Ongoing treatment tips

Posted Tue 27 Oct 2020 14.35 by Martha P

Hi everyone, I'm not new to Psoriasis, but I'm new to the forum. I've had Psoriasis and Hashimoto's Disease from 2014. Both initially difficult to manage but eventually treated successfully and kept under control until recently. I'm looking for practical advice on what to do when symptoms worsen. I've got the creams... The never ending creams... But I've got symptoms like Nausea, headaches, ear pain, dizziness, fatigue, muscle aches that are consistent and ongoing but the Dr never seems to address these or offer help or advice. I get the impression it is just accepted by the Dr that these are part and parcel of having autoimmune disease. Regardless of whether treatment is considered optimal. Has anyone else found assistance with the symptoms that are just simply daily aspects of autoimmune disease? Has anyone else found they are just left to muddle through finding their own coping mechanisms and ways to manage such daily issues? Mine have become something that is affecting my ability to work daily and this is obviously a concern. Yet I'm struggling outside of work to find the support, advice and crucially treatment that will resolve or at least minimise these daily symptoms. Any advice very much welcome

Posted Tue 27 Oct 2020 17.10 by Steview
A P sufferer for over 30 years, through good and bad times.

Hi sorry to hear of your current problems. I must say I have never heard of Hashimotos disease but a quick search looks like it is a condition affecting the thyroid. The symptoms you list look like being afforded to that disease rather than P. I could understand if you were treating you P with certain oral or biologic medications where side effects are common but you say you are only using creams. Thinking aloud there maybe possible links with Psoratic arthritis with some of the symptoms but like any illness/condition I think you should seek professional guidance or ask for a specialist refferal if you are worried or struggling. Are you a member of any Hashimotos Disease forum? Maybe they could also offer hints and tips. Good luck.

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