polyglandular auto immune type 2
Hi, wondered if anyone can help, diagnosed with polyglandular autoimmune disease type 2 last month, was put on Levothyroxine 125mg before christmas for my thyroid, started on Hydrocortisone nearly 3 weeks ago when I got diagnosed, I started on 20mg, 10 in the morning, 5 at dinner and 5 at tea but after 2 weeks felt I was going downhill, specialist put me up another 5mg at dinner but still waiting for some effect. Still feel fatique, swollen glands, migraines, can only go a little walk, cry alot etc, Has anybody had that trouble, how long does Hydrocortisone take to work, when it does work, do you get your normal life back, so you can do everything you did before. My specialist hasnt been through how I should feel after and how long. It would help if anyone could tell what do I expect to feel like. I read peoples stories and they sound that in a few days after taking hydrocortisone they are back to they feel great.!!
Last edited by benanddi; 04-08-2012 at 06:53 AM.