The Petechia is back and rashes ... still don't have a clue... Rashes, Brusing, Petechia, lowe back issues, hips issues, does it EVER END with AI Illnesses??????

 The first two photos are from a couple of years back. I developed "bruisinng and petechia" on my legs and arms.... portions appearing as huge bruises, others appearing to be like "blood blisters", such as you may get if you "smash" your finger etc... it forms a "blood type blister".... I went through every test in the world and specialist and no one really ever came up with anything other than "Lupus" causing it. They only appeared on my arms and legs... no where else on my body at all..,

I have that same strange "blood blistering" like stuff suddenly on my arm last night...  here are some new pics, along with the ones from a few years back... This one ABOV as I said is NEW... this just appeared a couple of nights ago as almost the same type of "petechia" blood blistering as before... no apparent reason I can come up with... and below is the "rash" the developed on the inside of my right knee about 2 weeks ago. It was like tiny blisters, but they were "lined" up in rows... I also had a few on my right ankle, and my 1st thought was shingles. I had happened to of course been on and stay on pain meds, and have those in my pain pump internally also, plus I was on the generic form of Valtrex. Since I began with the Lupus, RA stuff... I developed blisters around on the corners of my mouth. My doctor thinks it is a "herpes" type virus because my immune system is a mess with the AI illnesses, thus he treats me with the Valtrex for them... but as soon as the "2 day" dose is through, I develop them again. I am going to ask him about a "daily dose" to see if that is possible and it it might keep these mouth corners from being bright pink and sometimes blistered... they hurt and try to crack open at times, and I've put just about any and everything imaginable on them trying to see if I can stop it from happening....

Costochondritis - another "possible new problem"? With Me and the Lupus, RA, Sjogren's, Osteoporosis, one may never know....

I "think" I may have "Costochondritis".... I started having pain under my RIGHT arm a couple of days ago, and kind of around to the front of my right chest... it hurts to take a huge breath in, or if I hold my arm a certain way etc... it can bring on the pain. I noticed a moment ago, I had the hiccups... and OMG! WHEW!! Did that ever make it worse..... I figured I must have "pulled" a muscle underneath my right armpit and then around and it even hurts some into my back, but not like right at the arm, where your armpit meets your chest, and then a bit around to the front. an NO, I do not think this is a "heart related" issue at all. I already thought about that, but since I've had 2 of those, I am pretty well, educated on certain things to look for if heart related... that is why I am trying to stress this is under my right arm, kind of around to my right chest, and then into my back some also. I went to pick up Tazzy - my Pug, a couple of days ago. I have to help her onto the sofa,She no longer can jump, so she puts her feet up on the sofa and then I gently pick her up so she can get on the sofa. The other morning, I kind of had an "off" moment, where I lost my balance in helping her up. I really didn't think much of it until I began to get out of the shower a bit later and OMG I was like WHAT THE HECK????? Then of course I have been so busy doing about 15 of more things around the house etc... so I am already sore and achy due to all I am trying to accomplish also. But, ALL of it woke me up at 5AM! MY hips, lower back, my shoulders, under my right arm, and I was so achy and so stiff I didn't think I could even get up and do anything. I really didn't do a whole lot today, other than a few very "easy" things.... anyway, I had not even tried to look up what the "symptoms" might mean, so a bit ago, I though in between a movie and getting some sherbet I would look it up.  I think it appears almost like I do have "some swelling" on back on that side... it appeared to kind of look "puffy" comparing it to my left side under my arm.  The Costochondritis and was about the 1st thing that popped up and that seems to kind of describe what I am feeling. I gather since I am on pain meds, corticosteroids etc... that unless something else plays out or I get worse, or have different symptoms it will dissepate on its own over a few days. If not, I have an Ortho doctor appt on Wed to discuss my "test results" from the discogram, plus Mom is going to the same doctor about her hip severe pain, and cano't barely stand any pressure on it Then we also see our PCP at the same time o Friday, next week... so I will have a chance to ask about it, if it is still here by then.... Happy Fourth to ALL!!!!!!! May our Nation and World over find peace and harmony, and NO threats of any kind.... that is truly my 4th of July holiday wishes... I am probably spending mine either doing some stuff around the house, or resting, depending on how I feel tomorrow morning.... Hugs, Rhia Steele​

Necrotizing Myopathy: Are Statins to Blame? Article from Med Page Today! Something you may need to know more about... "Muscle Pain"? Not sure why? On a "statin"?? This maybe the answer...

 

This is very similar to what I went through a couple of years ago. I was on a statin, NOT for cholesterol issues. But, a statin, a small dose of blood pressure medication, and Lasix has became a "norm" for many who suffer a heart attack. IT seem the combination help to lessen chances of another MI. But, when I went in with severe muscle pain, especially in my calves... plus fatigue, weakness, and so forth, my PCP checked to see what my levels were to make sure I was not suffering not just from Myopathy, but worse, it can turn into Rhabdomyolysis. plus due to the fact that I also suddenly had double vision which grew worse as the days went by, my blood tests confirmed I had "muscle damage" in my blood. Much like the "enzymes" they look for immediately when the suspect an MI, also basically the same he found those enzymes and I should have not had any. Of course my situation was even more complex. I already had 2 "heart attacks" not just one. So, it was even more important to try and do any and everything to NOT risk another. Yet, the myopathy can be dangerous.... and it can cause permanent damage if left unchecked... so I had to go off the station for 3 months, or until my blood work showed NO muscle damage. So, just like "Prednisone" as my PCP calls it for me a "necessary evil"... without it, I honestly think I maybe unable do do much of anything. It helps to keep the severe inflammation down, but also again in turn, now I have severe osteoporosis due to the Prednisone and I am also "pre-destined" to have it due to genetic reasons and even the AI illnesses. Seeing this article once again brings to mind HOW MANY COMPLICATIONS, other illnesses in "tandem"... the meds and their side effects... all come with Autoimmune Illnesses, and arthritic illnesses, and many other chronic diseases, such as FM,CFS/ME and MANY others.... as PATIENTS so MATTER "what" a doctor might "tell me" I AM STILL going to be an EDUCATED patient~~~ I thoroughly believe some of my treatments, and even maybe some of my diagnosis, would NOT be right.... had I NOT became an EMPOWERED and EDUCATED Patient! I also know there is LOTS and LOTS of "bogus" material out there in the WWW... so you truly have to be diligent when it comes to what you think is accurate... but I NEVER hesitate... IF I Read, or see something online I feel "maybe" something my doctor had missed or not thought about and so forth... I PRINT IT, TAKE IT and Ask him to either allow me to ask questions, or let him read it.... or us just discuss the "main" issue whatever I bring in maybe relative to my situation.... of course I AM NO DOCTOR and by NO MEANS think I "know it all" ... YET, when it comes to OUR BODIES most of us especially women KNOW things very well..... Sometime I feel as if I am "educating" my doctors, and sometimes they tell me, that I am helping to bring new light to the subject.

http://www.medpagetoday.com/Rheumatology/GeneralRheumatology/52416?xid=nl_mpt_DHE_2015-07-03&eun=g773630d0r

In Remembrance, Reflection, Pride, and & Celebration. May YOUR July 4th Holiday be all you want it to be...

Have a Happy, Safe, and Wonderful July 4th Holiday Weekend!

 

I want to wish everyone a very SAFE, HAPPY, and reflective July 4th Holiday weekend! As I watched what the news had to say yesterday evening, it was pure shame I felt (even though I am not one of ""them") that our Grand Nation, has have to endure such horrific hate crimes, terrorist acts, and again "credible" threats enough to warrant each and every "celebration" especially in our huge cities, like Washington DC, New York, LA, and more to either have so many "patrols" out, or some have even cancelled their events due to the fact they feel it is NOT safe enough to even have a beautiful celebration of our Country, the USA! That also makes me mad, sad, and also even a bit fearful. Our small town has a "celebration" planned for tomorrow. We have now had a "Farmer's Market" that opens every Saturday to local growers, who come and sell their fruits, fresh veggies, and so forth. So, our town also is including some out of town vendors, even a small concert, and then a fireworks extravaganza* in the evening,, as well as one out of the Texas Motorplex, that they have been putting on for years for the holiday. Yet, even here, just because we are a "small town"... you NEVER KNOW... who could be a "lone wolf".... we have had our share of close calls in our country and the surrounding ones, and we don't live but about 35 miles from Dallas. So, we want to put aside our "fear" and think, "Oh, this would never happen here, not in our small community"... alas, sad but true, it only takes ONE person to create a horrific scene even in a small town.

So as we ready ourselves for cookouts, family gatherings, going to other celebrations, the lake, camping, and all of the many activities going on throughout our nation, be "viligant", watchful, and don't be afraid to "report" something you feel is "not right".... those types of "mindfulness" is what keeps us safe, happy, and being able to celebrate with family and friends...

I bid you ALL A Wonderful 4th of July Holiday Weekend... whether traveling, or at home cooking, wherever you are, be safe, be happy, we do still have much to celebrate and in so many ways... and Enjoy your Holiday! Hugs to All, Rhia Steele

 

FROM THE IFAA - Results from an in-depth study to IMPROVE EARLY & ACCURATE DIAGNOSIS of Autoimmune Arthritis diseases, as well as other AI disease that often are in Tandem!

Here is the link to this extremely important study of the importance of EARLY and ACCURATE Diagnosis when it comes to Autoimmune Arthritic Diseases, and other Autoimmune illnesses that often are in "tandem" with them. This report had hope of educating more of our Medical Professionals, Dentists, and Others, about these illnesses and diseases. It is SO Crucial to have an EARLY and ACCURATE diagnosis, so more Aggressive and targeted medications and treatments are done early, before so much damage has been done.

We have also seen and witnessed over the past couple of years SEVERAL often "very young people" are either extremely ill or even pass away due to the possibility that they were not diagnosed early enough, and had the proper treatments. That is just another reason why the report and others to follow are critical for all of us that suffer from these hideous diseases, syndromes, and illnesses.

Please see the report in its entirety at the URL below:

Early Symptoms of Autoimmune Arthritis Investigation