B12 specialist?: Hi, I'm newly... - Pernicious Anaemi...

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B12 specialist?

JillMaryC profile image
5 Replies

Hi, I'm newly diagnosed with B12 def. In addition to fatigue, memory fog, muscle stuff, tinnitus, and I now now laid up with severe dizziness and low BP 82/53. My GP only recommended three monthly injections, no load dose. Help! Feel I need monitoring. Anyone recommend a consultant in SW who is specialist in B12?

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JillMaryC profile image
JillMaryC
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wedgewood profile image
wedgewood

I hate to tell you that there is no such consultant in the whole of the U.K.. it is not an interesting subject for the medical profession. If there was such a person , most people on this forum would be beating a path to his/ her door .You will get better advice from the advisors on here who have no medical qualifications , but experience . They can give you chapter and verse on what action you should take.

JillMaryC profile image
JillMaryC in reply to wedgewood

Aaaagh! Thought this was the case. Was just hoping! My GP wouldn't explain fully, or clearly B12 and/or if I had Pernicious Anaemia. But a nurse in family says sounds like I have PA. it's a minefield. I am going to get another nurse friend to show me how to self inject. But... Is it also useful to get tested Intrinsic Factor? Many thanks

wedgewood profile image
wedgewood in reply to JillMaryC

Yes, it could well be useful , if you test positive . Trouble is, a negative test doesn’t disprove PA . You can still have PA with a negative test result. But if you have the the symptoms and do not receive any benefit from oral supplements , it’s likely that you could have PA . I’m taking it as read that you are not on any medication that inhibits B12 absorption (Google for that info ) don’t have Helicobacter Pylori infection or fish tapeworm infestation . Veganism and strict Vegetarian diet included obviously . I recommend you read books by our chairman Martyn Hooper obtainable from Amazon.uk .Very best wishes

JillMaryC profile image
JillMaryC in reply to wedgewood

Thank you so much. Appreciated.

kmalbasich profile image
kmalbasich

Hi Jill I was diagnosed over two years ago with PA mine is genetic runs in the family.

I keep a diary from day to day so I know what works for me.

I self inject twice a week, or my symptoms of shortness of breath horrid dreams,tripping when walking tiredness return very fast.

Mine was so bad while under the treatment of a Dr I knew I would be in a wheel chair within weeks from the muscle spasms.

So trial and error and much research I find twice a week best suits me to inject

I take mthf (active folate)

Maltofer iron tablets as they don't cause constipation and easier on the stomach

Magnesium malate,great for muscle and nerve repair

lipoic acid for cellular energy

l glutamine in powder form ,great for healing the gut but also energy

Hope that helps for info to search out for yourself.

Good luck on healing yourself

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