Uphill battle symptoms and conditions

UPDATE from Calybo ! ! ! ! !!!!!!!
The post below this (or a couple below ) is one that I added to this site almost a year ago!
After having Mirena removed in OCT. 08' it has been a very long uphill battle reclaiming my health. I feel I am now 90% better. I still experience some of the symptoms - just much, much,much milder than they were at first. I feel like Mirena has taken nearly a year away from my life! I've had to focus so hard on my health that I feel everything else has been put on hold. I just feel so disappointed in conventional medicine and pharmaceuticals for allowing this to be sold to women without doing more studies and not adding more warnings on adverse affects. it wasn't until I went to see a holistic doctor that I really started to make progress.

My son (14 years old) was given levaquin for a sinus and ear infection
2 weeks ago. Around the same time he began practices for his high school baseball team. He complained about his legs being stiff and aching. We assumed it was the intense practices causing his muscles to ache. After a week on the drug, he could barely walk and his knees were swollen. We were very concerned and looked up the side effects of levaquin on the internet. We were shocked and angry when we found out that levaquin should not be given to children under the age of 18 because on the possibility of joint and tendon problems. Today we went to the orthopedist and he drained a lot of fluid off of both knees (it looked like about a 1/2 cup from each).The doctor thinks it has to be a side effect of the drug, because the symptoms began at the same time. He doesn't
think after examining the knee and having him perform certain tasks that he has damaged any tendons. He has all the symptoms of rheumatiod arthritis. He is very athletic and plays competitive sports and we are praying that his knees are not permanently damaged by this drug. Parents please research all drugs and there side effects before giving them to your children! Doctor's DO make mistakes!! The pharmacist failed us too.

I was on Avalide for a while did not like side effects of tiredness, vertigo like side effects, went to my doctor she took me off and put me on lisinopril 20mg I have to say I rather have the symptoms from my first BP meds than this one! have been on it 2 and a half months. It sucks! I watch what I eat exercise on a regular basis, I lost a total of two pounds in a two week time period whoopeee!!! I should have lost two pounds in the first week never mind the second week but two lousy pounds! its like an uphill battle, I am done and going back to the Avalide, oh yeah and I have that irritating dry scratchy cough I thought was due to allergies, it wakes me up or never let's me sleep through the night. This Med stinks!!!!

I just read the article in question ,i am not sure what on earth they think mood changes and anxiety is,but i am not surprised as the doctors do not believe us,this has been a complete uphill battle,what would prove it to them,children have died, been poisoned tortured and imprisoned in there minds,and yet they say there is no evidence,the evidence is clear when your child improves when not taking this drug,what do they need.They agree this can happen in rats,but turn a blind eye to children.This article and findings of these so called specialists makes me want to vomit.The researchers should have to take the drug for 3 years and then tell us how they feel

My thyroid troubles started in 1993. I am not sure how long before the discovery I had the problem. Mine started as a nodule on one side. I was immediately put on Synthroid and had to go see the Endo every 6 months for a biopsy. In 1995 I became pregnant. I had one more biopsy until after the birth of my daughter. The Endo told me he wanted to see me right away after she was born to do another biopsy. I had my suspisions, but didn't think anyhing until after she was born and went for my biopsy. Well, I had cancer. I went through the whole thyroidectomy, the 3 days isolation with radio-iodine, and every year to every few years after I had to go back and get the radio-iodine treatment, while not the high dose as the first time, it went with the complete body scan. In fact, I am due now, but don't have health insurance. My dose has been switched a lot, I have probably been on every dose from the lowest up to .200mcg, which has been the highest for myself.

Symptoms: pre-thyroid disease, I am 5'2. I was always 110-115 lbs, I was 22 yrs old and 120 lbs. when I married in 1993. I did notice gradual weight gain, probably because of my thyroid problems. I am sad to say that now I am around 180 lbs. I cannot seem to lose the weight unless I go on a total starvation diet. I managed to lose 10-15 lbs over the past summer, but unfortunately for me it has come back over the winter. I tried to stay as active as possible by going to stores and malls to walk around. I do for a fact notice that when my dosage for Synthroid goes higher, so does my weight gain. I was on .137mcg over the summer, and I think that was a good dose for me, that was through the regular dr. The Endo is the one who put me back up to .150mcg. My Endo told me the thyroid is a regenerative organ, so it CAN grow back. I guess they don't want that in case of cancer again, and I guess that is why he keeps me on higher doses.

I personally cannot stand it. I feel it is a horrible curse. I feel very robbed of my previous active life. I have been dealing with this now for 12 years not having a thyroid and being on this medication. I feel angry that I do not have the energy to do things with my 12 yr old and 3 yr old. I miss the way I was before having thyroid disease. I feel very sad when they come up to me asking to do certain things and they (nor anyone else I know for that fact) can understand that I just feel so whooped, and no energy. All I ever seem to want to do is take a nap. I have migraine headaches constantly, I am constantly tired. I cannot concentrate, I have some memory loss. My ex-husband, and my current husband too for that fact think I am just being lazy. Well, that is not so. There are moments when I do feel a burst of energy, but then, I have to use that burst to do the things I need to do around the house.

Pre thyroid disease I was always active, never tired, could do anything. After: TIRED, I was 24 in 1996 and felt like an old lady, dry skin, no matter how much lotion I put on. The tub is full of hair, while it doesn't come out in clumps and I still have thick hair, I have hair all over the place. Irritable, mood swings, happy to angry and the snap of a finger. I can have insomnia some nights, constipation, lots of the same stuff others have listed on this forum. Those side affects are the same no matter what dose I am on. And like I said the higher the dose for me, the more weight I pack on. It is instantanious. Over Christmas, and no, it wasn't from eating all the goodies, I gained a lot of the weight I had lost over summer back, and that was because a few weeks before, the Endo had put me on the .150 mcg.

As a pediatrician I write for singulair every day.
The medication is for allergies.
Allergies cause adenoidal swelling, which cause sleep disturbances which makes the child tired the next day with makes him over weight, less attentive, hyper and eventually act out.
This in turn makes the child experience parental, peers and teachers criticism/ abuse, with leads to the child feel inadequate, embarrassed, frustrated and eventually depressed and suicidal.

Yes, singulair does cause behavioral change but they appear within the first couple of peels, the rest is due to allergies, lack of medical care, i.e. sleep, singulair, and zyrtec deficiency.
Allergy shots cause 4 times the incidence of suicidally than singulair, and Ritalin 10 times more.
They say in hebrew "once a stone is thrown into a well, thousands of smart people won't find it".
Check it, it's true.

Hi Danielle here, I have posted in the past, I was wondering if any of you that suffered from anxiety, and nausea post Mirena, when did you see an improvement, was it after a couple cycles? Are any of you on an anti- anxiety meds? They say that when the anxiety goes that the rest follows, is there truth to this? I am 4 weeks post removal and I still wake up with the feeling of dread, I take Lorazepam to help, but I am sick of taking a med I just want to feel like "me" again, what an uphill battle, while I do notice an improvement these pat 2 weeks to the 1st two weeks I am still very concerned about the anxiety and nausea, I went to the mall yesterday for 3 hours, and came home a wreck! crying, dread, I hate it, can anyone please tell me when I should expect to see an improvement? I know it is different for all but any information would be appreciated.