Nails symptoms and conditions

Everyone's posts have really helped me. I got Mirena inserted a year and a half ago right after my son was born. I thought it was the best option of BC because everyone was doing it. and only today I found out about it's symptoms from a friend. I am very moody and mean to my husband and son and I don't even know why. I have had HORRIBLE acne on my back and arms and sometimes my face.. It started out with just really oily skin like i could literally scrape off the oil with my nails and losing wads of hair with every shower. I thought it was my water and I even went out and got a shower head water filter and started using organic shampoo and soaps but the problem never went away it just got worse. I am constantly popping tiny wax balls from under my skin. I have a weird odor that i thought i would always have now because i had a baby or something. Sometimes I have a really thick mucus discharge that i have to pull out with toilet paper. And lastly I can't sleep through the night to save my life unless i take a dose of melatonin. The doctor never told me any of these side effects at least i would have known what was going on. This site and your posts helped me because i thought i was going CRAZY. and i thought that my marriage was just going to have to be the way that it was (unhappy with a side of no libido) because now we have a baby... coincidentally we also have Mirena. I'm getting it out ASAP I'm glad i'm not alone.

I love It! I have been experiencing low back pain when standing for over a year. I could hardly walk when I crawled out of the bed in the mornings. I was diagnosed with one point away from osteoporosis. The supportive tissue between my discs was deteriorating. I was given Evista to drive the calcium into the bone along with Limbrel 500 mg twice a day for the arthritic pain. My nails have become stronger which to me indicates my muscular structure must be getting stronger. I took Naproxen and Arthrotec previously to Limbrel and experienced severe stomach distress. I am 65 and I see a daily improvement from my previous condition. I have never experienced fever or chills. I am almost totally pain free and look forward to the future continuing to take Limbrel!

I am 29 years old and started taking Yasmin in January 2009....by month 2 I had severe pain in the nail bed of both hands....I kept hoping it would just go away...then 2 weeks later both hands hurt not just the nails...I started having to take advil just to get through the day...I figured it was the side effects of Yasmin b/c it was the only change in my lifestyle...I kept taking it thinking perhaps it was just my body trying to adjust....a couple weeks later my arms started to hurt....long story short, I stopped taking the pill in June 2009 and had to fly to my mother's house for help b/c I had gotten to the point that I was barely mobile and everything hurt...I felt like I was in an 80 year old's body....I had severe joint and muscle pains everywhere and I starting looking like Professor Klump, my hands and feet where so swollen I couldn't do anything (even picking up a pillow to make the bed hurt)...I asked my doctor if it could be the Yaz and he insisted no....I was told that it looks like I have arthritis...but I stuck to my guns and said that it was way too much of a coincidence that my health started deteriorating around the start of Yasmin.....my doctor decided that he could help me detox my body to get rid of any Yaz left in there and to see how I felt after....he did put me on celebrex (arthritis med) to relieve the inflammation and pain...I am also taking a diuretic to flush out my system...I am on day 2 and already feel better...I'm not sure if it's b/c of the celebrex or the detox, but I will know in 2 weeks when I finish all the meds.....after reading all these stories I feel a bit of relief...I'm not crazy, these symptoms really could be b/c of the Yaz!!

I was given Cymbalta to help me deal with chronic pain. For the last 7 years I have tried one thing then another.....this was a drug I actually asked for...I thought I knew the side effects. Well my nails look like I filed groves into them after 2 weeks and now I have all but lost the hearing in my left ear. I have quit taking the cymbalta...and have been seen twice now for my ear(s). Nothing is adding up....it came on all of a sudden. It has been very hard to cope with and now my right ear is acting the same as the left. I am scheduled to see a ENT in a week.
Anyone else had these type of symptoms...and did your hearing come back??? I'm only hearing out of one ear.

I an 34 and have one child, 7 years old. These are the changes I have experienced since I started the Mirena in December 2008. Each is something that wasn't the case before.

Until now, May 2009, I have gained 15 pounds. My stomach is bloated, my hair oily, no sex drive, and depressed and tired all the time. I get a lot of infections, and a yellow-brown discharge all the time. Spend a fortune in pads/pantiliners. I get joint pains on my legs and hips, and my nails have become brittle. I itch a lot like something bit me. My period is lighter.

I was on Topamax for migraine a few years ago and had to go off of it because my insurance changed. I was crushed!! I was on a lowww dose- only 25mg. morning and night. It helped soooo much- and really- the only side effect was some weight loss and the tingly fingers and maybe weird taste in foods.Also- and maybe it's because I;m relieved of constant headaches- I have MORE energy and even better breathing, seemingly!! ( just now had a problem spelling 'taste'- and have read where that is a side effect but think for me it's just being 51 and a tad flaky with menopause. :) ) I'm back on it now- 25 mg. morning and night- and am very happy. The several times a week migraines ( the real thing) are gone- as are the constant floaters I get in front of my vision, and the things like vertigo and photo-phobia that I have constantly even when I'm not in a full-blown migraine. I just don't get the fatigue, headaches, etc. other people do- in fact, almost nothing by way of side effects. That is no doubt due to the low dose and also because everyone's system is different. I am lucky to have found the one med which nails my migraines! I've read all the posts and am definitely upping my water intake, however- thanks for that head's-up! It never hurts! I would say that anyone with intractable migraine should at least try it- although at a low dose. My doc is very cautious and started at the lowest possible end luckily for me.If you're one of the fortunate people who toleates this med it definitely works beautifully to prevent the majority of migraines in chronic sufferers! It IS expensive, though-even in it's generic form- and I really hope to keep affording it!!
Blessings- A.

No question, Cymbalta caused me to have psoriasis of my nails and on my feet. My nails started looking funny and ridged a few weeks after taking the Cymbalta, and I could not get the callouses off my feet to save my life, and they were so itchy and flaky. I took it for about 6 months and the psoriasis got worse and worse, I had a few spots in other places on my body but they were small. I switched off the Cymbalta and immediately my nails started growing back normally and the callouses and dry spots on my feet and elbows went away.

I received my first shot on Kenalog three weeks ago, for a bulging disc in L5, and it took me from a 8 out of 10 pain scale, to a 2. After two weeks , I received my second shot, and now I feel about 98% better. As an added bonus, my Psoriasis of 15 years, that no Doctor could seem to control, has all but disappeared! Also a severe pain in my r/foot under 2nd tow area, has completely gone away, after 10 years of misery! I also am seeing my two toenails, and one fingernail restoring themselves to normal again(the nails had fallen off years ago, like a fungus, but it was not fungus). My dermatologist told me it had no cure and that I would have to deal with it! Kenalog benefits have FAR outweighed the negative effects so far... I have lost about 5lbs in 3 weeks, and anxiety is a mild issue, as is mild night sweats, but for me, this is a small price to pay for pain relief that was making my life miserable!

This post is directed to anyone who has contacted me regarding a possible class action lawsuit, which I was trying to initiate, as stated in my Oct 17th, 2008 post.
After contacting as many as 10 law firms, from NY to San Francisco, I have virtually "thrown in the towel". In essence, what they are saying is, this will be too expensive to litigate. The pharmaceutical companies have "teams" of lawyers, and I believe they are reluctant to go up against them.
I find it diabolical that this drug Kenalog is causing so much suffering, some emotional, some esthetic and some, like myself, sheer physical pain...but nothing can be done about it.
For all of you who have emailed me and I was unable to return your ems, I apologize....but I have been waiting to hear something positive feedback to relay. Unfortunately, that was not the case. If anything does develop I have stored your information and will get back to you. I would hope you would do the same.

I've been taking lamictal for btwn 2 and 3 years now, for depression and as a mood stabilizer. I was on wellbutrin 300 mg, and then I had an episode of severe depression (crying all the time) while on the wellbutrin. So my doctor added lamictal, gradually going up to 200 mg.

It works, and I haven't had a really severe depressive episode since (except for circumstantial reasons), although I'm generally mildly depressed.

Side effects: My fingernails have weakened, and some have ridges down the middle that are so weak they become cracks even if there is only 1 mm of white nail growth. I thought it might be a nutritional deficiency, but I eat healthily, and I finally decided to look into the side effects of my meds. Others on this site are talking about hair loss -- I'm quite sure the nail problem is from the lamictal, as hair and nails are produced in similar ways.

I yawn every few minutes, whether or not I'm tired, which at least one other person on this forum mentioned as well, as a less common side effect. (I'd figured this was due to one of my meds -- now I know which one it is.)
I've also been concerned that I'm klutzier than normal lately. After reading everything on this site, I've just decided to start weaning myself from 200 mg towards a lower dose of 100 mg. I don't think I'll go off of it entirely, b/c it works.
One last thing I have to say is that I really recommend ACUPUNCTURE for any mood disorders. I get it for free at a school in Chicago (it's often a long wait, but free!), and many bigger cities probably have an acupuncture school where it will be cheap, if you're on a budget like I am. Occasionally, insurance covers acupuncture. Anyway, I try to go once a week, and it helps tremendously with my depression, migraines, and general energy level-- it has a very powerful cumulative effect! When I stop going, I notice huge differences emotionally, and I get a lot more migraines. My mom and sister have also had very positive experiences using acupuncture for depression and anxiety.

I actually ask to be treated for my headaches, not specifically depression, but it helps me a lot with both issues. I really can't say enough about how wonderful acupuncture is, and how much it's changed my life. Last time I was medication-free, 5 years ago, I was going to acupuncture every week for many months, and it was enough! Just don't expect it to work overnight -- just be consistent and give it some time. When I first started going every week, I noticed a difference after a month or so, although the treatments generally leave me feeling relaxed and good right afterward as well.

terry's nails, white nails,half and half nails and smell like ammonia, lactaid milk. made lattes with it.

lactaid milk for a NON lactose intolerant person! eating regular dairy all day long, lots of normal cheese and ice cream daily... bought the lactaid for my cat..but ended up making COFFEE with it..latte style.. a full 8-10 ounces...
for a month now... and ended up with an ammonia smell to my urine and underarms..skin in general.. afraid of kidney problems as I also developed TERRY's NAILS..or "half and half nails" WHITE nails!!! the ammonia smell and the white nails indicate kidney troubles... my tests came back normal for kidney and liver... I attribute this to the lactaid so I hope this helps someone who may read this!!! these symptoms 100% coincide with the lactaid, NOTHING else is different in my diet..maybe my body got confused having lactase enzyme..AND normal dairy at same time.? maybe its not for people who are NOT lactose intolerant or for people who will ALSO include some regular dairy in their day... (without use of tablets) from what ive read here, you people are mistakenly believing you are intolerant... when all you need is probably PROBIOTICS after a course of antibiotics..which killed your healthy bacterias..and rendered you ineffective at digestion. That happened to me. takes months to re-establish the bacterias..and can even be a YEAR or two even, AFTER you took antibiotics that your digestion finally gave up..your antibiotic use didn't have to be "recent"
Thank you

okay;; im sure your supposed to stay on these pills for awhile to get used to them. but i was on apri before;; and hated it and im considering switching back. this was the worst pill i had ever taken! im only done with my first row and half of the second and so far here is what happened :: im having a lot of aggression didn't happen until i was on this pill. i have grabbed my sister and dug my nails into her and i bit myself;; why i don't know. i drew blood both times. normally im the type of girl who cries when upset and im always happy. i don't ever do those things. i already got my period and i take them at the exact same time every day! never missed any of them. with bad cramps. they are putting me on Yasmin;; which idk about. if Yasmin don't work im switching back to apri. oh and this pill didn't help with acne at all;; it actually broke my face out. apri helped me with that. anyways i don't think it was for me and other websites have shown its clearly not for a lot of people.

I have been taking 300mg of Wellbutrin XL since 2005. The doctor prescribed it to me due to major depression. Ever since then my hair is thinning, I used to have really thick hair and now its very thin. I have severe ringing of the ears, if I am in a quiet room I can't concentrate. The worst of it all is that I have extreme paranoia. I constantly worry about EVERYTHING! I have to sleep with the lights on and have to have the TV on at night as well. Sometimes I hear things or see things that aren't there. I can not sleep on this medicine what so ever, so they put me on another medicine to help me sleep. I am going to tell my doctor I want off of it now! I can't stand it! I get so worked up over it I feel like I am going to have a heart attack. I also shake like crazy when I get scared. When I go to get my nails done my hands tremble and they ask me to relax when I can't.

I Just started the lupron injection 2 weeks ago. My side effects have been coming one by one immediately after i had my shot my whole right side felt sore like my arm down to my leg. two days later i felt really sleepy and kept getting headaches that would come an go through out the day.a week into it i had to leave work because i was vomiting constantly it was horrible a just felt so sea sick. i just want to know what else am i in store for? an i'd like to know how much hair loss is it going to be?

For me having the Mirena removed just last Thursday was the right decision. I was not using it for birth control but as hormone therapy for heavy, crampy periods. I had it inserted in July 2008 and bled every single day for the entire time, I had it removed last week and now I am bleeding very heavily but hopefully that will stop once all those hormones are out of my body.
While on Mirena I lost all sex drive, I became severely anemic and with that fatigued terribly, and moody, crying at nothing and screaming at my kids or husband for stupid reasons, I felt bloated and gassy and didn't have those problems before.
I am 42 years old and I hate my heavy bleeding in fact I want a hysterectomy, but not sure now what I will do.

For those of you who had the Mirena removed, how long did it take to stop bleeding afterwards? This is draining every last ounce of energy for me and I am taking iron supplements.

What sucks is the cost of this, Even with insurance I ended up paying a lot out of pocket to get this thing and then all the Dr. visits due to bleeding and side affects in the 4 months it was in and now the removal of it. I am wondering if there is any way that we can get a Class action lawsuit against Bayer for this horrible thing they are trying to sell to women.
I know there are some out there who have not suffered all these horrible side effects at least not yet or that they are aware of, but I truly believe that there is nothing good about this IUD and those of us and there are a lot of us who have suffered with this should be reimbursed or compensated for the pain and loss of parts of our lives and expenses with this. Does anyone else have any thoughts on this?

Three years ago I was prescribed Levaquin for an infection. After the Levaquin I was unable to stay up in my wheelchair for more than two hours. I started taking two extra strength Tylenol and I was able to increase that to three hours. I added Naproxen 325 mg and that has decreased the pain and has also increased the time in my wheelchair by about an hour. I am also on a drug called Lyrica 150 mg which has decreased the pain further. I am a quadriplegic so I cannot feel anything below my shoulders but my body responds to pain. I can tell that my body is in constant pain but of course I cannot feel were it's coming from. Ever since the Levaquin I also have a condition called Terry's nails. I looked at this condition on the Internet and is says that Terry's nails occurs when the body is in distress usually with kidney disease or liver disease or cancer. I've had more blood tests than I can count and all of them are normal. My body's sensitivity to pain appears to be getting worse. I'm not sure what can help anymore, have any of you found anything out about pain management?

I love the vitamin...23 y/o not trying for pregnancy but was looking for a multivitamin, Prenate Elite was recommended by my doc. I've been using for about 6-7 months and I've seen extra growth in my hair and nails. The pill goes down easy and doesn't have a bad taste either. Is not too hard on stomach and has also relieved my occasional constipation.

Taking nicomide while taking Celexa and a b-complex for hair and nails. I read somewhere that nicotinamide may have anxiolytic effect. Not sure if this combination of vit B3 along with the other B vitamins and an SSRI is causing the SSRI to be less or more effective, but have experienced I think a tranquilizing effect, more noticeable at night. But at the same time I feel some depression and anxiety so I wonder if the Celexa concentration is being decreased secondary to the vitamins. I will stop taking all B vitamins for a few days and see how I feel. My work environment lately has been more stressful, too, so it's hard to say what exactly is going on. But will stop all B vits and see how I feel.

I took Yasmin for about two years, and never felt great on it. The first year, I was about 45 pounds heavier than the second, and the second, I started developing terrible side effects (depression, weepiness, paranoia, mood swings, general lethargy, extreme fatigue). I had the worst abdominal bloating (remember, all diuretics have a rebound effect) and most annoying, my nails started shredding and about 1/4 of my (lucky it was thick to begin with) hair fell out! Turns out Yasmin can affect the follicular cycle. THEN, my doctor pushed Yaz on me, though I expressly did not want to take it knowing it was simply a lower dose of Yasmin. She made me stick with it for four long, horrible months--it ruined my life!! It make me cry at the drop of a hat, practically suicidal, extremely moody, gave me TERRIBLE PMS like I hadn't had since I was 17 (I'm 33) and nausea, dizziness, and a spaced-out feeling. I became paranoid about all my friends, and have been jumping on my dear boyfriend for everything and overreacting to the slightest thing. From other stuff I have read, Yaz only works for people with terrible PMS already, or who have acne--I had neither. Whatever chemical is in this pill should be taken off the market--I am furious I was subjected to this, and horrified and so sorry to hear of the losses of loved ones above. Yas is terrible! I just finally switched to Loestrin, and am crossing my fingers. Yaz also gave me terrible bloating, gas and digestive problems.

Placed 6/19/08. Started period two weeks later. Daily period since. Now I am certain I am anemic. Extreme fatigue, weakness, bruises, nails chipping, hair falling out and I've lost 8 pounds. Also experiencing bizarre anxiety attacks - especially at night - almost panic with numbness in arm and tight chest.

I wish I could stick it out like some of you did but I am throwing in the towel. I will have it removed next week.

My 9 year old son only took Singuliar for about 5 weeks. He had side effects almost immediately, he was so aggressive, angry all the time, headaches, stomach ache and feeling like he was going to throw up, bad nightmares, a horrible rash, biting his nails, not focusing in school and got into trouble all the time, no appetite but his little body seem puffy all over. He has been off this medication for 3 months and he is still not 100%. He cries at little things and still has the same rash and with meds it is not going away. He had to change schools as he still was having problems in school. He just seems like he is not the same little boy and something is just not right. I do not know what to do at this point. Doctors say it should be out of his system by now, but if it is than there is permanent damage to his brain as he is just not the sharp little guy he was. We have had to take him out of all sports. Anyone else having these same problems???

WOW!!! I am glad I came across this website. I have twin boys that will be 7 this month. One has been on Singulair for about 3 years for allergy induced asthma and my other son has been on it for 9 months for allergies. I am taking them both off of it today. The son that is taking the medicine for 3 years has become increasingly angry and gets upset over small things. Over Memorial weekend, he lost a game he was playing on the wii and exploded. He was banging his head and then started to hit me. NEVER in my life have I seen him attack anyone. A few days later he threw rocks at his friend because he wanted the wagon. Over the past 3 years I have noticed some change in him and just took it as growing pains. He has always been a strong will child. However, over the past 3 years he has gotten worse and since he has physically attacked me and his friend, I have decided to send him to counseling. Now I firmly believe it is the Singulair.

My other son has been on it since August. He started to have anxiety within a month of taking it. His behavior has been stressed, depressed and not wanting to play with other kids. He was biting his nails to a nub, licking his hands, not talking to anyone at school and rubbing his head. I have also noticed he does like to look at the person he is talking too. Of course I thought the worse and thought he was being molested. I went to his Teacher and she has worked very hard with him, but he is still a loner. If you knew him before, he played with everyone and enjoyed life. I was told by his Ped. that he had anxiety and to have him see a shrink.

I am hoping that after taking them both off this medicine, I will see improvement.

I am 54 years old and on simvastatin for the past year. My nails have become brittle and break off easily. I have never had this problem before.
On the up side, my symptoms of GERD are better and my joint pains have also improved. I also used to have bleeding from gums while brushing (I do realise it is from plaque build up) but that has disappeared since I started simvastatin. When I stopped the medication for a month, the bleeding re-started from my gums. Simvastatin seems to have an anti-inflammatory effect, but I am worried about what it is doing to my nails. If my nails are getting brittle (? dehydration of cartilage), is it doing the same to the cartilage in other places too, e.g. knees and hips etc?