Re: Chronic all over muscle pain, joint pain, fatigue and headaches
Ladybug...less than 5 typically Hun? Yeah so I guess there is a bit of a difference. I'm sure your right about his back peddling since something has shown up. I can guarantee that from now on, I be making sure whatever dr I choose, will actually have my best interests in mind. Again, thanks for the info and the support!
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
So I guess he ran a metabolic panel - everything in the normal range. My CBC showed my MCHC low, just barely, but at 30.6 when the range is 31.0-36.0 . The Hemoglobin AIC is just barely low at 5.3, the range is 5.4-6.5 , as we know my SED rate is high at 35 , range 0-20. The only other test was thyroid stimulating hormone (TSH), which is inormal 1.79 , range .35- 5.50.
The dr told me about the SED rate, but nothing else...I guess it's not low enough for him to pay any attention to it. I briefly looked up the MCHC which I guess has to due with your red cell count...possible anemia?
I go to the rheumatologist on March 11 th...soonest appt. so that's where I stand. Any ideas what other tests the rheumy will run? Thanks
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
I hope the rheumatologist can give you some answers... your GP sounds like the orthopedic doc I saw who said I was fine - and then handed me a copy of my MRI report to give to the neurologist and I was shocked to see the length of the write up.
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~ asthma, allergies, anxiety, arthritis, back problems, high blood pressure, fibromyalgia
The Following User Says Thank You to Kaji For This Useful Post: KG5634 (02-16-2013)
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
Rheum should check you for lupus (ANA) rheumatoid arthritis (RA) thyroid disease for starters. He will likely repeat sed rate do urine check comPlement CRP and a bunch of specific antibodies. Some good clues should emerge from all that.
The Following User Says Thank You to ladybud For This Useful Post: KG5634 (02-16-2013)
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
I had gone to my primary care doctor for migraines (and even though I had medical records dating years w/migraines and meds for it) he wanted me to come in every time I had a headache because he needed to see it for himself. I went to him for leg pain and he told me it was bursitis, rest and take ibuprofen. I could tell more stories with regards to him but what ultimately happened was I had to go to the walk-in clinic that he also was tied in to, because of extreme back pain. The nurse there told me to go to a pain specialist, one that she also worked at. At my next appt I TOLD him that I wanted a referral to go there. He huffed and puffed but by the end of the appt he gave me one. That was the best thing I could've ever done! I was recently diagnosed with FM and although I'm still in pain, I at least have a doctor who believes me. I am being treated for it with meds, infusions, etc. Exercising is my next step. Because its winter here and its C ~ O ~ L ~ D I haven't been walking but soon it will warm up! Good luck to you!
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
Quote:
Originally Posted by Stufftie
Good luck!
I am setting an appointment with a primary that specializes in internal medicine. Maybe I will have better luck with her.
I know my ex-primary kept blowing off my hypothyroidism. I recently found out that she has kept me on a dosage that is a starter point for someone over the age of 50 with heart issues.
35 years old and no heart issues - I also read that birth control pills bind with my hypothyroid medication (T4) and she recently prescribed that without increasing dosage. Also, a blood test to check the levels should be done every 2 - 4 months when first diagnosed. She checked once a year. My Free T4 was only 8% when it should be around 50 - 80-% No wonder I kept getting worse!
It has been a painfully rough and medically stressful three years, but I was very relieved that I failed the fibromyalgia tender point exam. I did get the Rheumy to let me try a new thyroid medication and am taking the old and the new. I still need to give it time, but am hopeful! I am hoping the internist will help me with this.
I am seriously going to be angry if it was my thyroid all along! I kept bringing that up to the primary and her response was, "Levels are fine"
All for a search for an answer - things just kept getting worse.
I think someone owes me a refund for not just trying a higher T4 in the beginning.. lol
I am not implying that yours is all thyroid - I would have no idea. I guess what I am saying is that I wouldn't of found all this out without having a copy of all my bloodwork and some wonderful women on the thyroid disorder board!
I was initially here - and everyone was so helpful - so I am still lingering. How can so many doctors be so wrong?
I wish you the best!
Your post reads like I wrote this. I started having problems at 39, not counting the migraines at 37, and now I'm told it's Fibro. I found a functional medicine doc who takes my insurance, he's trying me on Diflucan and checking me for coinfections (bloodwork at Qwest labs, nothing expensive), and I'm hopeful he can get me back up and running. I have been sick since 2010. I just stopped taking pain meds last month, I was tired of them, so now it's me dealing with all this. It's hard to have a good quality of life when you're in pain. That heel pain you have, I have it too, if I'm on my feet too much (like at a theme park) I am barely able to walk, for those days I need pain meds I'm afraid. I wake up feeling some I've been in a wrestling match, or other things just hit me and it's confusing. I know this is hard, takes the wind out of your sails. I see a very mild imporvement with the start of my Diflucan, mainly in the muscle aches (my stomach is the worst but tonight it's not so bad). Check out a new doc and see if he or she can run some tests on your, I am learning that those of us with fibro can have another bugs at the same time, mainly because our immune system is down.
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
I really appreciate all the posrs from all of you. Each of you have lifted my spirits some with the fact that my dr apparently isnt the only idiot out there and there are good ones too, that actually listen and help. Too bad you have to go through the bad ones to find the good ones! Its nice to hear so many of you are finding out what's going on with yourselves and getting some relief. Thanks and I'll keep you posted!
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
Quote:
Originally Posted by KG5634
I really appreciate all the posrs from all of you. Each of you have lifted my spirits some with the fact that my dr apparently isnt the only idiot out there and there are good ones too, that actually listen and help. Too bad you have to go through the bad ones to find the good ones! Its nice to hear so many of you are finding out what's going on with yourselves and getting some relief. Thanks and I'll keep you posted!
I spent 2500 each year for my deductible since 2010, probably going to do hit it again this year too. I finally found a doctor who's an MD but he focuses on functional medicine. I'll post any positive results I get from this experience. He's the doc who told me I had Fibro, the Rheum blew me off, totally blew me off, and others said I had anxiety, which of course I do because I am ill all the time and I'm upset about it. Makes sense to me. I don't know if the new treatment plan will help me out, and I'm still going to see my neurologist and gastro, but it can't hurt at this point. I have a blood test scheduled to test for any coinfections. Pain, illness and stress can bring down our defenses, plus a lot of antibiotic use (or even a little), and we can get smacked with all sorts of stuff that just won't go away. It can't hurt to find a doc like this and consult with him. If you're like me, you've seen everyone in town anyway, what's one more. I know it gets embarassing. I don't even tell anyone when I'm seeing a doc now, and when friends ask how I am, I just say I'm great. I hope to be one day.
The Following User Says Thank You to stcloudmom For This Useful Post: KG5634 (02-28-2013)
Re: Chronic all over muscle pain, joint pain, fatigue and headaches
Oh I totally do the "smile and say...oh I good, how are you!" to people. They ask out of politeness but not real concern. I know that Many members of my family literally just think I'm lazy. Now I'm not referring to my husband, children, or mother....but I have 3 sisters and a father that have distinct opinions. Of my 3 sisters, only 1 will actually ask me how I'm doing am mean it. She is the only one that shows any sympathy or concern for my physical well being. I think she understands more because she struggles with drugs and alcohol. I was always trying to wake my parents up to what was going on...obviously we were younger than, around college age. She resented me for a VERY long time after she was basically made to go to rehab...but it was the only way at the time to assure we'd have more time with her- she partied REALLY hard...a lot! She had actually been put on a ventilator in the hospital on 2 seperate occassions, among MANY other things. Ok...back to the topic...she is literally the only one that will ask me how I'm doing, and actually mean it. My back issues are major and have been going on for a really long time. These other issues seem to have been creeping up on me over the past 5+ yrs. Thank goodness for the family that do actually support me, they have made things much more tolerable. I even met a stranger a few weeks ago who only lasr week did we realize we both suffer from back problems and she's been diagnosed with FM almost 10 yrs ago. We spome at lenth and exchanged numbers ( she's a parent of another child that one of my childen participate in the same sport). She actually texted me after my rhuemy appointment to see how things went.
Soo...to the appointment. She obviously had actually read over everything on the forms I had filled out...and they were very in depth, specific, and lengthy forms!). So, according to her, my best case scenario is that, yes, I do have Fibro. However, that is only being said without blood work being back yet. Yes she retested the SED rate and was hoping that it would come back lower, she said it it came back the same or higher...she'd have to look further into an autoimmune issue. She will be running other tests as well, took 4 viles of blood, but can't recall exactly what she said...she did say she would run a number of tests and see where we stand. Apparently I had at least 12 of the tender points for FM. Blood work should hopefully be back on Fri. Glad I brought a copy of my blood work with me because my idiot of a regular dr apparently never sent it to her...how hard is that? She also told me my regular dr. said he prescribed pt for me for my neck issues (car accident 2yrs ago), however he never called me to say if the xrays taken last week were clean or not nor did he call to tell me I should go to pt.(we know my feelings on him now!).
So basically that's were I now stand..hopefully I'll hear from her tomorrow...if nothing else come up in the blood work, I guess FM it is. Of course she mentioned trying to do some type of exercise would benifit me tremendously - and in there lies the catch 22 for me. My back issues are so bad and extremely limit what I can do. Even a simple little walk in our neighborhood isn't really possible because of the slightest hills. Now, in the summer when we go to the beach, I ALWAYS feel better and it allows me to go for short walks (the sand is hard so it's easir to walk on it as opposed to soft deep sand. People are always riding bicyles and walking along. It's the warmer weather in the summer that is easier for me, the cold, damp weather kills me (as I'm sure you ALL can sympathize with.)
So know I just wait another day and hope to hear something. It was very nice to go to a dr that actually listened to me and examined me! She asked tons of questions and it was nice to have a dr that seemed to understand what I was saying, even if I wasnt saying it exactly as I should...when I was stumbling to find the words about how stiff, tight, sore, my joints and muscles were...especially when trying to get up out of bed. My total lack of energy...she loomed at me and said, " many people say they feel they feel like they fought a fight in their sleep, and lost.." ..exactly I said! So, I'll keep you posted! Thanks