Showing posts with label clammy night sweats. Show all posts
Showing posts with label clammy night sweats. Show all posts

Saturday, January 6, 2018

After "many" strange" symptoms, DO I ADD yet "another diagnosis" to me endless list of crap wrong with me??? "CPRS"????

I finally made a trip to Urgent Care with what I feel is a very bad Lupus and RA flare, but there are several "symptoms" strange that add into the mix of it all... I was telling my friends on Facebook about the ordeal and one lady mentioned that I should be seen by a Neurologist who specializes in "CPRS"???? Complex Regional Pain Syndrome! I look it up and guess what, MANY of my weird symptoms "fit the bill" - I am just about ready to scream and run, I am so fed up with health problems and the "list" is endless.....


 I had not even thought about that. could it be caused by a very severe sprain? Actually I've had three sprains in that right ankle. The 1st one when I was 40... I had just gotten home after my 1st heart attack, and went toget out of the bed. That foot was "so asleep" I didn't realize it, so when I stepped up I twisted the hell out of it, and it was bad. In fact I had to make a trip to the ER thinking it may have been fractured. Then about 5 years later I stepped crooked on it, when the wind blew me out of a car door at a store here. I was dressed for work, and had went into a store at lunch. The wind was terrible, and when I opened the car door, the wind caught the door and made me twist it again. 

Then in 2016, the day before Mom's funeral in June, I stepped off my front porch, talking on the phone to my daughter, and my neighbor had called to me, and the grass was so wet with dew, both feet came out from under me, and I sprained both, but the right one was bad again. It was so swollen it looked like I had a softball on it. I had to wait, and that Monday after her funeral, went to have it X-rayed at Urgent Care. It was not fractured, but I pulled it again so badly, for 6 months it continued to swell. It was really after I fell fractured the right hip, and then early last year, I went to a foot specialist. He put an injection of corticosteroid in it, and I went for PT about 3 weeks. It went down and "seemed" fine, after that injection. Then last week, I went to the market, and when I got home I noticed my sock I had a bad indention in that foot and ankle.

 I didn't think much of it until then I noticed this week every time I am up on it, or sit at the computer, with it down, it swells terribly again. And I've noticed it hurting now, yesterday it was huge again when I went to Urgent Care about the Lupus and RA flares. I hoped the injection of corticosteroid for those would help reduce the inflammation, thinking that the Lupus, RA and just the very bitter cold weather, that was swelling my fingers and other joints may have caused it again to swell after it being so injured. 

But it never dawned on me, other than I was fearful my "heart" may be causing it to swell. When I had my 1st heart attack, for about 8 weeks before I had it, every day my ankles both of them would swell horribly. That was when I was in "great shape" watched my weight, exercised daily, and never thought I would have a heart attack, yet I did on Jan 8th 2001! So anytime unless I've sprained them etc it worries me that my heart could be acting up, but I've just had an echocardiogram, and a check up with my heart doctor about 3 months ago or less... 

so between knowing it is so damaged from the sprains, and the RA and Lupus, it will swell and hurt, especially with such very cold weather... my fingers, and every joint feels "swollen" and stiff and hurt like hell. So, last night I took one of the Metoprolol's that is for the "extra beat" of my heart. I had slacked down taking them daily because my doctor felt that they were causing me to have a very slow heart rate. In fact we talked about putting a pacemaker in, so I could take the medication and not have to worry over the heart rate problems. Then I will be damned I had one of the damned very cold, wet night sweats!!! Those are the reason I had cut down on the Metoprolol anyway. 

IF my heart rate gets too low at night, we feel my body compensates, by one of those horrid, cold, drenching night sweats, I was wrapped up all night in a heavy robe, and blanket, because then I get so cold after that sweat, I shiver all night, and I feel so bad, I can't even get up to change my clothes, I am just so cold, it just almost hurts to get up and have to change... I swear I thought 2018 would be "better" and it sure has not started off very well for me... I think I am just freaking cursed....


Strange enough, when I look it up, much of those symptoms are true... for one my "OTHER LEG" from the knee down has hurt now for about 10 days, it wakes me up at night, but it is in the other leg from the knee down into that ankle! Also, it looks so purple, but I thought it was spider veins, I suddenly have them in both ankles, and I've asked before because up until I sprained them, I didn't have those terrible ugly looking things, but that ankle and foot looks purple especially when it swells or I have problems with it... 

it has been injured badly twice... and it will even give way with me at times if I am not very careful with it... the "sudden" swelling was strange to me... unless it has just been swelling due to the Lupus and RA... 

so I guess even my Rheumatologist may not really be able to tell me, nor really the foot and ankle specialist... that does seems and I've heard of it of course due to Barby Ingle and many others that have the problem, I just didn't put two and two together thinking that could be what is going on with the ankle in itself... but now that you have said something, and I read the "symptoms" I am wondering if it may be something else like that  and I will definitely check on it. I see my PCP who was the one who diagnosed my Lupus and RA. He really knows a great deal about "other problems" such as something like this... he is a younger doctor and he is very well educated in other illnesses, syndromes, and things that some PCP may not know much about. Plus if I talk to him, he will know of a Neurologist who could look at me and see.

What is even stranger about this, is that suddenly also i about the past two weeks, I've had severe problems with my left arm, from the elbow down to my wrist and fingers. It wakes me up every night, swollen, and throbbing and like it's "asleep" with that pins and needles type of pain. It did it again last night, along with everything else, needless to say I was up since about 2AM, between everything hurting, the night sweat mess, and such I got up and turned on the television again, and said to heck with it... 

and of course I also have the "autoimmune issues" which I knew often go along with "CPRS" again I guess out of everything, I never put this together with the other problems and symptoms. Of course my first thought it dammit, I DON"T NEED ANYMORE FREAKING HEALTH ISSUES!!!! So, if this is the case then I just "chalk up" one more to the never ending damned list of crap wrong with me... again I feel totally "cursed"!!!!!!!


And here is one link talking about CPRS....  https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets/Complex-Regional-Pain-Syndrome-Fact-Sheet