Candida :: Can A Vitamin Cause Die-off?
Feb 6, 2015
I have struggled for a long time with candida. I've tried a few cleanses and better diets over the years, but haven't stuck with them.
Recently, I began taking a good "Living Green" multi-vitamin, three times a day as directed, along with more water and less unhealthy food. But instead of feeling increased energy, I felt more fatigued. I stopped the vitamin for a few weeks, then started it again a few days ago. The deeper fatigue returned, and my body feels stiff and sore, feet are always cold.
These symptoms match those of die-off. Can a vitamin/supplement have this great of an effect?? if it is die-off, should I muster through or back off?
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Any of you deal with this while breastfeeding? If so, do you have any dietary pointers to help prevent fussy baby (caused by carbs), Yet continue to maintain supply?
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Since I was 13 I've been plagued by Candida. I told my mom about it when I first found out what it was and asked her to take me to the doctors. She never did so I thought it would go away on it's own. 2 years later I was sick of it and went to my school nurse for help. She had given me the cream that's inserted deep into the vagina and I had started treatment, but then after one dose, I got my period so I had stopped treatment. I went back to my school nurse and she gave me the pill telling me it would get rid of the symptoms but it never helped. Unfortunately I moved to the country where I was then taught at home and I had no one to go to for help. And so I read online that Greek yogurt helps alot and so I started eating one pot a day like it said as well. That helped with the symptoms but it never got rid of it. I'm 18 now and I have moved back to the city and I have tried the creams twice, but every time I've started bleeding, which is unusual because I had the Jadelle inserted. I am literally stuck on what to do next
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I think I have balanitis - I have had a sore and red penis for over a year. It gets worse after sex because the thin skin covering the glans has bonded to the foreskin due to the infection and during sex it tears, causing an open split or wound. Some days it is very smooth and normal looking. It's like the thin skin of the glans has continued to grow over the ridge so I no longer have a ridge around the bottom of my penis - it's covered over. I feel like tearing it all around so I can expose the ridge but it is raw flesh underneath and would be a nightmare.
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I have had great success calming my gastritis , which can be troublesome from time to time , coconut oil , taken on a spoon , up to 5 tablespoons per day , has greatly eased a recent flare up of my gastritis , which i never had prior to a helicobacter infection , , just wanted to pass this info on , hope it helps other sufferers , i do watch what i eat and i have been quite well , but every so often , my stomach is very painful with gastritis , coconut oil seems the most reasonable way to help relieve the problem , read up on yeast infections ,candida , as well as gastritis , buy a good quality oil try Holland and Barrett
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I was diagnosed with with B12 and Vitamin D deficiency. Both levels quite low. I have been taking my Vitamin B12 shots for three weeks now. Also I am on supplements for Vitamin D 60000 IU once a week. Most of my symptoms like tingling numbness and headache have gone. But since a few days i have been experiencing this weird feeling in my chest and entire body, the kinds when we are nervous, with palpitation while sleeping. I wake up and sit for sometime and then I seem to be fine. However, it happens again when i am about fall asleep. My GP said its anxiety and prescribed clonazepam. It did help for three days. But yesterday I tried sleeping without taking clonazepam and the same feeling of anxiety and palpitation came back. Is it a part of the vitamin D recovery process? I don't want to take clonazepam regularly. Any suggestions?
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My most recent hemogram shows that my ferritin is at 0.7, and that scared the pants out of me. I also have low hemoglobin, my serum iron is nearly at normal levels, just a few points below normal. I have to wait for my doctor to come from his medical absence before I can show him the tests.
Until then I'm taking the iron supplements I was prescribed 2 months ago. I want to take some vitamin C to help with the absorption, but I have a little issue: I'm allergic to citric acid, so orange juice or other citrus fruits are out of the question.
Any suggestions on what I should eat to give my iron levels a push? Or should I just get a vitamin C supplement as well?
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Hi I have recently been diagnosed with vitamin D deficiency after years of pain and tiredness. I have quite a long history but have had surgery twice on my right foot. The first time was a straightforward bunion op and the second one I am now wondering if was caused by Vit D Deficiency as I was in so much pain after first op I needed the 2/3/4 metatarsals cuttings and replacing into different positions.
I also have Carpel Tunnel in right hand and been told I need surgery on it due to muscle waste, inflamed tendons and slight loss of sensation.
There isn't a part of my body that doesn't hurt and I am a 36 year old female. I am self employed and a mum (which can be very challenging with all the pain and tiredness at times!).
I have been prescribed pre d3 20,000 iu 3 times a week.
It turns out that I had a blood test in 2011 that showed I was low on vit d then so I have spent the past week battling between my GP and hospital to try get the levels and find out who did the original test and find out why nothing was done years ago for me. I am starting to feel fobbed off as no one is giving me a clear answer. The hospital won't give me the answers and told me they have to be faxed to GP which I asked for and after waiting days for this and chasing up twice the GP rang today to tell me they have recent blood test result which showed vit D below 30 if that makes sense to anyone?
They weren't sent the 2011 results so have had to chase up again!
I am concerned after having pain for years that this may have done damage. How long does it take to see a difference on that dosage?
My main pains are in lower right back, back right rib, hips, feet, hands, neck.
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I started taking cod liver oil and coconut oil supplements as of last week, but after taking them I couldn't sleep. I'm going on 5 days of not sleeping. I took the recommended dose at night and I noticed on the bottle that it has alot of energy in it. I stopped taking them 6 days ago but I still can't sleep good. I'll be lucky if I can get more than 4 hr. What can I do please? I never had sleeping problems until now.
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I know vitamin d deficiency can cause depression but can it affect anxiety. my doctor put me on vitamin d and i've noticed a drop in my anxiety. i am taking it once a week and forgot to take it yesterday. today i noticed my anxiety had increased. could it be related?
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I am male and so likely have had less severe autoimmune manifestations than females since they seem to have stronger immune responses. However, I have had some difficult times with autoimmunity. It started in 1972 with antiphospholipid antibody syndrome which caused deep vein thromboses in both legs. I started taking coumadin at this time but the dosage was not high enough to prevent some further clotting and a number of the clots travelled to my lungs causing pulmonary hypertension. Eventually, in 1994, this became severe enough to cause heart failure and the clots were removed via a pulmonary thrombo-endarterectomy. Subsequent to this, I developed lupus symptoms and lost both my adrenals and thyroid to it. The other lupus manifestation was regular pleurisy attacks. Also by this time, despite the coumadin, I was getting regular small blood clots on the skin on my feet and ankles, many of which subsequently turned into painful ulcers. In 2006, after reading an article on the internet by a doctor in charge of a hospital ward who was giving his patients 5000 units of vitamin D3 to prevent them getting sick, my wife and I started taking 5000 units of D3 ourselves hoping to avoid colds and flus. The vitamin D3 worked in stopping the colds but, in my case, it had another even better effect. The blood clots on my feet stopped and I have had none since.
In addition the pleurisy attacks almost ceased. With some additional experimentation, I found 10000 units of vitamin D daily (in split doses morning and evening, stopped the pleurisy attacks altogether. I remain free of the autoimmune effects since I started on the higher D3 dosage. I discussed the dosage with my hematologist and he felt up to 15000 units a day should present no problems in causing calcium over-retention (stones). I would recommend to anyone with auto-immune problems to try at least 5000 units a day of vitamin D3 to see if it reduces autoimmune problems. If you are concerned, you can discuss it with a doctor first but I have been taking 10000 units a day for several years now with no ill effects.
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It all started with the feeling of hot water being poured on my right foot. Started out slowly, then became very frequent and has slowly gotten better - now I only feel a sensation of "heat" pressing on my right foot occasionally. The worst of it lasted nearly 8 months. During that time I also had a worsening of many other symptoms such as: fatigue, horrible tremors, dizziness, nausea (from the dizziness), brain fog, chronic headaches/migraines, weakness in my entire right side, thighs that twitch and "pop" when I get warm, severe muscle cramping, vision changes also when I am warm, and urinary frequency problems. I say worsening because I have had some of these symptoms for years and just blew them off. In fact, I had a period of time about 20 years ago when I believe I was having something like the "ms hug" (really sever and unexplained pain in my ribs), as well as a hot feeling on half of my face, and my neurologist at that time said "you probably have some autoimmune disease that will show up later in life". I've had chronic daily headache and migraines for more than 20 years, and an essential tremor for about 10 years that has worsened lately. I also have an unrelated autoimmune disease, which I have been told makes it more likely that I have another (but which one?!). MS was suspected so...
I've been seeing a neurologist (and a PCP and a rheumatologist) for these symptoms for a while now and feel like I've had every test under the sun. I've had a normal cbc, sed rate, hemoglobin, basic metabolic panel, tsh, b12, all kinds of vitamin and mineral levels, folate, lyme test, MRI of brain and lumbar spine, MRI of brain, and an EMG. I have not had a c-spine MRI and wondering if there is a reason it was not included in these tests. So far the only thing that has come back was a positive ANA (which I believe is from my other autoimmune thing) and a low vitamin D (23), which fell from a level of 58 in under a year. I've been supplementing for more than 4 months. My neuro did not think that ALL of my symptoms could be from the D. Some, perhaps, but not all. Why does he think this, I don't know!
I recently finished a taper of prednisone and feel like the "fog" has lifted, like my brain is working again - hooray. My main symptoms now seem to be fatigue (it's insane), urinary problems, and some newer problems with my left foot (not the foot I was originally having problems with) - where it will cramp up for days and days (two and a half weeks one time), just like a never ending cramp. When it's not cramping I get feelings of heat, or sometimes just a vibrating feeling. The cramping can be very painful, the "hot" feelings are just strange. I've also now started having problems with jumping/twitching muscles in my left hand and arm (different than my normal tremor). I continue to have some right-side weakness.
So I'm wondering, do these symptoms sound as though they could all be because of the vitamin d? I've got a month until I see the doctor again, and he has been trying to push some meds on me, but I wouldn't want to start something if it's all because of the D. Since supplementing, I have had some improvements in my cognitive symptoms, but not much else.
Lastly, my neuro said he may send me to an MS specialist for a second opinion if I am still having problems next month... but if my MRIs are all clean, then there surely must be a more likely explanation, right? I just don't know why he is so sure that the low d couldn't be causing everything. He said that it was very unlikely because my levels had previously been ok and the severity of my symptoms would more match someone who had been very deficient for a much longer time. Does that sound logical? Would an MS specialist be able to tell me anything new?
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What are the causes of vitamin B12 Deficiency?
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In May I was told I had a vitamin d deficiency. My level was 11. Right before i was told about my low d i had burning pain throughout both of my thighs. If anything touched my thighs it felt like bees were stinging me. I went to the neurologist because I was also getting numbness in my arms. He told me i had mp or another name for it is lcpn from wearing tight pants. I bought new pants and waiting six weeks. Saw him again and now he thinks it's because my d levels were so low. D is up to 50 s now so why am i still in pain. I had an emg done on my legs and it was normal. Emg on arms showed mild carpal tunnel. I was tested for hiv 5 months after any exposure results were negative. He tested me for a bunch of other stuff all was negative. Could all of this be vit d
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I wanted to ask about vitamin d deficiency and possible side effects of it .
I am a 25 year old male , and my vitamin d level was very low (7ng/ml)
compared to the one I tested a year and a half ago that was 25 ng/ml.
The problem is that I had very little or even no sun exposure the past year and half because of medications I was taking for my acne including accutane , I wanted to test my levels six month ago but my doctor basically said that there was nothing to worry about , now that I know that my vitamin d levels were this low , I want to find out what is the possible damage that was caused by a year and a half of deficiency ?
and should I urge my doctor for more tests like calcium levels or bone density?
I'm just really worried that I've done damage to myself
of course now I'm taking supplements and I can also go back in the sun so I hope my vitamin d level will become normal , but it's very important for me to know if I need to have more tests done or what kind of damage may have been caused ?
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my wife is 13 weeks pregnant. And her B12 levels are 81 and Ferritin is 31.2. kindly Suggest that is it ok or any treatment will be need to be taken for it as Haemoglobin is 12.2
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I had sinus allergies , brain fog, inability to gain weight and just general fatigue when i was diagnosed with celiac disease an year back through biopsy and blood tests. I have been gluten free since then.
I weigh around 130 lbs. at 183 m.
My other test results are:
1.Severely deficient in vitamin D at 5.4 levels, for which i am taking supplements.
2. Normal T3 and T4 but T3 in the in the lower range at 112 (80-200 is normal).
3. High Anti peroxidase antibodies at 104
4. High TSH at 7.1
I don't know what to make of low Vitamin D and thyroid tests. Do i have a thyroid condition too or is it just due to my celiac disease? Despite being gluten free, i have not put on any weight until now. I feel just generally down, fatigued, anxious, and have difficulty keeping up with demands of day to day life. I was just wondering if i could do anything to rectify these symptoms.
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Had a blood test for this the other week and got my results back. It's says 200 but next to it says (180-900). Is mine low and need medical attention.
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Have suffered from RH for 2 years very badly, it has basically taken over my life.
Recently I read somewhere that it can be caused by vitamin D deficiency. Well that would make sense timing wise, I live in Scotland (no sun here) and I stopped sun holidays 3 years ago due to drop in income.
I was excited by this discovery but well 8 days in (5000iu) and no improvement. I know it probably takes a lot longer and I'm still going, but I hope it's not just a red herring.
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So I just got blood tests back and my vitamin d was 26 which is low and my calcium was 10.3 which is a tad high. I am 25 year old female. Should I be concerned about hyperparathyroidism?? I didn't get my PTH checked but my thyroid is normal. I don't know if they have anything to do.
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So my next appointment with my endocrinologist is in 2 weeks. I need to stock up on some vitamins and wonder which brands/mixes are best for hypothyroid/hashimoto's. My ferritin, vit d are low and I'd like to take calcium/magnesium/zinc too
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