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Magnesium deficiency
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Chillblains
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
GerryPL
in
CLL Support
10 months ago
FINALLY found a scientific study that supports my theory about Brain Iron and Serum Iron. Finally!!!
First, the relevant quote from the article: “The serum iron concentration was significantly higher in the RLS group than in the control group, but remained within normal ranges in both groups. In this study, there was a significant correlation between serum and CSF iron concentrations, both in the RLS
First, the relevant quote from the article: “The serum iron concentration was significantly higher in the RLS group than in the control group, but remained within normal ranges in both groups. In this study, there was a significant correlation between serum and CSF iron concentrations, both in the RLS
DesertOasis
in
Restless Legs Syndrome
10 months ago
Update
Hi Ladies, l hope you are as well as you can be! I haven't posted for some time as things have not been to great.After the chemo last July l had to have several blood transfusions and magnesium infusions. Well to cut a long story short l had to go for a bone marrow biopsy and the outcome of this was
Hi Ladies, l hope you are as well as you can be! I haven't posted for some time as things have not been to great.After the chemo last July l had to have several blood transfusions and magnesium infusions. Well to cut a long story short l had to go for a bone marrow biopsy and the outcome of this was
Lewisriley47
in
My Ovacome
11 months ago
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Supplements - Dangerous, Essential or Useless?
Wizard recently made an interesting post on the "drive to minimize supplementation" that I wanted to respond to in-depth. The post: https://healthunlocked.com/pasoc/posts/150006558/the-drive-to-reduce-minimize-supplementation I decided a long form response would be better, thus my separate post here.
Wizard recently made an interesting post on the "drive to minimize supplementation" that I wanted to respond to in-depth. The post: https://healthunlocked.com/pasoc/posts/150006558/the-drive-to-reduce-minimize-supplementation I decided a long form response would be better, thus my separate post here.
Technoid
in
Pernicious Anaemia Society
11 months ago
b12 iron relationship?
Hi friends…I was diagnosed with a b12 deficiency in June, which is thankfully improving with injections (I had horrible neuro symptoms). I had my iron tested twice over the summer, both well in the good range (over 100). However, this week I had an iron panel showing my iron is 40 (literally the bottom
Hi friends…I was diagnosed with a b12 deficiency in June, which is thankfully improving with injections (I had horrible neuro symptoms). I had my iron tested twice over the summer, both well in the good range (over 100). However, this week I had an iron panel showing my iron is 40 (literally the bottom
MuppDog
in
Pernicious Anaemia Society
10 months ago
Iron deficiency
Hello I’m asking a question with regards to low ferritin levels (17.4). I’m confused whether I should be prescribed folic acid or iron?!
Hello I’m asking a question with regards to low ferritin levels (17.4). I’m confused whether I should be prescribed folic acid or iron?!
sewingroom
in
Thyroid UK
10 months ago
Insomnia
I'm waiting to see the gp again this morning, this has been a nightmare since May and I now don't sleep at night, I've no idea what to take,how to take my iron,my magnesium,my gabapentin, I'm not eating because I'm not sleeping, I'm paranoid and demotivated and nothing is working I feel desperate and
I'm waiting to see the gp again this morning, this has been a nightmare since May and I now don't sleep at night, I've no idea what to take,how to take my iron,my magnesium,my gabapentin, I'm not eating because I'm not sleeping, I'm paranoid and demotivated and nothing is working I feel desperate and
Baz33
in
Restless Legs Syndrome
11 months ago
Results Advice
Hi I’m looking for some advice on my recent bloods please, since my last test I dropped my levo back to 100mg a day and increased my lio by 5mg so I’m a little confused as to why my T3 has dropped🤷♀️the only thing I can think of is that I’ve been using Morningside lio for my 10mg dose in the morning
Hi I’m looking for some advice on my recent bloods please, since my last test I dropped my levo back to 100mg a day and increased my lio by 5mg so I’m a little confused as to why my T3 has dropped🤷♀️the only thing I can think of is that I’ve been using Morningside lio for my 10mg dose in the morning
PrincessAnnie
in
Thyroid UK
10 months ago
Targinact
I have had RLS for over 20 years and have tried most medications, the latest being Pregabalin, which was good but is now not working so well. I therefore asked my GP if I could try Targinact as I read this is now licensed for RLS. He has agreed and I just need to taper Pregabalin. Can anyone
I have had RLS for over 20 years and have tried most medications, the latest being Pregabalin, which was good but is now not working so well. I therefore asked my GP if I could try Targinact as I read this is now licensed for RLS. He has agreed and I just need to taper Pregabalin. Can anyone
Quiltingmum
in
Restless Legs Syndrome
10 months ago
Naproxen
Naproxen felt like it was burning a hole in my stomach due to not being given the gastro liners. I stopped taking the naproxen for about 4 months, I'm now back on them with the liners, not had a problem since.I've also discovered the joys of magnesium oil on my most painful joints. I'm on a very long
Naproxen felt like it was burning a hole in my stomach due to not being given the gastro liners. I stopped taking the naproxen for about 4 months, I'm now back on them with the liners, not had a problem since.I've also discovered the joys of magnesium oil on my most painful joints. I'm on a very long
KMatrix
in
Fibromyalgia Action UK
11 months ago
Night cramps
does anyone have excruciating night cramps? I’m trying to work out if it is because I’m doing too much exercise during the day. I’m tapering very very slowly down to 2 1/2 mgs pred that seems to be working I do take a little more magnesium every day. Thanks for any ideas
does anyone have excruciating night cramps? I’m trying to work out if it is because I’m doing too much exercise during the day. I’m tapering very very slowly down to 2 1/2 mgs pred that seems to be working I do take a little more magnesium every day. Thanks for any ideas
ellarowan
in
PMRGCAuk
11 months ago
Arginine and Taurine
Has anyone here had success with Arginine/Taurine/Magnesium? My Naturopath is willing to have me try but I am wondering if anyone has any firsthand knowledge out there of how long it takes to see results or not? Thanks!
Has anyone here had success with Arginine/Taurine/Magnesium? My Naturopath is willing to have me try but I am wondering if anyone has any firsthand knowledge out there of how long it takes to see results or not? Thanks!
MeganMN
in
AF Association
11 months ago
Restless legs
Morning hun. Iv had it for around 20 years iv always managed okBut Last Tuesday it started really bad and its day and night. Drs have given me some tablets for Parkinson they ste Not working. I'm just in the lounge walking all night 1-3 ,hour sleep a night Went to hospital Saturday they done bloods
Morning hun. Iv had it for around 20 years iv always managed okBut Last Tuesday it started really bad and its day and night. Drs have given me some tablets for Parkinson they ste Not working. I'm just in the lounge walking all night 1-3 ,hour sleep a night Went to hospital Saturday they done bloods
Frenhies
in
Restless Legs Syndrome
11 months ago
UTI/AF
Since having a kidney transplant I am bothered with UTI's which quickly clears up after taking antibiotics. I also have a PAF episode more or less within a day or two of this. Has anyone else noticed having AF when also having an infection? My potassium and magnesium levels are lower than normal when
Since having a kidney transplant I am bothered with UTI's which quickly clears up after taking antibiotics. I also have a PAF episode more or less within a day or two of this. Has anyone else noticed having AF when also having an infection? My potassium and magnesium levels are lower than normal when
Mismarswe
in
AF Association
11 months ago
Repeat blood test - Subclinical hypothroidism?
Hi, So I’ve had repeat blood test (5 months since last test) and results as follows TSH 4.99 FT4 17.3 pmol/L ( 10.8-25.5) FT3 5.2 pmol/L (3.1-6.8) Gp advised by text: Dear xx your thyroid function showed a mildly raised thyroid stimulating hormone level TSH at 4.99, with a normal free T3 and free
Hi, So I’ve had repeat blood test (5 months since last test) and results as follows TSH 4.99 FT4 17.3 pmol/L ( 10.8-25.5) FT3 5.2 pmol/L (3.1-6.8) Gp advised by text: Dear xx your thyroid function showed a mildly raised thyroid stimulating hormone level TSH at 4.99, with a normal free T3 and free
Busybee342
in
Thyroid UK
11 months ago
Diarrhoea saga continued
I've had diarrhoea on and off for over a year. It started after breakfast and stopped around lunch time, not every day, but about 3 days a week. It's been slowly getting more frequent. A month or so ago I spoke to the GP who first diagnosed me with PMR/GCA. She tested me for coeliac and cancer, both
I've had diarrhoea on and off for over a year. It started after breakfast and stopped around lunch time, not every day, but about 3 days a week. It's been slowly getting more frequent. A month or so ago I spoke to the GP who first diagnosed me with PMR/GCA. She tested me for coeliac and cancer, both
Broseley
in
PMRGCAuk
11 months ago
Promethazine Hydrochloride
hi I have been desperate for sleep but my RLS has been so bad that I’ve found it impossible I managed to get a GP appointment and told her my story and background and although she was sympathetic said the RLS I’d very difficult to control I told her I had no desire to go back on to a DA and my problems
hi I have been desperate for sleep but my RLS has been so bad that I’ve found it impossible I managed to get a GP appointment and told her my story and background and although she was sympathetic said the RLS I’d very difficult to control I told her I had no desire to go back on to a DA and my problems
Hoochybaby
in
Restless Legs Syndrome
10 months ago
Gabapentin
have been on Gabapentin on and off for approximately 6 months, I’ve tried to keep the dose as low as possible. I started on 100 mg before I went to bed this seemed to work with me only waking up once. It then got worse and I now suffer with pain across my shoulders at night aswell as in my legs, I upped
have been on Gabapentin on and off for approximately 6 months, I’ve tried to keep the dose as low as possible. I started on 100 mg before I went to bed this seemed to work with me only waking up once. It then got worse and I now suffer with pain across my shoulders at night aswell as in my legs, I upped
Catbennie
in
Restless Legs Syndrome
11 months ago
Can anyone shed light on my blood test results? Taking NDT. Thank you!
Hello all, Would someone be able to offer any insight to my blood tests results here at all? Many thanks. I take 310mg of Erfa NDT. I have hypothyroidism (hashi) and am a 46 year woman (so perimenopausal) and have two children. I exercise daily for at an hour. I have coeliac disease and am gluten free
Hello all, Would someone be able to offer any insight to my blood tests results here at all? Many thanks. I take 310mg of Erfa NDT. I have hypothyroidism (hashi) and am a 46 year woman (so perimenopausal) and have two children. I exercise daily for at an hour. I have coeliac disease and am gluten free
DaisyJones1
in
Thyroid UK
11 months ago
Weak legs along with neuropathy!
Hi, I have Pernicious Anaemia, and SACD a lot of neuropathy in mostly in my feet and legs I am noticing that my legs have been more and more weakening and stiffening Is this normal for neuropathy and will it get better? also am chronically exhausted! I am SI daily B12 and taking 5mg of folic acid,
Hi, I have Pernicious Anaemia, and SACD a lot of neuropathy in mostly in my feet and legs I am noticing that my legs have been more and more weakening and stiffening Is this normal for neuropathy and will it get better? also am chronically exhausted! I am SI daily B12 and taking 5mg of folic acid,
brenanddave
in
Neuropathy Support
11 months ago
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