabethwright5650
      @elizabethwright5650 หลายเดือนก่อน

      @@chronicallyfit_withjill I just got my acth back. 118 with a reference range of 7-63. I’m still waiting on the rest of my labs.

    • @elizabethwright5650
      @elizabethwright5650 หลายเดือนก่อน

      My cortisol, Na, and K came back normal.

  • @sandrawheeler1521
    @sandrawheeler1521 3 หลายเดือนก่อน +1

    I still dont feel well on hydrocortisone Jill? Tabs? Not sure if dose is correct yet? Do you ever feel well with Addisons? Jill.xx

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      Ups and downs..but look into getting your meds adjusted...the pump is a BIG difference for me. I find dealing with stress levels a HUGE help. Keep fighting friend.

    • @sandrawheeler1521
      @sandrawheeler1521 3 หลายเดือนก่อน

      @@chronicallyfit_withjill Thanks Jill. Yes i wish we had the pump in the UK. I am very good at not getting stressed. I had years of training with cfs/ ME. Of calming my nervous system down... I cant se the point of worrying or stressing. Total waste of time and energy. Nothing is more important than our mental or physical health is it? Xxx

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  3 หลายเดือนก่อน

      @@sandrawheeler1521 Hey there...the pump was actually developed in the UK to been used for solu-cortef. Definitely an option for you!

    • @sandrawheeler1521
      @sandrawheeler1521 3 หลายเดือนก่อน

      @@chronicallyfit_withjill i can ask. Its not being used in the the UK? Just trialed in one area of the UK???

    • @bettyperez470
      @bettyperez470 3 หลายเดือนก่อน

      Greenstone brand Big Difference

  • @c.k.1530
    @c.k.1530 หลายเดือนก่อน

    Have u checked ur iodine levels
    Usually always being cold is a sign of iodine defiency

  • @jfouts1979
    @jfouts1979 2 หลายเดือนก่อน

    I may not have full blown Addison but believe I have adrenal insufficiency...doctor's won't listen to me. Do u have any suggestions?

    • @chronicallyfit_withjill
      @chronicallyfit_withjill  2 หลายเดือนก่อน +1

      Hey there...so you have not been diagnosed then...I would suggest if not done yet blood ACTH test and possibly ACTH stimulation test and to consider primary and secondary adrenal insufficiency testing. Monitor through symptoms and blood work (acth, cortisol, sodium and potassium) at least with your health care team. MRI are often helpful on the adrenals and the pituitary. Hope that helps a bit...keep fighting and trust your instincts!

    • @jfouts1979
      @jfouts1979 2 หลายเดือนก่อน

      @chronicallyfit_withjill Well I have like twenty plus other diagnosis so it's more complicated than that. I've been looking for a unified diagnosis for many years. I think I might have something called auto.Immune polygland dealer syndrome type two. Adrenal insufficiency is part of that syndrome. I will look into the AC.T.H stimulating test. Thank you for your reply. I have felt like adrenal insufficiency problems for years but doctors don't care...I've even shown them where at the mist stressful time in my life....my cortisol had spiked and then went down to hardly anything at all....still...they won't even consider further testing....is there an inexpensive panel I could order on my own?? I have been unable to work for years...and also unable to collect ssdi for years...mainly bc I am under age 50....also what is the best way to test cortisol? Serum? Urine? Saliva? Combo? And besides cortisol and acth and now acth stim and na and k what else should I have? I regularly have cmps and have intermittent hyponatremia and have had low phosphorous too...many of my hormones are affected by whatever...testosterone...shbg....lh....fsh...tsh...etc...