Thyroid storm symptoms and conditions

The first time I took Zoloft, it was a brand new drug with a high price tag and people were just beginning to talk about depression--openly. I had a positive experience with it. I have PTSD and severe depression due to trauma as a child and later from an abusive husband. I had a major depressive episode shortly after the birth of my 2nd child, exasperated by postpartum depression and thyroid storm. I became suicidal at a time when I seemingly had all I ever wanted. It saved my life in that regard.

I had stubborn baby weight that needed to come off. Also, I tend to be an emotional eater. Zoloft helped curb my emotional eating and I lost weight. Some people say overeating or eating disorders are akin to OCD behavior, both anxiety based, so in that way it makes sense. When Lithium was added, then changed to Depakote, I had a tremendous weight gain--I was PUFFY! At that time Bi-Polar was the flavor of the month--not that it isn't real--it just seemed that at the time, everyone was BiPolar. I later went off all meds and was OK for about 3 years when the ugly beast reared its head again.

Zoloft at one point both saved and ruined my life. The first time on Zoloft as a young wife and mother I think the verdict was still not out with all the side effects. I was unable to engage in sex. Not only did I not have any sexual urge but my body couldn't. I talked to a therapist and psychiatrist to no avail--it was MY problem--that the birth of a child brought up abuse issues--men are the only ones with sexual side effects! After being sexually NORMAL my husband and I were told that it was psychological. That didn't do a lot for our relationship. It also made me more distant and quiet. The new Me-on-Zoloft was like my repressed alter ego. The new me was all the more reason to need to stay on meds--just see how depressed and troubled I am. My husband and I divorced due to bad medicine and I didn't know any better. Had all the information been out there at the time, things could have been different.

I went back on Zoloft with mixed results. As a creative writing major at the university, it was like someone flipped a switch and all creativity left me. I found it increasingly difficult to concentrate and recall information for discussion or tests. I was however , more focused in the mundane--dinner, dishes, laundry, regular exercise, all the routine stuff. The anxiety before going back on zoloft made me want to rip my hair out and I was overwhelmed by everyday stuff. I would wash a dish and fight the urge to run around the table before washing the next one. Part of that, I think, was the pressure of being a single mom with 3 small children, going to school full-time and working part-time. Whew! and with little support from anyone, no dad in the picture.

Through the years I have been on many other things and this will probably be the pattern for the rest of my life. Paxil made me a suicidal zombie to the point that my kids cried and made me go to the hospital--they didn't know the suicidal ideation at the time. Effexor caused flabby weight gain and myalgia. Last year I went in the hospital again for depression (job loss, 2nd divorce, mother's death & all at once). The psychiatrist talked me into going on Pristiq claiming it was like Effexor but with none of its bad side effects. BS!!! Once again, I was duped and still weigh 33 pounds over what I did. I am AGAIN back on Zoloft and it seems fine. The devil you know is better than the one you don't know--I guess. I haven't been back on it long enough to know what will happen this time but it can't be worse than the other things out there. I'm tired of being the psychiatric community guinea pig. Everyone is different; my best friend gaied 25 lbs. on Zoloft and takes Paxil (I can't), my sister only does well on Welbutrin, my friend's mom has been on Effexor for years and it keeps her sane. You just have to find your fit. My problem has been from the medical community not being forthcoming with information and the reluctance to listen to a 'crazy' patient.

A couple of other symptoms I didn't mention before are I still get cold a lot and ibuprofen is my best friend because of all the aches and pains. But running on 3-5 hours of sleep a night with the occasional 7 hours has definitely diminished the quality of my life.

I suggest to anyone that has Hashimoto's Thyroiditis (type of Hypothyroidism) to have a blood test done for Celiac Disease. There has been research done linking Celiac Disease and Hashimoto's Thyroiditis. Celiac Disease can be controlled by a gluten-free diet (wheat, rye, and barley free). In the US, not many doctors recognize/know of this link. I have been hypothyroid for 20 years (had Hodgkin's Disease (cancer) - radiation/chemo at age 16) I have 2 sisters with Hashimoto's Thyroiditis and were iron and B12 deficient. I was diagnosed with Hashimoto's Thyroiditis 3 months ago with iron and B12 deficiency. I have been on a gluten-free diet for 2 months now. My dosage of synthroid (levothyroxine) was 175 mcg and now is down to 137 mcg. I hope that I am one of the lucky ones that will have their antibodies to their thyroid normalized (no more synthroid!) I have a couple of days left before my next blood test and I hope that it goes down more. I am feeling better now than I have in a very long time. I have attached a link for those of you interested. It is an endocrine article from Finland outling the link between Celiac Disease and Hashimoto's Thyroiditis (among other things). I hope that this helps some of you. http://edrv.endojournals.org/cgi/content/full/23/4/464

I have been on synthroid for 30+ years. It has steadily been increased throughout the years. Last April 2007 I ran out of medication and was going through a stressful move. I hadn't been on the medication for about 6 weeks. Once I got my new doctor they checked my levels and instead of putting me on the same dosage of .175 they increased it to .2mcg. I gained 10 pounds overnight. I looked like I was pregnant, mood swings, aching joints, insomnia, etc. I went back in 2 weeks to have it rechecked. That was the second problem. It takes 6 weeks for the medicine to level out in your system. So not only did they increase my dosage after telling them I had been off of it for some time they retested my levels too soon. So it was again increased to .225...more weight gain...another test...another increase .25mcg. Now my neck is swollen and I have an enlarged gland, hard to swallow, shortness of breathe, 43 pounds of weight gain, severe anxiety, acid reflux, gerd, on top of the other symptoms mentioned above. In 8 weeks of increments I have been retested and the dosage has gone down and as of last week it was finally decreased to the original amount of .175mcg. It has only been a week but I have lost 2 pounds. Oh Lord please let it keep coming off! My neck isn't as swollen and my 5th doctor who finally could see the light explained that I was having a thyroid storm. It is very important that when your levels are checked you wait 6-8 weeks to let the medication level out in order to get a true reading. He also said that you need to take your meds on an empty stomach...which I knew...sort of. I took my synthroid on an empty stomach but I also took my other vitamins with it which can effect the absorption of the synthroid throughout your body. He also gave me a beta blocker to help with my symptoms until my levels even out. It is called metoprolol succinate (Toprol-XL) 50mg. My gut doctor put me on Paxil as well to help with the acid reflux and gerd which he felt was caused by the anxiety due from the synthroid levels being off. I hope this info helps but it makes sense to me.

Hello, I had a TT two weeks ago. I had hyperthyroidism. I was diagnosed three years ago after ending up in the hospital because I had a thyroid storm. I started taking synthroid the day after my surgery. I feel like a nut job! I don't know if it is because of the medication or because of the TT. Could it be a combination of both. I don't remember my numbers but I know that I was in a hyper state when I went in for surgery. Since I have been home...I can not fall asleep without meds, can not stay asleep, my day starts around 4:30 AM, have night sweats (big time) and chills (although, that symptom seems to be improving), I have been so irritable that I can't stand myself, my husband and kids are ready to kill me. I know that my behavior is totally unreasonable but I can not seem to control myself. I feel crazy! I see my Endo next week, I just hope that I can make it until then. I feel like I need to pack my bags and head to a hotel and spare my family from me! Please someone tell me that this will get better.

Had total thyroidectomy 9 months ago and started taking Synthroid immediately thereafter. For the last 4 months I have noticed significant hair thinning. I have always had very thick, healthly looking hair but now it's just dry and brittle all of the time. I always feel tired and bloated around my stomach area in particular. I have always been a size 4-6 but have inexplicably gained 6 pounds in the last month. Is there an alternative to snythroid without these side effects?

I have been on prednison since l980. I was told I had steroid dependent asthma. I briefly had moon face. I was very organized. I even typed my honey do list for my spouse. I was "driven" to get tasks done. I had difficulty sleeping, muscle cramps, frequent night time urination. easily bruised on my forearms when I bumped into things, lots of 3 corner skin tears and recently had a bone density test and now I have to take Boniva. I did not gain weight. Over the last two years I went from 140 to 120. I did experience two very serious illnesses (Throtoxic with Thyroid Storm and a spinal tumor and surgery.) I finally weaned off about 3 weeks ago. I went from 10 to 5 to 2.5 to 1.25 then 1.25 every other day - very slowly. No asthma symptoms yet. At this time I fatigue very easily. I have lost subcutaneous fat in my forearms, feet and face. I still have some muscle cramps in my feet and somethings deep in legs. I am sleeping much better. I am wondering if the loss of fat has anything to do with the long term use of prednisone. Has anyone experienced or heard of this connection to Prednisone?