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Yes - i've been diagnosed

Posted By: taxydeer on 2007-04-23
In Reply to: So you do think you have FMS or CFS? - Stephanie

for many years now - just was not aware of this somatization disorder and its correlation with fibro and CFS. I would skip the rheumatology route and go straight to pain management - you will save yourself a lot of time and money. I live in a large metro area and have access to many very good doctors, but until I went to a pain management group of anesthesiologists, I never got any relief. My internist who I fired kept me on prednisone for 8 years and he actually got mad when I told him I was taking control and going to a PM specialist - that I was tired of him jerking me around and I resented having bought his car and put his kids through private school because of his inability or unwillingness to treat my pain issues. Yes, I am on narcotics - don't let that deter you - they work and not everyone that takes them becomes an addict. My life has been much better since I have been out of pain and am mostly bothered now only by the CFS - which no one has found anything really to help that. I sleep a lot and have learned my limits - I would just really hate for you to waste your time with a rheumatologist - they are for people with arthritis and inflammatory conditions. Fibro is not an inflammatory process and the rheumies don't offer any real treatment for what ails you.

Just reread your post - I would be interested to know what treatment the rheumie has planned for you -


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While I've never been diagnosed with

lupus, I sometimes think I do, but when my rationale kicks in, I realize it is the wear and tear my body has taken over the past 40+ years, in addition to overwhelming perennial stress.  Stress can cause lots of symtoms that mimic other diagnoses.


I do wish you the best and hope you get to the bottom of it and feel better.  You are a delight to have on this Board.


no, was diagnosed 8 yrs ago but have had...

I have had it since my 20s, I remember my LFTs were crazy then, they had no test for this in the 70s-80s.  I didn't KNOW I had it.  My husband had it (ex) and he was tested in 1992 and many friends had it and all told me to get tested, but I felt/feel like a million bucks so I laughed them off or poo-pooed the issue


In 1998 I decided ok - get tested and my case was so mild that it looked like I was only a *carrier* but on further testing I had it.  Last year I went to that GREAT specialist (who really specializes in C and is an older MD-I like that, not *green*) who confirmed my suspicions.  My tests are excellent and for decades now, I take care of myself.....and I don't eat raw fish...(my ex did and still does and another MD told me he's nuts to do so), and I will NOT die from it - because I have had it forever....


I also read that online years back......that if you've had it for 30-40 years and doing great, you'll die from something else......but if one continues to drink and drug - well, then, you will die from the disease.  


My dad has been diagnosed with

a bacterial infection that is very rare.  The word sounds like Narcartia but I am not able to find anything on this bacterial infection so I'm probably spelling it wrong.  Does any one have any suggestions or know where I can go to get this info?


He became very sick, had a couple of episodes of losing his sight.  When I found out about it (a week later) and he went to the ER, the initial diagnosis was spinal meningitis.  This diagnosis eventually "evaporated" for the lack of a better word.  CT scan revealed a lesion on the brain.  This was not able to be identified.  Brain surgery ensued and this biopsy was sent across the nation to multiple labs.  One lab finally made an association with "agriculture, ground, farming."  About six weeks ago, my dad had spread chicken manure on his garden.  What complicates the matter is that he has arthritis and is on Remicade with a depleted immune system.  This is probably why this affected him.  They are treating him with an antibiotic IV every six hours around the clock.  There is only one antibiotic that will treat this bacterial infection.  This is making him very sick.  The antibiotic does contain sulfa and I don't know that he is allergic to that but I have heard that sulfa medications can make some people very sick. 


One other note to help in getting info on this.  This must be something that is sometimes seen in AIDS patients because of the depleted immune system.  I have tried to Google it in conjunction with AIDS and still cannot come up with info.


That's the story and any info that anyone can help me with would be appreciated!


They are probably diagnosed with
lung cancer because either they had it when they quit or because they are susceptible to it because of the smoking. My dad quit and died 2 years later. Either way something is going to get you. When it is your time, it is your time--that has always been my philosophy.
Anyone diagnosed with shingles and if so
how long had you had before the diagnosis and have you had any complications from it, such as constant pain, etc. Thanks
I have been diagnosed with fibro but
I have fatigue sometimes and don’t know if from that or from the hypothyroidism that I have, double duty so to speak. I have appointment this week to see what exactly is happening with me. Terrible, terrible pain for days on end- thought fibro, now not sure. I have some hydrocodone and take 1/2 pill of that when severe pain with fibro, supposed to start rehab for mild exercises but too much pain involved now with ?? I had a boss 1 time and she said she started exercising and that was the only thing that helped her. I just have had some setbacks to where I have not been able to start yet (including shingles!!). Hurt so much with the fibro and think the shingles started because of that. I can sleep at night, no problem there but some mornings unable to stay in bed because of hurting. I will give a follow up when I visit my physician this week and see what he has to say about if this is fibro, what does he think is problem, things you might do for fibro, etc.
Yes. I was diagnosed 10 years ago
with early stages of cervical cancer. Had a cone biopsy done which showed that the cancer did not spread or in situ. I decided to have a total abdominal hysterectomy, kept my ovaries, because I did not want to go back to the DR. every 3 months for testing and the chance that the cancer could return. No chemo or radiation. I was very lucky.

What makes you think you might have cancer?

Have to get those PAPs every year ladies. This is a very treatable disease.
Has she been formally diagnosed?
I get an outbreak on my nose every now and then, and the doctor prescribes Acyclovir. Don't know if it's the same when it's on the lips. Acyclovir works great, and you can use it either prophylactically and take it every day so you won't get any outbreaks, or you can use it when an outbreak is coming on and it's gone within a day or so, and it never has a chance to get bad. Again, I don't know if the lips are different than outbreaks on other body parts. My husband gets one on his leg and he takes Acyclovir too.
I have been diagnosed with fibro about 9 SM

years ago. You mention the pain is in your ribs. When I was diagnosed that was not one of the key points, of which there are many. I have pain all over, really. I have very much pain in my neck, wrists, elbows, shoulders, lower back, etc. I have terrible burning and pain in my muscles in my arms and legs as well. I have advanced osteoarthritis and chronic fatigue, which can also accompany fibromyalgia, as I am sure you know.  Symptoms can certainly vary from one patient to another.  I wish you luck and success in your efforts to control pain. I wish I had the answer for everyone suffering daily with chronic pain.


Anyone here diagnosed with Lupus?

I've been getting worse and worse physically and am in the process of being ruled out for all sort of stuff and this (Lupus) is one of them...some test came back positive but it's not definitive and I may have to see a specialist.  I should really pay more attention but it's so hard to focus when a bazillion things are racing through your head while you're sitting nekkid freezing your hiney off on a paper-lined table. 


So, yeah, anyone got this disease and, if so, how are you dealing with it?  I'm just bummed out with the amount of pain and fatigue I have.  I mean, I'm all crippled up and can't even sit here at my desk for more than an hour at a time anymore and chores that used to take 20 minutes or so now take up to 2 hours.  I actually was so exhausted and in so much pain I curled up in a ball on my living room floor in front of the wood stove and slept for almost 2 hours before my husband found me and got me up on my feet.  I'm only 35 and this just ain't right!  Any advice is much appreciated.



she's been diagnosed as bipolar
of course, that's according to the press.

My dad is bipolar and has s/a and alcohol problem. I know how heart breaking that can be. It's like people who overeat. We all feel sorry for fat people but if you chose drugs then you are such a bad person but it's the same thing, really. A compulsion is a compulsion, no matter what you are taking into your body.
Diagnosed with this since the late 80s,
in fact I went in and told the doctor what to check for, had the classic symptoms, intense itching (waking me at night with urge to scratch), terrible coldness all the time, having to sit under blankets. Mine now has turned into Hashimoto's thyroiditis, I was told just a few months ago, thyroid totally gone. Now with the Synthroid, I told my physician did not want to take any more, loss of hair really bad, heard Synthroid noted for that. I asked and now on Armour thyroid and seems like loss is not as bad but still some. People on here have posted against Synthroid.
I was diagnosed 11 years ago and that along with SM
other physical conditions is why I cannot do a full day. I support myself and still  have to do it without benefits, etc. I have tried different things for pain, but they either upset my stomach or were even taken off  the market. I know exactly what you are going through. Sometimes I feel so bad I can't even put it into words. Good luck to you.
some people never get diagnosed at all because they
x
i was just diagnosed with diabetes

No insurance.  Went to the doc yesterday to go over lab work I had done in November.  My blood glucose was 127 (upper limit of normal being 126).  I am 45 yeard old and overweight, but I never had this happen before.  He then did a glucometer reading (after I had had three cups of coffee, each with two sugars, of which I was still sipping on as he took the reading).  He then ordered new lab work as a recheck, but stated he had to put NIDDM as a diagnosis on the requisition form.  I don't feel a diagnosis can be made that simply.  What's really upsetting is the fact that he informed me that now since I had been diagnosed with NIDDM that I would probably never be able to get health insurance with a pre-existing condition such as this.  I feel that through correct diet and exercise over the next few months I can easily lose ten or more pounds, and that this more than likely will change the status of my next lab values.  I feel so very sad about this.  What do I do??


My mother was diagnosed back in her 40's..
Hers came on after a stressful injury, as I've read this tends to come on after a very stressful situation, injury, or illness, and she got progressively worse. She hurt all over, was so tired she could barely move, was trying to work while this was going on and it was about to make her crazy. There would be days she would cry she hurt so bad all over and then would fall asleep into exhaustion. This did go on for several years and then began going away little by little. She just has a flare now and then, but mostly under stressful situations. My doctor did tell her that she should continue to exercise, force herself to do what she can, and then she definitely needed to rest, get enough sleep, eat a proper diet. He said there could be a day or two flare, weeks of a flare, or years, as in her case.

To answer your question, she did get much better and doesn't hurt all over all the time. She was just so tired she couldn't function, which I had never seen in her before.
I have been diagnosed wth fibro about 10 years ago SM

and know what you are going through. I read somewhere that it is impossible do describe the pain, and that is how I feel. It is a gnawing, pulling, burning, aching, fatigue all the time. No one has helped, and what meds I have tried gave too many other bad side effects, stomach upset, etc.


My daughter was diagnosed with ADD in 2nd grade
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In other words, before you even think about medication, I would monitor his diet and make sure that he's eating healthy and then make sure he's eating every 2-3 hours (if possible at school) and see if this helps.
Adult ADD? Never diagnosed but wondering (sm)
So all my life I have been disorganized, first it was papers hanging out everywhere from my notebook, now it is everything in the world stuffed in my purse.  My mind wanders all the time. I do transcription but flip back and fourth between here and my work and my e-mail and other things on the net that interest me.  And i have to have background noise while I do all this.  My house gets very cluttered and than I have to work like a maniac to get it cleaned up but still things are kind of in haphazard places, not really organized. I just always feel overly busy, overly tired, and behind on everything.  So....could I have ADD? Or am I just too busy, bored with sitting in front of the computer, and disorganized??
I had a "slow Mohs" in 12/00 after being diagnosed sm
with melanoma in situ on my left cheek near my eye. I had about 8 shots and I didn't feel a thing. I guess it was called a slow Mohs' because the procedure was about 4 hours long. The wound was open for 1 week until results came back that he got it all out. So for a week I was doped up, as I had a hole in my face that I could put my finger in. I barely have a scar there, he did an excellent job. And so far, no return of the cancer.
My cat was just diagnosed with lymphoma last night.

She is 10 years old.  I noticed that her back hind leg looked very swollen last Friday.  When I felt it, it was a huge lump.  She has not been eating and not drinking any water at all. I think it has been there a long time and just did not notice it until last Friday.  I was given the option of amputating her leg, which I cannot do.  Give her prednisone and start chemotherapy, but how much time will that give her? She looks so sad and sleeps all day and it not using the litter box, about once a day.


I had to make a very hard decision this morning, and I am having her put to sleep.  It makes me so very sad, but I do not want her to suffer.  I am going to bring her home today and place her to rest in my garden under a park bench I have out back. I could not think to just leave her there.  I am going to miss her greatly.


Just needed to talk as I have been crying all morning and trying to work.  I am not going to get much done. 


I was diagnosed with GAD in 2005. I think everybody's different as far as meds go. SM

I am on Effexor XR 150 mg a day and it works wonderfully for me, although when I forget to take my pill, I do get that strange dizzy, buzzy feeling that someone below described.  I also have Klonopin if I need it.  It's not as strong as Xanax, but it takes the edge off and helps with sleep.


I'm curious what was the catalyst for you being diagnosed?  I have always been a "worrier" ever since I can remember.  I bite my nails, but it was always manageable worrying.  Then in the fall of 2005, I had a full blown panic attack.  It was the worst experience of my life and I hope that I never have to go through it again.  I had a gallbladder attack.  I new it was my gallblader.  I knew I wasn't have a heart attack and yet it was like one half of my brain could not convince the other half.  I started feeling lightheaded, dizzy, and like I was in a tunnel.  I was at work and someone told me I should go to the employee health nurse.  I did and my BP was through the roof, my pulse was 130, and the nurse just ripped that BP cuff off my arm and said you need to be seen in ER and made sit in a wheelchair and wheeled me down there!


The irony is the more urgent she acted, the worse my panic got.  Finally, it was established that I was not having a heart attack, but still my body was freaking out.  I could not calm down.  Then I started crying and cried for two weeks straight.  I couldn't sleep at night.  I didn't want to be home alone.  I didn't want to go out in public.  I just basically sat in my house, on my couch for two weeks straight crying and fretting.  My doctor tried me on several different medicines including Lexapro and Zoloft, both did nothing for me but make feel nauseous.  Then he wanted to prescribe an antipsychotic which made me freak out even more.  Being a medical Transcriptionist and knowing about drugs, side effects, etc. was NOT conducive to my anxiety disorder!


Finally, I found a female nurse practitioner who was wonderful.  She new exactly what I was feeling.  Told me her daughter had the same issues and started me on Effexor.  I have been panic attack free going on three years.  I get what I call mini panic attacks where I can feel myself starting to freak out, but I've taught myself relaxation and breath techniques that calm me down.


I'm just jazzed to meet people who have the same "disorder" as me, ya know.  When I've described my anxiety and panic attack to my family and friends, they just look at me like I should be committed and when I was going through it, my family didn't have a clue what to do with me or to say to me.  They were afraid of me, really.  My mom kept saying "you need to snap out of it."  Yeah, ma.  If only it were that easy!


My lab was diagnosed with an allergy to pine needles and had the same
symptoms you are describing. Now, I live in North Carolina where pine trees are as common as grits, so I thought the poor things was doomed!! My vet suggested a cortisone injection in the early part of the season before it got to really take off and then 2 tablets of Benadryl twice daily, which seems to have worked great for the past 6 years, but if I delay that darn shot and she starts that itching then I run into problems because not only is she itching from the allergy, but from the irritation caused from the scratching.
I studied the disease back in 98 when diagnosed

and thank goodness for the web!!!  I continually get educated all the time from being online.  I love it.  Glad you're feeling well!!!!  Attitude has much to do with it.....


Hope you aren't diagnosed with fibro
because no one believes you anyway. I had heard about before, did not know really much about, if I typed on it paid no attention, diagnosed in 2004 and not having fun yet. This is so far uncontrollable for me-mine might have been better controlled if diagnosed with rheumatism- I would suppose rheumatism feels a lot better than being over the entire body.
Have any of you been diagnosed with generalized anxiety disorder?

I have within the last week or so.  Just wondering what meds your doc put you in and if it is helping and how long it helped all of your symptoms.  I guess I was expecting "a feel-good feeling", too, but not really.  The anxiety is definitely better.  Had gone to the ER 3 times in less than a week, thinking it was my heart, but not.


Any help would be appreciated.


My husband diagnosed 1 time with diabetes, get this
he ran 1 high blood sugar and was diagnosed. He did have elevated blood pressure but for years and years controlled his blood sugar and the elevation was always and I mean always low- the insurance company would NOT cover him because of that 1 only diagnosis. I tried talking to them- they told me 2 counts against him- unable to get life insurance on him. This diagnosis was made on a job entry and for 7 years he kept his blood sugar average or below, made no difference. I have been there.
I read MRSA first diagnosed in 1961
There are things that unless you pick them up, may never know. I have an example: Had carotid ultrasound done. I asked for and got the report (I save any and all that I can including lab work) and the neurologist said ok. Well, happened to have 50% stenosis of the left carotid artery. I asked is that a concern to you and he said well, it should be watched ever so often. Another time, going to have elective surgery done, got EKG and lab done ahead for that. The EKG read abnormal (this was one I was picking up from a previous appendectomy surgery I had). I then asked my internist about it. Never mentioned to me at all. Needless to say when I see abnormal on something, only surgery is a have to surgery, not elective. I see mistakes all the time on my records, not sent out but diagnosis for a scan- had it showing me having hypotension and I have hypertension. Even when the people in the office doing the click and go reports before seeing the doctor, have found errors there. These are not outsourced reports, done right here in the USA. I always get copies of everything.
I was diagnosed with fibro but the rib pain, front and back
started 2 years ago when I got back from vacation and has been there off and on since. Sometimes horrible pain, sometimes just there but never completely gone. I went for 1 acupuncture but it is $70.00 out of pocket for each treatment, insurance does not pay so instead I am doing the 70% chocolate, 2 pieces a day because read that might help because of the antioxidants and flavinoids. As long as I am not touched anywhere around the ribs do pretty good. Have tried the chocolate for a week now, cancelling doctor appointment this Tuesday and will see if that holds the pain. The chocolate lot less costly than the treatments. I have found absolutely no assistance with any physician I have gone to, none including pain specialists, rheumatologists, ortho, etc. I sometimes have extreme fatigue, can lie down for a while and it seems to go away. I have hurt all over with the fibro but now my pain issues are the ribs (oh, forgot about the feet but too long story on that). Did your physician give you anything for the costo? I do not take anything for the fibro nor the costo. I had to dust my fatcat today and I thought she weighed a lot, she is only 20 but still had to pick her behind up and put her in the bathtub.
How funny! I have clinically diagnosed my hubbie as Bipolar too!! LOL! We really are in the wrong fi
s
Senator Kennedy diagnosed with malignant brain tumor.
He has to have radiation and chemotherapy.  Hopefully he can recover from this.
Yeah, tons of info online. I have a friend diagnosed
nm
If you've got one, you've got bunches!

How do ya feel about cats?  That's what I'd do...get a cat...but I love cats and love it when they bring me 'presents' of dead varmints. 



If that's not an option, and you're not comfortable with baiting, glue traps, or that sort of thing, it'd be worth it to hire a professional 'cridder ridder' or exterminator.  Those things will chew up your walls and floorboards like you have no idea and cause incredible amounts of damage.  Good luck in your jihad! 



 


 


I've done this 12 yrs and I've had to take breaks sm
Took a break and worked at my kids preschool one year, worked at a hospital one year, took a couple months off once. It does burn you out because it takes all of your concentration. When I worked at the hospital as a secretary I could not believe how easy the job was ;-) I was sooo used to just getting paid for actual work that when I had a conversation with a coworker or a phone call or took lunch, I felt like I was getting away with a lot! I hope your break works out!! I wish you lived close-by, we could take turns watching each others kids ;-)
I've been using...
Zicam severe congestion. It gives me temporary relief and I've been taking Singulair, but originally nasal discharge was clear, this morning it was yellow (don't mean to gross anybody out). Could it have turned into a sinus infection? And if so, is it time to see the doctor??
I've tried that...

I've done that along with changing my diet but still no relief.  I just received an e-mail saying to try vitamin E which is what I am going to try next.


Thanks a bunch.....


I will try that too, I've had enough of this...sm

where to I go to do this, remove IE7 and reinstall IE6.


TIA


oh yea, we've been through that one . . SM
My husband is the type of person that avoids conflict, does not want to face it, because if you pretend it's not there, it isn't, right???? Yea. He was in counseling for a while, but never went back after a few times. He really felt like last night was a punch in the face, like it's a game or something . . . like if you look the part, you ARE the part.
I've been there...
Hang in there...
I have one, but I've only had it for a day
I definitely can't do more than a minute on it, as it REALLY targets my inner thighs. I can really feel it working already, but I don't know what the benefit is going to be to everything it states, i.e. thighs, abs, back. I did a lot of research before I bought it and the only negatives I found were about ordering it through the company's website. So, I ordered it through QVC and saved a lot of money. Plus I received it only 3 days after I ordered it with no extra shipping charge.
A few I've seen....
The Wedding Date
Must Love Dogs
In Her Shoes
The Family Stone
In Good Company
What's the most you've ever won? sm
How did you win it?
I've with you on that! --nm
nm
LOL, I've seen some of those!
  I admit it, I must be a pervert 'cause I think it's hysterical.
I've been on it
now going on 3 weeks and love it. I never use up my points and am always full. Best thing is you can still eat the foods you love. I only purchased the starter kit and did not join. I feel better and have lost weight and best of all I'm never hungry. But, like everything else, 1 diet doesn't fit all. I've tried Nutrisystem, Adkins,Right Size Smoothies, and Medifast and they didn't work for me. So far WW has worked. Also, you don't have to give up the "cool ones" on this plan.
me too - I've been doing this for over 9 (sm)
Same problem, and it doesn't go away overnight. Mostly my right (pedal) foot. Is yours?
I think I've seen something like this
But can't remember which one...a bride having her bridesmaids sign a contract, yeah right...I'd tell her exactly where she could put all her demands...geez!
We've actually done that (sm)
There is, unfortunately, an "out", meaning that if they have ever been invited to call (We refi'd our house and had been calling mortgage brokers, etc) they are exempt from the list, at least in New York. So it could be a brokerage or something trying to drum up business (not my problem)but all I have is an 866 number to go by, no name on the caller-ID. I wonder if you can get them back on the list after your business is finished.
I've been there

I understand.  For 17 years I dealt with this, always feeling like I was never doing enough, if only I could do more then maybe....  I became very ill myself because of it.  I had no life of my own, -- I lived for the next crisis, just like you -- and no one could understand, not even my doctor.  I didn't find peace until I took the burden off my shoulders and put it on His--until I realized I had a responsibililty to God for my own life and I was losing my life, my freedom to find His Will for me and do it, to someone else's addiction.  In this case, it was my mothers's.  She was there night and day as well, no escaping.  I gave up my outside job and worked from home too.  I finally had to move in order to remain sane and THEN other family members had to start doing their share of helping out while I tried to regain some sense of self. It wasn't until then that she even got a clue that I had a right to my own life. 


Your daughter, loved though she be, is robbing you of your life.  That is not right.  But I don't know of a stronger bond than that between a mother and a daughter no matter what problem may arise.   One can never really walk away, forget it, etc. like so many will tell you to do.  Inside, that bond lives strong.  All you can do is find a way to deal with it, a way that is fair to you, healthy for you, a way that will keep you strong or else she will take you down with her. 


For me, it was distancing myself physically and praying for her.  I realized for all my love of her, only He could make the changes in her, and He did once I acknowledged how true the words are, "Without Me, you can do nothing."  Now I pray for and expect miracles if it so be His Will when I have problems I cannot resolve.  It brings great peace and strength -- and HOPE because I've seen first-hand how prayer made with faith truly does bring them and I don't feel like I am carrying the burden all by myself anymore and then I accept whatever He lets happen, realizing He in His wisdom knows more than I.   


Talk to a therapist -- tell them what you've just written here.  Again, they might have access to resources you don't know about.  If their advice sounds harsh, and it probably will, listen anyway.  Consider it.  Your life DOES matter too.  But don't ever lose hope in God.  Ask for the strength and courage to do what must be done for the sake of the both of you and grace for her to change.  Nothing is impossible for Him to do.  Nothing. 


Have you read the books by Melodie Beattie?  They help.  Feel free to e-mail me if you wish. 


Oh thank God. I've been following this sm
and have been just sickened by the whole thing. What a pretty little girl. Such a terrible thing to happen to an innocent child.
N/T - That's what I've been doing
I've been watching a lot of episodes, or at least bits and pieces of them online to get caught up. Some things still confuse me. The new season looks really good.