December Update....

Hi all! Hope everyone is doing well since my last post. I do apologise for the lack of posts as I'm having laptop issues and waiting on a part to be delivered. But on with the update....

So I didn't update through November, which was also due to being busy with work. I had another visit back to my Rheumatologist. I had experienced quite bad stiffness in my elbow in the days leading up to my visit, and unfortunately my skin hasn't been behaving lately. With the winter setting in, it could be down to the changes but it has been fairly mild temperature wise here. 

My rheum did discuss with me about changing medication, to which I wasn't open to. As previously posted about, my current medication, Stelara, is the third different biologic I've tried this year. I was told about a different oral medication I could try but due to being of 'child bearing age' it was not something he would be comfortable putting me on.

We decided that it would be best to give the higher dosage a fairer chance (only one 90mg had been taken at that stage). I was due to take my next dosage the first week of December but due to not being well, I was put on a course of antibiotics and could then take Stelara. I got a steroid injection to my side to relieve the stiffness and pain I had been feeling in my joints and sent on my way.

A week later and I was feeling better, I then waited another 3 days before I took my next injection. The 90mg dosage came as one injection, instead of two, which made life a lot easier. I have become more confident at injecting, considering at the start of the year it was something I felt sick at the thought of but I'm am grateful for having learnt this.

As previously mentioned above, my skin hasn't been agreeing with me lately, especially on my legs, upper arms and lately my scalp. I find scalp psoriasis to be one of the more annoying things, as well as being itchy, you have to deal with flakes through your hair and on your clothes. I have found one or two dots appearing on my face lately as well, so I'm hoping it is not reappearing there but I guess this time I am more prepared for it. Last year when my face was covered, I took it very badly, hated going out in public and felt the need to avoid certain situations. I have found some very good foundations and good application techniques which would help if I feel the need to cover it, as well as becoming a stronger person to be able to deal with it uncovered in public.

Have you found your skin/joints to be flaring up this time of year? What do you find helps?


I hope to update before the year is out, but if I don't get the chance to, I hope everyone has a lovely flake-free Christmas! Stayed tuned for bigger and better to come in 2016 :)

Until next time.....

Sarah x

World Psoriasis Day 2015....

If you didn't know, now you do! Today, October 29th is World Psoriasis day. A day celebrated worldwide by many a Psoriasis sufferer, to educate others, and also to acknowledge how far treatments have come over the years with so many options now available.

I know Psoriasis is something, if we all could choose, we wouldn't want to have it. But there are positives to come from it and for me a bit part of that was how much of a community you will find from fellow itchys. People are so eager to educate as well as share their own experiences and advise when times are tough.

For myself, the Psoriasis Ireland group on Facebook has been so helpful and so welcoming, be it to rant or rave, you'll always find someone who will set you on the right path. There are plenty of forums out their also, as well as other Facebook pages/groups from different countries.

I want to end this by sharing a video by a beautiful little girl named Pearl, who is an inspiration in speaking out about how it feels to live with Psoriasis and deal with it from a young age. I wish I had her confidence. When I developed it at age 17, it was the awkward years, in high school and a lot of focus on how you look. I wish I was a brave as this girl back then, thankfully I have grown a lot as a person since :)

Until next time......

Sarah x

Double the fun.....

I must apologise for the lack of posts lately, there has been a few bits going on in my personal life that I have had to deal with, so I chose to take a break from blogging for a while.

While one issue I was dealing with is something I hope to deal with in a future post, it's not exactly psoriasis related, but stress related....so in a way I guess it is psoriasis related.

To update on my ongoing treatment, I took my 45mg Stelara as usual in August and had a return visit to my Rheum in September. He was happy with my progress, but unfortunately my arthritis was active, in my knee, elbow (which doesn't straightened properly these days) and now my ankle. My ankle had been giving me trouble for a while, and I found an ankle support did help when at work. When I bought new runners to replace my old, falling apart Golas, I found my ankle to be better supported.

With my PsA being active, but my skin coming along well, my rheum decided to up the dosage from 45mg (1 injection) to 90mg (2 injections). I was prescribed one injection to boost me up to 90mg from my old dosage a month earlier. I have been feeling great, my joints feel a lot better in that I have been doing more things that I couldn't do as well in about a year or so. My skin has had its ups and downs, mostly on my right leg but still nowhere near my worst flares.

I am due back to my rheum in November, to see how I'm finding the higher dose. I am due to take my next 90mg on Nov. 21st, all going well. In the mean time I hope to post a bit more often as I have had a few ideas during my blog break.

If you have an suggestions on any topics or issues you would like to see covered, leave it in the comments below :)

Until next time.....

Sarah x

Quick update.....

Apologies for the lack of updates lately, life has been quite busy with work, outings and a friends wedding. I wanted to update on my progress with my skin and my treatment as of late.

It wasn't too long ago I wrote about my experience with Stelara so far. Two weeks ago, I did my third Stelara injection. I did feel it this time, but didn't hesitate for too long because the sooner you do it (once prepared) the quicker it's over with. I had found my skin to be getting worse, but now I do see improvements going forward. There are still some stubborn patches near my ankle that aren't cooperating.

As for my joints, I find that I am not wearing the right shoes for my feet, therefore I do get a lot of pain in my knees and more recently my right ankle. I have also found my right elbow to be fairly painful also, especially when lifting etc. in work. I am due to see my rheum just over a weeks time, so I look forward to seeing what he makes of my progress.

I don't think the recent spate of bad weather has helped either. Do you find your skin/joints acting up when the weather worsens? Feel free to share your experiences in the comments below.

Until next time.....

Sarah x