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Pneumonia/cancer
Hi I'm new to this forum but great to hear other peoples experiences. I was diagnosed with pneumonia after an x-ray. Had antibiotics and fingers crossed, not feeling too poorly. Doctor said it was a small showing on the x-ray and that no cancer concerns at all. He said I will have a follow up x-ray in
Hi I'm new to this forum but great to hear other peoples experiences. I was diagnosed with pneumonia after an x-ray. Had antibiotics and fingers crossed, not feeling too poorly. Doctor said it was a small showing on the x-ray and that no cancer concerns at all. He said I will have a follow up x-ray in
Scooby1967
in
Lung Conditions Community Forum
9 months ago
second opinions
hi, I hope everyone is ok ❤️🙏🏼 Sorry if this is a ramble, but I just wanted to thank everyone who responded to my posts of despair following my last 2 failed egg retrievals. 2 egg retrievals, 19 eggs, and just 1 fertilised, including one ICSI round with total fertilisation failure. The consultant
hi, I hope everyone is ok ❤️🙏🏼 Sorry if this is a ramble, but I just wanted to thank everyone who responded to my posts of despair following my last 2 failed egg retrievals. 2 egg retrievals, 19 eggs, and just 1 fertilised, including one ICSI round with total fertilisation failure. The consultant
Hidden
in
Fertility Network UK
9 months ago
Severe Lung Scarring from Pneumonia
Hello, I have posted about my dad who is in his late 70s in ICU for severe pneumonia here before, but here is the current situation. At the moment, he is stable and he is close to weaning off sedation completely and starting ventilator weaning (trachy) soon. His ventilator setting is O2 35%, Saturation
Hello, I have posted about my dad who is in his late 70s in ICU for severe pneumonia here before, but here is the current situation. At the moment, he is stable and he is close to weaning off sedation completely and starting ventilator weaning (trachy) soon. His ventilator setting is O2 35%, Saturation
ForMyPapa
in
ICUsteps
9 months ago
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Very low AMH at 41
I am in a bit of a state right now as I was told that my AMH is 0.3 yesterday. I know a lot of ladies have success with low AMH but is there anyone who had a baby with own egg with such a low level AMH? Age isn't on my side either as I turned 41 this month. We are lucky to have a daughter I conceived
I am in a bit of a state right now as I was told that my AMH is 0.3 yesterday. I know a lot of ladies have success with low AMH but is there anyone who had a baby with own egg with such a low level AMH? Age isn't on my side either as I turned 41 this month. We are lucky to have a daughter I conceived
Beakbeak
in
Fertility Network UK
9 months ago
Severe Scarring From Pneumonia
Hello, First time posting in this group! I have posted about my dad who is in his late 70s in ICU for severe pneumonia in the ICUsteps group, but here is the current situation. At the moment, he is stable and he is close to weaning off sedation completely and starting ventilator weaning (trachy) soon
Hello, First time posting in this group! I have posted about my dad who is in his late 70s in ICU for severe pneumonia in the ICUsteps group, but here is the current situation. At the moment, he is stable and he is close to weaning off sedation completely and starting ventilator weaning (trachy) soon
ForMyPapa
in
Lung Conditions Community Forum
9 months ago
5th Covid Vaccine has affected me
Hi I was advised to take up a 5th Covid Vaccine and I had it last week. In the last few days I have been feeling unsteady on my feet, Has anybody experienced this? I was given the Pizer Vaccine. Because of this I have not taken my Metraxate injection. I thought I would hold off for a few days. Worried
Hi I was advised to take up a 5th Covid Vaccine and I had it last week. In the last few days I have been feeling unsteady on my feet, Has anybody experienced this? I was given the Pizer Vaccine. Because of this I have not taken my Metraxate injection. I thought I would hold off for a few days. Worried
cpt13
in
NRAS
1 year ago
newly diagnosed with autoimmune underactive thyroid
Sorry for the long post but I’m a newbie and wanted to give a decent background… I had covid at 38 weeks pregnant in December 2020 and ever since, i have suffered with crippling fatigue, lightheadedness, brain fog, nausea, headaches and muscle aches and pains. Initially told it was long covid but then
Sorry for the long post but I’m a newbie and wanted to give a decent background… I had covid at 38 weeks pregnant in December 2020 and ever since, i have suffered with crippling fatigue, lightheadedness, brain fog, nausea, headaches and muscle aches and pains. Initially told it was long covid but then
RoseStar
in
Thyroid UK
1 year ago
Advice on increasing Pred for breathlessness and persistent cough
My GP told me that breathlessness is a symptom of PMR, so I can't seek her advice on how to manage this cough etc. Some people are saying that Eris Covid is around and it presents as a bad cough which does not show up as positive on home covid testing kits. I have had a persistent productive cough
My GP told me that breathlessness is a symptom of PMR, so I can't seek her advice on how to manage this cough etc. Some people are saying that Eris Covid is around and it presents as a bad cough which does not show up as positive on home covid testing kits. I have had a persistent productive cough
Motida
in
PMRGCAuk
11 months ago
Pentamidine?
I am on V + O treatment. My last Obi infusion is July 3. A month ago I developed a rash on my chest, neck, and face. My oncologist had me stop Bactrim to confirm it was the culprit. The rash cleared within a week. Now he has me scheduled for an oral inhalation of pentamidine. I am concerned about this
I am on V + O treatment. My last Obi infusion is July 3. A month ago I developed a rash on my chest, neck, and face. My oncologist had me stop Bactrim to confirm it was the culprit. The rash cleared within a week. Now he has me scheduled for an oral inhalation of pentamidine. I am concerned about this
Tabbytabby
in
CLL Support
1 year ago
Swelling back after knee aspiration
Hi everyone,I have had a diagnosis of inflammatory arthritis for about 10 years now (although the symptoms had been there many years longer like so many of us). I am on a weekly Metoject 20mg and 6x 500g Sulfasalazine daily. It tends to be my knees that are particularly affected and over the last 10
Hi everyone,I have had a diagnosis of inflammatory arthritis for about 10 years now (although the symptoms had been there many years longer like so many of us). I am on a weekly Metoject 20mg and 6x 500g Sulfasalazine daily. It tends to be my knees that are particularly affected and over the last 10
BillyJayDuncs
in
NRAS
11 months ago
New cycle for ivf
hi all, I need advise I am confuse and stressed. As I already had one ivf cycle failed with icsi privately as I payed for it. But luckily now nhs contacted me for appointments I want to know am I tell them about failed ivf cycle so they further investigate and give treatment accordingly or shall I don
hi all, I need advise I am confuse and stressed. As I already had one ivf cycle failed with icsi privately as I payed for it. But luckily now nhs contacted me for appointments I want to know am I tell them about failed ivf cycle so they further investigate and give treatment accordingly or shall I don
Nabsal
in
Fertility Network UK
9 months ago
Post flu jab
Has anyone else had a flare up of asthma or cold since having their jabs
Has anyone else had a flare up of asthma or cold since having their jabs
Sars28
in
Asthma Community Forum
9 months ago
Bile acid malabsorption
Hi , has anyone here had a seHCAT scan for bile acid malabsorption. Been having bad stomach issues for a while and with back log seeing consultant took ages . In March finally had a consultation and lots of test all clear . Not sure if this is last hope but having seHCAT scan for bile acid malabsorption
Hi , has anyone here had a seHCAT scan for bile acid malabsorption. Been having bad stomach issues for a while and with back log seeing consultant took ages . In March finally had a consultation and lots of test all clear . Not sure if this is last hope but having seHCAT scan for bile acid malabsorption
andepande
in
Pernicious Anaemia Society
1 year ago
Hello
Hi I have been diagnosed with an anti synthesase syndrome with features of myosotis. This was diagnosed following what was initially thought to be a chest infection / covid pneumonia in December. my rheumatologist thinks that exposure to covid has triggered my autoimmune disease which includes lung
Hi I have been diagnosed with an anti synthesase syndrome with features of myosotis. This was diagnosed following what was initially thought to be a chest infection / covid pneumonia in December. my rheumatologist thinks that exposure to covid has triggered my autoimmune disease which includes lung
Bronte007
in
Myositis UK
1 year ago
Steroids not working?
I’ve just had a 5 day rescue course of prednisolone due to an asthma flare. However, my peak flow is still only about 70% and I have an itchy, scratchy throat and cough. I don’t actually have a cold so I’m not sure what’s going on. I’ve never had a course of steroids before where it hasn’t made me completely
I’ve just had a 5 day rescue course of prednisolone due to an asthma flare. However, my peak flow is still only about 70% and I have an itchy, scratchy throat and cough. I don’t actually have a cold so I’m not sure what’s going on. I’ve never had a course of steroids before where it hasn’t made me completely
Gymbearo
in
Asthma Community Forum
9 months ago
Every story matters - UK COVID-19 public inquiry
[i]The pandemic affected every single person in the UK and, in many cases, continues to have a lasting impact on lives. Every one of our experiences is unique and this is your opportunity to share the impact it had on you, and your life, with the Inquiry.[/i] [i] [/i] [i]Every story shared with us will
[i]The pandemic affected every single person in the UK and, in many cases, continues to have a lasting impact on lives. Every one of our experiences is unique and this is your opportunity to share the impact it had on you, and your life, with the Inquiry.[/i] [i] [/i] [i]Every story shared with us will
bennevisplace
in
CLL Support
1 year ago
Anti virals and AF
I have just had Covid , inspite of 6 boosters. Apart ftom Persistent AF I have Ankylosing Spondilitis . I was put on Lagevrio ( anti viral) I think it was later than the 5 day’s limit . I did feel really unwell with Covid , still feel exhausted . I have one more day of anti virals but , apart from
I have just had Covid , inspite of 6 boosters. Apart ftom Persistent AF I have Ankylosing Spondilitis . I was put on Lagevrio ( anti viral) I think it was later than the 5 day’s limit . I did feel really unwell with Covid , still feel exhausted . I have one more day of anti virals but , apart from
Luludean
in
AF Association
1 year ago
November Webinar
We hope you will join us and ask your questions during the November Live Webinar with Dr Yusuf (JP) Saleeby with a presentation on LDN, Long Covid and Lyme Disease Update. Register here https://form.ldnresearchtrust.org/232812335487964 for a $5 donation.
We hope you will join us and ask your questions during the November Live Webinar with Dr Yusuf (JP) Saleeby with a presentation on LDN, Long Covid and Lyme Disease Update. Register here https://form.ldnresearchtrust.org/232812335487964 for a $5 donation.
Shewulf
Administrator
in
LDN Research Trust
9 months ago
Colesevelam
I am on colesevelam for bile acid malabsorption and all these tablets do is make me constipated i know they is alternatives to these tablets and thinking about changing but will the others do the same constant belly ache i do take laxitives to make me go but i cant live my life like this ,
I am on colesevelam for bile acid malabsorption and all these tablets do is make me constipated i know they is alternatives to these tablets and thinking about changing but will the others do the same constant belly ache i do take laxitives to make me go but i cant live my life like this ,
Netbet22
in
IBS Network
1 year ago
Foot/mouth hand or something else??
Does anyone know what this is. It started with red burning spots then turned into patches. Then I had chicken like pox all over my body and face. Hands rashes are similar to feet. But my thumbs are going white too and thin skin. Anyone know what's happening. I'm very stressed. Doctors are not helping
Does anyone know what this is. It started with red burning spots then turned into patches. Then I had chicken like pox all over my body and face. Hands rashes are similar to feet. But my thumbs are going white too and thin skin. Anyone know what's happening. I'm very stressed. Doctors are not helping
Shine54
in
LUPUS UK
8 months ago
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