Cod liver oil symptoms and conditions

52 years never had a problem sleeping, began lisinopril for blood pressure which was very high. Began five weeks ago.

Thank you for this website and for all your contributions. It has certainly informed me about what is causing these recent problems.
Side effects so far:

Insomnia
Excessive stomach gas
Hideous Smelly gas
Bloat
Diarrhea
Indigestion / acid reflux
Irritating cough
Vomiting twice so far.
Dry throat and mouth
Dry eyes

typo's on keyboard becoming an irritation, can't believe so many mistakes since medication was increased to 10 mil.

Required: Huge saucepan / stockpot, Hawthorn berries and leaves, plastic screw top fizzy drinks bottles clean.
Taking Hawthorn syrup

Which is made from berries collected locally leaves and berry's, "carrier bag full" washed and boiled for 20 minutes, allowed to cool, strained water / juice and then more water added repeating and boiling for 10 minutes more again allowing to cool and strained and press out all liquid using small plate pressed into the strainer. Combine both lots of liquid in saucepan and Re-boil adding preserving / jam sugar to taste, allow to cool and fill clean plastic bottles 3/4 full and compress bottle until all the air is gone. screw on cap and store in freezer over the winter so you can make lots. The flowers and leaves can be harvested the following year to make lighter syrup. I drink about half a cup 3 times a day.

Tastes very nice too.

Blood pressure is now normal most of the time so going to ditch the lisinopril and report findings back to doctor who happens to be a good friend of the family.

Also taking chelated potassium, cod liver oil and fish oil, calcium, garlic pearls and making own bread using Black Salt instead of sodium chloride. Use Black salt on everything now.

Check out my research on “Inclined Therapy” or google “Andrew K Fetcher” this may help your BP also.

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

I was using every excuse possible for what I have been experiencing. I started NR in May, now it's December, I was scheduled to take it out. Since I started I noticed acne, which I never had even in my teen years. I blamed it on the towels in the gym, stopped using those, then on the sweat from workout... kept trying new acne treatments, but acne magically disappears during the ring out days. I'm not sure if I can call depression, what I felt, it was like I'm never happy with anything and many days in a month my thoughts were very dark, unhappy. I noticed serious decrease in energy, blaming it on 2 children, but my son was a year old when I started NR and I had more energy before with newborn and a toddler daughter. Again I thought, he's so active... I have hard time getting out of bed, sometimes sleep is ok, sometimes no sleep for hours, but this happens to many people. night sweats I was blaming on the blanket, the thinnest one we have(my husband uses 2 at night), I was waking up many days in a month drenched in sweat. No discharge, yeast infection for me, lower sex drive. Even more interesting- I noticed the smell of my partner to be less attractive... Then I read in a magazine that BC messes up with the smell as well. I had horrible headaches, feeling I'm going to pass out< dizzy< especially if I was trying to rush(blamed it on rushing too much). I was growling(like my daughter said) at the kids with the smallest mischief, it's like a little bomb heating up and bursting in my head, I felt rage, not anger, total rage.Life has lost any appeal for me, this is not living, just suffering, I thought all the time. But here I am at home with two little children, hardly ever see friends, always doing work around the house, laundry. Hot flashes during the day are frequent and I feel like I want to tear my clothes off. Recently I started to have a lot of pressure in my chest, like it's hard to breathe. Just last week I almost went to the ER, because I was laying on the couch unable to speak out loud, just whispering, could not move. Then couple of days ago my heart started to ache, it aches now, so last night I looked up the side effects of NR, because I didn't even know where to start with this condition, that has all these symptoms I have been listing. I was planning to go to the doc for all the test. My stomach has been hurting slightly in the last 3-4 weeks(I thought it was food, but no one in our family had any problems). I am 28year old in great shape(I cut back on my food intake to keep th weight the same), I work out 2 times a week and have a very active lifestyle. My relationship with my husband is great, my children are well behaved for their age, So I'm stopping NR before I get divorced like some other women did. If you want to try NR go ahead, it's really convenient, but be aware of all these side effects, so you know, it's not something else, before it's too late.

My now 17 year old daughter was prescribed Yaz back on 7/12/07. Since then she has had an extreme problem with constipation. She has been to the doctors several times, and is now seeing a gastrointestinal specialist because she can only have a bowel movement if she takes a laxative. The pediatric doctor had her on miralax from April to October trying to get this problem under control. It has not worked. We are seeing the specialist and they are running her through a battery of tests, which will now possible include a colonoscopy (at 17 !!!!). She has been extremely moody and aggravated - which I attributed to her age of course. She is no longer extremely athletic, she doesn't really do a lot. She is not the same person, definitely is a homebody now - never going out hardly with friends,etc. She has also had a 20 pound weight gain and for a tiny girl, this has had a huge effect on her. I have watched all of this, and never really thought about the yaz connection until today when a friend sent me this email with a link to this site:
******

that is when I got scared thinking maybe her problems were all caused by yaz. of course her acne cleared up, but her periods are still irregular and spotty. has anyone else experienced the bowel problems???

I was on prednisone while getting over pneumonia to help with my breathing. I was only on it for 7 days and the doctor didn't have me go off of it gradually. I missed the last dose on the 7th day and by bedtime, my muscles were sore enough it almost hurt to lay down. I took the last pill that night before I went to bed and had no muscle soreness in the morning. After that, the muscle soreness came back, along with dizziness. My pulse was also higher than normal. Two days later at night, I was still having muscle soreness and dizziness, although not nearly as but, but I was having a lot of trouble breathing and my pulse would refuse to go below 100 no matter what I did and the problems continued thought the night. The next morning I went to the clinic that prescribed me the predisone because the information they gave me said to see a doctor if these problems persisted. I told them I thought I might be having a predisone withdrawal because my mother, a nurse, said it was the most likely problem from experience. They completely ignored that saying it had been several days since I've stopped the steroid and kept asking me about my asthma (inhalers weren't working and it was definitely not an asthma attack -- I've had plenty of those, to all different degrees) and ended up giving me medicine for anxiety, which helped the closing of my throat, but none of my other symptoms. Three days later, my resting pulse is down to 80, but my breathing is so much worse than it would be with just my normal asthma and taking my inhalers as much as is allowed. I had no noticeable symptoms when I was on the prednisone except being less able to sleep. If it keeps up, I intend to go to a different doctor to see what is really happening, but I don't think it's 'normal' to have the withdrawal symptoms for this long after only having it for 7 days. I know I took it when I was younger (I'm 22), but I don't remember ever having issues going off of it before.

I was prescribed Zocor for high cholesterol. Almost immediately I began to experience body aches -- some days more severe than others. I would take ibuprofen and it would help. Then, I started getting a pretty strong pain on my hip which radiated down my leg onto my foot. The pain was so severe, even the Motrin 800 mg. pills didn't help it. I am 53 years old, but I felt like a 90 year old. I had problems walking, especially after sitting for an hour or so. I had problems with stairs. Even laying down was painful. I tried heating pads, ointments, etc. When I told my doctor about it, she said that this was a typical side effect of statins, and that because I am diabetic, I need to continue taking Zocor to keep my cholesterol down. Just the other day, I stopped taking Zocor for 3 glorious days and guess what? NO pain!!! I resumed it because my doctor insists that I stay on it, but I wish there was something else I could take that wouldn't cause pain.

I stumbled onto this site while trying to find a reason for these headaches I get sometimes for no" apparent" reason. Imagine my surprise to find your testimonies about your lives on warfarin sodium.At 38, I had surgery to repair a congenital defect of the aortic valve and had to have a hema-shield graph to repair an aneurysm of the aorta. That was in Oct.2002. Warfarin has been a part of my life since then. I was also put on anti-depressants because my family Dr. thought I was depressed since I repeatedly complained of not feeling well.(I took myself off the anti-depressants a couple of years ago.) Extreme fatigue , serious memory issues, thinning hair,dizzy spells and numerous other ailments continue to plague me.Add to that a large weight gain ...and, well, you get the picture. If anyone knows of an alternative to taking this "poison", PLEASE, PLEASE let me know. I just WANT MY LIFE BACK!!! I actually cried after reading this blog. As I explained to my husband, I suppose it was from the sheer relief of knowing I was not going insane!!!

My symptoms are the same as all (anxiety, mood swings, low sex drive) and I plan to have this thing taken out ASAP. It has been so bad lately that I cannot function. I've had more panic attacks than I can count in the last couple of weeks. What I want to know is how people fare on the other side of things. I would imagine it takes a while for your body to regulate after removal, but how long. And to echo- no more artificial things in my body.
Side note- has anyone tried cold shower therapy, apple cider vinegar or lemon balm for the anxiety? (******)

I have taken, for the first time in my life for poison oak, prednisone- 60 mg for 3 days, 30 mg for 1 day, and 20 for 1 day. A week after the dose ended, I took another dose of it. As soon as that was over, the symptoms began with extreme low energy and dizziness, and eyes not feeling to well. I have been like this for a week, and would like to know how long this will last? And what can I do to speed up the process?

I took Lipitor for about 2 years- 5 mg.
Leg cramps-soreness throughout my muscles- very sore buttocks-
my legs are shaky- if I use them too much; (as in walking 3 miles)
I am (was ) an avid body builder that could squat with 100 lbs- and now ( I am a health conscious -non drinking- NO other medication 104 lb slim female) have quivering legs if I stand for too long. I even had a muscle biopsy- and it cam back negative- I have not had a statin for 6 months- but I still have cramps- and abnormal liver values- and I have NO other conditions-I have been scanned from head to toe - open MRI- closed MRI -but the muscle stiffness- soreness- especially legs- continues-
does anyone know how long it lasts? I have also been tested for liver cancer- thank God-negative.
I really feel that Lipitor did this- has anyone else gone from fit as a fiddle to a quivering -achy person- I have gone through 5 doctors- internal - gastrointestinal - neurologist- hematologist and all is negative- just high liver values and muscle pain. Thank you so much.Maxine

Hello.

I was started on Prednisone on Saturday (3/15) for Bronchitis. So far I have taken 40mg, 40mg, 30mg, 30mg, 20mg, - I am to take 20mg for two more days than 10mg for three days. I also just finished a Z-Pack of antibiotics and am taking Mucinex and Ventolin HFA...

I have head pressure, dizziness, and weird visual disturbances. The problem I am having is my breathing feels WORSE on the Prednisone??? Is this possible??? I feel like I am losing my mind. I have insomnia and am extremely jittery. I have never taken Prednisone before - but want so badly to breath better - but it is not helping and in fact seems to making the problem worse?

Has this every happened to anyone? Please help I am so frightened.....

Thank you

I'm a 47 year old male and have been on 20Mg Daily Lipitor for about 4 years. Everything was mostly fine until about 1 year ago when I started experiencing severe hip and groin pain. I played hockey regularly up until that time and assumed the problem was a hockey related injury, though never remember any specific incident that may have been directly responsible. I told my doctor I thought it was a sports hernia because the symptoms and suspected cause held a close resemblance. X-Rays, MRI and Bone Scans were all negative. Physical Therapy was a useless waste of money. I was in agony for over a year and barely able to walk some days. Could no longer participate in hockey or other sports. Even coaching youth sports was a challenge due to the pain that greatly limited my mobility. The maddening part of it all was the doctor's had no explanation and just wanted me to continue with Physical Therapy. My wife casually suggested to me that maybe it was the Lipitor as she had heard some recent news on TV related to Lipitor and muscle pain. I told her she was being ridiculous and that's when I started to do some internet research and came across this site. It's all starting to add up. I've been off Lipitor for a week and the pain on my left hip is almost completely gone while the pain on the right side has shown significant improvement. While I am seriously happy that I think I have found the cause of my pain, I am incredibly angry that not a single doctor (I saw a total of 3) even suggested the possibility that the problem might be the Lipitor. They all new I was taking it. I know the drug has had highly positive affect on most people and saves lives but I feel that I've lost a year of my life to it.

My mother was put on Prednisone 3 weeks ago because of severe muscle pain (15 mg at first and increased to 60 mg). After she starting taking it she began to have weakness in her muscles/joints and was unable to walk by the end of the week. She also had severe water retention and could not catch her breath. Most of all she was very weak all the time and could not seem to sleep at all. She wound up in the hospital and was classified with a type of Congestive Heart Failure due to the excessive dosage given by a pain doctor. She had to be admitted to a Rehabilitation Center where they have now cut her down to 10 mg a day and she is trying to take Physical Therapy to walk again. She is fighting with depression and overwhelming feelings of anxiety. She still cannot sleep and wonders if she will ever by back to normal again. Just a month ago she was living a normal life and because of the pain, was given this medication. I wonder if the benefits outweigh the horrible side effects she has experienced. After reading some of the responses above I see others are having similar side effects.
Any encouragement from someone with a positive long term outcome would be beneficial at this time to her. She feels very helpless in her situation.

Firstly, there is hope! I have been off the evil Advair for 8 months now, I have my Ventolin at the ready but typically I use it one or twice a week...and when I do I hold it at arms length away and only inhale a tiny amount.

Okay a little rewind to the start of my recent problems. I went to an allergy doc since my asthma seemed to be getting worse, he did the test where they scratch your back with 70 or so allergens, from the reactions he determined what some of my trigger are. Turned out to be house dust mites, mold, grasses, cats, horses, shrimp etc. Then the idiot put me on Advair rather than dealing with the real issues.

After 2 years on this evil substance, my chest was so tight when I didn't take it, and generally my breathing was the worst it had been my whole life. I felt like there was something in my lungs that I just couldn't cough up...this gradually did subside. Long steamy showers helped me a little here.

So this is what I did.
Bought a copy of Reversing Asthma by Richard Firshein, a must read, he was a chronic asthmatic and reversed his own condition, you must buy this book.

Armed with my known allergies, I cleaned up the house, bought the pillow covers that keep the dust mites out. I sprayed all the carpets and duvets with an anti-allergen spray. And of course avoided my other known triggers.

I bought a Microlife digital peak flow meter to map my progress.

On Richard Firshein's advice I take a whole host of daily supplements, cod liver oil, vitamin C, magnesium, beta carotene and so on.

I exercise 3+ times a week and I bought a PowerLung Lung Trainer to build up my breathing muscles (I haven't been using this a whole lot so far though).

I'm still working on finding my triggers, so I still have days that aren't as good. I think something I occasionally eat or drink is bothering me. Oh and I found being dehydrated seems to cause my breathing to go downhill.

All the best to you all.

Hi I'm 26 years old and just started 60mg pred treatment for Kidney condition called Nephrotic Syndrome. This is my 8th Relapse since i was 7years old.

Started Tabs 27th Dec and now they are really kicking in with side effects! I have a beautiful little boy and just got married and was soooo Happy. Now I'm feeling so depressed, I cant sleep , My Face has started swelling and I've eaten all inside my mouth cause I'm so hungry!! Been having a few Cramps but nothing like I've experienced in the past.
I'm trying to reduce the tablets myself so I'm not on them too long but its just not working!
I just WISH I could stop the moon face I'm developing, Its the main problem for me (causing depressed thoughts)

I was diagnosed with Crohn's disease in July. I had my colonoscopy/endoscopy the day before 4th of July. Got sick with what I thought was the flu on June 26th. That's when I first landed in the hospital (dehydrated & sick). After the diagnosis I was first put on Entocort and Pentasa (Pentasa is supposed to be a remission drug - keep you from having flare-ups). Entocort didn't work so they switched me to Prednisone. I've been on Prednisone for about 6 months now. Going from 20 mg to 40 mg and then I'm finally weaned down to 5 mg. I get to go completely off of it Jan. 13th. Scared of what other side effects might occur from coming off the drug. While on it I've had emotional problems, acne(never had a problem with it before), moon face, gained 30 pounds, joint pain (I was in therapy for as long as insurance covered. - I recommend water therapy, it helps for some people as it did me), trouble sleeping (haven't slept a full night since I got sick), certain days I'm really really thirsty, I've had sort of what I'd call restless leg (I had this before I was on this medicine but it has gotten significantly worse - mostly at night or when lying down), and dry skin.I have to say though that the WORST side effect is the FOG. It's horrible. I enjoy learning and using my brain and when I'm on this I can't think, I mix up words, and it feels like my brain is covered in cobwebs.I had to drop a calc 2 class and that got me off the track I'd set with my academics. My inflammation rate is down where it's supposed to be as of the last blood test a couple weeks ago. So I guess the Prednisone and Remicade are doing what they are supposed to - but I still don't feel as if the pain (not associated with Prednisone - caused by the disease) has gone completely away even if the inflammation has gone down. And Prednisone's effects are just horrible. Some nights I feel depressed and just want to cry and cry. The past months have been trying because of several hospital stays, switching to many different doctors (gastrointernologists, nephrologist, urologist (kidney stones), primary doctor - and they think maybe I should see a rheumatologist), and Pentasa (it began shutting my kidneys down). I just hope that when I come off the Prednisone the side effects will fade (hopefully quickly but lets be realistic - ill just be happy if they go away sometime in the next few months) and I won't flare up again. Anyone know the best way to get rid of the weight? I'm already drinking lots of water and I go walking and do exercises everyday.

QUESTION: When tapering Prednisone does anyone have a place(s) on their stomach that are sunken in and feels dry compared to the skin around it?

Anyways, I hope that everyone overcomes their difficulties, whatever they might be or concern. It's hard to have a life when you are constantly fighting your own body to stay healthy.There are plenty of situations in life that are already hard enough to deal with without medical issues of your own. Best of luck to all!

I was just wondering...I've been weened off Prednisone the last month or so and today is my last pill. YEAH!!!!!!!!!!!!!!!!! AMEN!!!!!!!!!!!!!!!!!!!!!.
However, I've noticed that my joints hurt and my feet oh the pain. Is this normal. I feel like my muscles are weak. walking up a flight of stairs is painful. Anyone know how long this will last or if this is something I will have to live with.

After bith my childrens births I have experienced a enigmatic skin disease / disorder which has been unclassified by dermatologists and specialists. First I experienced blisters on my torso, which crusted over and followed with severe urticaria-like wheels all over my body. Doctors placed me on Prednisone 5mg tablets ( 40mg daily) for 4 months, in which time the symptoms subsided , but the side -effects for this Mother was terrible!!! I experienced a 12kg weight-gain, uncontrollable appetite, excessive sweating, dizziness , shortness of breath and extreme hairloss. My skin thinned and OI bruised very quickly. No diagnosis could be made. After the induced -birth of my second child now, I have the same episode and had been placed on Prednisone for the second time just to cope with the swelling.

I am currently in my 7th week of using 10mg - 15mg daily with an anti-histamine. I hate the re-occuring side-effects and am very scared of all the long-term damage. Does anyone have any idea how to boost your own natural immune-defence system while being bombarded witha immuno-suppressant like Prednisone??!!!!

I believe that your own body ws made to heal itself or be healed by natural means... but how and what?? I am desperate, and have been following a anti-candida like diet ( no yeast + sugars + preserved foods) Thus far I have not been able to kick the symptoms. Any help out there would be much appreciated. Have someone experienced the same sort of symptoms???

I have been taking 20 mg. Lipitor for so many months now and continuously experiencing sore muscles and my wrist seems to have arthritis. I have told all these symptoms to my cardiologists and just told me it is not from lipitor. Iam a Veterinarian and I am not convinced with his response. The only good thing is that he is monitoring my blood chem and my cholesterol is within normal level. I am taking antioxidants (cod liver oil,Vit C and E,Mg,CoQ10,Chromium) and lots of olives and nuts. I am also taking those expensive drug- acid reflux and BP lowering drugs. I stopped using Lipitor for 7 days now and will go organic.

I have been suffering from almost consistent sinus infections since moving to the Virginia area. I never had one before moving to this new climate, where I have been told there a more mold spores and other allergens in the spring and summer. Having no doctor here I went to a walk in clinic for some relief. I was prescribes a 10 day course of Levaquin. The course ended three days ago, and the sinus irritation is still present, now it is more like sinus pain.

Although the yellow and green mucus cleared up, I still have the sinusitis it seems AND side effects from the Levaquin including light-headedness, blurry vision, heaviness in my legs and stiffness in my joints/hands. I also for the past few night have not been able to sleep, waking up every few hours with nervousness or anxiety for no reason. I am only 39 and otherwise was healthy. I am taking vitamins, drinking alot of water and taking cod liver oil now hoping these symptoms will go away.

I have been taking 30 mg a day for 5 weeks now...great results shredded up fast.......but my hair seems to be falling out and i cant get an erection..is this normal? it also looks as if my penis has shrunk and my joints hurt

You know, I almost feel guilty at being the only success story to date here. Still taking 5mg. Zestril before bed every night. I insisted on this brand with my doctor as others were causing side effects. Having said that the British National Health Service contributes to supplies so it costs me just over £6 every order which can last up to two months. Interested to read opinions that Lisinopril is not necessarily for High BP. Now, if it's any help to you at all, can I suggest dietary changes too. I have for some weeks switched to Soya Milk and ceased (nearly) all dairy products (farmers practically stuff fat down your throats in the UK!). No chocolate either. Switch to a Soya based spread for putting on bread. Fish oils are also greatly beneficial, i.e. sardine, tuna, cod (cod liver oil) etc. I took my BP the other day (12 hours after the last tablet) and it still gave me the satisfactory reading of 122/75. The highest it seems to go now is about 140/85. Last year readings were around 150/98. I'm not so sure about taking lots of Coke (caffeine) to stay alert as someone suggested - doesn't this actually RAISE BP like smoking or alcohol? Good luck, stay well.

mijie, - I personally don't think increase in Lisinopril could actually increase BP. But there again this is a question for a doctor. A definite YES, it can cause a dry cough! I was very interested to read your nausea comment. I read somewhere that Lisinopril only affected 0.9 per cent of users this way. Well I believe it did affect me this way too. But these Lansoprazole tablets are an absolute miracle as far as nausea, acid, feeling like death warmed up in the morning etc. My Lisinopril is now always Zestril and is 5mg a day. Combined with dietary adjustments and a dose of cod liver oil a day I am expecting to enter the 'safe' area at last after my next blood test.