Fingertips symptoms and conditions

I feel so relieved to have found this website. I am going to call the doctor and have my Mirena removed ASAP! I have been experiencing many different random health problems lately. Which is strange because I am an extremely healthy person. My husband was laid off from his job and we lost his health insurance, so through all my symptoms I have just been suffering through it because I couldn't afford to go to a million doctors and have a million different tests run to find out the source of my symptoms. It started with itchy hives on all of my joints, elbows, knees, knuckles, toes and fingers. Then a symptom I had gotten during my pregnancies called PUPPP which is basically ugly, little, red bumps that ooze a clear liquid and itch like the dickens on my hands, fingers and legs. Then a big knot developed under the skin on my right wrist. The pain started on top and started radiating all the way around my wrist. Then the numbness, tightness and pin-prick pain occurred in my fingertips, then my hand, then my entire arm went numb from the elbow down. I also had horrible pain in my reproductive area on two different occasions that had me doubled over in pain. It felt exactly like contractions. I also have been bleeding every day for several months. Not enough to call it a full blown period, but bleeding every day. Some days, blood streaked mucus, other days full on blood clots would drain out of me. I've has horrible back pain and have been very fatigued even when I am careful to take care of myself. I also am naturally a very optimistic person who can handle bumps in the road of life, but lately, even though I hate to admit it, I have been down-right depressed. I have lost interest in all my interests, have a hard time shaking off life's set-backs, find myself on the verge of tears a lot, and basically have just wanted to pull the covers over my head and not wake up until I can just feel like myself again. Then last night my lips started to tingle, numb and swell. Then the same thing happened again tonight. I told my husband I am just falling apart and don't know what's wrong with me! I have never had any health problems before and now it's a new symptom practically daily. He said he had been doing some research and that he thought I was allergic to my IUD. I immediately Googled "Allergic reactions + Mirena" and found this website. It is such a relief to know that I might actually have an answer to all my problems. I can hardly wait for the doctor's office to open in the morning, I want this thing out right now and I want my life and ME back!

My experience was a seven day short-lived trip through hell on Topamax.

I began experiencing a constant headache for several months in February 2009 (no prior history of headaches). I am healthy 32 y/o male. After multiple MRI's and CT scans came back negative I had a very severe headache that sent me to the ER. The ER helped arrange for me to see a Neurologist, who after patient listening to my laundry list of symptoms concluded I was having migraines (even though I had no sensitivity to light, sound, or nausea). I had been doing a decent amount of research on headaches and didn’t agree that they were migraines but decided, he’s the neurologist, I should trust him. Let me also say at this point, I am not a person looking for a pill to cure my problems, but I was getting desperate as my headaches were ruining my life. I was prescribed Topamax.

I was suppose to start with three days at 25mg, then go to three days at 50mg, and finally up to 100mg per day. The first three days were uneventful when I hit 50mg and then 75mg…I was out of my mind. I read these messages and see people at 400mg with no problems…it makes me cringe to think of dosing that high. I stopped at 75mg…here were my side-effects. Tingling in my face, lips, hands, arms, and fingertips, chest pains (I do have GERD and it jacked up my GERD bad!!!), pain in the back of head, taste confusion (soda tasting flat), and pressure in my eyes and temples…But those are NOTHING compared to the complete feeling of anxiety that over took my body. I had a mild nervous breakdown at work, became paranoid to the point where I was afraid to do routine tasks. And the MUSCLE SPASMS…those are the worst part. I have muscle spasms all over my body, just random fluttering of muscles in my chest, arms, back, neck, head, and face! I became suicidal and had the worst night terrors ever, of things, that I wasn’t even afraid of.

I have been off Topamax cold turkey for four days now and the anxiety has significantly subsided. I have worked through a lot of the anxiety with my wife and I now believe that stress is the cause of my headaches, not migraines like I tried to tell the doctor…but the muscle spasms have not stopped (they have decreased) yet…but I can’t wait for the Topamax to leave my body.

I used to think these messages boards were part of the problem, but they are very helpful. Do your research before you put anything into your body…trust yourself and if you disagree with your doctor, get a second opinion. This has been a life changing event for me.

Health and Happiness to all

I have been taking half an Ambien (5mg) each night for roughly 3 months. The other day I woke up, and I just felt out of it. Like I was dreaming or something. I started to think I was getting sick, and I think I had a panic or anxiety attack. I'm not sure those words describe what I felt correctly though.

It was like I was in a nightmare. My fingertips and limbs started to get cold, and I couldn't feel anything. I started to sweat really bad. My chest felt really tight. I started to hallucinate a little, and this caused me to freak out even more. It was like I completely lost my mind for a few hours. I just remember thinking that something snapped in my head, and I was never going to be the same.

I called my husband and told him I went crazy, and I was afraid I would never be the same. I told him about the hallucinations, and he thought I might have a really high fever. I tried to take my temp, but I couldn't get my mind to slow down enough to do it. I would start, and then I would think I need to take a cold bath to lower my temp. I would then think of something else and get sidetracked.

My mind was freaking out so fast that I could not keep up. I was talking to myself to try to tell myself there was nothing wrong. I was trying to over-power my thoughts, but this made me think that I was in fact insane. So I would tell myself to shut up. It felt like I was battling myself or my own thoughts at least. My husband came home, and I went to sleep. I woke up feeling just fine a few hours later.

I have been so scared to tell even my Doctor. I am no longer taking the Ambien, and I feel fine. I am just embarrassed by the whole thing, and I don't want to tell anyone about it.

I've only been taking this drug for two days - 25mg in the evening - and I've already got side effects. I get tingling in my fingertips, and all down along the bottom of my fingers. I've been feeling nausea as well, and writing this, my brain feels a little blocked and slow. I also think I'm losing my appetite, which could be a good thing, considering that I do need to lose weight. But I don't think it is worth it if I end up getting side effects like the ones that have been posted by other people.
I'm a writer, and I cannot afford to lose my memory, or suddenly not remember how to spell words, or to communicate effectively. Should I stop taking Topamax?

I've only been on topamax for about a month and a half and already I'm feeling some interesting side effects. In the first week of taking the medication I had such pressure behind my left eye I thought it was going to pop. It eventually went away and has not come back (thank the Lord). I also experienced some pretty nasty numbness, tingling, and uncomfortable pins and needles in my fingertips and toes/sole of my foot. The tingling in my hands usually lasted a few hours and the tingling in my feet only lasted for a couple of minutes. This tingling is never predictable.

Eventually the tingles went away and I was tingle free for a while. But in the past few days they came back. It actually coincided with my PMS. The tingles came back and with intensity about three days before my period started. I was wondering if it was common to have a side effect return or increase in intensity around your menstrual cycle? My hormones are pretty nutty and the reason I'm on topamax is to stop severe migraine auras and slight seizures that are tied to my menstrual cycle.

The feet tingles are the worst. It feels like I'm being jabbed with needles and I hate when it happens while I'm sleeping because it wakes me up and I can't fall back asleep again until they go away... they are that irritating. The hands I can deal with because I'm used to my left arm going numb when I was having the auras.

My sleep patterns have been disturbed because of topamax... I'm not too peeved about that. I still manage to get enough sleep. However there are times when I'm out with friends or having conversations and I'll know the word I want to say and I'll just bust out the wrong one. Like for example saying symphony instead of sympathy. My friends have gotten used to it and know what I'm trying to say. It cracks them up when my word salad produces sexual innuendos on accident when I really mean something else. BUT it's really messing up job interviews at the moment. I'm a bright and articulate person who is getting her BA in Anthroplogy and Archaeology, minor in History and am trying to get research assistant jobs at museums and universities. It's really hard to get a job when you are sitting there sounding like an uneducated moron high on crack.

I haven't had problems with memory, thank the Lord. Even though I've got the word salad going on (and it's strange... the word jumbles are only when I'm speaking... I'm super coherent when typing) I'm not forgetful. I was able to make it through finals week perfect, while juggling a full work load. I hope I don't start losing my memory.

I haven't lost any weight (AW SHUCKS!!!!!). I was looking forward to that one. How soon should I expect to lose weight by, if I do in fact lose weight? I'm a difficult duck when it comes to weight loss. I've been at a stable weight since I was 13. I'm an athlete so my body is my temple sort of thing. But in the past two years I've put on a little bit of unwanted weight in certain areas when I stopped hitting the weight machines :( My question is, if I haven't lost it yet... will I lose any?

I'm also classified as type II bipolar, obsessive compulsive, and anxiety disordered. I've noticed my mood has stabilized. I'm not as all over the place as I used to be. My highs could get pretty high and when they would get up there my obsessive compulsive would almost go on a little joy ride. And when I was low, I was super low and my anxiety would take the depression out for a spin. But now I feel a calmness and a zen that I never felt previously. It's not an apathy I can certainly tell you that. I feel like I am in control of my life. I thank topamax for that.

Reading all of these posts I just worry that the honeymoon period of my medication maybe over. I worry about other side effects cropping up. I think that I can deal with my tingling extremities and that I can manage my word salads. I don't want the pressure in my eye to come back. I also don't want to start exhibiting the other side effects. What is the possibility that I will start exhibiting more side effects or are you generally stuck with what initially presents in the first month or so? My doctor also does NOT intend on increase my dosage. He thinks 50mg once a day will do me just fine. Oh and one last question, anyone else experiencing the side effect increase coinciding with PMS?

Sorry for the super long post! All replies are welcome!

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.

As a Doctor myself I think drugs are NEVER the answer except in EMERGENT issues in Heroic life saving... YOU however and all individuals are and should be MORE accountable for your own health and STOP DEMANDING the Drugs and look to LIFESTYLE changes in DIET and EXERCISE to achieve the GOALS so necessary for quality and quantity of life.... The tools are at your fingertips ... The almighty internet ... And your OWN imaginative mentation is your TRUE limitation... So TAKE control of yourself and BE accountable .... Sorry so blunt but MORE tough love and Educating people is whats needed.... NOT more drugs....

MDG

I had some really odd-ball side effects from Lyrica. I was on 150mg twice a day for fibromyalgia, and it seemed to work initially. I was feeling pretty good, and thought I, too, had found an answer to my aches and pains. After about two months, I noticed that my hair was falling out and turning gray (I was 39 at the time). I hadn't had a menstral period that second month, either. I told every doctor I saw about these strange symptoms, but was prompty ignored.

The third month, I began to gain weight like crazy. I ended up gaining a little over 20lbs during the year-long treatment. My skin was dry and thickening around my thumbs and heels. My energy level began to really go down (it was never that high to begin with). My fingernails became brittle and broke with the slightest provocation. The grayer and falling out hair was coarser, too. I also was either sleeping all the time for days, or then couldn't sleep at all for days.

By the sixth month, I noticed that my wounds were also taking longer to heal. Being diabetic for the last 29 years, I thought that maybe neuropathy was starting to set in. Up to that point, I had never had any signs of neuropathy, and always was in good control of my blood sugar levels. Now, I was beginning to get worried.

The eighth month forward brought cracked heels, cracked toes, cracked fingers and thumbs. I began to have pitting edema, which I immediately informed my Rheumatologist about. I have chronic renal insufficiency, though not diabetic related. It was a gift from my OB/GYN during pregnancy when I became eclamptic. The edema was so bad that blisters appeared on my ankles and would not go away, no matter how high up I rested with my legs. My skin hurt all around my legs, and soon started to notice my face also swelling. Still, no comments from any of my numerous doctors.

After a year of all this strange stuff, I took myself off of the Lyrica. It was a hard choice, as the meds helped to silence the strangling pain in my muscles. Within a month after discontinuing the drug, my period came back. Three months later I noticed that both my hair and nails were stronger, and my hair wasn't falling out as much.

Six months later, and I notice now that my wounds heal like they used to. My hair isn't as coarse, and my nails are much stronger. My sleep schedule is still not right, and I still have the deep cracks and crevices to my thumbs and heels, but it is much better than it had been. I have also since tried Lamictal, but am having tachycardia and shortness of breath, along with a marked rise in my blood pressure. This, too, I discontinued and am feeling somewhat better. The muscle aches and pains and fatigue are back with a vengeance, but I will put up with them as long as I can. I am on so many meds anyway, that my body is probably kissing my toes in thanks!

Luck to all who are on this drug, and hope it works for you without all the weird side effects I put up with!

I have been on Vytorin for about six months. I just recently started experiencing numbness/tingling from the waist down to my feet. I have also experienced it in my forearms and fingertips. Two days ago, I woke up and my face was tingly. My muscles are very week, and I have no energy. I stopped taking it two days ago, but haven't seen any improvement, yet. Hopefully, I'll see some soon. I am drinking lots of water to try to get it out of my system. I am done with statins.

Have any females suffered from decreased sexual desire with this med? I have had the cough, weakness, dizziness, sore throat, runny nose, numbness and tingling in my hands, weakness in lifting with my arms, coughing, and catch my breath a lot. I thought it was just "getting used to the med". I am convinced this is a dangerous med, I am off it for good.

This is an update from my first posting earlier this year. I still have localized pain in my neck and shoulder area sometimes extending down my arms to my fingertips. I am 58 years old and stopped taking Lipitor 5 months ago. I am always in discomfort but the very severe pain comes in waves at least 3-4 times a month and lasts for about 1-2 days. I have noticed an improvement since stopping Lipitor but my cholesterol count is on its way up so I am trying to control that. Not an easy task but at least I am not totally debilitated as I was in January and February. I am totally off all meds and vitamins as of this writing. I am trying to cleanse myself and start over with diet and exercise. Hang tough ... this is definitely the battle of your life!!! KooKoo

I took Doxy last summer for cystic acne. It worked fine and I didn't have any problems, and my skin cleared up nicely. I had some left over (bad, bad, I know but it hasn't yet expired!) so I started taking it again about 4 days ago. I noticed, almost immediately, severe tingling and burning in my fingers and hands and up into my arms when I am out in the sun and for hours afterwards. Also water (like washing my hands) makes the tingly feeling much worse. Weird, right? My two index fingers are bright red and any touch burns.

It's weird because last summer when I was on it I was out in the sun all the time with no problems at all.

I am a 56 year old man who has been suffering of asthma for several years. This spring my doctor put me on Singulair as an additional medicine to my cortisone-inhalator. After one month I have the same experience as many here has told about - depression and periods of "swinging mood", ups and drastical downs.
AND - a growing problem with feeling in my fingertips, seem that with accelerating speed i am loosing feeling in fingertips and now even the hold fingers and parts of my hand, which feels "cold".
Anyone here who recognize these symptoms?

I am upset because neither the Pharmacist or my Doctor were any help. I thought I was going crazy. I have been on this med. for 6 or 7 weeks of which have been absolute misery. I have experienced numbness and tingling in my finger tips, headaches, yellowing of my skin, severe nausea but never throwing up, unable to eat and yet gaining weight, severe dizziness and nearly passing out, fatigue, pain in my legs when I exert myself (climbing stairs to my bedroom), unable to stay asleep at night, leg cramps, stomach pains, anxiety!!, depression, grouchy, extreme bleeding with my monthly cycle (my normal cycle is 3 to 5 days this cycle lasted 3 weeks and counting), coldness, heart palpitations, chest pains, wheezing and deep dry hacking cough. I just felt like I was going to die also thought it could possibly be menopause, low blood pressure (90/60). Because BP was low I took 1/2 the dosage day before yesterday (5mg). Yesterday I stopped taking it altogether and I was able to eat (yeah!!!!) with only minor nausea. Today my legs are not hurting as bad going up and down the stairs and my bleeding has really slowed down. I don't have a headache but I am still coughing and am having the problem with the numbness and tingling in my fingertips. I see dramatic improvement. I believe if my husband had not researched the side effects of this drug online, it would have killed me. Also he thinks that women should not take this drug because of the emotional impact on the husband! Also I am so angry that his happened to me in full sight of the medical professionals !@!@!@ I will be posting this message on as many medical sites that will take it.

I first posted about 6 weeks ago when I began taking Topamax at 25mg a day. I'm now up to 100mg a day, 50mg am/pm and surprisingly it seems that most of my side effects have subsided. I have the tingling in my fingertips and feet now that I didn't have before, but it is rare and not something that keeps me from any normal activity. Sodas still taste flat but I've adjusted to that, beer is something that also tastes flat and that is rather disappointing. The only thing I've noticed is that I tend to have a slight headache most of the time that taking Advil will cure. I don't know if this is caused by the Topamax. When I do feel a migraine coming on, it seems to take days and never fully matriculates and I have to get a shot of Toradol. All in all, this is much better than the weekly migraines I was having.

I am having tingling burning sensation in my feet, legs and hands and arms. My blood pressure was not improving on 5 mg so I upped it to 10 and those symptoms are much worse. The tingling sensation goes all the way up my left arm and up above my knees on my legs.

I have tried to take the Lisinipril before and stopped for these same reasons. My doctor does not seem to think that it is due to the Lisinipril. so I tried it again and the burning, burning sensation is driving me crazy and keeping me awake. I have to get up and stand in cold water for a while to get some relief.

I have not read about anyone with the same symptoms. Does anyone out there have these symptoms??

I have been on topamax since Nov. 06. My psychiatrist started me on 25 mg and moved me up to 100 mg. He put me on this medication because I asked him about undergoing a gastric bypass for weight loss and wanted me to try medication first. My symptoms are tingling fingertips and feet. I have also had a chronic cough (sometimes so violent I vomit) from a cold that I have been unable to get rid of. I read on a web site that Topamax can cause a chronic cough. Also, carbonated beverages taste flat to me now. I have lost about 20 pounds but I don't think the sides effects I am having are worth the weight loss.

I was on 10 mg. of lisinopril for about 2 months when I noticed that my left foot and my left hand frequently felt heavy, as if they had fallen asleep. My PCP checked me out and confirmed that I was not having heart problems. Then, I also experienced the "buzzing" sensation in my left hand and left foot. This happened frequently while I was taking the drug. I also experienced a burning sensation in the fingertips on my left hand and the muscles in my left arm ached.

Finally, I stopped taking the medication about four weeks ago and the sensations in my hand and foot greatly subsided, athough they did not go away completely. Ironically, a week after stopping the medication, I developed the achy joints (hand, knees and elbows) that many of you have complained about. Now, four weeks later, all symptoms have lessend substantially. I occasionally get a transient achiness in my knuckles and occasionally I feel some of the strange sensations in my left hand that I have listed above.

I just wanted to let those of you that are experiencing strange neurological reactions to this drug know that you are not alone; I went through what you are going through and possibly more and endured some of the worst weeks that I have ever experienced in my whole life; For weeks I was gripped by the fear that I was developing lupus or MS.

So, if you are struggling with some of these problems, be brave and stand up to your PCP and tell her that you WILL NOT take this drug anymore. I'm sure that you will find as I have that quitting lisinopril will restore your sanity and hope of having a happy, healthy future.

I am a 41 year old woman who has been on Toprol for 2 years. At first there were no problems, and a pleasant side effect was that my chronic migraines were greatly reduced! However, of late, I have been experiencing EXTREME sleepiness, sometimes even first thing in the morning after a good full night of sleep! I have been nervous to drive because of how sleepy I feel. I can barely keep my eyes open anymore, and the muscles of my eyes are even tired from trying to keep them open! I also have extremely dry eyes, atrial flutter, numb and tingling fingertips. The symptoms definately got worse when I went from taking 50 mg to 100 mg per day. I am glad I finally got worried enough to investigate the side effects on the internet. Thanks for your site! I will be talking to my doctor about slowly getting off Toprol and trying another medication for my high blood pressure. The best medicine is Exercise!

my doctor just put me on lipitor two weeks ago i have been hurting all over my legs are killing me cant sleep they ache all night cant hardly walk if i stand very long and i too have trouble lifting my arms up it hurts to my fingertips dont know if this is a side effect of it or not but i also am having swelling in my lymph nodes below my armpits does anyone have this problem im going to stop takin this drug as of now and see how it goes i cant take this pain anymore and function

During the first month of use I had a severe migrane headache. It was the worst headahce of my life. I litterally could not stand up for an entire day, if I did I felt light headed and my heart rate was very fast. I also had a numbness in my fingertips. It only lasted one day but it was VERY severe. My Dr. said to discontinue Nuva Ring

I am having tingling and numbness in feet and fingertips. Additionally my period has stopped coming on.

I have very high blood pressure. I was on a beta blocker for years (my heart runs extremely fast) to slow the heart down. Too many side effects - asked the doctor to change. First of all NEVER go off of a beta blocker cold turkey (yuk). Anyway, my heart is really fast (I am on 240 mg). It seems that my heart still is running extremely fast and I have developed the most horrible pain in both of my arms. It is from my elbows down to my fingertips. It feels like someone is squeezing my arm really tight. My fingers are tingly. Is this a possible side effect or has anybody ever experienced this before?????

vasculitus churg-strauss syndrome resulting in the amputation of two fingertips and diabetic neuropothy in both feet.

@twogirlsmum:

I'm very relieved to hear that you're not goin to take Mirena, because I really read of so many women suffering in a very similar way as we all do here from Yasmin...

<<<>>

Well, I had that feelings, too. Not in the tops of my arms, but in my feet and fingertips. Most of the time just ONE finger or one little point at my feet or such. Felt just like someone had dropped a little bit of warm water on it for a second... VEry strange feeling which always made me look at my finger or foot to reassure myself, that there isn't anything on it, that could have caused that warm feelings... Seems to be another nice Yasmin symptom...

Girls, better times are ahead. I'm so glad to see, that every day more and more women come around here and are finally able to put 2 and 2 together and get off that Yasmin poison as fast as possible!! well, not glad to hear, that most of you are going through the same or similar torture as many of us... But glad to see, that they all finally have a solution for their health problems and see a light at the end of the tunnel!!

I really thank god for this and other sites in the www helping us that way where doctors don't seem to be able to do anything for us, but tell us, that it's all just us!!! Here they could find so much evidence of their mistakes...

Greetings to all of you out there, especially chrissy, lisa,
and every other woman here, that is finally guiding others here on their way after being very anxious about the future and not believing that there will be better times after Yasmin!! :) I think of you all every day and pray for you!!

Big hugs go out to everyone!!

Silke