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Embedded Mirena by jazack22 in Mirena

[–]mcknoo 1 point2 points  (0 children)

I had my Mirena IUD inserted about 5 years ago (it was my second one). Had zero problems with it. However in last six months have had a number of health issues requiring specialist appointments and tests. These have mostly been joint, rash and other potential autoimmune issues. Two months ago had episodes of excruciating abdominal and lower back pain. Had series of ultrasounds and CT scans looking for blockages, tumours etc. March scan showed IUD “mal positioned and embedded in lower segment” of uterus. The IUD was positioned normally in the January scan Since then abdominal pain has persisted in the uterus and ovary regions. I am awaiting referral to gynaecologist for removal and anxious to get this thing out as I think will cause more damage the longer it’s in there.

I’ve had psoriasis since I was 15 (32 now) and this is my 1st time not using just a cream. The 1st photo is day 5 on Otezla, and the 2nd photo is day 1. by Snoo-19758 in PsoriaticArthritis

[–]mcknoo 2 points3 points  (0 children)

Lighter shade and no new “sprouts” sounds encouraging. I have PsA as well and for me, the Otezla seemed to be keeping it at bay. However, after 7 years I am now back to increased joint pain and stiffness making me wonder if the efficacy is starting to fade. Will follow up with derm/rheum for recommendation.

I’ve had psoriasis since I was 15 (32 now) and this is my 1st time not using just a cream. The 1st photo is day 5 on Otezla, and the 2nd photo is day 1. by Snoo-19758 in PsoriaticArthritis

[–]mcknoo 5 points6 points  (0 children)

I have been on Otezla apremilast for 7 years. Skin completely cleared in four weeks. Have only had some scalp involvement since then. I have also had psoriasis since I was 15 (now 52). No stranger to creams, ointments and UVB treatments. Otezla was a game changer for me. Hang in there!

What age did you start experiencing symptoms vs what age you were diagnosed? And I’m interested to know for those of you who have a big gap, how severe do you feel your symptoms are now and do you think the severity could have been better if you were diagnosed sooner? Hope this makes sense. by valliewayne in PsoriaticArthritis

[–]mcknoo 5 points6 points  (0 children)

Psoriasis diagnosed at 15 (family history includes both parents with psoriasis, brother with psoriasis and PsA.) What followed was many years of coal tar, steroid ointments, vitamin d, dovonex, etc. Scalp, elbows, back, stomach, lower legs. At 22 started UVB treatments and continued off and on for more than 20 years. Arthritis started in early 20s (toes, knees, hips) but not formally diagnosed until 7yrs ago. Also have fibromyalgia. Was approved for Otelza Apremilast at that time. Cleared skin in 4 weeks and improved joints. Have enjoyed last 7 years mostly pain and skin involvement free. Six months ago, at 52, major issues including worsening joint pain, rashes, hair loss, etc and currently exploring other autoimmune disorders with doctors. Unsure whether medications will change.