One of the lucky ones symptoms and conditions

It has been interesting for me to read this posts. I have been wondering about the long term side affects to singulair- mostly because my 11 year old has been on Singulair for several years now. We spent many of nights in the ER for asthma when he was little and no Dr. did testing. When he was 5 his pediatrician tested him for allergies and put him on Singulair. We have had a great experience with it. I find it interesting that many of the health issues on here- joint pains, bouts of depression, weight gain...I personally experience all of them and i am not on any medication. My 11 year old does not experience any of the mentioned side affects. I wanted to find out long term side affects for my own personal knowledge. Prior to Singulair, he was on Zyrtec which was not a good fit.

I'm 47 yrs old now, & have been on Methadone since 92'. My journey with pain started at age 11 yrs, when i had a disease that totally screwed me up. From 11 yrs to 24 yrs, I was prescribed everything from Tyl #3 to Fentanyl patches. I don't know how many of you were around back then, but the 70's & 80's for pain patients wasn't easy. Lots of us put bullets into our brains because the Government made Doctors afraid to treat us "humanely" (so to speak). I was one of the lucky ones because I had outward physical signs of being in pain, so Doctors treated those outward pain symptoms. If i had not had those signs, I know I would wouldn't be here typing this now. I'm relaying this history, before my methadone side effects, because its important pain patients know something.

When I was 21 yrs old, got married & had a child. He didn't live very long, and it was at that point i started using my pills to stifle my feelings. At first I didn't realize what I was doing.. but.. it didn't take to long, and I realized it. Up to that point.. after losing both limbs, skin, and bone grafts, ulcer surgeries up the wazoo, fusions, countless medical procedures, hospitalizations, and operations.. to many to remember.. I had three surgeons, and a internist. All of them knew about one another, but it was up to me to keep each informed as to what they were prescribing.. and I didn't do it. Cut to the chase... About two years after my child dying, my internist retired, so I had to have my records transferred to another Doctor, at another Clinic. Everything with the Dr/ Patient relationship went well, up to about a month. One day.. Something in my head told me I should go to the clinic office, and read my records (i.e. Chart). So.. for the first time in my life, I listened to my head, and went into the clinic, told them what I wanted.. they directed me to medical records.. I told the lady there what I wanted.. she took me to a private room.. handed me a waiver to sign.. kind of stupid waiver, since I was reading my own file.. but.. none the less, signed it.. she handed me my three volume chart. It didn't take long for me to see why, and I'm sure most veteran pain patients will know why too. Right there in Bold Red on the very first piece of paper was "Drug Seeker! Abuses Opiates". Now.. I'm not saying I'm not deserving of that title, but what I am saying is.. "They don't let you know you've been labeled, they let everyone else know, but you." So.. If you are a pain patient.. read your chart once in a while, because once you get that title.. life gets much harder, & you have no idea how judgmental people (even Doctors) are. To most M.D.'s your too big of a liability, & a "criminal" Lastly.. be very careful with these medicines because, it's not that far of a jump from, you controlling them, to them controlling you." Once it happens, its not easy to turn it around again. From age 24 yrs to 27 yrs.. it was hell. I came close many times. Loaded my 30-06 three times, & My 45 twice that I remember. My wife came home early from work on that second time, and found one live round that had fallen on the floor, bent down to pick it up, then found the revolver under the couch.. took me to the hospital.. the E.R. doc admitted me for the pain, and actually treated it with Methadone. With the first dose, I noticed a relief, as I had never felt it before. Not all pain was gone, but after a could days of upping the dose.. it was. When my pain was controlled, it was time for discharge. The doctor that took over my care during admission sent me home with a week supply, & wanted to see me in a week. When I went to his clinic, he had read my previous doctors notes, & now wanted me to come off, & go back to something else. He told me, "that people like me, have to go to Methadone clinics to get methadone." I had been conservative with hiss discharge meds, so I left his office, went home, looked up the nearest methadone clinic, and stayed there for over 7 years (ME BEING STUPID AGAIN!). During those 7 years, I met 4 "pain patients" who were only guilty of being in pain, & having a doctor that didn't want to deal with them, so (like my doc) they mention the only real place, they can get it without bothering them (Methadone clinic). What I didn't realize until the day I walked out, and never went back (and never will), is that Methadone Patients are treated like criminals.. not patients.. AND by being a methadone criminal, you give your state permission to be part of your treatment (And believe me.. you may not see or hear from them,, but they know you by name). I found out after my pain doctor at the time got authorized to prescribe to me, supplemental Methadone at bedtime. After about a month, I get called into my councilors office, & she tells me "the State Methadone Authority says, I have to go back to Phase I because, apparently the pain doctor had been prescribing to other methadone patients without their permission, and that all of us patients had to go back to Phase I". There was no way I was going back to driving 90 miles a day 6 days a week, for something I had nothing to do with. I'm guessing the State was thinking I spread the news about my good fortune with this new pain doctor.. but everyone at the Clinic knew, I came there, sat & waited for my turn, & left. I might say Hi as i passed someone.. AND.. none of the 4 pain patients I mentioned above, were the patients being punished by the State.

The Country says, "its doing better when it comes to treating chronic pain patients." and to a point, I'd say its better.. but there are still miles to go.

METHADONE SIDE EFFECTS:

Someone here mentioned that by taking methadone, he doesn't feel the need for any other opiate. Thats very true. I felt it, & its why they use it for heroin addics. THe first month, I felt really sedated after about 20 minutes of taking it.. But that went away, & now all i get is pain relief.

Constipation-

When I have a operation, I stop taking them about two days before. Three if its possible, because its also true.. after the operation the pain increases, but you get little pain relief from anything.

I can't think of anything else.. except.. soon my only doctor since being on methadone is leaving to another State 3000 miles away, so soon, I'll be back to unthinkable thinking again, I'm sure. Who's going to take a past "drug Seeker-Methadone clinic patient? No Body that doesn't know me.. thats for sure.

I'm sorry this is so long. Good-Luck All

I was started on Bactrim 7 days ago. The first two days I felt fine, but the 3rd night I got cold...very cold and could not stop shaking for about two hours. My heart was racing and I was nauseated and couldn't focus. This went on for about 8 hours before going to the ER. Upon arrival I had elevated BP and pulse, but after a couple of hours it went down to normal. I saw a new doctor who said it sounded like I had a hypoglycemic attack!! I never had one of those before!! So, I'm figuring I'm getting sicker and maybe it is not from the Bactrim so I take it again and last night was another horrible night!! Racing heart, confusion, and urinating every 30 minutes. Thinking maybe I'm having another attack I get up and eat some applesauce and my husband gives me some sweet tea. I promptly threw up a few times and then we went to the computer to look for ourselves the side effects of this drug. Guess what? It causes hypoglycemia, racing heart, confusion and does something to your kidneys and makes you urinate too much and could be very dangerous!! That was it for me!! I didn't sleep the rest of the night but slept on and off during the day and felt like myself today for the first time since taking the drug. I don't know if it has done any permanent damage, but I will let everyone I know about this awful awful drug!!

Wow, I'm a bit fr***ked out after reading all these posts. I must be one of the lucky ones, as well. I had my Mirena put on 1 year ago after my first child. It did not hurt and I have had very few of these complications listed. However, I have suspected that my weight gain and inability to lose was a side effect of Mirena. This is what brought me to this site. I've gain 15 pounds and no matter how much I exercise or stage myself...it stays! I also notice now that I read....that I have had a lot of hair loss. I now have a few questions:

I lost my milk supply after going on Mirena and my Dr. assured me this wasn't the cause. Anyone else experience this?

Also, I'm concerned about the effect this will have on my next pregnancy. What has been your experiences once you've started trying again? I was told I would have no problems and should go off 1 month before TTC, but now I'm pretty worried!!

I have just been put on Neurontin and found out about this weight gain thing!! I am freaked out. I have come off of Topamax due to I could not handle the side effects and I was like I was in a coma. I am also on lexapro for depression so the topamax really effected me. The Neurontin has said to be given to bi polar patients but from what I have read people are having depression problems on it. So the whole weight gain and the depression thing is scaring me.

I just completed a 10 day cycle of one tab at 400mg a day with minimal side effects. I experienced some dizziness in the evenings and some tightness in the chest. That was it, no weird dreams, no nausea or vomiting. I was prescribed avelox to lessen the possibility of pneumonia, (sp) as part of a bad cold. I have weaker immune system after being diagnosed with multiple myeloma 5 years ago. I guess I was just one of the lucky ones. I took my last pill yesterday so am waiting to see whether the side effects I experienced are gone.

Wow, I can't believe the bad experiences everyone has had. I guess I was one of the lucky ones because my experience was WONDERFUL! I had it inserted about 2 months after baby #2. I lost all 60lbs I gained during pg PLUS and additional 10. I have to admit the insertion was awful but the almost non-existent periods for 5 years were wonderful. If my insurance hadn't changed, I'd have another one in a heartbeat. I don't want to be on the pill because I just had an allergic reaction and my husband is resistant to get his end taken care of. So, we're still looking.............

I had my Mirena IUD inserted two weeks ago today. I had it inserted on day three of my normally five-day period. My period stopped for 2 days following insertion and then I spotted for one day. After that one day, I have been bleeding heavily ever since, and I'm talking super jumbo tampon every 2-3 hours bleeding. Before receiving Mirena, I talked to my GYN, read the pamphlet and researched online. Each resource told me to expect spotting - so I expected spotting for 3-4 weeks after and I am completely blown away by the constant heavy bleeding that I am now being told could potentially last 3-4 months.

I normally do not use oral contraceptives because of my problems with High Blood Pressure, but my doctor felt the low dosage of hormones in Mirena was "ok" for me. Since insertion, I've experienced a slight raise in my blood pressure but the doctor doesn't seem too concerned about it because I am supposedly "adjusting" to the Mirena. I am slightly worried that my constant bleeding and increased blood pressure are not going to subside in the 3-4 months the doctor is recommending I wait it out.

Not to mention how the constant, constant bleeding is ruining my sex life.

I honestly have no idea what kind of standards or limits I need to be setting here for myself. It has only been two weeks, but how much is too much..? I also have to say I am worried as well since I have to have minor surger in 4 weeks and would hate to have HBP/Anemia complications because of this.

I started reading the posts with all the side effects and kept thinking I'm not having any of these problems, except a slight increase in the number of pimples I get - then someone mentioned how they're tired constantly no matter how much sleep they get. My doctor's been jumping through hoops trying to figure out what's wrong with me and now it looks like it might just be the frickin' Mirena! I've had it for three and a half years and the worst side effects I've thought I had was cramping around the time I usually get my period (something I've NEVER had before - I was always one of the lucky ones) and my skin was oilier. But the exhaustion and increase in my Bipolar symptom may be side effects too? I need to get this stupid thing out.

Although I experienced some mild headaches and sever joint pain for a few days, I am over all very happy with my treatment. As with all medications, there are side effects. I am one of the lucky ones that has seen success with this medication. My appetite has decreased dramatically and I am seeing some pounds fall off.

I am so sorry to those of you who have suffered serious illness from this drug. I wish each of you the best of luck in getting healthy!

well today i got the mirena put in and i didn't feel anything and so far everything is great i go back in a month to make sure its where its suppose to be but as for it being painful it is so not painful its just like getting a pap done you don't feel them put the mirena in at all

I HAD NO PROBLEMS WITH MIRENA. I got it in November of 2007 so a little over a year now. I was 19 when I got it ( and I've never had children). The doctor put numbing spray on me, then gave me a small shot to numb the area before he put it in. It was 10 seconds of REALLLY uncomfortable pain but nothing too unbearable. However, my sister just got it about 2 weeks ago and was put on Vicadin because the pain was so bad.. I bled for about the first 2 months straight.. and after that, nothing. I hardly have any cramps, headaches, mood swings,etc. The day after I got my IUD put it, I went on a similar web site to find these same complaints. I told my boyfriend if he noticed any mood swings, depression, etc. then to let me know and I would have it taken out. Over a year later, it is still in. I am definitely one of the lucky ones that seemed to have no bad experiences. I break out a few times a month but I'm a 20 year old girl and acne runs in my family.. but nothing out of the ordinary. I don't know if maybe the symptoms will come later.. or If i just got really lucky. Everyone is different I guess. My heart goes out to those who weren't as lucky as I was with this.
(If it makes you feel any better, the birth control patch made me break out in hives and puke for 6 hours, the pill made me bleed almost every day, and the shot gave me a bad reaction and I spent the night in the hospital.. so I've had my fair share of bad birth control experiences).

I had a Mirena inserted October 2007. I had it removed in October 2008. I am SO GLAD I had it taken out!!!! When the device was in my body, I had instant weight gain. 5 pounds the first two weeks. Put on a total of 10 in about 3 months. I was working out liek a fiend!! I even did two a day cardio sessions for a month and did the Special K diet with it. Couldn't lose a pound. It was awful.

I had horrible acne. Not just on my face. On my scalp, my back, really gross on my neck. I even had occasional zits on my legs. AND I have DRY skin.

I had no sex drive. And just felt generally in a funk and had frequent headaches. I still had weird sludgy periods at irregular intervals. It just wasn't right. It was a grey mucky color. It was thick. I had never had a single yeast infection in my life until Mirena. I can't tell you how awful this thing is.

Since having it removed a little over a month ago, things have gone back to normal. My face cleared up in a week. I just feel better. I lost about 2 lbs. of water weight the first week. I have since lost another 3 that just slipped off (I cardio about 30 min. 5 times a week and lift weights 3 times a week, but that's not new. It is my routine with or without Mirena.). My husband even commented the other day how much healthier I looked.

DO NOT PUT THIS THING IN YOUR BODY!! My new GYN said to me, "If I won't do it to my wife, my mother & my sister, I won't do it to my clients." He doesn't recommend Mirena and won't use it except in very rare cases. He said if you have one you're unlikely to have your pap come back normal as long as it is in because of the strings. Really, don't listen to the sales pitch. These devices are high profit items for the Doctor's so that's why we women are getting the big sales pitch on them. Don't fall for it!!!

Well, I'm kind of nervous reading these postings now. I just got the Mirena put in today and I had my first child in September. It didn't hurt at all when he put it in, because he used a local anesthetic, but I started having a little cramping after he finished up. Now I'm home and I've noticed that the cramping is a little bit worse than before. I was already on my period (because they said you have to get it put in during your period or immediately after it stops), but it was almost over. Now i'm bleeding a little more, and I'm feeling aching pain in my pelvic area and back. I can't afford those major side effects that have been discussed here. Should I keep it in and wait and see if I am different, or get it out now? I'm worried!

I was prescribed Levaquin yesterday for a severe bronchial infection. I woke up at 3:30am this morning, and my arms were numb from the shoulders to my fingertips. My hands were tingling as if they were "asleep," and my thumbs were drawing inward toward my hand. I could not lift ANYTHING. Also, the joints in my elbows were extremely stiff. I immediately woke my husband up, and we started searching for Levaquin on the internet. I AM SO THANKFUL FOR THE POSTINGS I FOUND ON THIS WEBSITE. I am scared to know what might have happened if I had continued the use of this drug. My fingers, wrists, shoulders, and elbows are so sore right now. I just hope there is no permanent damage to my body.

FINALLY I FEEL LIKE I AM NOT INSANE!!!!!!!!!
I am 27 years and had my Mirena inserted 2 months after my son was born. It has been over a year and I feel so crappy at times I don't know how i get through the day. I have been feeling apprehensive about removing it and thought maybe all of these symptoms have nothing to do with Mirena. I feel dizzy at times like I am drunk, mood swings, my hair is thinning out, i look like I am 9mon pregnant especially when i am PMSing, and have gained weight around the middle section, I don't feel attractive anymore, i don't feel good wearing clothes I once looked good in and always have to wear girdles which do not always work. I have always had acne but now it is ten times worst. I was a very sexual person but now it sucks. It hurts sometimes and I am very dry down there and that is not like me. I have leg cramps every now and then. I am gassy constantly and bloated, which I thought was because of my acid reflux (which existed before mirena). My breast hurt and gets swollen, sometimes one even looks bigger than the next. I just basically feel like I am having an out of body experience and not in a good way. My boyfriend has been nagging me to remove it if I feel so bad, but I am sacred that if I do and the symptoms still persist then what. I have spoken to my gyn so many times about this and he keeps insisting it is not the mirena. He has recently sent me for some lab work related to my breast pain and prescribed some medication to dry out my breast milk, but I have decided against it. Now after reading this site, I definitely am not going to waste money doing this, I am just going to be adamant about it and go get it removed. To think I am a nurse I should know better but I guess I am a woman first. I AM HAPPY I DO NOT FEEL ALONE ANYMORE. CAN ANYONE OUT THERE WHO HAS THIS REMOVED AFTER ALL THOSE SYMPTOMS TELL ME HOW THINGS HAS CHANGED FOR YOU. PLEASE SEND ME A PRIVATE MESSAGE.

SINCERELY,
WANNA GET RID OF MIRENA IN THE VI

I don't know what is wrong with you people but its like you can't handle anything. I had the mirena put in November last year and yeah ok i had cramping for the first month or so and yeah i had spotting. But unlike some of you fools i knew what the side effects were i read what came in the package which means i knew what to expect before i got it put in. And yeah there are loads of possible side effects but if you read everything and know what could happen you shouldn't complain if something does happen. Not everyone who has the mirena has these things and for people who are considering it i would recommend trying it and after 3 months if it doesn't feel good then get it removed. That especially goes to people that have just had a baby... i mean really in the first 3 months after having a baby who is really seriously interested in sex right away. The reason i am here was to see if there was more information about them now because UNFORTUNATELY i had to have mine removed for an operation. I had a cyst on my fallopian tube which was not mirena related. In fact almost all women get them when they are menstruating but they go away. Unfortunately with me they don't go away and this is the 2nd cyst to be removed in 3 years. I am planning on getting a second mirena inserted next week. Because frankly i find it ideal. And yeah i may have had mood swings on occasion while i had it but come on think about it what woman doesn't have mood swings. So sure you can blame everything on the Mirena but for the most part besides then for the people where the mirena got stuck or moved during the time you had it... its all in your head. And like i said before i would recommend the mirena and if after 3 or 4 months it doesn't suit you then go for something else... but don't dismiss it because some people have too much time on their hands and like to spend it whining over everything on the net. Remember with the Mirena you have a 50/50 chance of having symptoms or not. Take that risk before taking the risk of going on the pill and forgetting to take it or going on depo provera and putting on 20 pounds.

okay ladies, I'm not sure what you all are experiencing since I'm not a doctor. But I will tell you that a huge amount of your symptoms can either be age related or post baby related. I have four children ages 15, 6, 5, 3.
The beginning stages of the Mirena granted are not pretty and can last for months. I was having a terrible time with my periods and was out of commission for the first three days of every cycle each month. I have had my Mirena for almost 2 years now and am going on 41. I had to wait it out for about 6 months before seeing any huge improvements. I will tell you this, over eating and NOT eating a healthy diet of fruits and veggies will aggravate bloating and mood swings. You could have these with or without the IUD. I never lost my hair unless I was 3-6 months post partum.
A diet rich in potato chips, bread, meats and cheesy pizza will show on your hair skin and nails. The typical American diet will leave even your special guy moody. As we age the expectation is that we will always feel 18 and I have had to come to grips with how my body ages and how I take care of it. A new baby whether it is your 1st or 4th will cause unwanted fatigue. I still struggle with fatigue because not everyone sleeps thru the night including my hubby so my sleep gets disrupted a lot. There are several things you can do to help your Mirena work for you and not scare you. I NEVER lose my sex drive unless I fail to exercise even a little each week and have fought back with a super charged diet. I'm not perfect at it but boy does it ever help. Sugar has a HUGE impact on your hormones and fatigue level. Limit it. Got to bed as early as you can and avoid late night TV. Don't give your precious zzz's to some silly show that won't help you be a better person any way. Get moving and add a little (or a lot) of weight training to your days- your sex drive will soar and your body will thank you. Pray for wisdom. God will help. Sometimes he uses fatigue to slow me down and focus on what is really important. Granted not everyone can handle an IUD. But if you try a little self care and be patient you might find that it works for you. I had heavy bleeding and at my age the doc said I got it just in time because from 40-50 I could expect more of the same. I am grateful for it because I felt like I was dying every time I had a period. A little fatigue is worth the benefits. Keep in mind that even your little ones get tired. They need naps and they are kids. We need rest in the afternoons too. It's okay to stay off the phone and rest a little if you can. My energy drainers are TV, negative people, talking on the phone too much, eating too much especially when I'm not really hungry, the wrong foods when I do eat, and not getting sleep or exercise. Start small and see if over time it doesn't make a big difference before you throw in the towel. Blessings to all and especially the new mommies.

My Daughter has been the same way .. she had the headaches, stomach pain, very depressed .. she has missed 6 months of school she was afraid to go to school, shopping, and being left alone.. I have put her on medication for her depression, and anxiety . i have her in therapy for this... she is not the same child i just want my beautiful daughter back..We are having a hard time with her from school to he social life.. and from her tring to kill herself.. My daughter is only 13 years old...I think someone needs to pay for this... please there must be help out there...How long must this go on before people (FDA, Merck, ALA, etc.) will take this seriously?!?!?!?!
I want my beautiful katelynn back........................
--

I have decided to get mine out after 10 weeks, going next week, fed up of stomach pain, cramps and weight gain, does it hurt

I wish I would have read the side effects before trying this med on my 4 year old. I've been receiving complaints from his preschool teachers in the last few weeks about him throwing things, hitting kids and adults, yelling, spitting, name calling and the length of time it takes him to calm down. He can't tell me why he is doing these things but can give me a detailed account of all he is doing and to whom and admits its wrong. I've ignored the messages he's sent me saying his stomach hurts even to the point of crying about it 1 day, complaining of headaches that he is sleepy at home and school no matter how early he goes to bed or how late he wakes, a little vomitting, eye swelling occasionally, stuffy nose, thirst leading to increased accidental bed wetting and all this has been going on since he started the med in late July. I even took him to a child psych who said he couldn't find any reason he would act out and that he is well spoken, mannared, entertaining and knowledgeable for his age. Starting today he will never take this med again! The doctor says give him 5 days for the med to be out of his system. I hope this is the problem and feel terrible for putting him, his classmates, and teachers through this.

Have been experiencing the same serious behavioral issues (screaming, launching every toy he has out of his room, knocking over his night stand, hitting, kicking and just being hateful) with my 4 year old who has been on Singulair for 2 years as I'm noticing many of you have here. My wife and I have a wonderful relationship and happy home and tons of love and support from other family that's close buy so the kid has a very nice environment. We have taken him off the medication as of yesterday. I have consulted his doctor but I'm anxious to hear what methods of treatment for the asthma all of have chosen in replacement of Singulair or did you just maintain with an inhaled maintenance program with something like Pulmicort? Also, how long was after taking your child off of Singulair did take to for the outburst to subside and the behavior to become more mellow and normal (what is normal for a 4 year old?). Any info would be greatly appreciated.

Hi,
I am 50 years old. I was diagnosed with as hypo at age 39. My doctor prescribed Synthroid at 25mcg and I have (proudly-ha!) worked my way up to 125mcg. I was always one of the "lucky ones" who could eat any and everything and my weight stayed the same. I am a busy mom of two and a first grade teacher, so the 33 lbs. I have gained since age 39 has not been due to diet changes or sitting around with a bag of chips in front of a TV all day. I also questioned my doctor about this and he just brushed it off. Well, I am tired of not feeling good about myself. My life is in good order except for my weight. I want someone to take this seriously. Should I see a specialist rather than my regular internist?
Wow! I think I just lost a little weight telling you great people about this!
jf

I was a healthy 42 year old male who took Levaquin for a sinus infection. The same day as the Black Box Warning was issued; I was having my third tendon reattachment surgery. I have to wait at least 6 weeks before I can undergo yet a fourth tendon rupture reattachment. At least it takes my mind of the Achilles Tendinopathy, joint pains, headaches, uncontrolled muscle twitching etc. I consider myself one of the lucky ones since so far it has not affected my kidneys, liver, heart, eyes and other side effects that many are dealing with from this class of drugs. I would urge a real journalist to take the time and look at the real number of cases. The Fda numbers are misleading. The clinical data coming from other counties are showing much higher rates of tendon ruptures and other life threatening side effects.

I'm back.. I posted back in June when I've had my Mirena for a few weeks... I go to my GYN on july 29 for my check up.
I can actually be one in a million to say I'm very happy I had this IUD inserted. I have never been able to take the pills. I tried the shot once and had a period for 6 months straight... and that was only ONE injection....
The first couple of weeks I did feel like I had a yeast infection... it burned when I pee'd... It hurt to shower... I started to get frustrated..
I didi wait it out.... I told myself that I would tough it out until my check up appointment and IF I didn't feel better I woudll discuss removal ASAP !!!
but I'm fine ... I did cramp for a couple days after insertion. That is now gone .... I was moody for a few days ..... moodiness is gone.... I still get tired but I notice that is getting back to normal also....
I FOR ONE AM GLAD I HAD MIUD INSERTED !!!!
I say good luck to the rest of you...