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unknown rash
hi everyone! Last week I posted pictures of my son’s face rash asking if it looked like cutaneous lupus. For those who are just reading now, he had this rash for about two months now— started on his ear which was raw red then went away. A few weeks later the rash developed bright red spots on his face
hi everyone! Last week I posted pictures of my son’s face rash asking if it looked like cutaneous lupus. For those who are just reading now, he had this rash for about two months now— started on his ear which was raw red then went away. A few weeks later the rash developed bright red spots on his face
Demaso33
in
LUPUS UK
3 months ago
Has anyone seen Prof Dorota Dworakowska in London?
Has anyone seen Prof Dorota Dworakowska in London and would she treat with T3? Please direct message as per rules. Thanks.
Has anyone seen Prof Dorota Dworakowska in London and would she treat with T3? Please direct message as per rules. Thanks.
samaja
in
Thyroid UK
3 months ago
Negative test results - Gutted
Hi, I'm new to this group but have found it very useful during the TWW. I've just undergone my first ICSI cycle and today did a pregnancy test. It was negative and despite trying to be prepared it's hit me hard. I'm 39 years old, turning 40 this year. Had an ecoptic pregnancy 2 years ago and after almost
Hi, I'm new to this group but have found it very useful during the TWW. I've just undergone my first ICSI cycle and today did a pregnancy test. It was negative and despite trying to be prepared it's hit me hard. I'm 39 years old, turning 40 this year. Had an ecoptic pregnancy 2 years ago and after almost
Letis
in
Fertility Network UK
3 months ago
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MediAlert bracelet for private T3 anybody?
A post by Rapunzel mentioned someone who was left untreated with T3 in hospital as they were on a private prescription. It made me think on the idea of getting a MediAlert bracelet for the private T3 issue. I wondered if anyone does this already and am interested in opinions as to whether the hospitals
A post by Rapunzel mentioned someone who was left untreated with T3 in hospital as they were on a private prescription. It made me think on the idea of getting a MediAlert bracelet for the private T3 issue. I wondered if anyone does this already and am interested in opinions as to whether the hospitals
inthedoldrums
in
Thyroid UK
3 months ago
Technical question-is there a difference between making your own T3 or taking synthetic T3 physically?
Could you feel a difference between the 2? I wondered whether making your own might reach other places the synthetic stuff might not be able to reach? Or are they both exactly the same? Thanks.
Could you feel a difference between the 2? I wondered whether making your own might reach other places the synthetic stuff might not be able to reach? Or are they both exactly the same? Thanks.
ockerdoc
in
Thyroid UK
3 months ago
ferritin level
hello, this is my ferritin level from my medichecks test. Is this ok?
hello, this is my ferritin level from my medichecks test. Is this ok?
Kimmi01
in
Thyroid UK
3 months ago
WHEN YOUR SPUTUM TEST COMES BACK ‘CLEAR’
How many times have members (particularly those with bronchiectasis)written that they feel ill, have purulent sputum and lots of it and yet have been told that their sputum test has come back ‘clear’ and so have been left with no or insufficient antibiotic treatment to battle on, knowing full well that
How many times have members (particularly those with bronchiectasis)written that they feel ill, have purulent sputum and lots of it and yet have been told that their sputum test has come back ‘clear’ and so have been left with no or insufficient antibiotic treatment to battle on, knowing full well that
Swizzy
in
Lung Conditions Community Forum
3 months ago
New Post, community only please
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
Dawnm10
in
Hughes Syndrome APS Forum
3 months ago
Wait time for food and drink after thyroxine
hi I have just been diagnosed with hypothyroidism and will start taking thyroxine tomorrow morning. I usually wake at 6.30 and will take then. NHS and endocrinology guidance says wait half an hour before having any food and drink, but I notice this forum advises an hour. I’m not worried about eating
hi I have just been diagnosed with hypothyroidism and will start taking thyroxine tomorrow morning. I usually wake at 6.30 and will take then. NHS and endocrinology guidance says wait half an hour before having any food and drink, but I notice this forum advises an hour. I’m not worried about eating
Bluesew
in
Thyroid UK
3 months ago
Carbimazole dose
Hi all, Back again! As always, grateful for thoughts. I've been on Carbimazole 10mg BD and Propanalol 40mg TDS for about 10 days now. My heart rate before treatment was sitting around 130/140 with a peak of 167. Has been sitting 55-75 since starting Propanalol. Bloods before treatment for free T4
Hi all, Back again! As always, grateful for thoughts. I've been on Carbimazole 10mg BD and Propanalol 40mg TDS for about 10 days now. My heart rate before treatment was sitting around 130/140 with a peak of 167. Has been sitting 55-75 since starting Propanalol. Bloods before treatment for free T4
Someday_maybe
in
Thyroid UK
3 months ago
1 1/2yrs of treatment and I’m getting worse again.
Need advice. I’m concerned. I was diagnosed with PA (lack IF via blood test) a year and a half ago. I have been on daily Hydroxo injections since. I started at a high concentrated dose (I’m in US) of 5,000mcg day and dosed it down to 1,750mcg day. I maintained this dose for 6 plus months and still
Need advice. I’m concerned. I was diagnosed with PA (lack IF via blood test) a year and a half ago. I have been on daily Hydroxo injections since. I started at a high concentrated dose (I’m in US) of 5,000mcg day and dosed it down to 1,750mcg day. I maintained this dose for 6 plus months and still
lb9999
in
Pernicious Anaemia Society
3 months ago
vitamins to help thyroid
Hello, has anyone got any tips of vitamin complexes to help under active thyroid? I have recently upped my vit d, my B12 and found a complex that says it helps the body convert t4 to t3. I’ve been taking them all about two weeks and I do think that I’m less exhausted than I was. I’m hopeful that it
Hello, has anyone got any tips of vitamin complexes to help under active thyroid? I have recently upped my vit d, my B12 and found a complex that says it helps the body convert t4 to t3. I’ve been taking them all about two weeks and I do think that I’m less exhausted than I was. I’m hopeful that it
Kimmi01
in
Thyroid UK
3 months ago
Buy t3
Coild someone dm/direct message me with a supplier they've used? Desperate.Tjx
Coild someone dm/direct message me with a supplier they've used? Desperate.Tjx
lesleyfromkent
in
Thyroid UK
3 months ago
out of date liothyronine T3
my T3 goes out of date 31st May and I still have a whole box left. I could do without another £99 cost 😭 do you reckon it would be ok for the next 2 months?
my T3 goes out of date 31st May and I still have a whole box left. I could do without another £99 cost 😭 do you reckon it would be ok for the next 2 months?
RoseStar
in
Thyroid UK
3 months ago
T3 Capsules
I,ve actually been given a NHS prescription for t3 after all these years.There in a capsule.I,ve always split my dose.Can you split the powder and just take it with water?
I,ve actually been given a NHS prescription for t3 after all these years.There in a capsule.I,ve always split my dose.Can you split the powder and just take it with water?
sylus_911
in
Thyroid UK
3 months ago
First PSA post surgery
Hello, Just had my first 3 month PSA test post surgery. <0.01. Good news but need to monitor every 3 years due to intraductal component. I just want to thank everyone that has been so supportive and has given me positive feedback on this forum. I am also getting genetic testing done this week as well
Hello, Just had my first 3 month PSA test post surgery. <0.01. Good news but need to monitor every 3 years due to intraductal component. I just want to thank everyone that has been so supportive and has given me positive feedback on this forum. I am also getting genetic testing done this week as well
Granolaberry
in
Prostate Cancer Network
3 months ago
Sometimes the solution is simple !
Getting through the winter isn’t isn’t easy, is it friends ? This one was a long one and once the spring is on its way my energy levels, enthusiasm and motivation get going and life opens up again. It didn’t happen this year though. Asthma COPD for 21 years….was it all getting to the body ? No energy
Getting through the winter isn’t isn’t easy, is it friends ? This one was a long one and once the spring is on its way my energy levels, enthusiasm and motivation get going and life opens up again. It didn’t happen this year though. Asthma COPD for 21 years….was it all getting to the body ? No energy
PaulineHM
in
Lung Conditions Community Forum
3 months ago
Confused about relatives diagnosis and treatment for colon cancer
Grandad is 87, diagnosed with colon cancer at the beginning of the year. Only symptom was rapidly decreasing iron in blood.They said he had stage T4 and that they were going to do an operation to remove the cancer. They did just that last week. Doctors said they had removed the cancer and he was released
Grandad is 87, diagnosed with colon cancer at the beginning of the year. Only symptom was rapidly decreasing iron in blood.They said he had stage T4 and that they were going to do an operation to remove the cancer. They did just that last week. Doctors said they had removed the cancer and he was released
Fenella34
in
Colon Cancer Connected
3 months ago
This is not how I am 😕
I saw my rheumatologist yesterday. A couple of weeks earlier than scheduled because I've felt very depressed. I feel no joy, no focus, no energy/vibe. My blood and urine tests were OK, but my skin is the worst he's seen it. 😫 He even, with consent, took a photo of my hands to show them to his medical
I saw my rheumatologist yesterday. A couple of weeks earlier than scheduled because I've felt very depressed. I feel no joy, no focus, no energy/vibe. My blood and urine tests were OK, but my skin is the worst he's seen it. 😫 He even, with consent, took a photo of my hands to show them to his medical
AnonLupi
in
LUPUS UK
3 months ago
Both LH and HCG positive
This is my 6th week since first miscarriage. I have confirmed negative hcg 3 times before. Have been tracking my LH just to see how my body is reacting, which as usual started with very low LH. I'm getting high LH now since 5 days, I never ovulated on my own before (atleast never checked) and I was suspicious
This is my 6th week since first miscarriage. I have confirmed negative hcg 3 times before. Have been tracking my LH just to see how my body is reacting, which as usual started with very low LH. I'm getting high LH now since 5 days, I never ovulated on my own before (atleast never checked) and I was suspicious
Hope_1996
in
Fertility Network UK
3 months ago
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