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Allergic reaction To preventer inhaler
I have been on Symbicort pressurised inhaler for over 3 years but am Now getting side effects of pins & needles in my lips and fingers. I have eliminatedall my other medication and tried fostair and ellipta and they too are causing the same. Can anyone advise me of any other inhaler that does not contain
I have been on Symbicort pressurised inhaler for over 3 years but am Now getting side effects of pins & needles in my lips and fingers. I have eliminatedall my other medication and tried fostair and ellipta and they too are causing the same. Can anyone advise me of any other inhaler that does not contain
pam7974
in
Asthma Community Forum
4 months ago
slightly anxious and just looking for moral support
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Abcd123455
in
PMRGCAuk
4 months ago
What to do after prednisolone rescue ended?
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Merryroundabout
in
Asthma Community Forum
4 months ago
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How effective is fenofibrate for itch?
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
Carly92
in
PBC Foundation
4 months ago
I thought it was just a cold!
Not on ocrevus anymore, but I had the 1st of my monthly tysabri on the 20th, and I've since got a chest infection 😞 a couple of nights of not being able to sleep properly had really affected me, to the point where on Monday just gone I was wanting to get in to see a GP! But, when I called them up, they
Not on ocrevus anymore, but I had the 1st of my monthly tysabri on the 20th, and I've since got a chest infection 😞 a couple of nights of not being able to sleep properly had really affected me, to the point where on Monday just gone I was wanting to get in to see a GP! But, when I called them up, they
Cwright170994
in
My MSAA Community
5 months ago
Trimbow inhaler
I have read a few people having symptoms of a soar mouth, bleeding and thrush etc from this inhaler or steroid inhalers and wanted to share a tip I had . Use a spacer , never suck in hard as the medicine will hit the back of your throat and not go down your windpipe to your lungs , take the second inhalation
I have read a few people having symptoms of a soar mouth, bleeding and thrush etc from this inhaler or steroid inhalers and wanted to share a tip I had . Use a spacer , never suck in hard as the medicine will hit the back of your throat and not go down your windpipe to your lungs , take the second inhalation
Julesc12
in
Asthma Community Forum
5 months ago
Rash any advice?
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
I have noticed this rash over last 2 or 3 months. Its not itchy or raised. Any advice most welcome. Im taking 100mcg teva levo and 15mcg thybon henning. Vit d, magnesium glycinate. Any advice most welcome 🌸🌸🌸🌸🌸
Geegee777
in
Thyroid UK
6 months ago
Hair issues
hi I forgot to ask my rheum nurse about my hair. I’m on methotrexate and seems to be ok with no abnormal hair loss but since taking it I haven’t had my hair highlighted . Anybody advice with this ? I have left message on advice line but wondering others people’s experience. Thanks
hi I forgot to ask my rheum nurse about my hair. I’m on methotrexate and seems to be ok with no abnormal hair loss but since taking it I haven’t had my hair highlighted . Anybody advice with this ? I have left message on advice line but wondering others people’s experience. Thanks
Teddyboy17
in
NRAS
6 months ago
Chillblains
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
GerryPL
in
CLL Support
6 months ago
ANyone taking Prolia for osteoporosis?
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Pumpkin2009
in
LUPUS UK
7 months ago
Alvesco and fostair
I am currently on fostair 100 mart, with the ability to switch to fostair 200 when I need it. Along with spiriva. My asthma is relatively uncontrolled, but spiriva has helped a lot. My consultant has just put Alvesco 160 into the mix twice a day. Any idea of what he is doing, apart from just increasing
I am currently on fostair 100 mart, with the ability to switch to fostair 200 when I need it. Along with spiriva. My asthma is relatively uncontrolled, but spiriva has helped a lot. My consultant has just put Alvesco 160 into the mix twice a day. Any idea of what he is doing, apart from just increasing
Homely2
Administrator
in
Asthma Community Forum
7 months ago
Is this Scabies?
Please tell me if this looks like scabies? This is right under the armpit. I have tried to crop and focus on the problem area but can share another version of this photo if it is not clear. I am morbidly obese so a lot of skin stretching is happening.
Please tell me if this looks like scabies? This is right under the armpit. I have tried to crop and focus on the problem area but can share another version of this photo if it is not clear. I am morbidly obese so a lot of skin stretching is happening.
TryingItOn
in
MY SKIN
20 hours ago
Slapped Cheek Disease
My nine year old Grandaughter has Slapped Cheek Disease. I am on my final 3mg of Pred a day for PMR. Is it ok to be in contact with her. Thank you. Jenny
My nine year old Grandaughter has Slapped Cheek Disease. I am on my final 3mg of Pred a day for PMR. Is it ok to be in contact with her. Thank you. Jenny
Attic
in
PMRGCAuk
13 days ago
Advice please...
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
My fibro always gets worse in cold weather so bath soaks are my best friends at the moment, however, my boiler and heating stopped working few days ago, I called my housing association and they fixed the heaters, but for hot water I was told its not considered emergency as you can boil kettles of water
YMEPLEASE
in
Fibromyalgia Action UK
2 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
8 months ago
PBC and nails / gel polish / acrylic
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
hi everyone, just a quick question.. I wondered has anyone had any issues with having their nails done with gel polish. I had to switch from gel polish to acrylic as my nails kept having a reaction to the gel - and often developed a fungal infection. Once I switched to acrylic they were much better
Deemum
in
PBC Foundation
3 months ago
Mouth thrush
Does anyone else suffer from thrush in the mouth, due to taking antibiotics. I think l may have it as my tongue is coated in white and l have lost a lot of my sense of taste. I have just started taking colomycin in Nebuliser for pseudomonas infection.
Does anyone else suffer from thrush in the mouth, due to taking antibiotics. I think l may have it as my tongue is coated in white and l have lost a lot of my sense of taste. I have just started taking colomycin in Nebuliser for pseudomonas infection.
falcon68
in
Lung Conditions Community Forum
8 months ago
Question on tapering
Everytime I start reducing my pred I develop a Cold sore on my lip, does an yone else have this problem?
Everytime I start reducing my pred I develop a Cold sore on my lip, does an yone else have this problem?
Kiwisufferer2019
in
PMRGCAuk
4 months ago
More red spots on nails
Still don't know what these are. Anyone else get them?
Still don't know what these are. Anyone else get them?
Brychni
in
NRAS
5 months ago
Sezary Syndrome.
After many months of fighting a complete body rash, I was visually diagnose with Sezary Syndome and had to discontinue my CLL treatment with Venetoclax, only did 8 months out of 24 months due to the rash condition. Is there anyone with knowledge of this or was there any previous postings? I greatly
After many months of fighting a complete body rash, I was visually diagnose with Sezary Syndome and had to discontinue my CLL treatment with Venetoclax, only did 8 months out of 24 months due to the rash condition. Is there anyone with knowledge of this or was there any previous postings? I greatly
Champlain
in
CLL Support
20 days ago
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