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Devestated - empty looking sac at 7 week scan
Hello, I’ve had a whirlwind of a few weeks which included a totally unselected BFP following our last round of ovulation induction before moving to IVF in the new year. Of course I was anxious but really thought this could be my lucky break and naturally got carried away imagining future baby. Today
Hello, I’ve had a whirlwind of a few weeks which included a totally unselected BFP following our last round of ovulation induction before moving to IVF in the new year. Of course I was anxious but really thought this could be my lucky break and naturally got carried away imagining future baby. Today
CarlottaD27
in
Fertility Network UK
7 months ago
Iron deficiency symptoms..? GP says not.. advice please !
Hi there I've been unwell struggling after catching covid with those iron-deficiency like symptoms for long time GP has done some blood tests then told me Im fine all time but Im worst ever..too much weird dizziness & headaches can't standing bit long mostly have to sit down at least extremely tired
Hi there I've been unwell struggling after catching covid with those iron-deficiency like symptoms for long time GP has done some blood tests then told me Im fine all time but Im worst ever..too much weird dizziness & headaches can't standing bit long mostly have to sit down at least extremely tired
Snqanq
in
Thyroid UK
11 months ago
Need mental help or support about sharing the ivf procedure with parents and in laws
I'm Indian 36+ ttc since 2016 and moved to UK in 2019. 2 iui + 1ivf icsi FET failure. My parents torture me to the core to share all the details of my process and everytime I tell them they have no rights to ask and I'm not obliged to tell, they start up their drama of being silent. Already my childhood
I'm Indian 36+ ttc since 2016 and moved to UK in 2019. 2 iui + 1ivf icsi FET failure. My parents torture me to the core to share all the details of my process and everytime I tell them they have no rights to ask and I'm not obliged to tell, they start up their drama of being silent. Already my childhood
positivityonly
in
Fertility Network UK
4 months ago
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A friend said to me “It sounds as if your heart has rebooted?”; Is this possible?
Here is the background. I had Covid from my partner following a visit of his to the hospital and 48 hours after it went negative, I had a fast pulse with an irregular heartbeat (only traceable using taking a wrist pulse, no palpitations, no breathlessness). Was put on apixaban and bisoprolol both of
Here is the background. I had Covid from my partner following a visit of his to the hospital and 48 hours after it went negative, I had a fast pulse with an irregular heartbeat (only traceable using taking a wrist pulse, no palpitations, no breathlessness). Was put on apixaban and bisoprolol both of
LindyMc
in
British Heart Foundation
11 months ago
covid
hi. Has anyone got Covid gone off ibrance and feel worse. I am so tired it’s nuts. My blood work today was good although my tumor markers went up 3 points but I’m really nervous. Thanks so much. Marianne
hi. Has anyone got Covid gone off ibrance and feel worse. I am so tired it’s nuts. My blood work today was good although my tumor markers went up 3 points but I’m really nervous. Thanks so much. Marianne
marianne88
in
SHARE Metastatic Breast Cancer
11 months ago
Microbiome in PD, RBD and 1st degree relatives
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
As much as I'd like to believe that one "bad" bacteria (desulfovibrio) is responsible for Parkinson's, I suspect the situation is more complicated than that, as this recently released study suggests; https://www.nature.com/articles/s41467-023-38248-4 Certainly the evidence is accumulating though, that
Rufous2
in
Cure Parkinson's
1 year ago
cutaneous lupus
I have got subacute cutaneous lupus and coeliac and my question is I got covid back in October and was quite poorly and I would say just over it now. As a nurse I took all covid vaccines but was never sent by my GP to get them as they said I was not high risk. Can you clarify. I never got the very
I have got subacute cutaneous lupus and coeliac and my question is I got covid back in October and was quite poorly and I would say just over it now. As a nurse I took all covid vaccines but was never sent by my GP to get them as they said I was not high risk. Can you clarify. I never got the very
No2Sunshine
in
LUPUS UK
11 months ago
Covid Vaccines
Hi Anyone have any comments about taking a 6 covid vaccine? After 5 vaccines is it necessary to take another one? Will it really protect CLL people?
Hi Anyone have any comments about taking a 6 covid vaccine? After 5 vaccines is it necessary to take another one? Will it really protect CLL people?
Kmegood
in
CLL Support
11 months ago
thrush……again
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
For the past three months I’ve been trying to get rid of a bad taste in my mouth. The roof of my mouth feels like I’ve burned my mouth on a too hot pizza. The middle of my tongue is coated the tip is somewhat red. My dentist said X-rays show no infection. GP looked in my mouth and said
Mstiles
in
PMRGCAuk
10 months ago
Change from Nucala to Dupixent
Hello all! I don’t post much but read daily. I have eosinophilic asthma and chronic sinusitis. I’ve been on Nucala for the last 5 years and have been relatively well controlled. After a mild case of covid I developed bronchitis and was treated, but after that, I can’t seem to stop coughing. I have constant
Hello all! I don’t post much but read daily. I have eosinophilic asthma and chronic sinusitis. I’ve been on Nucala for the last 5 years and have been relatively well controlled. After a mild case of covid I developed bronchitis and was treated, but after that, I can’t seem to stop coughing. I have constant
kdr112
in
Asthma Community Forum
8 months ago
FLU VACCINE
I am in the UK on Venetoclax and have just spent 5 days in hospital with COVID. Is it safe to have the flu vaccine and is it hit or miss whether the vaccine is actually for the strain of flu which is going to be around this winter
I am in the UK on Venetoclax and have just spent 5 days in hospital with COVID. Is it safe to have the flu vaccine and is it hit or miss whether the vaccine is actually for the strain of flu which is going to be around this winter
Marisa
in
CLL Support
8 months ago
prednisolone 3 week course followd by surgery
Hi please can anyone advise how long to wait in between a prednisolone course and surgery ? I have heard from the nurses that if you have an IM steroid injection they postpone surgery for 6 to 8 weeks to allow the imunosuppresant effects to wear off before surgery. my RA consultant seems to think
Hi please can anyone advise how long to wait in between a prednisolone course and surgery ? I have heard from the nurses that if you have an IM steroid injection they postpone surgery for 6 to 8 weeks to allow the imunosuppresant effects to wear off before surgery. my RA consultant seems to think
lindyloo2018
in
NRAS
11 months ago
Out of Remission
Well, I got some not so good news today. I had my CLL check today and I'm out of remission. My WBC is now 14K. My platelets are 152. My doctor wants to start me on Zanabrutinib now. I know it seems silly when just getting out of remission and I'm not even close to a WBC of 30K yet, and I have no other
Well, I got some not so good news today. I had my CLL check today and I'm out of remission. My WBC is now 14K. My platelets are 152. My doctor wants to start me on Zanabrutinib now. I know it seems silly when just getting out of remission and I'm not even close to a WBC of 30K yet, and I have no other
MyCLLJourney
in
CLL Support
8 months ago
Covid and the NHS
Late april this year I contracted Covid again (previous time was just before the first lockdown). I slept for 4 days feeling cold and exhausted with lack of appetite I lost a stone in weight in 4 weeks. It did not seem to effect my chest so much this time (I have emphysema) but here I am 6 weeks later
Late april this year I contracted Covid again (previous time was just before the first lockdown). I slept for 4 days feeling cold and exhausted with lack of appetite I lost a stone in weight in 4 weeks. It did not seem to effect my chest so much this time (I have emphysema) but here I am 6 weeks later
Daisytime
in
Lung Conditions Community Forum
11 months ago
Third fresh failed (6th embryo) 😢
Good morning all Firstly I wanted to say a big thank you to everyone that responded to my posts and shared their experiences over the last few weeks (sorry I've not managed to reply to everyone but I have read your responses). It's been an incredibly anxious time and just doesn't get any easier the more
Good morning all Firstly I wanted to say a big thank you to everyone that responded to my posts and shared their experiences over the last few weeks (sorry I've not managed to reply to everyone but I have read your responses). It's been an incredibly anxious time and just doesn't get any easier the more
J0J0123
in
Fertility Network UK
5 months ago
Change clinics after failed first attempt?
Hi all! I’ve just completed my first ivf cycle and I’m looking for some advice from more experienced ivf ladies. in a nutshell, I’m wondering if I should change clinics or question them further. I am 40 and had previous successful pregnancy and miscarriages (12 years ago) good amh, afc and retrieved
Hi all! I’ve just completed my first ivf cycle and I’m looking for some advice from more experienced ivf ladies. in a nutshell, I’m wondering if I should change clinics or question them further. I am 40 and had previous successful pregnancy and miscarriages (12 years ago) good amh, afc and retrieved
Ses9
in
Fertility Network UK
5 months ago
embryo freezing day 1
hi all, First time posting and needing to hear from others with similar experience. Please help My partner and I have just completed our 3rd round of icsi. The first round we got one embryo make it to transfer but it failed. Second round we got a poor response and none of the 4 eggs were suitable for
hi all, First time posting and needing to hear from others with similar experience. Please help My partner and I have just completed our 3rd round of icsi. The first round we got one embryo make it to transfer but it failed. Second round we got a poor response and none of the 4 eggs were suitable for
Emjem84
in
Fertility Network UK
5 months ago
Hoping for some reassurance
Hit my head falling off my (not moving) bicycle a couple of months ago and have been suffering from severe nausea triggered by lights, high contrast and moving things since then. I'm seeing a physiotherapist specialized in head injury recovery and have exercises to do (which I do) and I know I'm in
Hit my head falling off my (not moving) bicycle a couple of months ago and have been suffering from severe nausea triggered by lights, high contrast and moving things since then. I'm seeing a physiotherapist specialized in head injury recovery and have exercises to do (which I do) and I know I'm in
capibaras
in
Headway
11 months ago
crp 6.7
Hi, I went to see my gp yesterday with suspected uti. I did a urine sample which was showing Leucocytes present, I was given a three day course of antibiotics and blood test sent. I have seen the results of blood tests on nhs app today and is showing abnormal result for crp at 6.7. When I last had
Hi, I went to see my gp yesterday with suspected uti. I did a urine sample which was showing Leucocytes present, I was given a three day course of antibiotics and blood test sent. I have seen the results of blood tests on nhs app today and is showing abnormal result for crp at 6.7. When I last had
Lynlea
in
PMRGCAuk
11 months ago
HU and prefibrotic myelofibrosis
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Apple238
in
CLL Support
1 year ago
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