I studied the disease back in 98 when diagnosed
Posted By: vaginal vs. cesarean.....sm on 2007-07-27
In Reply to: Mine were C-sections too but (sm) - Anonymous Mom
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.....
Complete Discussion Below:  marks the location of current message within thread
The messages you are viewing
are archived/old.
To view latest messages and participate in discussions, select
the boards given in left menu
Other related messages found in our database
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 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.
That seems to be debatable even in the medical field. Disease or not disease?
things that could lead to diabetes and hypertension are true, they are still diseases and could obviously occur with or without staying away from known causes.
But for you to come here and say alcholism is "NOT" a disease is a little extreme and maybe should have been accompanied by IMO? That is my opinion anyway.
I studied to be a scopist years and years ago
Back in the early 1990s I took a course called Note reader Scopist. They read court reporter notes (those long skinny papers that looks like a cash receipt) and types them into documents. I had found the course through something called At Home Professions but just didn't finish it because it was too expensive for me. But I am familiar with them and even found my book from the first course I took. Looking back I think it would have been a blast if I had kept up with it.
It is definitely legitimate. A lot has changed since the early 90s, so I'm not too familiar with the industry now. I do remember what was really weird was it didn't take a lot for me to learn it. For instance I could look at a line of court notes and see something that looked like: NV p srn - and I seemed to know exactly what it said. Just weird. My DH used to say that I understood it because I was an alien and my ship crashed in Roswell. HA HA HA Anyway...that's what I know about it. But if you Google note reader scopist or at home professions i'm sure you could probably find a lot of info.
It IS NOT a disease. The use of it causes disease but
alcoholism in itself is not a disease. My husband was also predisposed to it by *genetics* (his mother and father were also alcoholics). He should have had better sense than to ever pick up the first drink, but he didn't. Now, for the rest of his life he will have to battle with the fact that he is an alcoholic (albeit, a recovering alcoholic). He CHOSE to drink. He CHOSE to take the chance and it caught up with him. It's just like cigarette smoking. That's not a disease, but the effects of the cigarettes cause disease. If one is predisposed to something harmful, they need to take control of themselves and stay away from whatever causes the problems associated with it. Both of my parents are diabetics, so that predisposes me to diabetes. They are both hypertensive (as am I). I'm predisposed to have hypertension, but I have to use my common sense and stay away from things that could cause the hypertension to blossom into something much more serious. The predisposition to alcoholism has to be handled the same way. STAY AWAY FROM IT!!!!!
Does anyone have a dog who has Cushing's disease? sm
My mom and dad's daschund was diagnosed with Cushing's disease. She's 15 years old. She's going to have to be medicine for the rest of her life. I've read on a web site this can be fatal. Has anyone ever had any experience with their pet having this? thanks.
lyme disease
Friend's dog was chewing paws because joints were sore from Lyme disease.
Disease question
As someone in recovery for more than 9 years this is my take on it. Addiction (alcohlism) is a combination of nature (genetics) and nurture (environment). One can be predisposed to addiction but never know it if they never ingest the substance. Many people drink but not everyone is an alcoholic. Drinking the alcohol is a choice that one can control, but once an alcoholic or addict makes the choice to drink, they no longer have control over how their body reacts to it.
If classifying it as a disease is a way for health insurance companies to pay for treatment and healthcare for the alcoholic or addict, then that is fine with me. But it is NOT an excuse to drink and once one admits or realizes one is an alcoholic they ARE responsible for what happens after they take a drink.
To the original poster wife: The best way you can help your husband is to take care of yourself and your children through Alanon, Alateen and/or counseling. The only person YOU can control is YOU. Lives by example. Your husband just might find his own way to changing his life by watching you change yours.
thyroid disease
I have hypothyroidism and take Unithroid. I'm up to 150 mcg a day. The only thing I am sensitive to is hot and cold. My internal thermostat does not work well. No medication sensitivities though, but that does not mean much as each person is different. We all reactive diferently from each other. Good luck though. Hope things improve with this.
Foot-in-mouth-disease
At one time or another we have all suffered from it. Sometimes, things just pop out of our mouths before we have had a chance to edit them. What was probably a poor attempt at conversation turned out to be an embarrassing situation for both of you. Accept his apology and move on.
A lifer here, too. It used to be called a disease!
That really freaked me out on hearing that diagnosis. Cysts and pain come and go - supposedly we are to avoid chocolate and coffee/caffeine. yeah, right! No way! I do not do breast self-exams, and was also instructed not to do them as well by my OB/GYNs and surgeons, as we will always find a lump and then freak out. I have yearly detailed mammos - dozens of shots for surveillance. Had a cyst aspirated now and again, and have always been fine. In my 50s now and have gotten used to it - not lazy about it, but just not so afraid. Information is power! It is a very common "condition", by the way! We are all in good company!
Polycystic kidney disease....
My husband was just diagnosed with this. It is the mostly common inherited disease there is and many people don't know they have it. It generally leads to renal failure later in life. There is a new clinical trial beginning right now for a drug that is supposed to shrink the cysts. This is the third phase and so far it has been extremely successful. The clinical trial is at Johns Hopkins University in Baltimore. Let me know if you need more info.
...going on here, including a few disease processes. nm
s
My thirst is Sjogren's disease! sm
I am always, always and forever chronically thirsty, but I don't have the polyuria to go with it.
I have dry eyes, dry nose (to a point where it is usually pretty full of scabs), dry mouth with caries at the gumline. I have gastroparesis and proctalgia fugax which often go with Sjogren's just like the rest of it. Dry skin and feeling like you are drying out from the inside out is part of it. I even get a nasty, clay-like sludgy feeling in my mouth and throat from my stomach being too dry to digest.
It is misery and even better than a gallon of water a day doesn't fix the dry feeling, but it keeps my kidneys from shutting down from being dry.
Lovely huh?
My 13 y.o. niece has just been dx with Grave's disease. Does anyone here have any info or sm
advice on what I can tell my brother about this? They are such a precious family. Brother visibly upset over this because he has been disciplining her for behavioral problems, etc., when all along it's been here thyroid. They want to do radiation right away to help shrink it? Or possibly remove thyroid altogether. She is so pretty. I spent the summer with them and yes, she did act diff. from other 13 year olds, looked very developed for her age (to me), and her eyes weren't bulging to me. I'm so glad they caught it today. It sounded like she was in the early stages of shock with fever, shakiness, etc.
Anyone with experience in this? Thank you so much.
Every woman in my family has thyroid disease...
and only about half of them are overweight, so that's just another excuse. You really need to stop blaming other people for your weight problems and take control of your own situation. I too have hypothyroidism, but I am a size 6 and was only overweight when I was eating unhealthy and not exercising. If you're really only eating one meal a day, I can guarantee this is why you can't lose weight! Your body is probably holding onto everything you eat because you're starving it!! You absolutely need to eat 3 (small) meals a day and 2 snacks. There's a book called The 3 Hour Diet that can really help you with what you should be eating, how much and how often. You sound like a very angry person and like you don't want accept that you're responsible for your own health. Honestly, you're not overweight because of what the government does or doesn't do, it because of what you're doing to your body.
And the scariest part is, they then carry this disease
among many others without even knowing and spread them around.
absolutely. its a disease, and a super prevalent one also.
.
Absolutely, it is a disease, but one that a person can recover from if they
have the desire to be sober. Unfortunately, there is no test to tell you prior to your first sip of alcohol that you area an alcoholic and will suffer from this disease and hurt everyone, including yourself. Fortunately, however, there are steps to recovery and, albiet it not a cure, it does not have to debilitate you. I am a recovering alcoholic and have been for 13 years. My recovery started with admitting my problem and taking the necessary steps to change and find other ways to deal with my self-esteem, problems and anxieties other than a drink. Since my recovery I have not only become "sober" but a much better person and very serene with my life, which of course has made a very producitve member of society and not "disabled." I think someone who accepts disability based on their alcoholism has not only accepted their fate, but accepted its consequences and not willing to change. I really think that is very sad.
Anyone with thyroid disease experience sensitivity
I have had thyroid disease for about 5 years now and am on Synthroid for it. I find that I cannot tolerate caffiene very well and narcotic/anlgesic medications, such as Novocaine make my heart race and make me feel so weirded out I can no longer tolerate this. I cannot even have a wisdom tooth pulled because of this.
Anywa, I thought it was just me but I recently read in a magazine that thyroid disease could cause sensitivity to medications. It would stand to reason once your thyroid levels were adjusted this would go away, but such is not the case with me. Does anybody else have this problem?
If you have a child with a life threatening disease
you possibly would think a little different about this issue. I do and saying full steam ahead.
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.
Thank you for sharing that. Yes, thyroid disease left untreated can sm
be a very serious thing. I appreciate your response. Good luck to you!!
My daughter has hand, foot and mouth disease
She has 4 ulcers in her mouth and, of course, is in pain and won't eat anything. I put some cereal and milk in the blender this morning and she drank that okay, but her poor little mouth is really painful. We tried the saltwater rinses, but that didn't help. We have been using Orajel on the biggest sore, but was wondering if anyone has any other ideas for pain relief. She's been coping pretty good with the blisters on her hands and feet so far, but this is only the 2nd day. Hopefully, this will be over soon. Thanks for any help!
Check out celiac disease from gluten allergy
Many times it is mistaken for IBS - my grandson is being tested for this by GI doctor on the ball!
Incidental finding, polycystic kidney disease
Not something that I would have liked to hear but being as older, told the doctor maybe can outlive the cysts, i.e. having to be on dialysis and/or dying because of them. I had an MRI of another region and those picked up, told someone in my family had to have and know of no one. The cysts I have can go anywhere in your body so they will watch them every few months, no abnormal lab tests or the like, found those about 2 years ago. The kidney cysts are the only ones I know of.
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've been diagnosed
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 -
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.
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.
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??
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
We took her to 3 different doctors who did a bunch of different tests and all three said without a doubt she has ADD (without hyperactivity). So, we put her on medication. The medication made her VERY cranky and she was a holy terror to live with!!! So, we went back to the doctor and he switched her medication. This medication made her mood better, but her appetite was virtually nonexistant. My husband and I read every book and website we could find on ADD to see if we could help our daughter. We ended up taking her off the medication and changed her diet, making sure she eats every 2-3 hours. We eat pretty healthy anyway, but we really have to make sure that we don't let her eat too many carbs or junk. She also has to eat pretty frequently to keep her attention span up. It has been 2 years now and she is doing great at home and at school. She just started a new school this year and this teacher is excellent at letting the kids have a healthy snack during class so the kids stay focused all day long.
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.
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.
|
