Make mine a double…

I've been having a rough time with my autoimmune diseases lately.  I'm chronically tired, with swollen and hot joints that seem to move around my body without much rhyme or reason.  It's exhausting.  My rheumy wants me to start taking Enbrel twice a week.  I'm really not sure that Enbrel is the biologic for me.... Continue Reading →

Hiding in plain sight….

When people look at me they never see a person who is "sick".  I'm often told, "But you don't look sick!".  Who suffering from an autoimmune disease hasn't heard that statement a few hundred times.  I try to prevent people from seeing how hard life with my body has been lately. It's been so easy... Continue Reading →

My enemy is my friend…

Living with autoimmune diseases is a never ending journey.  I've had people tell me that "But you don't look sick", and "Do you know that you are limping?"...hmmmm....you really think I didn't know that I was limping?Each day is a journey because I never really know how I will be feeling.  It's the same with... Continue Reading →

A needle in the haystack…

We survived our first round of acupuncture.  Georgia was very well behaved and seemed okay with having needles sticking out of her head.  The vet was thorough and really seemed to listen to me as I spoke about my concerns/fears/hopes.  I think it is a good fit.  Time will tell if Georgia benefits from this... Continue Reading →

Who’s on first

Since Georgia has been sick, I've been putting my health on the back burner.  I think focusing on her illness has been good and bad for me.  I was so focused on Georgia that I didn't realize how bad my shoulder were.  Two cortisone shots later and I'm a new person.  Now I have to... Continue Reading →

In over my head…

Many things have happened in the last few months.  In August of 2010, my sweet little Cavalier King Charles Spaniel, Georgia Grace was diagnosed with a Chiari malformation that causes syringomyelia.  Syringomyelia (SM) is a horrible, progressive and painful neurological disease.  Basically, she has a malformation of her skull that puts pressure on her brain... Continue Reading →

I’m back…I think…

So, I 've taken some time off from writing this blog.  I think the combination of living with RA/Fibro/Sjogren's/Graves'/& DSAP in addition to writing was wearing on me.  I'm thinking that I will change the name of this blog.  I don't just live with RA.  I live with autoimmune diseases.  Each take a significant part... Continue Reading →

Humidity is not my friend…

So I'm now fully into the 2nd month without Humira. The summer heat and humidity has been rough but overall I'm hanging in there. My ankles might not agree (they are swollen and sore) but for the most part my RA is cooperating with my decision to travel to Africa. On another note, I recently... Continue Reading →

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