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I come from a highly dysfunctional family. Emotional Abuse is the norm in the family. It is carefully covered up.
I figured only people who worked in the manufactoring and mining were really at risk. *shrug* thats why i'm asking here.
Some people are "hidden hyperventilators", I am and it took 10 years to find a doctor who recognized the problem.

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Eventually your testoserone levels will drop, like they do for all guys, and THEN you'll really want to look into supplements. But wait till you need them.
I think you can purchase this stuff on the net, easier than buying it in the shops.
You know the deal is Yes I am emotional. This neck injury came right after a 3 1/2 year battle to recover form a very long and difficult injury to my arm. I am tired. I am emotionally and mentally and physically zapped out.

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So basically, the only thing that was abnormal in the testing was the 2 EEG's, which showed mild slowing in the temporal lobe areas. It was NOT indicative of epilepsy, though (and I never had a seizure before), but the neuro still tried me on Dilantin, which seemed to slow everything down even more. I was on it for a month before getting off of it. They also tried me on Neurontin which had the same "slowing" effect as the Dilantin. During this time, my head felt like it just needed to be "jump-started" to get the neurons going again in the temporal lobe region.
my boyfriend has not been feeling great lately and i think that some of his symptoms may point to diabetes? but i am not sure. i am trying to convince him to go to the doctor, but in the meantime:
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Hey gottagetbetter,
Here's why.
I have secondary hyperaldosteronism due to another underlying condition (crf-acth defect).
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Hello. I've been posting on the Depression board for a couple of months now, and have been encouraged to post here by several people. (Hi Sannah) I'm usually not one to just open up, and pour my heart out, but I've found that on the depression board, the people are so welcoming, and really do try and understand. So, here it goes.
The majority of Lyme doctors and Lyme testing labs no longer take insurance because insurance companies often do not reimburse them. People usually pay up front and submit the bills to their company for reimbursement. Some pay more than others. You may want to see what percentage your company will pay ahead of time.
I have narcolepsy w/ mild cataplexy, hypothyroid (due to radiation treatment for Grave's disease) and severe depression caused by the on-going medical.
I can also comment on what I believe is an ingrained bias at Johns Hopkins against *********** for prostate cancer, but that's another story involving my own personal experience. I had hoped the Johns Hopkins community had come up to speed on 5-ARIs, but now I'm thinking that that has not yet happened. Also, I'm no longer surprised when I see true experts making faulty calls when they venture beyond the areas of their expertise. These are very smart folks at Johns Hopkins - wonderfully dedicated and talented, and when they take off the blinders that we all wear from time to time - often blinders created by obsolete or misinterpreted experience, I'm confident they will climb on board the 5-ARI bandwagon.
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Hello to all. I am a regular "old timer" on the Thyroid boards and recently switched Endos. This new endo seems to be more interested in pursuing the sex hormone problems and does not seem to think my thyroid issue (wicked case of Hashi's) does not seem to be all the causes of my trouble.
Can you please assist me in locating an experienced Da Vinci Robotics surgeon in your Texas. I am willing to travel out of my Dallas for the surgery if necessary.
This is where I stand now. The numbness isn't that severe unless I drink alcohol or touch something cold (taking something out of the fridge, etc). Slight "breezes" of cold air also cause the numbness/tingling, but not for long. For example, when I take off my pants, my legs feel numb but it quickly subsides.
You were probably all excited about possibly getting some at this party, right? So I guess this hasn't been the kind of advice you were hoping for. Unfortunately I'm just going to add to it...

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I have ostea-arthritis. But my rheumatologist keeps doing sed rate tests and RA tests, just to make sure that it does not become/change to Rheumatoid Arthritis. I also have other blood tests too. I have been diagnosed for about 1 yr. I take Skelaxin, Tramadol (Ultram), Glocosamine/Chondroiten, and just this week she added Relafen. I have also had a couple of shots, which you can only have about 4 per yr. They only help with the pain and especially swelling (in my hands and wrists) for a few weeks.
I am worrying so much lately that sometimes i go to bed and worry about if im going to wake up or not as sometimes i feel like i am poutting too much poressure on my heart, brain and body in general with all this non stop stress, i have been getting headaches loads and occassionally get heart flutters/palpitations but right now im convincing myself that maybe i deserve it for being so stupid and if i hurt someone else then why should i have the right to worry about my own health
I take depakote 3 times a day and have noticed an amazing difference. I still get headaches but not every day and sometimes not every week! I take Maxalt MLT 10 mg with a Fioricet to get rid of the pain when I do get one. And the pain is usually gone in less then 30 minutes.

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I have posted before but not really about my problems. My husband and I are separated due to his anger and violent behavior. It has been a long time and we have kept contact. We have been to several therapists and have had it said that he is bipolar, borderling personality, bipolar/borderline and one said he could not diagnose him. He is a loving person and yet can call me names and damage the house. Since the separation he has not improved in any way or grown. He still says he is living in hell without me and does not help himself. He does not believe he has an illness but believes he is the way he is because of me or things I say and now contributes it to being alone. He is not the type to kill himself but says he does not want to live. He does not take care of himself and eats wrong foods, does not exercise or try to better himself as far as how he lives. My question is this most of the posts mention how the person with bipolar or borderline seem to run hot and cold as far as how they feel about the spouse. The opposite is true in my case he will not let go and professes undying love always. Is this common in bipolar and I have not heard about it? Or is this a symptom of something else. He also has problems spending money at times other times is tight with the penny. He rages at things and calls names. He has strange ideas about many things and usually does not agree with what most people do. Any ideas on this would be appreciated. Thank you in advance.
Thanks for your replies -- both of you. My boyfriend is probably going to be getting a BMT in the next month or so. Can you tell me more about what this process was like from the inside (we're hearing such scary stuff from the doctors about what this process will be like...)? How long did it take you to recover? I know you have to be isolated from germs for a long time even after you return home from the hospital. But, when did you remember starting to feel a little bit better after your BMT? How are you feeling now? I am so glad to hear you are doing well and still in remission.
I'm not sure what that means, my consultant was so busy that day that I was in and out in ten mins. He told me I will going back into the clinic for more tests, something to do with finding out which side of the pituitary is affected, posterior or anterior??? so confused.
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They laugh at me, comment on things, argue with me, taunt me, and say things very fast and strange.
C6-7; Mild disc dessication. Combination broad based posterior spur and 1-2 mm broad based posterior disc bulge, no spinal stenosis. Mild bilateral facet degerative changes. Moderate right neural foramin narrowing. No left narrowing.
Our Experiences: happy childhood / harsh judgemental parents / abuse / neglect / these things affect our psyche because reactions to these provide messages to us about our sense of self and place in the world.