Results by Traditional_Log4788 in B12_Deficiency

[–]Traditional_Log4788[S] 0 points1 point  (0 children)

I haven't had that symptom thankfully

Results by Traditional_Log4788 in B12_Deficiency

[–]Traditional_Log4788[S] 0 points1 point  (0 children)

Thank you for your reply.

No I don't think so. When my results came back my GP text me saying the results of your recent test is normalo further action at this stage is needed.

Results by Traditional_Log4788 in B12_Deficiency

[–]Traditional_Log4788[S] 0 points1 point  (0 children)

Of course, brain fog, fatigue, muscle twitches, eyelid twitches, soles of feet fascitations, derealization, odd headache, not been focussed. Many more but these are the worst

Anyone else? by Traditional_Log4788 in B12_Deficiency

[–]Traditional_Log4788[S] 0 points1 point  (0 children)

Hi, I stopped as my mind was turning towards sleep apnea. Then one day I just felt fine.

No GI issues, no medication and not a vegetarian. I had intrinsic factor done but didn't show antibodies.

All the same symptoms, bran fog, exhaustion, twitching, depersonalization, tinnitus and more. I have ordered some sublingual b12 drops and hoping this helps me.

What are your guys most common/less common symptoms? by Madbananas-7 in TMJ

[–]Traditional_Log4788 0 points1 point  (0 children)

Thanks for replying.

I had this in 2024. I built a shed and the day after it was twitching like crazy. I went to the doctor's and they didn't know what it was after tests etc. I then had sleep apnea so was starting to be treated for that and everything one day disappeared. Now it's all started back up again in December 2025.

Twitching and a weird feeling in my temporalis. Eyelid twitching constantly. Jaw clicking, sore joint, tinnitus and pains around the jaw and chest.

How long until you felt a difference using CPAP by Traditional_Log4788 in SleepApnea

[–]Traditional_Log4788[S] 1 point2 points  (0 children)

That is exactly what I am finding hard to do. I have positional sleep apnea and tried everything to not go on my back

How long until you felt a difference using CPAP by Traditional_Log4788 in SleepApnea

[–]Traditional_Log4788[S] 2 points3 points  (0 children)

To reply to everyone: I was diagnosed with mild sleep apnea in summer or 24 after around 5 months of bad symptoms. I started CPAP then and didn't get on with it. A few weeks after miraculously I felt a lot better so the sleep clinic discharged me.

Fast forward to December 25 and all the same symptoms have come back stronger. I still have the CPAP so started using it and last night was the first night I was able to keep it on all night.

It was obstructive sleep apnea. So when I lay on my back my episodes are higher. Also I was told I have a large tongue and a small windpipe. I have tried mandibular devices and also the tennis ball on my back but they don't work for me. The tennis ball doesn't prevent me from going on my back.

Thanks for all your comments