Hi everyone, new to site but love the helpful posts. Cumbria have withdrawn funding for T3 for all patients and I've now been on an increased T4/reduced T3 for the past month. I'm now only taking 100mcg of T4 (for the past 3 days) upshot is I feel awful. Painful joints, aches, really bad indigestion type pain, and random back ache. I'm tearful, anxious and seriously worried how I'm going to manage this change. Next bloods are start of Jan 17. Any help, advice?? Thx
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