Crohns disease and Vit B12 deficient Need Help!
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I was diagnosed with Crohns in 09 and prescribed mercaptupurine 6. 1012 built up my B12 injections (every other day/weekly/monthly) 2 days after my first 3 month jab you could split my brain in half! Sharp pain on left side of head and right side completely numb with stiff neck. I was so dizzy i dropped to the floor and the right side of my face went completely mumb and was dribbling. It went after afew hours and Doctor said nothing to do with the jab and left it, but since then it seems the b12 jabs dont seem to work. Always feel im not in my own body, confused (Taking 2/3 minutes to recognise my own toothbrush and then putting toothpaste on the wrong side! Had to throw the brush and paste in the sink to stop myself doing it then my temp raised that i looked purple! Extreme exhaustion, dizzy spells, jelly legs, pins and needles in hands and feet, palputations which are so bad sometimes they wake me up! Sometimes chest pain with it, Blurry, light sensitive eyes feeling like im going mad thinking everyones against me and crying for no reason! Today i have a nasty shooting pain on left side of head shooting to back of my neck and temp up and down to the extreme!! Cant go out on my own anymore and cant go to parents eve with my 3 children!! Very upsetting Please Help!!
0 likes, 18 replies
julia24711
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isabel1 julia24711
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julia24711 isabel1
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marion29181 julia24711
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julia24711 marion29181
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marion29181 julia24711
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julia24711 marion29181
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There are no dietry triggers with my Crohns they think it's hereditry (Dad died from Bowel Cancer and Brother had UC at 16 has now had bowel removed) so will try vitamins. Only reverted to soup when these latest symptoms of dizzyness, eratic blood pressure and palpitations started as i found eating food agrivates it for about an hour. My GP has categorically said She will Not refer me. Happy Days
isabel1 julia24711
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cant you get in touch with your consultant and as him to re send letter to your GP. Its a pity some GPs have this "I am always right" syndrome. It would be nice to be properly listened to as a person and not just a number on the GPs daily list. I do hope that you get sorted soon.
julia24711 isabel1
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He said he has re sent the letter but my GP insists the letter does not state that I shouldbe refered then went on to say "So what if your diagnosed with something? Thats just a name for the way you feel" Was in complete shock. This is why I joined this forum last ditched attempt at not feeling so isolated.
d39719 julia24711
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Have a look at crohnsforum.com. There's a wealth of stuff there about vitamin deficiencies.
julia24711 d39719
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d39719 julia24711
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Most parts of the world seem to get monthly B12 injections, but the NHS is insistent on sticking to 3 months. I found B12 patches do make a noticeable difference; not so much the pills or lozenges which rely more on your bowels working properly. It doesn't seem there's any problem with getting too much of the stuff so you don't have to rely on the GP completely.
julia24711 d39719
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isabel1 julia24711
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julia24711 isabel1
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