Anaemia? Exhaustion For Long Years?
Jul 7, 2015
I'm suffering from exhaustion for long years.
Lately I noticed that in my blood tests there are a results that might indicate of an Anemia.
RBC-Red Blood Cells 4.46
Hemoglobin 13.4
Hematocrit 39.9
Fe - Iron 82
Ferritin 81
Are those results indicate os an Anemia?
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I have recently been diagnosed with fairly mild iron deficiency anaemia, which was picked up incidentally prior to an unrelated issue, and I was told it is a type that usually stems from bleeding. I was advised to speak to my GP about treating this, and on doing so he first asked me if I'd had any worrying symptoms, well I haven't noticed any obvious blood spurting from anywhere, or any blood in my bowel movements/vomit, so I said no. He then seemed to put it down to periods. I don't really have periods, and when I do they are pathetically light, so I don't think its that, but he didn't seem concerned. I am now on a 1 month course of ferrous sulphate and need to have more bloods after that to see if it's sorted it, but I am just worried about what caused it in the first place. I don't think my diet is particularly bad, so where on earth am I bleeding from!! My GP doesn't seem concerned, so I'm guessing I shouldn't be either, but just wondering what other people's experiences are of the causes of their anaemia?
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I found out I had a B12 deficiency 5 years ago. My levels were very dangerously low at the cellular/functional level. I was told I was near paralysis. Now, after 5 years, they are still low. They have come up to almost borderline, but it still flags red on my tests. My serum levels though are too high for the lab to measure! Its just not getting into my cells so it's not able to be used. I do twice a week injections plus twice a month IV B12 and still it has taken my body 5 years just to go up a little bit. I feel the effects of the shot for about 15 hours barely then I just feel awful again, thankfully it's prescribed every 2 days. But I don't want to do it every 2 days forever!
In the beginning I was told it would take a month or two to get my body back to normal and then just a shot every few months for maintenance. My drs have not only increased my dose but also the frequency and STILL after all these years I'm deficient.
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I have been taking Tibolone for 7 years, and there has always been fors and against taking them. I would like to share my personal experience, I was told by my Doctor to try and wean myself off them as I had hit that crucial stage of 5 years where they do not recommend that you take them any further! I did what they asked and for three months I reduced to half per day, recommended rather than one every other day, I have to admit I managed well, didn't really have a huge impact, so I thought I would try half every other day to reduce it further, within a week, my symptoms came back with a vengeance, I felt generally unwell, my bones hurt, headaches, mood swings and panic, it was horrific, so on that basis I spoke to my Gp and I have restarted my Livial, one per day, to say that these tablets change my life is an understatement, for me personally the benefits far outway the supposed risks, I am happy I will take them for many years to come as long as you are checked I really don't see why you should suffer if you don't have to? Good Luck to you all and I hope that this post will at least make you feel a bit more relaxed. My Gp said that some women can manage after 5 years of HRT but some need it up until ten years depending on the severity of your symptoms, All Gp's are different, I think they just have to stand on the side of caution as with any drugs, For me, no-one knows my body like me, and if it makes me feel well and able to function normally then I am all for it, Tibolone for me has been a lifesaver and long may it be prescribed for us Girls.
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I suffer from bipolar and sleep disorders. My dr. prescribed many different things and nothing worked until the dosage of Seroquel was up to 600mg per night. Even at this dose I'm not sleeping more than 2 hours at a time. My weight has soared from 130 to 195 over the past couple of years. I'm afraid to try something different but am also scared of long term side effects
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So how are we expected to exercise when we're so tired? I'm 22w,2d and always exhausted. I get less than an hours worth of energy a day. If I try to push past that I feel very ill. Even light stretching or reading a book is to much. I've only had maybe two weeks this whole pregnancy that I felt normal energy wise. Anyone else going through this? If so, how do you get anything done? How do you exercise? And no, naps don't help replenish me.
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I am 20 years old and it's been at least 4 years since I started experiencing these symptoms. I am unable to perform normally in life (I have been struggling to live normal life up until now, I can't just take it anymore.) I'm from Czech republic so pardon my poor language skills.
These are symptoms I experience:
1) sore/stiff muscles, stiff neck, my muscles slightly hurt me when I stretch
2) being weak, tired, exhausted, feeling fatigue/nausea - nowadays basically to the point where I don't get up from bed whole day if I don't have to, this can go on for months even (when I have holidays)
3) permanently yellow/orange-ish stool no matter what food I eat. Eating fried food sometimes makes me feel worse. I think I also often go to the toilet - once every 3 hours. Similar for water: I drink usually 3 litres a day through the day and my bladder hurts me very slightly all the time - the more I drink, the more it starts to hurt.
4) symptoms as if I had mild cold all the time - permanently stuffy nose, sweating (it goes like this - I start to feel cold but when I get into warm environment, I start to sweat)
5) visual snow, feeling dreamy (aka depersonalization/derealization)
6) generally unspecified weird/unpleasant/painful sensations across whole body
Symptoms never go away, no matter how much I rest (when I don't rest, it obviously worsens them a lot).
Cold weather feels very bad to me so symptoms probably get little worse when its fall/winter.
I have undergone mononucleosis over a year ago, but as I said, I had the symptoms even before. It's however possible that mononucleosis worsened it.
I have been to several medical places during this year including gastroenterology (stool/blood/gastroscopy, ultrasound of my guts), oncology (blood test, it's known that I have 2 genes that make me more prone to cancer - family origin), immunology (blood test) and infections department (blood test).
All the results were negative except the few that had border values - smooth muscle antibody and something that indicated that I must have undergone lyme disease some time ago. (and the results from oncology)
I tried taking vitamins, magnesium (with B6 and B12 vitamins or so) and supplement that supports liver function (contains choline and few other things). It does not do anything.
As of the fact that I must have undergone lyme disease some time ago, I was prescribed antibiotics for 15 days, I have been taking them for 7 days now but I don't feel any better. Well they make me feel somewhat fresher, but all my symptoms persist.
I tried I think 2 or 3 kinds of probiotics but it did not help. I was also prescribed pills at gastroenterology to slower indigestion process (or something) 6 months ago, but I haven't started taking them yet.
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I'm 8 weeks post TKR and not doing too badly apart from the usual sleepless nights, stiffness and ache at back of knee, etc etc but I wondered if anyone else experiences getting to about now (7pm) ish and feeling absolutely exhausted, and every part of my body hurting? I had to go to bed this afternoon and slept for an hour but still feel dodgy. Is it still my body recovering from the operation? Lord knows how I'm going to be able to go back to work in four weeks time - not gonna happen.
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My 23 year old girlfriend has a urinary tract infection/kidney infection. She has had the infection a year ago brought in by excessive alcohol and exhaustion which is possibly what was to blame this time. She has the usual symptoms, stomach pain, lower back pain, low appetite etc but she also has psychological symptoms that are presenting predominantly as paranoia. From what I've read, this last symptom is seen mainly in the elderly and not such a general symptom And my question is, am I worrying unduly and it's just how she reacts to the infection or could this be something more that just an infection?
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I'm 9 weeks post TRHR and although I'm back driving, doing most regular activities I'm getting wiped out in the evenings.
It's not just fatigue. It's like I'm going to pass out and I feel very nauseous.
I was just wondering if this was normal or if maybe I am anaemic. I was anaemic after surgery but I was in a supplement and I had recovered.
Basically I'm wondering if it's due to me overdoing things prof maybe I should get my bloods checked.
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I'm a 28 year old male. Over the past couple years my health has been steadily deteriorating.
Physical Issues:-
- Weight gain. 1-2 years gained 40lbs. (Now closing in on 295lbs)
- Unable to lose weight. Cut calories, ate better food, worked out with a trainer 4-5 days a week, 2.5 hours a day for a month and lost 2lbs. Muscle gain did not account for the lack of weight loss.
- knee pain (for 4-5 years). X-rays came back negative.
- legs are constantly overheated, and warm to the touch.
- exhaustion, all the time. To the point where it affects my life.
- no interest in anything due to always being tired.
- caffeine has no effect. Never drank coffee in my life, but started drinking black coffee and had no effect.
- constantly feeling 'I can't', whenever something comes up.
Doctors suggestions:-
-Doctor treated this as depression. I went on Celexa for 5 months and all that did was make things worse. Increased weight gain, more tired, more emotional, more depressed.
- I also saw a psychologist for about 10 sessions, but this was not very effective as I didn't have any specific trauma events.
- blood work and urine came back normal. No thyroid issues, no diabetes, nothing.
I keep trying to get healthy, but I can't shake this 'cloudy' feeling and exhaustion all the time.
I don't know if anyone can think of what this could be? I know I need to get more active, but like I said above my body and mind keep telling me 'I can't'...and no amount of caffeine helps.
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I really feel ill after almost three days taking Primethoprim.
Following a hip replacement in April, my pre-existing (1959!) lumbar spine problems came back worse than ever. I now have Lumbar canal stenosis.
To help the intolerable pain, I was given Baclofen, then Diazepam and nothing made any difference. I was admitted to hospital one day when I couldn't move at home and was given an injection of Ketorolac plus Tramadol and Paracetamol tablets and discharged back home where I live on my own.
Supplied with a prescription for Tramadol 50mg to a max of eight in 24 hours, the pain continued to lessen.
But then I began to have a slight pain when passing urine. After testing my urine, the GP said I have a bladder or urethral infection. She prescribed ten Trimethoprim 200mg, to run over five days, i.e. one morning and one evening.
Ever since taking the Trimethoprim 200mg I have had extreme exhaustion, nausea, mouth-breathing and panting and therefore very dry mouth, complete loss of appetite, etc, and general misery.
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I currently take 30mg of adderall xr every day and was put on strattera, which i took for about 18 days. On april 9th i had an episode of really bad vertigo where i stood up and the room started spinning and then i got really nauseous, light headed, started sweating a lot, and my pulse dropped about 30 bpm. I have thyroiditis and my pulse is typically between 95 and 105 and during this it dropped down to about 66 but started to go back up after about half an hour. and an hour later i was fine and felt great the rest of the week.then this past sunday the 17th i had another episode of vertigo with the same symptoms. I ended up going to the ER to get checked out because my pulse was not going up at all after about 45 minutes. It took about 1 1/2 hours to get in to see someone at the ER and by that time i was starting to feel better. They told me the vertigo episodes could be caused by the strattera so my psychiatrist took me off of it on monday. Since sunday/monday i have felt completely exhausted emotionally and physically, and i had been having some chest pains. I went to the nurse practitioner at my doctor's office and she told me that it is probably all related to my thyroid. She did an EKG that looked normal, of course when i wasn't having any chest pains. Has anyone else had similar symptoms or experiences with strattera?? I felt so much better when I was on the strattera than I do now, and it really was helping me a lot.Any suggestions I should bring up with my doctor or psychiatrist?
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Two months ago I was diagnosed with a sinus infection and took antibiotics but after I finished them I still wasn't feeling great so my doctor put me on another round. Finished those and then began having slight headaches, lots of nausea, sometimes vomiting and diarrhea and extreme exhaustion. I have had two blood tests and nothing shows up I have an ultrasound this week but does anyone have any idea of what this could be? I am a normally healthy twenty year old and this is keeping me from work and school!
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I'm a mum of 6 and have had bleeding from the bottom on and off for years but never had it dealt with I was given suppositories for haemorrhoids but never took them I have been feeling really unwell lately and doc said I need to have a op to remove the haemorrhoids but after reading the posts on here im really scared but then im also worried that i am not running on all cylinders due to my low blood count what's worse operation or feeling this low its really hard as i have a family to take care off and not sure if i can deal with the recovery needed as per the stories on here is the operation really as bad or worse Than childbirth? i had 2 c sections and was ok after those but this sounds so much worse
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Hb 3.7 iron deficiency anaemia
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my son was diagnosed with B12 a year ago he got the 6 booster jabs last September he had been getting sore heads that were lasting up to 8 weeks his joints ache his shoulders and neck are really sore he was getting ear infections had 10 in last 6 months pins and needles in his hands and feet he is sleeping about 15 to 18 hours a day they started to give him 3 monthly jabs and after 6 month put him on monthly also done a blood test went back to get his second monthly jab but said his b12 levels were normal so put him back to 3 monthly but he could hardly get out of bed they have now put him back to monthly jabs which are only lasting a week if that asked if they could be given weekly the doctor said he would not be happy giving the jabs sooner he got his last jab on the 17 sep and its only lasted till yesterday the are treating him for chronic migraines and now telling me they think it is ME I am sick getting put of by doctors as my son has no life now and i was wondering if I could give him tablets in between jobs because when he first gets his b12 jabs the symptoms all disappear and he gets a week of feeling a lot better but they won't listen
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I have found reading the posts about PA very helpful, i was diagnosed early last year with PA and have injections every 3 months they have helped enormously with my symptoms, please could any one tell me about the side effects of the B12 injection, i have had various syptoms which i have just put down to the whole PA thing, but would like to know....
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I have to go for a gastroscopy and want to have sedation. Will I be allowed to as I am anaemic, Hb of 5.3. Can anyone advise me?
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I have historically had iron stores of .5 my gp said my hemoglobin levels are fine and has gave me iron supplements. He is also checking levels every three months. I am very dizzy all of the time, have shortness of breath, I have constant feeling of brain fog and often get my words mixed up. My gp says this is not a result of my low iron stores. I am really struggling is anyone else experiencing similar
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I have been low iron since i was born. Only recently has my doctor been checking my levels and trying to raise my iron from anaemia. My doctor says that i should be getting between 800 - 1000 mg of iron a day. That means i have to take an iron pill four times a day. So when should i take the pills? Do i take them right after or before meals? I will go back in two months and they will draw blood to see if my iron has improved. I am just wondering what to do in the meantime to improve my iron results?
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