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Anybody tried 'the Breather' device?
Hi all, anybody tried the 'Breather' (https://www.pnmedical.com/product/the-breather/)? I bought it like 11 days ago and have been trying to use it at least 2-3 times a day since. I'm actually struggling to use it the specified amount of times, but am finding it easier to blow into after using setting
Hi all, anybody tried the 'Breather' (https://www.pnmedical.com/product/the-breather/)? I bought it like 11 days ago and have been trying to use it at least 2-3 times a day since. I'm actually struggling to use it the specified amount of times, but am finding it easier to blow into after using setting
DaveT81
in
Lung Conditions Community Forum
4 years ago
Lupus/APS and cod liver oil
Hi, I'm 49, and have lupus with antiphospholipid syndrome. I'm currently on lifelong warfarin, statins, vit D, hydroxychloroquine and methotrexate injections. The inflammatory arthritis is very painful, would cod liver oil be safe to take with anticoagulants? I think the oil would help with the inflammation
Hi, I'm 49, and have lupus with antiphospholipid syndrome. I'm currently on lifelong warfarin, statins, vit D, hydroxychloroquine and methotrexate injections. The inflammatory arthritis is very painful, would cod liver oil be safe to take with anticoagulants? I think the oil would help with the inflammation
Gerardina
in
LUPUS UK
4 years ago
HAS ANYONE WITH PD HAD SPINAL CORD STIMULATOR IMPLANTED FOR POSTURE CORRECTION,PAIN MODULATION AND MOTOR FUNCTION?
Hi,friends,this procedure might be relatively new. I have read that it is similarly to DBS,but it targets the spinal cord instead of the brain.I was wondering,if anyone had this procedure done,please share your experience. How effective is it?Is it safer ,compared to DBS? Thanks in advance.
Hi,friends,this procedure might be relatively new. I have read that it is similarly to DBS,but it targets the spinal cord instead of the brain.I was wondering,if anyone had this procedure done,please share your experience. How effective is it?Is it safer ,compared to DBS? Thanks in advance.
OREOLU
in
Cure Parkinson's
4 years ago
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Circumscission post op 6 weeks
6 weeks post circumscission. Finally got to see surgeon. My inner foreskin attached to glands, gave me fucibet cream.anyone have any tips how to speed process of freeing foreskin. Fucibet cream just applied, do I need to stretch it? Help, please guys I'm at wits end.
6 weeks post circumscission. Finally got to see surgeon. My inner foreskin attached to glands, gave me fucibet cream.anyone have any tips how to speed process of freeing foreskin. Fucibet cream just applied, do I need to stretch it? Help, please guys I'm at wits end.
Monty555
in
Men's Health Forum (Penis Health)
4 years ago
6 months post circumcision
Hello again everyone. I’ve been through alot with my circumcision and even though I dreaded my foreskin because it started to get balanitis, I wish I go back. Also a bit off topic but I read online thar Balanitis is not something you can catch or it’s due to poor hygiene but i only got after I i rubbed
Hello again everyone. I’ve been through alot with my circumcision and even though I dreaded my foreskin because it started to get balanitis, I wish I go back. Also a bit off topic but I read online thar Balanitis is not something you can catch or it’s due to poor hygiene but i only got after I i rubbed
StupidMo
in
Men's Health Forum (Penis Health)
4 years ago
Chilblains or ulcers?
I’m getting lots of painful bumps on my hands/fingers at the moment (see photo). Are these chillblains or ulcers? I’m on sildenifil for my raynauds but wondering if I need to do something more?! I have a bad chillblain on my toe but using balmosa cream for this.
I’m getting lots of painful bumps on my hands/fingers at the moment (see photo). Are these chillblains or ulcers? I’m on sildenifil for my raynauds but wondering if I need to do something more?! I have a bad chillblain on my toe but using balmosa cream for this.
Dancingc21
in
Scleroderma & Raynaud's UK (SRUK)
4 years ago
Balanitis/Fungal/Bacterial Infection - Solution Found
After 1 year of misery, I have cured myself. The solution/cure that worked for myself: Fucidin ointment 2%, applied on the glans and foreskin once a day for two weeks. For those that are interested, here is my story: It all started after I used my fleshlight the second time. I didn't clean it after
After 1 year of misery, I have cured myself. The solution/cure that worked for myself: Fucidin ointment 2%, applied on the glans and foreskin once a day for two weeks. For those that are interested, here is my story: It all started after I used my fleshlight the second time. I didn't clean it after
Daniels95
in
Men's Health Forum (Penis Health)
4 years ago
Shingles vaccine
I'm in Johannesburg South Africa. Shingrix is not available in SA only Zovirax. As a CLL sufferer who has had one session of Shingles has anyone been able to obtain Shingrix in South Africa??
I'm in Johannesburg South Africa. Shingrix is not available in SA only Zovirax. As a CLL sufferer who has had one session of Shingles has anyone been able to obtain Shingrix in South Africa??
Alpha66
in
CLL Support
4 years ago
Fed up with always getting colds and bugs
I ended 2018 with a nasty chest infection which took months and a ton of medication to budge. After that I seemed to have a cold or a bug every few weeks, all through the year. 2019, I spent 2nd Christmas in a row, too poorly to get out of bed (with a cold, each time, rather than regular hypo symptoms
I ended 2018 with a nasty chest infection which took months and a ton of medication to budge. After that I seemed to have a cold or a bug every few weeks, all through the year. 2019, I spent 2nd Christmas in a row, too poorly to get out of bed (with a cold, each time, rather than regular hypo symptoms
Wetsuiter
in
Thyroid UK
4 years ago
Panasol 2 Light therapy?
ok, I have one of these 8 ft lights! It is for use by Doctors. I used it for a friends leg, for only 20 seconds at a time..with goggles and black cape over her body. Now it says these are good to destroy this virus! anyone know how I use it to be safe with my COPD, Heart Damage, Lung Damage, Diafram
ok, I have one of these 8 ft lights! It is for use by Doctors. I used it for a friends leg, for only 20 seconds at a time..with goggles and black cape over her body. Now it says these are good to destroy this virus! anyone know how I use it to be safe with my COPD, Heart Damage, Lung Damage, Diafram
JANET127
in
Lung Conditions Community Forum
4 years ago
Three-drug combination reduces COPD patient mortality.
Once-daily treatment of patients with chronic obstructive pulmonary disease (COPD) with an inhaler combining fluticasone furoate (FF), umeclidinium (UMEC) and vilanterol (VI) reduced all-cause mortality by 42 percent, according to new research published online in the American Thoracic Society’s American
Once-daily treatment of patients with chronic obstructive pulmonary disease (COPD) with an inhaler combining fluticasone furoate (FF), umeclidinium (UMEC) and vilanterol (VI) reduced all-cause mortality by 42 percent, according to new research published online in the American Thoracic Society’s American
2greys
in
Lung Conditions Community Forum
4 years ago
Losing lymph nodes after lung cancer
Hi firstly sorry about the long post. I'm hoping someone can help last year I had my lower right lobe of my lung and lymph nodes removed due to lung cancer. I already have secondary lymphodema of both legs due to a motorbike accident in my teens and lipoedema. After the operation I had a lot of complications
Hi firstly sorry about the long post. I'm hoping someone can help last year I had my lower right lobe of my lung and lymph nodes removed due to lung cancer. I already have secondary lymphodema of both legs due to a motorbike accident in my teens and lipoedema. After the operation I had a lot of complications
Loramay
in
LSN
4 years ago
Looking for advice (post-revision... frenuloplasty...)
I have been on this forum for a year now, reading what you've all been through so it really eased (as well as heightened) my own experience. However, I am still experiencing all sorts of drama. Let me know what you think... I'm 23. I knew I had phimosis my whole life, but I never said anything - daddy
I have been on this forum for a year now, reading what you've all been through so it really eased (as well as heightened) my own experience. However, I am still experiencing all sorts of drama. Let me know what you think... I'm 23. I knew I had phimosis my whole life, but I never said anything - daddy
buzz1333
in
Men's Health Forum (Penis Health)
4 years ago
Neuropathy pain and hoping for a spinal cord simulator
Hi there good evening to everyone, can anyone advise me on how and where I can find a hospital in the UK which would hopefully give me a trial for a spinal cord stimulator on the nhs, in so much pain for over a year now, has totally affected my life in every way possible, I was so independent, now I
Hi there good evening to everyone, can anyone advise me on how and where I can find a hospital in the UK which would hopefully give me a trial for a spinal cord stimulator on the nhs, in so much pain for over a year now, has totally affected my life in every way possible, I was so independent, now I
midashomes64
in
Pain Concern
4 years ago
Quitting smoking
Hi everyone.I have struggled to stop smoking as being diagnosed with copd year and half ago was a shock I never even heard of it. I had lung function test at the time which was I mild I not had one since due to my council cut backs so i cant even keep an eye on my lungs..I have now after year and half
Hi everyone.I have struggled to stop smoking as being diagnosed with copd year and half ago was a shock I never even heard of it. I had lung function test at the time which was I mild I not had one since due to my council cut backs so i cant even keep an eye on my lungs..I have now after year and half
Madonna1
in
Lung Conditions Community Forum
4 years ago
Thyroid & Weightloss
Hey all ... I’m sure many of you on here with hypo conditions will have something to contribute here. Précis of my story so far ... RAI treatment 12 years ago. Battle to lose weight gained. Lost a massive amount then gained it again. Feeling more like myself again now treatment plan corrected so
Hey all ... I’m sure many of you on here with hypo conditions will have something to contribute here. Précis of my story so far ... RAI treatment 12 years ago. Battle to lose weight gained. Lost a massive amount then gained it again. Feeling more like myself again now treatment plan corrected so
Aslangal
in
Thyroid UK
4 years ago
Complex regional pain syndrome
Hi all! I’ve had CRPS for 12 years in my leg and managed to get it under control. However last April I had an operation for endometriosis and have now been told that I have CRPS inside. None of the medication the Drs have prescribed (I’ve tried all the normal ones) work for me, so I’ve asked for spinal
Hi all! I’ve had CRPS for 12 years in my leg and managed to get it under control. However last April I had an operation for endometriosis and have now been told that I have CRPS inside. None of the medication the Drs have prescribed (I’ve tried all the normal ones) work for me, so I’ve asked for spinal
MiniRowls
in
Pain Concern
4 years ago
This might help
Hi everyone..I write on here from time to time..as I've had restless legs on and off for years. Recently it's been not soooo bad.. I've managed to take more iron and supplement that with rose hip and cod liver oil.. I also make sure I have enough magnesium.. These simple steps have made a difference.
Hi everyone..I write on here from time to time..as I've had restless legs on and off for years. Recently it's been not soooo bad.. I've managed to take more iron and supplement that with rose hip and cod liver oil.. I also make sure I have enough magnesium.. These simple steps have made a difference.
janland
in
Restless Legs Syndrome
4 years ago
Facet joint injection or not in North East Wales.
Good morning everyone, I hope you are all having a good day. I have a question, are there any people living in North East Wales who have fibromyalgia and have had facet joint radio ablation or spinal cord stimulator fitted for arthritis. I have been told by the pain team that I can't have either because
Good morning everyone, I hope you are all having a good day. I have a question, are there any people living in North East Wales who have fibromyalgia and have had facet joint radio ablation or spinal cord stimulator fitted for arthritis. I have been told by the pain team that I can't have either because
mimimouse
in
Fibromyalgia Action UK
4 years ago
Share your quitting success stories: What helped you quit smoking?
I am noticing a few posts lately about people who are trying to quit smoking. Being a former smoker myself I understand how hard it can be to quit. Truthfully, creating a lasting change in life is tough enough (for me at least) without the added burden of nicotine addiction making it even harder. That
I am noticing a few posts lately about people who are trying to quit smoking. Being a former smoker myself I understand how hard it can be to quit. Truthfully, creating a lasting change in life is tough enough (for me at least) without the added burden of nicotine addiction making it even harder. That
R2B_Joe
Partner
in
COPD Friends
4 years ago
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