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Daflon for Venous Leakage?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
baw1955
in
Prostate Cancer And Gay Men
5 years ago
Daflon for Venous Leakage?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
baw1955
in
Advanced Prostate Cancer
5 years ago
Daflon for Venous Leakage?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
I see a few posts on the "FrankTalk" site about using non-FDA approved drug called
Daflon
to help with ED issues. No hits on this site when I did a search. Any users with experiences to share?
baw1955
in
Erectile Dysfunction Support
5 years ago
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Itchy rash more
Folliculitis continues - wash fom Doctor doesn’t clear aloe vera savlon hydrocortisone Aveeno don’t work - using ice packs at night and will try oatmeal bath tonight - any ideas please?
Folliculitis continues - wash fom Doctor doesn’t clear aloe vera savlon hydrocortisone Aveeno don’t work - using ice packs at night and will try oatmeal bath tonight - any ideas please?
Daffodilia
in
PMRGCAuk
5 years ago
Feeling like hell
I posted a couple of weeks ago about being diagnosed with a diverticular disease flare up and the reactions to the Metronidazole antibiotic which I have never taken before, well last week I had the runs all week including the beginning of this week so decided to give my usual Laxido a miss for a day
I posted a couple of weeks ago about being diagnosed with a diverticular disease flare up and the reactions to the Metronidazole antibiotic which I have never taken before, well last week I had the runs all week including the beginning of this week so decided to give my usual Laxido a miss for a day
Doggie123-UK
in
IBS Network
5 years ago
I'm New - Boyfriend has EDS
Hello all! I do not know much about EDS other than what I've read online or what my boyfriend has told me about it. His EDS has always concerned me and it makes me sad because he believes his life expectancy is super short because some doctor told him this... It bothers me because not enough doctors
Hello all! I do not know much about EDS other than what I've read online or what my boyfriend has told me about it. His EDS has always concerned me and it makes me sad because he believes his life expectancy is super short because some doctor told him this... It bothers me because not enough doctors
Usako
in
Ehlers-Danlos Support UK
5 years ago
35 minutes and a blister
We planned a lazy morning in bed as i was at work til gone ten last night but woke early and decided to get it over and done with I put my favourite running trainers on and darn it they slipped a bit, not much but enough to cause a blister then rub the top off but hey we ran for 35 minutes and a bit
We planned a lazy morning in bed as i was at work til gone ten last night but woke early and decided to get it over and done with I put my favourite running trainers on and darn it they slipped a bit, not much but enough to cause a blister then rub the top off but hey we ran for 35 minutes and a bit
SueAppleRun
Graduate
in
Couch to 5K
5 years ago
Bitten!
so was out this morning, doing the stamina podcast and pondering life when I see 2 tiny dogs and their owner in the distance. I called out morning and she smiled but didn't call her dogs to her. I slowed down to go past and that was that.... or so I thought. not even 10 paces on, 1 of the dogs ran after
so was out this morning, doing the stamina podcast and pondering life when I see 2 tiny dogs and their owner in the distance. I called out morning and she smiled but didn't call her dogs to her. I slowed down to go past and that was that.... or so I thought. not even 10 paces on, 1 of the dogs ran after
speedylol
Graduate
in
Couch to 5K
5 years ago
Symptoms suggesting EDS
Hi I’m 24 years old and have a number of symptoms suggesting I have EDS but was brushed off by the GP that saw me because I have a history of health anxiety. Some of the symptoms I’m experiencing are: - bladder prolapse (I’ve never had any pregnancies)... I’ve had bladder leakage for a few months and
Hi I’m 24 years old and have a number of symptoms suggesting I have EDS but was brushed off by the GP that saw me because I have a history of health anxiety. Some of the symptoms I’m experiencing are: - bladder prolapse (I’ve never had any pregnancies)... I’ve had bladder leakage for a few months and
CC0507
in
Ehlers-Danlos Support UK
5 years ago
Joint hypermobility syndrome-what did you wish you'd known before?
Hi! So I'd been thinking today about what life could be for me in 20/30/40 years time as even in the last 5 years living with hypermobility syndrome has changed drastically for me. I know everyone's experience varies, but I wondered if anyone had any advice or things they wish they'd have done differently
Hi! So I'd been thinking today about what life could be for me in 20/30/40 years time as even in the last 5 years living with hypermobility syndrome has changed drastically for me. I know everyone's experience varies, but I wondered if anyone had any advice or things they wish they'd have done differently
orangesounds23
in
Pain Concern
5 years ago
Private Referral
Hi guys, So about a month ago my GP agreed with me that I needed to see a rheumatologist about the benign joint hypermobility syndrome diagnosis, to confirm whether or not for my own sanity if it was hypermobile EDS or hypermobility spectrum disorder. I don't know which resources I can send to my employer
Hi guys, So about a month ago my GP agreed with me that I needed to see a rheumatologist about the benign joint hypermobility syndrome diagnosis, to confirm whether or not for my own sanity if it was hypermobile EDS or hypermobility spectrum disorder. I don't know which resources I can send to my employer
emilyhedgehog
in
Ehlers-Danlos Support UK
5 years ago
*GRIM IMAGE* is this a normal post lap belly button?!!
Hi guys, I had my first lap 5 weeks ago and looked after my stitches as told too, they all came out last week but since then my belly button has been ‘leaking’ so I’ve been cleaning it with a cotton bud and savlon in case of infection.. tonight I noticed before cleaning there was dry blood around my
Hi guys, I had my first lap 5 weeks ago and looked after my stitches as told too, they all came out last week but since then my belly button has been ‘leaking’ so I’ve been cleaning it with a cotton bud and savlon in case of infection.. tonight I noticed before cleaning there was dry blood around my
Elv-Marv19
in
Endometriosis UK
5 years ago
Lungs and hypermobility
Just wondering if anyone with JHS has ever had episodes of haemoptysis?
Just wondering if anyone with JHS has ever had episodes of haemoptysis?
Gretna11
in
Ehlers-Danlos Support UK
5 years ago
Just been told i am hyper-mobile. hEDS? This might explain my chronic fatigue / post exercise malaise and more!
Hi EDS forum! For most of my adult life if have suffered with poor sleep, chronic fatigue and severe physical exhaustion after what might be considered normal exercise. I go mountain biking with friends who the next day would be feeling amazing but i am totally debilitated, limbs shaking/buzzing, can
Hi EDS forum! For most of my adult life if have suffered with poor sleep, chronic fatigue and severe physical exhaustion after what might be considered normal exercise. I go mountain biking with friends who the next day would be feeling amazing but i am totally debilitated, limbs shaking/buzzing, can
TranceW1974
in
Ehlers-Danlos Support UK
6 years ago
Diagnosis and support
Hello I am diagnosed with Behcet’s Syndrome and ‘primary hyper mobility syndrome’. I have excellent care and support from a specialist centre for Behcet’s but don’t know it understand hyper mobility that well despite having the diagnosis for over 7 years. The rheumatologist who diagnosed retired after
Hello I am diagnosed with Behcet’s Syndrome and ‘primary hyper mobility syndrome’. I have excellent care and support from a specialist centre for Behcet’s but don’t know it understand hyper mobility that well despite having the diagnosis for over 7 years. The rheumatologist who diagnosed retired after
VickiOliver
in
Ehlers-Danlos Support UK
6 years ago
Where to get help on diagnosing EDs.
Hi, Where can I go to get genetic testing done for Ehlers Danlos. I live in East Sussex in the UK. I am in my 50s but my 2 adult daughters have so many symptoms of EDs and one in particular is suffering severely with pain. Her g.p. has no interest and just tells her its in her head. She did see a Dr
Hi, Where can I go to get genetic testing done for Ehlers Danlos. I live in East Sussex in the UK. I am in my 50s but my 2 adult daughters have so many symptoms of EDs and one in particular is suffering severely with pain. Her g.p. has no interest and just tells her its in her head. She did see a Dr
honeybea22
in
Ehlers-Danlos Support UK
6 years ago
I am 28 Year old male and I have EDS (Ehlers-Danlos syndrome) Everyone tells me that I have a soft body like a female. Is it related to EDS?
Hi Everyone. Last year I found out that I have EDS. I had hypermobility since I was a kid but from Last 3-4 years I started noticing that my body especially my upper arms, chest and belly started getting softer by day. I know that soft, doughy, smooth and velvety skin is a symptom of EDS but my body
Hi Everyone. Last year I found out that I have EDS. I had hypermobility since I was a kid but from Last 3-4 years I started noticing that my body especially my upper arms, chest and belly started getting softer by day. I know that soft, doughy, smooth and velvety skin is a symptom of EDS but my body
Alcatraz
in
Ehlers-Danlos Support UK
6 years ago
Hypermobile EDS??
Does anyone here have hyper mobile EDS and sleep with eyes partially open, have blue scerla in their eyes, and/or irritated vessels in the whites of their eye?
Does anyone here have hyper mobile EDS and sleep with eyes partially open, have blue scerla in their eyes, and/or irritated vessels in the whites of their eye?
Apaigemarko
in
Ehlers-Danlos Support UK
6 years ago
Cellulitis and heeling process
I was in hospital for 2 weeks with cellulitis in my foot and leg, had a bad bout, sent home on antibiotics but went to doctors given more but different antibiotics I’ve had in the past along with other antibiotics to kill any bacteria, leg and foot peeling lots, doctor gave me savlon to apply daily to
I was in hospital for 2 weeks with cellulitis in my foot and leg, had a bad bout, sent home on antibiotics but went to doctors given more but different antibiotics I’ve had in the past along with other antibiotics to kill any bacteria, leg and foot peeling lots, doctor gave me savlon to apply daily to
Naomibling
in
LSN
6 years ago
Cellulitis and heeling process
Hi, I recently had a very bad bout of cellulitis in my foot and leg, this spread quick due to waiting 5 hours to see a doctor in our A&E department, I was in hospital for 2 weeks and was discharged on antibiotics, once finished those I went to my doctors and have been given another course of different
Hi, I recently had a very bad bout of cellulitis in my foot and leg, this spread quick due to waiting 5 hours to see a doctor in our A&E department, I was in hospital for 2 weeks and was discharged on antibiotics, once finished those I went to my doctors and have been given another course of different
Naomibling
in
LSN
6 years ago
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