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Iron info
Iron and RLS - and you There is by now no question that iron therapy helps many if not most RLS patients. This has been proven in numerous studies, dating back to the 1950's. Yet nearly all physicians have never heard of the RLS-Iron connection, let alone how to treat it. Many patients who have
Iron and RLS - and you There is by now no question that iron therapy helps many if not most RLS patients. This has been proven in numerous studies, dating back to the 1950's. Yet nearly all physicians have never heard of the RLS-Iron connection, let alone how to treat it. Many patients who have
fritzb43
in
Restless Legs Syndrome
19 days ago
RLS and iron
HOW TO HAVE YOUR IRON STATUS CHECKED IRON INFORMATION FOR RLS PATIENTS As we know, low iron in the brain is one of the two major causes of Restless Leg Syndrome. (The other is a dopamine imbalance in the brain. In any event, RLS occurs in the brain - it is manifested in the limbs.) With regard
HOW TO HAVE YOUR IRON STATUS CHECKED IRON INFORMATION FOR RLS PATIENTS As we know, low iron in the brain is one of the two major causes of Restless Leg Syndrome. (The other is a dopamine imbalance in the brain. In any event, RLS occurs in the brain - it is manifested in the limbs.) With regard
fritzb43
in
Restless Legs Syndrome
19 days ago
Recent blood š©ø results for my partner - Parathyroid issues
Hi everyone š Iāve just been and collected recent blood results from 29th August . Your thoughts on results would be very much appreciated . John is experiencing bone pain in his legs / tiredness / fatigue / brain bog - and GP just wants to watch and wait š I think we may have to look at a private
Hi everyone š Iāve just been and collected recent blood results from 29th August . Your thoughts on results would be very much appreciated . John is experiencing bone pain in his legs / tiredness / fatigue / brain bog - and GP just wants to watch and wait š I think we may have to look at a private
Kisca
in
Thyroid UK
19 days ago
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Neurology appointment today!
I have a follow up appointment with the NHS neurologist today. Saw her over 18 months ago when I had some tingling nerve pain in my abdomen/hip/groin. (Follow up was supposed to be 12 months, but not surprised itās longer). At the time she didnāt know what was causing it so referred me to Birmingham
I have a follow up appointment with the NHS neurologist today. Saw her over 18 months ago when I had some tingling nerve pain in my abdomen/hip/groin. (Follow up was supposed to be 12 months, but not surprised itās longer). At the time she didnāt know what was causing it so referred me to Birmingham
Chickens44
in
Pernicious Anaemia Society
19 days ago
Update on neurology appointment
Saw the local consultant here in Aberdeen (not a RLS specialist) had a thick pile of paperwork, journals etc to give him. However, these were not needed (yet!) I gave him my last week symptom severity scale and monitor (from RLS-UK.ORG) which he will scan into my notes and encouraged me to bring new
Saw the local consultant here in Aberdeen (not a RLS specialist) had a thick pile of paperwork, journals etc to give him. However, these were not needed (yet!) I gave him my last week symptom severity scale and monitor (from RLS-UK.ORG) which he will scan into my notes and encouraged me to bring new
Islay9
in
Restless Legs Syndrome
19 days ago
Insights on 4 years of results?
Hello to everyone on here. Does anyone have any insights to share on my results, please? I'm due another blood test with my GP next week and I have asked for a full thyroid panel, but so far they haven't agreed to that. I asked last year too, but they were only willing to measure TSH. I have read on
Hello to everyone on here. Does anyone have any insights to share on my results, please? I'm due another blood test with my GP next week and I have asked for a full thyroid panel, but so far they haven't agreed to that. I asked last year too, but they were only willing to measure TSH. I have read on
FrancesD
in
Thyroid UK
19 days ago
Hypo crash after going too fast with T3, saliva cortisol readings
Hi, community. So Iāve been on a bit of a wild run over the past 2.5 months trying to get my thyroid therapy back in good shape. To give you a bit of the context, I am a 25 yo female, have been diagnosed with Hashimoto and subclinical hypothyroidism since 2018, started combo therapy (T4+T3) around
Hi, community. So Iāve been on a bit of a wild run over the past 2.5 months trying to get my thyroid therapy back in good shape. To give you a bit of the context, I am a 25 yo female, have been diagnosed with Hashimoto and subclinical hypothyroidism since 2018, started combo therapy (T4+T3) around
anakondratenko
in
Thyroid UK
19 days ago
calcium and vitamin D
Unfortunately I never got round to joining the PMRGCA uk ( brain sieve forgets to do a lot of things!) and so didnāt hear the speakers from the latest AGM. I have joined today! I was never prescribed calcium when I was diagnosed a year ago. I was told to buy Vitamin D 3000iu and I take it daily ( vitD3
Unfortunately I never got round to joining the PMRGCA uk ( brain sieve forgets to do a lot of things!) and so didnāt hear the speakers from the latest AGM. I have joined today! I was never prescribed calcium when I was diagnosed a year ago. I was told to buy Vitamin D 3000iu and I take it daily ( vitD3
Mashed
in
PMRGCAuk
19 days ago
Anaemia anyone?
I am wondering if anyone with PMR and/or GCA (both of which I've got/had) has also been diagnosed with anaemia. I notice that Pernicious Anaemia is another autoimmune condition. My GP called me in as my monthly blood tests had suggested I might have anaemia. He's running more tests but of course I'm
I am wondering if anyone with PMR and/or GCA (both of which I've got/had) has also been diagnosed with anaemia. I notice that Pernicious Anaemia is another autoimmune condition. My GP called me in as my monthly blood tests had suggested I might have anaemia. He's running more tests but of course I'm
DogAgilityObsessed
in
PMRGCAuk
20 days ago
Feeling desperate
I'm feeling very low at the moment, and quite isolated. I'm hoping to get some advice here. I'm a 45 year old male, and have had Hashimoto's since my early 20s. After a terrible few years on thyroxin I found NDT and on the whole have been relatively well on it. However, since around 2019 I've had bouts
I'm feeling very low at the moment, and quite isolated. I'm hoping to get some advice here. I'm a 45 year old male, and have had Hashimoto's since my early 20s. After a terrible few years on thyroxin I found NDT and on the whole have been relatively well on it. However, since around 2019 I've had bouts
ci00aaj
in
Thyroid UK
3 months ago
Sore, swollen lips; lethargy and weakness
Hello all.... over the last year or so I have had worsening health. I have been managing ok for a good few years my hypothyrodism / hashimoto's / menopause via Thyroid-S x 2 grains / strictly gluten free for over 5 years / Oestrogel x4 pumps/day. Had reasonable energy levels, body composition, mood
Hello all.... over the last year or so I have had worsening health. I have been managing ok for a good few years my hypothyrodism / hashimoto's / menopause via Thyroid-S x 2 grains / strictly gluten free for over 5 years / Oestrogel x4 pumps/day. Had reasonable energy levels, body composition, mood
richar03
in
Thyroid UK
20 days ago
Problem absorbing T4/T3
Just wondering if anyone knows how you can tell if you are not absorbing thyroxine and liothyronine due to gut/stomach problems. Will your TSH and T4/T3 blood levels show you have enough hormone - i.e. will it still get into your blood but not other parts of your system. I currently have a diverticulosis
Just wondering if anyone knows how you can tell if you are not absorbing thyroxine and liothyronine due to gut/stomach problems. Will your TSH and T4/T3 blood levels show you have enough hormone - i.e. will it still get into your blood but not other parts of your system. I currently have a diverticulosis
JRosemaryW
in
Thyroid UK
20 days ago
IBSA USA debuts three new dietary supplements - FilmTec B12.
Having produced Tirosint and Tirosint SOL levothyroxine (under their various names - brands and re-branded), IBSA appear to see supplements as a money-spinner. I'm just putting this here for information - hopefully at some point we will find out more. Like whether there is some basis for their absorption
Having produced Tirosint and Tirosint SOL levothyroxine (under their various names - brands and re-branded), IBSA appear to see supplements as a money-spinner. I'm just putting this here for information - hopefully at some point we will find out more. Like whether there is some basis for their absorption
helvella
in
Pernicious Anaemia Society
20 days ago
Supplement absorption
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I havenāt yet managed to do all the recommended reading but Iām working on it. Iām still looking into
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I havenāt yet managed to do all the recommended reading but Iām working on it. Iām still looking into
SallyBeeBobs
in
Cure Parkinson's
20 days ago
PMRGCAuk Annual Meeting....I wasn't alone today~!!
After my dress rehearsal last week, I got up at 4:30 AM, Central Time in the States, and was the only person at the Zoom link. I'm thrilled to report that I remembered today, and there were quite a few people. It was wonderful to put faces to the names of HU staff, Trustees, and some 'soul sisters' from
After my dress rehearsal last week, I got up at 4:30 AM, Central Time in the States, and was the only person at the Zoom link. I'm thrilled to report that I remembered today, and there were quite a few people. It was wonderful to put faces to the names of HU staff, Trustees, and some 'soul sisters' from
Grammy80
in
PMRGCAuk
21 days ago
Latest blood results
Hi all, I've just had latest results back from medichecks, I like to get these before I go and see my GP for nhs testing! After my last set of results in March when I was feeling so awful I increased my levothyroxine from 50mg to 75mg - my symptoms have improved a little but I still feel that I am
Hi all, I've just had latest results back from medichecks, I like to get these before I go and see my GP for nhs testing! After my last set of results in March when I was feeling so awful I increased my levothyroxine from 50mg to 75mg - my symptoms have improved a little but I still feel that I am
FlamingoPenguin
in
Thyroid UK
21 days ago
test results help !
I have a gp appointment in 4 days , Iāve done private blood test through medicheck and wanted some help with results as I still feel that my bowels are slow and rubbish , low calorie careful diet , I weigh a stone and a half more that a year ago ! My levothyroxine is 100 micro-grams daily ( I didn
I have a gp appointment in 4 days , Iāve done private blood test through medicheck and wanted some help with results as I still feel that my bowels are slow and rubbish , low calorie careful diet , I weigh a stone and a half more that a year ago ! My levothyroxine is 100 micro-grams daily ( I didn
Gilbert2023
in
Thyroid UK
22 days ago
Morning update on so confused.....
morning all, thank you for your help. So have just got latest bloods in. this is the picture so far... begining of june started as week knees going up stairs, then more Hyper symptoms- Hot flushing, sweating, weeing alot, skin burning at night, loss of weight, right eye red and puffy. tremors
morning all, thank you for your help. So have just got latest bloods in. this is the picture so far... begining of june started as week knees going up stairs, then more Hyper symptoms- Hot flushing, sweating, weeing alot, skin burning at night, loss of weight, right eye red and puffy. tremors
KimyH
in
Thyroid UK
22 days ago
Blood test Results
My serum folate is 3.7 ng/ml. ( 1.5-20) Serum B12 is 312 ngl ( 180-2000 ) Serum ferritin 117ng/ml. Opinions gratefully received š
My serum folate is 3.7 ng/ml. ( 1.5-20) Serum B12 is 312 ngl ( 180-2000 ) Serum ferritin 117ng/ml. Opinions gratefully received š
foamfollower
in
Thyroid UK
22 days ago
low b12 borderline folate celiac test
does anyone know what these results mean I didnāt do diet doc didnāt mention that but says normal no action required. AvtiveMy b12 and folate low also mch and Mchc low and red transferring sats 14.4% Iām so confused as everything marked normal no action and Iām so tired gut issues constipation
does anyone know what these results mean I didnāt do diet doc didnāt mention that but says normal no action required. AvtiveMy b12 and folate low also mch and Mchc low and red transferring sats 14.4% Iām so confused as everything marked normal no action and Iām so tired gut issues constipation
ninja1
in
Pernicious Anaemia Society
22 days ago
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