Search
Search
About
Log in
Join
Experiences with
Lodine
Posts
Communities
5,568 public posts
Filter results
Mum in extreme pain
My Mum has been suffering with a Prolapse for the past 5 months and it has caused incredible amounts of pain. The pain seems to be easier when she first wakes up in the morning - to the point where she says she is completely resolved. For context, she has been diagnosed with a Stage 2 rectocele and
My Mum has been suffering with a Prolapse for the past 5 months and it has caused incredible amounts of pain. The pain seems to be easier when she first wakes up in the morning - to the point where she says she is completely resolved. For context, she has been diagnosed with a Stage 2 rectocele and
Concerned_Son1981
in
Pelvic Pain Support Network
1 year ago
Unbearable back pain
Hi - I am just wondering what pain relief people take for severe nerve pain? I have DDD. I had a badly herniated disc with was operated on. It caused nerve damage so I have sensation issues in my lower right leg. I get pain periodically in my back. I ended up in hospital on Saturday due to severe pain
Hi - I am just wondering what pain relief people take for severe nerve pain? I have DDD. I had a badly herniated disc with was operated on. It caused nerve damage so I have sensation issues in my lower right leg. I get pain periodically in my back. I ended up in hospital on Saturday due to severe pain
Devils_Advocate
in
Pain Concern
1 year ago
interesting podcast on hypothyroidism but I think equally applies to other conditions
https://theenergyblueprint.com/fixing-hypothyroidism-dr-eric-balcavage/?inf_contact_key=5a718d6cbeb6c85d6fdf4729841e4d16b7af0999dac2af6212784c39e05d2aef Imbalances are caused by cell danger response as a way of the body protecting itself. You can read the transcript if you prefer. In this podcast,
https://theenergyblueprint.com/fixing-hypothyroidism-dr-eric-balcavage/?inf_contact_key=5a718d6cbeb6c85d6fdf4729841e4d16b7af0999dac2af6212784c39e05d2aef Imbalances are caused by cell danger response as a way of the body protecting itself. You can read the transcript if you prefer. In this podcast,
LAJ12345
in
Cure Parkinson's
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
"re-Tweeted" by Simon Pearce ..'evidence' that long term T3 use risks heart failure /stroke ... can anyone get full access ?
Link to original tweet by ThyroidFederation: https://twitter.com/ThyroidFed/status/1540276641007550465?cxt=HHwWgoCysbfclOAqAAAA "The use of combination therapy with liothyronine and #levothyroxine in Asian patients was looked at and found that use of liothyronine was linked with higher incidence of
Link to original tweet by ThyroidFederation: https://twitter.com/ThyroidFed/status/1540276641007550465?cxt=HHwWgoCysbfclOAqAAAA "The use of combination therapy with liothyronine and #levothyroxine in Asian patients was looked at and found that use of liothyronine was linked with higher incidence of
tattybogle
in
Thyroid UK
1 year ago
A brief respite and now back with a vengeance
I suffer from restless legs syndrome and was prescribed pramipexole. I started a reduction program several months ago and by September I was down to half a tablet today. I was diagnosed with breast cancer and had to have a mastectomy 3 moths ago. Unbeknown to me the surgery temporarily raised my ferritin
I suffer from restless legs syndrome and was prescribed pramipexole. I started a reduction program several months ago and by September I was down to half a tablet today. I was diagnosed with breast cancer and had to have a mastectomy 3 moths ago. Unbeknown to me the surgery temporarily raised my ferritin
RestlessMe
in
Restless Legs Syndrome
1 year ago
Reduction of Ropinirole
Hello fellow sufferers where ever you are in the world. I have been reducing my Ropinirole dosage by 0.25mg every 2 to 3 weeks depending how it’s going and am now taking 4.75 mg / day a reduction of 1.25 mg / day from 24 October 2022 and am in for the long haul. I used to spread my dose out during the
Hello fellow sufferers where ever you are in the world. I have been reducing my Ropinirole dosage by 0.25mg every 2 to 3 weeks depending how it’s going and am now taking 4.75 mg / day a reduction of 1.25 mg / day from 24 October 2022 and am in for the long haul. I used to spread my dose out during the
HipHop1972
in
Restless Legs Syndrome
1 year ago
Plasma Metabolomics Reveals Systemic Metabolic Alterations of Subclinical and Clinical Hypothyroidism
This paper does what I have long been waiting for. Takes some blood, just the serum, and do a comprehensive analysis of pretty much everything they can detect in that serum. The subjects were divided into Control, Subclinical Hypothyroid and Hypothyroid groups. They found clear differences
This paper does what I have long been waiting for. Takes some blood, just the serum, and do a comprehensive analysis of pretty much everything they can detect in that serum. The subjects were divided into Control, Subclinical Hypothyroid and Hypothyroid groups. They found clear differences
helvella
Thyroid UK
in
Thyroid UK
1 year ago
generally fed up
bern to see prof D’Cruz at London Bridge as it looked likely I had sjrogens. He did his usual full checks thought dry lios dry eyes etc was likely to be APS but sent for blood test and now been referred as no sjrogens but high Gamma GT and high reactive c protein. Then on top of that had follow up lung
bern to see prof D’Cruz at London Bridge as it looked likely I had sjrogens. He did his usual full checks thought dry lios dry eyes etc was likely to be APS but sent for blood test and now been referred as no sjrogens but high Gamma GT and high reactive c protein. Then on top of that had follow up lung
Greenmil3
in
Hughes Syndrome APS Forum
1 year ago
Introduction and Preface to Comments
Hi, All. My first post. For several months, I've been reading your comments and empathizing with those who have suffered with this condition. To the extent that there is anything that may be unique to my circumstance, it may be the volume of medical experts with whom I have consulted and by whom
Hi, All. My first post. For several months, I've been reading your comments and empathizing with those who have suffered with this condition. To the extent that there is anything that may be unique to my circumstance, it may be the volume of medical experts with whom I have consulted and by whom
Hidden
in
Restless Legs Syndrome
1 year ago
More recent bloods & dose increase
After my last post regarding my private blood tests, my Endo increased my levo to 100/125 alternate days. I've just had more blood tests, 6 weeks on through the Endo so no Ft3 and again he says they're in range! I really lost my sh*t and got out my list and explained how I've been feeling since having
After my last post regarding my private blood tests, my Endo increased my levo to 100/125 alternate days. I've just had more blood tests, 6 weeks on through the Endo so no Ft3 and again he says they're in range! I really lost my sh*t and got out my list and explained how I've been feeling since having
JUUJOO
in
Thyroid UK
1 year ago
Been very hard to find a suitable multi-vit
I have been here long enough now to realise that I need only very select vits/mins in high quality and the right doses and absolutely do not need a ton of stuff that ordinarily gets put into the std packages eg iodine / iron/E/A/boron /B plus the rest etc etc But as I try to save packaging and costs
I have been here long enough now to realise that I need only very select vits/mins in high quality and the right doses and absolutely do not need a ton of stuff that ordinarily gets put into the std packages eg iodine / iron/E/A/boron /B plus the rest etc etc But as I try to save packaging and costs
Danielj1
in
Thyroid UK
2 years ago
bone,, muscle, nerve pain
I have just found the energy to write this, not sure what what is wrong with me apart from a huge list of the medical history I already know about, the main things are that I have had problems Hughes syndrome since about 1981 have problems with my memory really bad I had to retire early anyway gradually
I have just found the energy to write this, not sure what what is wrong with me apart from a huge list of the medical history I already know about, the main things are that I have had problems Hughes syndrome since about 1981 have problems with my memory really bad I had to retire early anyway gradually
daisyd
in
Hughes Syndrome APS Forum
1 year ago
Anagrelid to Interferon and Hashimoto.
I’m seriously thinking of changing from Anagrelid to interferon. I’ve always had heart palpitations from Anagrelide. All doctors to date said no interferon (I have Hashimoto) and no HU ( I have inborn anaemia). When I tried it once, I had nasty neurological side effects. Now I found a new MPN
I’m seriously thinking of changing from Anagrelid to interferon. I’ve always had heart palpitations from Anagrelide. All doctors to date said no interferon (I have Hashimoto) and no HU ( I have inborn anaemia). When I tried it once, I had nasty neurological side effects. Now I found a new MPN
Anag
in
MPN Voice
2 years ago
just When I thought all was OK
I am here again looking for some guidance. Doing well then started to feel anxious. I am currently taking 2 grains of NDT and 25mcg of T3. Decided to do a blood test and my results are below…I have been taking the exact amount for some time .. but my results are different and why? What shall I increase
I am here again looking for some guidance. Doing well then started to feel anxious. I am currently taking 2 grains of NDT and 25mcg of T3. Decided to do a blood test and my results are below…I have been taking the exact amount for some time .. but my results are different and why? What shall I increase
SophiaR
in
Thyroid UK
1 year ago
Newbie - confused and needing advice
I'm desperately confused and frightened, and looking for advice. Probably quite a long post coming up (sorry). I'm currently 42 and have been pregnant twice in ten years - once with my first boy naturally after three years TTC and again with my second son following an IVF cycle two years ago. I have
I'm desperately confused and frightened, and looking for advice. Probably quite a long post coming up (sorry). I'm currently 42 and have been pregnant twice in ten years - once with my first boy naturally after three years TTC and again with my second son following an IVF cycle two years ago. I have
Anonymoususername2
in
Endometriosis UK
1 year ago
Hashimoto's and CT scan with Iodine Containing Contrast Materials
I had a CT scan in August. No one warned me that this would involve an IV with an Iodine Containing Contrast solution. No one had any idea how this would affect me with regard to thyroid levels. In other words, I encountered the usual apathy with regard to being a thyroid patient and what my needs
I had a CT scan in August. No one warned me that this would involve an IV with an Iodine Containing Contrast solution. No one had any idea how this would affect me with regard to thyroid levels. In other words, I encountered the usual apathy with regard to being a thyroid patient and what my needs
kferrer
in
Thyroid UK
2 years ago
liquid radioactive iodine therapy
hello. I’m booked in at Mount Vernon hospital on November 14th for RAI. I’m totally rubbish at swallowing tablets so they have agreed to give it to me as a liquid. I’m now getting anxious it may be a massive beaker full and May taste disgusting Has anyone else had it this way and if so what was
hello. I’m booked in at Mount Vernon hospital on November 14th for RAI. I’m totally rubbish at swallowing tablets so they have agreed to give it to me as a liquid. I’m now getting anxious it may be a massive beaker full and May taste disgusting Has anyone else had it this way and if so what was
Titch121
in
Thyroid Cancer Support
2 years ago
TT or RAI
HiI have Graves disease - diagnosed 30 Sept 22 with zero TSH and high TRAB count. Carbimazole 40mg less than 3 weeks and neotrophils dropped with slightly raised AST and ALT liver enzymes. Endo told my GP to stop that and go on PTU. One week on only beta blockers then started 400mg PTU. Liver enzymes
HiI have Graves disease - diagnosed 30 Sept 22 with zero TSH and high TRAB count. Carbimazole 40mg less than 3 weeks and neotrophils dropped with slightly raised AST and ALT liver enzymes. Endo told my GP to stop that and go on PTU. One week on only beta blockers then started 400mg PTU. Liver enzymes
MsPeartree
in
Thyroid UK
1 year ago
lymphocytic colitis
hi there my husband has been recently diagnosed with lymphocytic colitis in his large intestine he’s in chronic pain he’s had tests mri biopsies done and he hardly eats he’s losing weight he has no energy his tummy is hard most days he’s in constant pain can anyone suggest anything to help him he’s been
hi there my husband has been recently diagnosed with lymphocytic colitis in his large intestine he’s in chronic pain he’s had tests mri biopsies done and he hardly eats he’s losing weight he has no energy his tummy is hard most days he’s in constant pain can anyone suggest anything to help him he’s been
Natsteveo
in
Bowel Disease Support
1 year ago
Iron Levels
I am on a reduction program for pramipexole, and it’s going really well. I’m taking gentle iron every other night. I also have some codeine tablets and I take one at bedtime. However I had surgery about eight weeks ago. I had my second full iron panel blood test about four weeks ago. My ferritin levels
I am on a reduction program for pramipexole, and it’s going really well. I’m taking gentle iron every other night. I also have some codeine tablets and I take one at bedtime. However I had surgery about eight weeks ago. I had my second full iron panel blood test about four weeks ago. My ferritin levels
RestlessMe
in
Restless Legs Syndrome
1 year ago
1
...
29
30
31
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
3060 results
Endometriosis UK
520 results
Restless Legs Syndrome
285 results
View top 10 communities
Sort by
Most Relevant
Newest