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Worse anxiety after B12 injections
I've been on B12 injections for 2 weeks and I'm sure it's made my anxiety and panic worse. I'm now in a constant state of panic and it's absolutely deliberating.
I've been on B12 injections for 2 weeks and I'm sure it's made my anxiety and panic worse. I'm now in a constant state of panic and it's absolutely deliberating.
Chocolatelover15
in
Pernicious Anaemia Society
4 days ago
After some B12 advice following results
Hi everyone, thanks in advance for reading. These sites and forums have been so useful since having found out I was deficient in a few things a few months ago. Following a blood test, it showed I had low B12, deficient in Folate and Vit D and low iron, but not deficient. This topic was not one I knew
Hi everyone, thanks in advance for reading. These sites and forums have been so useful since having found out I was deficient in a few things a few months ago. Following a blood test, it showed I had low B12, deficient in Folate and Vit D and low iron, but not deficient. This topic was not one I knew
BlackberryJam
in
Pernicious Anaemia Society
4 days ago
B12 injections dangerous?
Came across this whilst trying to find out if I can purchase b12 injections whilst in USA later this year. It may have already have been uploaded to site so apologies if I am late to the party https://www.wolverhampton.gov.uk/news/warning-illegal-use-vitamin-b12-injections-puts-city-customers-risk
Came across this whilst trying to find out if I can purchase b12 injections whilst in USA later this year. It may have already have been uploaded to site so apologies if I am late to the party https://www.wolverhampton.gov.uk/news/warning-illegal-use-vitamin-b12-injections-puts-city-customers-risk
Nonameme
in
Pernicious Anaemia Society
4 days ago
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Hi Again - b12 and Peripheral Neuropathy (PN) - its wasnt the Alcohol?
Hi again lovely folks, and a big thanks to those "constant" heroes in this forum; who stick around to help us "worried-up" trainee Health Detectives To set the scene my lovelies - I was in here a while ago looking for the cause of my awful symmetrical Peripheral Neuropathy (PN) in my hands, feet and
Hi again lovely folks, and a big thanks to those "constant" heroes in this forum; who stick around to help us "worried-up" trainee Health Detectives To set the scene my lovelies - I was in here a while ago looking for the cause of my awful symmetrical Peripheral Neuropathy (PN) in my hands, feet and
Treesong2023
in
Pernicious Anaemia Society
5 days ago
Vitamin D and Magnesium
I've got low vitamin D and one of my symptoms is severe anxiety and panic attacks. Not sure if these are related. Someone suggested taking magnesium alongside vitamin D to help with the panic and anxiety. Has anyone had any luck with magnesium citrate helping with anxiety?
I've got low vitamin D and one of my symptoms is severe anxiety and panic attacks. Not sure if these are related. Someone suggested taking magnesium alongside vitamin D to help with the panic and anxiety. Has anyone had any luck with magnesium citrate helping with anxiety?
Chocolatelover15
in
Pernicious Anaemia Society
5 days ago
Vitamin D and Anxiety
I've got low vitamin D and one of my symptoms is severe anxiety and panic attacks. Not sure if these are related. Someone suggested taking magnesium alongside vitamin D to help with the panic and anxiety. Has anyone had any luck with magnesium citrate helping with anxiety?
I've got low vitamin D and one of my symptoms is severe anxiety and panic attacks. Not sure if these are related. Someone suggested taking magnesium alongside vitamin D to help with the panic and anxiety. Has anyone had any luck with magnesium citrate helping with anxiety?
Chocolatelover15
in
Thyroid UK
5 days ago
Why no consistency when diagnosing B12D
Back in 2004 I tested low for B12 and had 6 loading doses, no follow up treatment. Then in 2018 same feelings of fatigue, tested low again (140) and again had 6 loading doses but again no follow up. As I hit 60 (but considered myself very fit for my age as always been keen sports person) I put fatgue
Back in 2004 I tested low for B12 and had 6 loading doses, no follow up treatment. Then in 2018 same feelings of fatigue, tested low again (140) and again had 6 loading doses but again no follow up. As I hit 60 (but considered myself very fit for my age as always been keen sports person) I put fatgue
Sailing63
in
Pernicious Anaemia Society
5 days ago
Delayed 2nd IVF Transfer
hi ladies I haven’t been on here for sometime and just thought I would post an update. I had a IVF transfer in my which failed unfortunately and I was due to half my second transfer in July, which would be a frozen embryo. I went on holiday last month and when I returned, my mindset had changed
hi ladies I haven’t been on here for sometime and just thought I would post an update. I had a IVF transfer in my which failed unfortunately and I was due to half my second transfer in July, which would be a frozen embryo. I went on holiday last month and when I returned, my mindset had changed
KFC1233
in
Fertility Network UK
5 days ago
Iron problem?
Hi,I have a low iron saturation - latest blood tests show range = just out (low side). Apologies I haven't got details atm. Although I do supplement with iron it's obviously not enough? I'm not too sure regarding Folate and Ferritin? What exactly do I purchase? Love to you all
Hi,I have a low iron saturation - latest blood tests show range = just out (low side). Apologies I haven't got details atm. Although I do supplement with iron it's obviously not enough? I'm not too sure regarding Folate and Ferritin? What exactly do I purchase? Love to you all
Booblet
in
Thyroid UK
5 days ago
New member -Dexa query
Background I was diagnosed with PMR in June 2024. Fortunate in having very supportive GP who quickly started me on 15 mg Predisolone which brought about dramatic improvement. Dose has been reduced to 14 mg after 1 month. GP plan is to reduce by about 1mg a month, depending on monthly blood test results
Background I was diagnosed with PMR in June 2024. Fortunate in having very supportive GP who quickly started me on 15 mg Predisolone which brought about dramatic improvement. Dose has been reduced to 14 mg after 1 month. GP plan is to reduce by about 1mg a month, depending on monthly blood test results
Crosswordsolver
in
PMRGCAuk
6 days ago
sublingual b12 and injection b12 new wakeup symptoms
good morning Everyone, I was wondering if when we treat b12 def. at first with liquid drops sublingual as I did for 6 months then realized I need to inject, I had strong wakeup symptoms with the sublinguals then a month and 1/2 ago I started the injections EOD and so I noticed I'm getting the wakeup
good morning Everyone, I was wondering if when we treat b12 def. at first with liquid drops sublingual as I did for 6 months then realized I need to inject, I had strong wakeup symptoms with the sublinguals then a month and 1/2 ago I started the injections EOD and so I noticed I'm getting the wakeup
JesusMercy60
in
Pernicious Anaemia Society
6 days ago
Things My Doctor Said in Notes./Rant On
I am abandoning this woman! (From January9, one day after a disabling super flare.) "Prednisone dosing - she is currently on 9mg of prednisone daily. She is trying to cut back by one milligram per month. Using naltrexone 4.5mg daily for pain as well. She remains convinced that her symptoms are due to
I am abandoning this woman! (From January9, one day after a disabling super flare.) "Prednisone dosing - she is currently on 9mg of prednisone daily. She is trying to cut back by one milligram per month. Using naltrexone 4.5mg daily for pain as well. She remains convinced that her symptoms are due to
Sandmason
in
PMRGCAuk
6 days ago
Low B12 and Anxiety
Has anyone experienced severe anxiety, panic attacks and disassociation from low B12. How long after starting injections did things improve?
Has anyone experienced severe anxiety, panic attacks and disassociation from low B12. How long after starting injections did things improve?
Chocolatelover15
in
Pernicious Anaemia Society
6 days ago
Be your own case manager
I was diagnosed with Behcets in 2018 followed by breast cancer in 2022. (Interesting to note inflammation in biopsy even for that). It was all fairly well controlled but I was not thriving as such and Nov 23 showed a new symptom - eye inflammation. Basically I read about a study in Birmingham where a
I was diagnosed with Behcets in 2018 followed by breast cancer in 2022. (Interesting to note inflammation in biopsy even for that). It was all fairly well controlled but I was not thriving as such and Nov 23 showed a new symptom - eye inflammation. Basically I read about a study in Birmingham where a
SCMW
in
Behçet's UK
6 days ago
Day 3 update (+hope)
The embryologist has just called with a Day 3 update and so far we have 4 out of 7 fertilised embryos at Grade 1 (the top grade) and 7-8 cells. The other 3 are Grades 3 and 4 so probably won't make it, but the fact that we have four front runners is such good news and means I'll hopefully have a decent
The embryologist has just called with a Day 3 update and so far we have 4 out of 7 fertilised embryos at Grade 1 (the top grade) and 7-8 cells. The other 3 are Grades 3 and 4 so probably won't make it, but the fact that we have four front runners is such good news and means I'll hopefully have a decent
neonpg
in
Fertility Network UK
6 days ago
British Vits
Hi all - I'm trying to optimise my
vitamins
but can't get Thorn Basic B from my normal supplier. I noticed in the process of attempting this that they come all the way from USA. I'm wondering if anyone knows of a British supplier to recommend. I am looking at BioCare presently.
Hi all - I'm trying to optimise my
vitamins
but can't get Thorn Basic B from my normal supplier. I noticed in the process of attempting this that they come all the way from USA. I'm wondering if anyone knows of a British supplier to recommend. I am looking at BioCare presently.
SilverSavvy
in
Thyroid UK
1 year ago
ME AGAIN
Hi so after hubby rang rheumatology clinic.. After all the issues abt appointments..I saw a different rheumatology.lady we spike about my symptoms and she said scalp tenderness is NOT part of GCA symptoms.....I was ..surprised and told her so...I got the look and we moved onso...from today I've dropped
Hi so after hubby rang rheumatology clinic.. After all the issues abt appointments..I saw a different rheumatology.lady we spike about my symptoms and she said scalp tenderness is NOT part of GCA symptoms.....I was ..surprised and told her so...I got the look and we moved onso...from today I've dropped
Alliekat65
in
PMRGCAuk
6 days ago
iodine/ Lugols ever ok for hypos?
I have numerous chronic health problems, most recent over last 4+ years being Long Covid with dysautonomia ( including hypertension with bad postural hypotension)…anyway on the look out for alternative health advice/ support , as NHS given up on me. I have come across Sarah Myhill’s advice to LC sufferers
I have numerous chronic health problems, most recent over last 4+ years being Long Covid with dysautonomia ( including hypertension with bad postural hypotension)…anyway on the look out for alternative health advice/ support , as NHS given up on me. I have come across Sarah Myhill’s advice to LC sufferers
Judithdalston
in
Thyroid UK
6 days ago
feeling anxious and alone
hey all I had my rhemotologist appointment this week after many months of my latest issue swelling in joints knees feet ankles wrists and fingers so full blood work taken talks of physio not sure how that would help ? To find out my CRP is high all of my liver tests are high and I have to start taking
hey all I had my rhemotologist appointment this week after many months of my latest issue swelling in joints knees feet ankles wrists and fingers so full blood work taken talks of physio not sure how that would help ? To find out my CRP is high all of my liver tests are high and I have to start taking
Jaq1971
in
Scleroderma & Raynaud's UK (SRUK)
6 days ago
Vitamin D & Calcium Supplements - current advice from Canadian Doctors.
Hello All, I thought this was worth passing on. I recently received the same advice from my family Doctor and CLL Specialist. "Make sure you take a vitamin D supplement at 1000 IU per day, but do NOT take a calcium supplement and try to ensure you get sufficient from your diet, not just diary but
Hello All, I thought this was worth passing on. I recently received the same advice from my family Doctor and CLL Specialist. "Make sure you take a vitamin D supplement at 1000 IU per day, but do NOT take a calcium supplement and try to ensure you get sufficient from your diet, not just diary but
PoisonDwarf
in
CLL Support
6 days ago
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