These socks were a ton of fun to knit. They kept my interest as I knitted my way through color changes and different textures. The red is “brickwork”, the grey stripes remind me of the siding on the house, and the light grey cable might be the gingerbread details on the cupola… (if you navigate to the Ravelry pattern for these socks you can see pictures of the house). The heels are Norwegian short row heels, which were new to me, but easy and fun to do. The best part of these socks?
I have lots of yarn left over from the socks, and I’m already thinking that I should whip out some matching arm warmers using these colors and textures. But first, I have a few sweaters to get finished.
Have a nice rest-of-the weekend, everyone. I’m off to do some knitting on my Nordiska sweater.
Last week was great; I finished up a big knitting project, read a good book, baked cookies, and began planting flowers and doing yard work again. Yay! The leaves are bursting out on my trees, the roses are looking good, and I think that we have finally had our last freeze warning. Spring is finally here! Good weather has arrived for a few days, I have energy, and I made lots of progress over some really excellent days.
And yet, there was a downside to getting things done… I suddenly found myself rattling around the house at loose ends. I aimlessly flipped between books on my tablet, unable to find one that would hold my interest. I listlessly looked through knitting patterns, unable to commit. Where is my next project, I asked myself. I dove into the yarn stash hunting for inspiration.
Enough of that, said the stash! Here are some nice yarns, truly excellent colors, and ideas galore. It really does pay off to have a well-fed stash at times like this. Look at what I am casting on for the next round of projects…
So, there we are. I have projects going again and I am excited with the drive to complete more knitted yumminess.
Still hunting for the book, but it is sure to come. I have two audiobook credits to burn, so as soon as I settle on some titles I will be in business.
After all, I need something to listen to while knitting!
Wow. How quickly time flies. It has now been two and a half years since I was diagnosed with the autoimmune disease limited systemic sclerosis (AKA scleroderma), and I joined the rare disease club. When last I reported on my progress I was at the end of a tough year; lung disease, oxygen, a referral to palliative care, gastroparesis, and constant pain. I was having trouble walking and my stomach was really acting up; I was losing weight at the rate of a pound a week. Ugh. I was somewhat upbeat by the end of the second year since I was off oxygen, but still, things weren’t really all that great.
What a difference six months can make. A change in medication made my Raynaud’s much easier to handle. I started doing yoga (carefully) a few months ago and added tart cherry extract as an anti-inflammatory that I can tolerate better than traditional NSAIDs. I bought shoes that felt better on my feet (Haflinger clogs) and got serious with stretching exercises for the plantar fasciitis I developed due to tightening on the bottoms of my feet. I switched to a gastroparesis diet that is mostly easy-to-digest, low fiber foods (got to love pasta and yogurt to do this one…) and began to add some blended fruits and veggies. My weight loss stopped and I started to gain back some weight. My skin has started to loosen up on my right arm (scleroderma literally means “hard skin” as the most obvious symptom is thick, hard skin that develops as the result of systemic scarring), which is pretty darn exciting! Over the last six months my energy has been slowly coming up and I have been managing with less pain; I can even walk normally! I’m breathing better and I rarely need to use the rescue inhaler. There was a Sjogren’s flare, but still, things are better.
I just finished making the latest round of testing and doctor visits, and I have to say, it is pretty exciting to visit with happy smiling doctors. My pulmonologist was almost giddy! My lungs and heart have maintained (scleroderma damage tends to be forever…) with almost no new damage; I am right at the edge of trouble, but I’m not there yet. I have good blood work, and even had the first NORMAL kidney function test in over 5 years. My red blood cell count is back down in normal range, and my muscle strength has improved so much I can now easily push shopping carts. It seems that the increased dosage of immunosuppressants has turned the tide and I am stable. STABLE!! What a wonderful word that is.
I will continue with all of my current drugs for now and there will be more testing in a year, but it is clear that I have definitely pulled up from the nose dive that they through I was in a year ago.