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Gorlin syndrome
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When should I tell me manager I'm pregnant
I want to wait until 12 weeks before telling anybody I am pregnant, but I work with complex, vulnerable individuals, often lone-working, and am not sure whether I should tell my manager earlier than 12 weeks. We have had a lot of ups and downs with IVF and so I am feeling anxious about sharing the news
I want to wait until 12 weeks before telling anybody I am pregnant, but I work with complex, vulnerable individuals, often lone-working, and am not sure whether I should tell my manager earlier than 12 weeks. We have had a lot of ups and downs with IVF and so I am feeling anxious about sharing the news
GranolaLover2000
in
Fertility Network UK
5 months ago
Update - pinning all our hopes on one embryo
Thanks for all your well wishes. We started with 5 eggs, which dwindled down to 2 embryos by day 3. As you know, we requested for a day 3 single embryo transfer against clinic advice. Well, it looks like my remaining embryo did not make it to blastocyst. We just got the call. My clinic feels that
Thanks for all your well wishes. We started with 5 eggs, which dwindled down to 2 embryos by day 3. As you know, we requested for a day 3 single embryo transfer against clinic advice. Well, it looks like my remaining embryo did not make it to blastocyst. We just got the call. My clinic feels that
Mrs_MT
in
Fertility Network UK
5 months ago
Lining 5.9mm on day 12.. not feeling very hopeful
Hi all, I had my cycle day 12 lining scan today. My lining on my day 9 scan (on Monday) was 5.3mm. Today on cycle day 12, it was only ay 5.9mm. I was told the lining was triple layer however have been asked to return for a scan on Tuesday 23rd Jan to see if there are any developments. I have been
Hi all, I had my cycle day 12 lining scan today. My lining on my day 9 scan (on Monday) was 5.3mm. Today on cycle day 12, it was only ay 5.9mm. I was told the lining was triple layer however have been asked to return for a scan on Tuesday 23rd Jan to see if there are any developments. I have been
lovetravelling
in
Fertility Network UK
5 months ago
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Views on my test results
New to this forum, so glad to have found it, I was beginning to despair with my GP who explains nothing to me. Shocked to learn how badly thyroid conditions are treated in UK. Began losing my eyebrows 2 years ago and my diverticulitis began flaring up after years of being stable. Various ultrasound
New to this forum, so glad to have found it, I was beginning to despair with my GP who explains nothing to me. Shocked to learn how badly thyroid conditions are treated in UK. Began losing my eyebrows 2 years ago and my diverticulitis began flaring up after years of being stable. Various ultrasound
Norash
in
Thyroid UK
9 months ago
Day five
Well,I wasn't going to do this but have just had a couple of things out of the ordinary happen. Last evening I ate pork, peas, carrots with garlic and sweet potato, larger than my usual size meal. Likely a normal size meal for most. I experienced abdominal pains but only mild and thought no more of
Well,I wasn't going to do this but have just had a couple of things out of the ordinary happen. Last evening I ate pork, peas, carrots with garlic and sweet potato, larger than my usual size meal. Likely a normal size meal for most. I experienced abdominal pains but only mild and thought no more of
Hidden
in
IBS Network
9 months ago
Nailfold infection
I have my second nailfold infection in 2 months - it is proving difficult to resolve and a few days ago a telangectasia bled profusely for no reason. Is this connected to my Systemic Sclerosis or just a coincident. Thanks for any thoughts on this.
I have my second nailfold infection in 2 months - it is proving difficult to resolve and a few days ago a telangectasia bled profusely for no reason. Is this connected to my Systemic Sclerosis or just a coincident. Thanks for any thoughts on this.
janetfmauk
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
Day four
Well what a journey, day 4 and still no kick back from IBS. So far the foods that have triggered my IBS that I have tried again. Tomato sauce, crisps/chippies, gingernut biscuits, water, saveloys, marmite/ vegemite and wholemeal bread. All in moderation except for the bread, love my bread. Not a reaction
Well what a journey, day 4 and still no kick back from IBS. So far the foods that have triggered my IBS that I have tried again. Tomato sauce, crisps/chippies, gingernut biscuits, water, saveloys, marmite/ vegemite and wholemeal bread. All in moderation except for the bread, love my bread. Not a reaction
Hidden
in
IBS Network
9 months ago
A newbie question about vitamin D3
Before discovering compression fractures due to osteoporosis, I was taking various vitamin supplements. ( this is going to sound like I’m a hypochondriac, but I was trying to stay healthy). I had Garlic tablets, Glucosamine& Chondroitin, vit B, vit D3 and zinc. After my DEXA scan, my old GP put me on
Before discovering compression fractures due to osteoporosis, I was taking various vitamin supplements. ( this is going to sound like I’m a hypochondriac, but I was trying to stay healthy). I had Garlic tablets, Glucosamine& Chondroitin, vit B, vit D3 and zinc. After my DEXA scan, my old GP put me on
Indigo2417
in
PMRGCAuk
9 months ago
Garlic and Autoimmune
I have antiphospho lipid antibody syndrome (CAPS) and a very high intolerance for Garlic, within 20 minutes of ingesting garlic I start vomiting and my intestines blow up like balloons and I have extreme pain. My daughter who has lupus was told by her doctor not to eat Garlic as it activates
I have antiphospho lipid antibody syndrome (CAPS) and a very high intolerance for Garlic, within 20 minutes of ingesting garlic I start vomiting and my intestines blow up like balloons and I have extreme pain. My daughter who has lupus was told by her doctor not to eat Garlic as it activates
Thick_Blood
in
Hughes Syndrome APS Forum
10 months ago
PLMD and RLS Update
25 + years ago, I began experiencing symptoms with leg jerkiness during sleep, causing me to rise and stretch and sit up until the movement stopped. The GP prescribed gabapentin, which led me down the road until 2016 with a move to Phoenix, and to visit a neurologist. After testing, and his patient for
25 + years ago, I began experiencing symptoms with leg jerkiness during sleep, causing me to rise and stretch and sit up until the movement stopped. The GP prescribed gabapentin, which led me down the road until 2016 with a move to Phoenix, and to visit a neurologist. After testing, and his patient for
vikkitennis
in
Restless Legs Syndrome
4 hours ago
Thyroxine uptake and Ehlers Danlos Syndrome
Hi all, any experience or advice on this would be much appreciated. I have been on thyroxine for 25 years since having Hashimotos at the age of 29. I've also been diagnosed a while ago with Ehlers Danlos Syndrome and Fibromyalgia (both connective tissue disorders.) My new GP is messing about with
Hi all, any experience or advice on this would be much appreciated. I have been on thyroxine for 25 years since having Hashimotos at the age of 29. I've also been diagnosed a while ago with Ehlers Danlos Syndrome and Fibromyalgia (both connective tissue disorders.) My new GP is messing about with
hcmoss68
in
Thyroid UK
3 days ago
7 days off Pramipexole
Two months ago I finally found a doctor (addiction specialist) who read all the literature I gave him (from this site) and he was very understanding and prescribed me the suboxone film. I’m taking 1/7 of the film each day and it has enabled me to get to this point of no Pramipexole! I kinda thought
Two months ago I finally found a doctor (addiction specialist) who read all the literature I gave him (from this site) and he was very understanding and prescribed me the suboxone film. I’m taking 1/7 of the film each day and it has enabled me to get to this point of no Pramipexole! I kinda thought
Itsatom
in
Restless Legs Syndrome
4 days ago
For those considering methadone
hi again everyone, I just want to give a quick update for anyone who may be considering methadone. After trying many other drugs, and after augmentation and withdrawal from dopamine agonists, I started mid Feb on 2.5 mg methadone and have titrated slowly over 4 months to allow my body to get used to
hi again everyone, I just want to give a quick update for anyone who may be considering methadone. After trying many other drugs, and after augmentation and withdrawal from dopamine agonists, I started mid Feb on 2.5 mg methadone and have titrated slowly over 4 months to allow my body to get used to
Mongolia2020
in
Restless Legs Syndrome
4 days ago
HELP Please
How do I find a GP who knows about RLS. I have been back again to my GP as I'm now in server pain all the time which has sent my RLS into overdrive, I'm not sure if I'm in augmentation, she said she would give me an antidepressant to lift my mood!!. I explained that they will make my RLS worse and
How do I find a GP who knows about RLS. I have been back again to my GP as I'm now in server pain all the time which has sent my RLS into overdrive, I'm not sure if I'm in augmentation, she said she would give me an antidepressant to lift my mood!!. I explained that they will make my RLS worse and
Marymill
in
Restless Legs Syndrome
5 days ago
Exercise that often helps
Although I have experienced intensification of RLS symptoms after heavy, prolonged daytime exercise, paradoxically I have sometimes found significant relief with short bursts of fairly intense calisthenics when symptoms hit at night. As mentioned elsewhere, I have had RLS since my teens. By about age
Although I have experienced intensification of RLS symptoms after heavy, prolonged daytime exercise, paradoxically I have sometimes found significant relief with short bursts of fairly intense calisthenics when symptoms hit at night. As mentioned elsewhere, I have had RLS since my teens. By about age
Cedarish
in
Restless Legs Syndrome
6 days ago
At a loss
I was prescribed Ropinirole .25 mg I took that for 4 days and could not handle the side effects. Day 4 was terrible. After reading the posts, it seems as if I am screwed if I don't take any medication for it so I guess I will just have to live with this condition drug free. I was never a pill popper
I was prescribed Ropinirole .25 mg I took that for 4 days and could not handle the side effects. Day 4 was terrible. After reading the posts, it seems as if I am screwed if I don't take any medication for it so I guess I will just have to live with this condition drug free. I was never a pill popper
Tree1228
in
Restless Legs Syndrome
9 days ago
levodopa and augmentation
I have had RLS for over 10 years and controlling symptoms with oxycodone. I have also been diagnosed with Parkinson’s disease and prescribed Levodopa. Can someone please confirm whether or not this is a dopamine agonist like Pramipexole. If so does it also lead to augmentation?
I have had RLS for over 10 years and controlling symptoms with oxycodone. I have also been diagnosed with Parkinson’s disease and prescribed Levodopa. Can someone please confirm whether or not this is a dopamine agonist like Pramipexole. If so does it also lead to augmentation?
Covenant1962
in
Restless Legs Syndrome
11 days ago
Solving Restless Legs
Medscape have a report issued on June 14th on some new interesting research It is entitled; Solving Restless Legs: Largest Genetic Study to Date May Help and is written by Lisa Marshall and published in Medscape June 14, 2024 I think it is worth our while to know something about it so for
Medscape have a report issued on June 14th on some new interesting research It is entitled; Solving Restless Legs: Largest Genetic Study to Date May Help and is written by Lisa Marshall and published in Medscape June 14, 2024 I think it is worth our while to know something about it so for
thorp
in
Restless Legs Syndrome
12 days ago
cryo-ablation update
hi everyone, Thought I would give an update. I had the cryo-ablation on the 13th of May. i felt fairly uncomfortable over the first few weeks, but thanks to all the support and info on here, I have got through it without panic. the main thing is pacing myself and not overdoing it. Get enough
hi everyone, Thought I would give an update. I had the cryo-ablation on the 13th of May. i felt fairly uncomfortable over the first few weeks, but thanks to all the support and info on here, I have got through it without panic. the main thing is pacing myself and not overdoing it. Get enough
Tilly1957
in
Atrial Fibrillation Support
12 days ago
RLS treatment Australia
Here is the latest I can find on treatment recommendations in Australia. It is consistent with the latest US advice and includes the option of opiods as last line treatment in refractory (including augmented) RLS. https://www1.racgp.org.au/ajgp/2023/september/restless-legs-syndrome To my mind it does
Here is the latest I can find on treatment recommendations in Australia. It is consistent with the latest US advice and includes the option of opiods as last line treatment in refractory (including augmented) RLS. https://www1.racgp.org.au/ajgp/2023/september/restless-legs-syndrome To my mind it does
ChickenTwisty
in
Restless Legs Syndrome
13 days ago
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