Pernicious Anaemia :: What Size Needles For Self Inject B12 Injections?
Sep 7, 2015
I've decided that I have no other choice than to self-inject B12. I am older and don't have the same muscle tone that I used to have. I will be injecting into my thigh muscle. What would be the best sized needle for this? Would a one inch needle be ok? Anything longer might be too long if my muscles aren't what they used to be. And what guage?
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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 only recently started having the B12 injections. Does anyone know if you can still give blood? I used to be a regular donor but now I'm not sure if I can still give?
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I was diagnosed with low B12 levels and further tests revealed that I had intrinsic factor.
I was given the 6 injection course and was told I would have another in 12 weeks then again and then blood tested again. 6 weeks since my last injection and my symptoms are back. Feeling vague, tired, lethargic, irritated etc. How can it be that I have intrinsic factor but obviously have low B12?
is it likely something else is going on? - any ideas/suggestions?
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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 was diagnosed with copper deficiency a few months ago and sent for further investigations prior to treatment. As all scans, eye tests and liver functions were fine and no signs of copper storage or damage anywhere else as might explain the deficiency in my blood, so they have now decided that I am not deficient after all and I have not been treated.
These were my results which are all pretty low within the normal ranges (in brackets):
Copper 9.3 umol/L (normal is 12.0 - 20.0)
Free Copper <1% (<25%)
Ceruloplasmin 0.20 g/L (0.20 - 0.40)
I also have Pernicious Anaemia (B12 deficiency) and the two conditions often appear together and have similar symptoms. I have very regular B12 injections so I am happy that is under control but as there are still outstanding neurological symptoms, I am wondering if this is due to the low copper levels?
Has anybody else had similar results, please?
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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 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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How many different places should I use for injection. When I was first diagnosed I only used arms and legs, however they are starting to hurt a lot when I use them. Should I start using my sides?
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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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Getting pins & needles in hands and feet, on 25mg for 5 days now. Anyone else had this? It's really annoying... IS it normal?
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Ten days ago I had a robotic laparoscopic myomectomy to remove four large fibroids from my uterus. The surgery went great, and I've been recovering at home and have been waited on hand and foot by my husband a bit less each day.
The only problem I'm having is occasionally in one specific spot I'm experiencing a pins and needles type of pain - sometime like shards of glass - in my abdomen. Yesterday I thought it was the result of overdoing it so I rested yesterday and still woke up in pain. My doctor is an hour and a half away (closest one I could find who does the Da Vinci robot!) so I'd hate to schlep myself all the way there if I don't need to. Anyone have any insight about this kind of pain following surgery?
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I've just taken my second tablet of the day about 20 mins ago and I'm having serious side effects. I've been on them since Thursday and have had a few issues with shaking, palpitations, insomnia and some mega weird dreams but nothing I couldn't cope with. in fact nothing I didn't have in one degree or another before.
Tonight I'm in serious pain with my chest. My heart feels like it's breaking out and breathing is hard. I'm light headed and dizzy when sitting but when I lay down my head starts pounding as if all the blood is being pumped in there.
My legs feel numb and everything below the knee has pins and needles.
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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'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 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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I've been on ferrous fumarate for 3 months and doctor says my results are improving (hemoglobin has reached normal and ferritin has went from 1 to 12)
My symptoms were continuing so I was tested for B12 deficiency and got result today. B12 came back as 276. The doctor left a message to say continue with iron for 3 months and that was it! I am really down as I don't know whether the iron will up my B12 or not? I don't know if this means my B12 is on the up or if the iron tablet has nothing to do with it?
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I have been taking this medication for nearly 4 weeks , the first 2 weeks with prednisolone as a treatment for nasal polyps. I am spaced out most of the time , have had weakness in my muscles, pins and needles and numbness in my fingers. My stomach was painful so I have taken omeprazole for that which eased that pain altogether. Clarithromycin also have me insomnia and mood changes. They made my skin greasy,eventually spotty, and I have headaches and think I am sensitive to the light.
I finish them in 3 days time thank the Lord. At times I felt like passing out and unusually for me zonked out at unlikely moments during the day.
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I have numbness in my left upper leg once a week, to the point where I cant feel anything when I touch the skin on my leg. I also have pins and needles in the same leg. I don't have any pain. I also have a slight case of scoliosis. Its not visible but it might be a contribution to the numbness in my leg?
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