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Gabapentin Gel. or other topical creams
Thu May 10, 2018 9:43 am by Rosie21
Hi I have been suffering for some years with this abominable pain. I have tried most of the systemic drugs , I asked specialists and Doctors if I could at least try a topical treatment but because this requires a special prescription have been refused Has anybody had a chance of trying these? Thank you I will try to put a link on to some of the research into Gabapentin Gel. Thanks.
Comments: 2
Putnams 'bony parts' cushion or Putnams 'Dr Huff' cushion - which is best?
Sat Aug 01, 2015 4:17 pm by Fielder
Hi everyone,
I'm a newbie. I live in the UK.
I'm trying to work out the best cushion to get for my vulvodynia. I suspect that I could have pudendal nerve involvement (the aching and burning pain is from vagina to clitoris) and I have rectocele and some tailbone pain too.
I have seen some good reports on older threads regarding the Putnams pressure relief cushions....with some ladies …
I'm a newbie. I live in the UK.
I'm trying to work out the best cushion to get for my vulvodynia. I suspect that I could have pudendal nerve involvement (the aching and burning pain is from vagina to clitoris) and I have rectocele and some tailbone pain too.
I have seen some good reports on older threads regarding the Putnams pressure relief cushions....with some ladies …
Comments: 11
An absolute success story- please read!
Fri Mar 08, 2019 10:57 pm by Persevere1990
Dear All,
I posted on here back in March 2017 having just got a diagnosis of vulvodynia after a few months of relentless and acute pain. I was desperate, I was hurting, I was scared I would never know life without pain there again.
I tried creams, acupuncture, numbing gels, frozen pads, baths with various internet recommended concoctions- convinced myself I had lichen sclerosus, herpes, thrush- …
I posted on here back in March 2017 having just got a diagnosis of vulvodynia after a few months of relentless and acute pain. I was desperate, I was hurting, I was scared I would never know life without pain there again.
I tried creams, acupuncture, numbing gels, frozen pads, baths with various internet recommended concoctions- convinced myself I had lichen sclerosus, herpes, thrush- …
Comments: 0
I'm sorry im rambling
Thu Feb 21, 2019 5:49 am by Jet227
hey, im 19, ive been struggling with this almost a year. The first week I became itchy I went in to check about a yeast infection another week later. I have been to 10 different doctors a total of about 15 appointments for this problem for the past 11 months. I have been tested for everything including having a biopsy. I was first told basically to just go home and use hydrocortazone, then I went …
Comments: 1
New member need advice please
Thu Feb 28, 2019 11:33 pm by PANDORA123
Hello, I have just been diagnosed with unprovoked vulvodynia. Im really scared and worried. It burns a lot and it hurts to sit down. I have been prescribed amitriptyle 10mg. Can anyone give me some hope that I can get better from this condition. Feeling low and depressed.
Thanks
Thanks
Comments: 5
MonaLisa Touch
Fri Feb 08, 2019 7:35 pm by rl2091
Hi All,
I'm wondering if anyone has any experience with the MonaLisa Touch treatment for Vulvodynia? My pain started when I went on HRT(pill) for anxiety mainly and my pain abruntly stopped when I stopped HRT. However, when I started on the HRT patch (at my dr's suggestion), the pain returned and has never left. That was 7 years ago. I found MonaLisa Touch on the internet purely by accident …
I'm wondering if anyone has any experience with the MonaLisa Touch treatment for Vulvodynia? My pain started when I went on HRT(pill) for anxiety mainly and my pain abruntly stopped when I stopped HRT. However, when I started on the HRT patch (at my dr's suggestion), the pain returned and has never left. That was 7 years ago. I found MonaLisa Touch on the internet purely by accident …
Comments: 3
Diagnosed Recently
Tue Jan 08, 2019 3:55 pm by flissyg
Hi All,
I’m so glad I’ve found a place where there are others who understand how I feel!
So this is my story:-
I’m 36, and 4 months ago, whilst innocently sitting in bed reading I experienced a very sharp stabbing pain in my clitoris. It last only a few minutes and then subsided as quickly as it came on. It put it down to “one of those things”. The following morning I woke up …
I’m so glad I’ve found a place where there are others who understand how I feel!
So this is my story:-
I’m 36, and 4 months ago, whilst innocently sitting in bed reading I experienced a very sharp stabbing pain in my clitoris. It last only a few minutes and then subsided as quickly as it came on. It put it down to “one of those things”. The following morning I woke up …
Comments: 4
New and need advice and help
Wed Dec 05, 2018 3:26 pm by Cin124
Hi everyone,
About three months ago, I started having vaginal and vulval itching. Then, about two months ago, my vulva started to feel painful and look swollen, so I went to the doctor. I was tested for herpes, chlamydia, and gonorrhea which all came back negative. I also had to do a vaginal swab test and the only thing that came back positive was yeast infection. I was prescribed hydrozole …
About three months ago, I started having vaginal and vulval itching. Then, about two months ago, my vulva started to feel painful and look swollen, so I went to the doctor. I was tested for herpes, chlamydia, and gonorrhea which all came back negative. I also had to do a vaginal swab test and the only thing that came back positive was yeast infection. I was prescribed hydrozole …
Comments: 6
New here would very much appreciate advice at the end of my rope
Wed Jan 09, 2019 9:09 pm by Jma990o
This might be a little long but it's been such a long time I've even been able to talk about my problems openly thank you in advance for any helpful advice.
So ok I'm 24 I've been having this problem for over two years seen quite a few doctors and obgyns alike and nobody will take me seriously I have had a few utis and yeast infections and even bv once and this all started after one of the utis …
So ok I'm 24 I've been having this problem for over two years seen quite a few doctors and obgyns alike and nobody will take me seriously I have had a few utis and yeast infections and even bv once and this all started after one of the utis …
Comments: 3
HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
+4
Rainy Day
Sarah001
Alana3
zarli
8 posters
Page 1 of 1
HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Hi All
Just wondering if any one else suffers from painful burning heels/feet when unprovoked vulvodynia is present?
Just wondering if any one else suffers from painful burning heels/feet when unprovoked vulvodynia is present?
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
I do sometimes...
Alana3- Posts : 1093
Join date : 2012-09-25
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Me too, the entire soles of my feet burn at times but more so in the winter for some reason. I'm not totally sure why it happens, could be crosstalk between nerves or could be misalignment of various areas, I can't really say for sure but I have found that even when my V isn't so bad my feet can be . I also get burning down the inner thighs quite often but more so if I have to stand for lengthy periods like I do at work.
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
BURNING FEET
So glad I'm not weird!!
I have been doing research on nerves, the genital area is close with the feet in the nerve passage in the brain. I am now looking into trapped nerves as I have always had a gut feeling this is my problem. Wouldn't that be so easy if some one could 'untrap' your nerve!!!!
I have been doing research on nerves, the genital area is close with the feet in the nerve passage in the brain. I am now looking into trapped nerves as I have always had a gut feeling this is my problem. Wouldn't that be so easy if some one could 'untrap' your nerve!!!!
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
There is a thing called nerve flossing which is supposed to free the nerves but it's very hard to find specific information about how to do each nerve online, however physios would know about this. The only one I know how to do is the sciatic nerve which isn't really one of the ones associated with V so it's very little help!!
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
still searching
Thanks Sarah I am still researching will let you know how I go. Im off to my specialist at the Royal Womens Hospital in Melbourne on Sep 9th I have a list of questions about it I will keep you posted kind regards Zarli
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Great zarli, I love adding to my geeky knowledge! The nerve flossing is sometimes called nerve gliding just in case they don't know what you're asking about. My physio did once mention she knew how to release the pudendal nerve but I didn't press her at the time so other physios should know too. Good luck!
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
nerve pain spreading
At my worst, I couldn't wear socks/shoes, since my feet were burning. My ENTIRE leg would sometimes burn...at times it would spread to my arms, chest, and back. I haven't had that happen for about a year...but when my flare was out of control it did happen. So, don't feel like it will be like that forever. Mine went away.
Rainy Day- Posts : 54
Join date : 2012-07-19
Location : US
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
I'm so glad I'm not the only one who finds an association with the two areas. I have always found that if my feet are too cold, more so if I place bare feet onto cold floor, I feel the burning in my genitals. Also if I walk a lot, when my feet have been rubbing,it can aggravate pain or burning in my genitals.
Interesting to know the two nerve pathways are close together. Let us now what you find out about it all.
Finch
Interesting to know the two nerve pathways are close together. Let us now what you find out about it all.
Finch
Finch- Posts : 10
Join date : 2013-01-02
update from appointment
Hi lovely ladies,
I have no news on nerve trapped or other?? I saw 3 specialist a psychologist, physiotherapist and a vulva pain specialist. It can get rather confusing and information can change a little from each person, nerve fact they tell me is my nerves are inflamed and it is tight muscles that are the cause so I should do physio to correct this (tried this 5 times). I am feeling rather dejected today although I insist on keeping a positive attitude. I would love a doctor (well I don't wish vulvadynia on any one) but yes I would love a doctor to suffer this condition so they could experience what we all go through, as at times I felt like they were so out of touch of a woman's mind that has this condition and that they had no idea what all the medication does to us, at the same time I appreciate there help!!!
I was sent away with more cream another to add to the list!! I am now taking Lyrica, nortriptaline, valium, amitriptyline cream and diprosone cream.
I have low pain while taking all of these which I am grateful. I do how ever suffer terrible constipation, bloating and am 20 kg heavier than 5 years ago, but I am in LaLa land so its not that bad!!!
I am not religious at all and have to confess I said my first prayer or what ever I can call it to who ever is up there or down there last night going to bed....." please god if you are up there, feed the starving, house the homeless and give rapist, murders, child abusers etc vulvadynia" I guess I have just wished it apon others.
I have no news on nerve trapped or other?? I saw 3 specialist a psychologist, physiotherapist and a vulva pain specialist. It can get rather confusing and information can change a little from each person, nerve fact they tell me is my nerves are inflamed and it is tight muscles that are the cause so I should do physio to correct this (tried this 5 times). I am feeling rather dejected today although I insist on keeping a positive attitude. I would love a doctor (well I don't wish vulvadynia on any one) but yes I would love a doctor to suffer this condition so they could experience what we all go through, as at times I felt like they were so out of touch of a woman's mind that has this condition and that they had no idea what all the medication does to us, at the same time I appreciate there help!!!
I was sent away with more cream another to add to the list!! I am now taking Lyrica, nortriptaline, valium, amitriptyline cream and diprosone cream.
I have low pain while taking all of these which I am grateful. I do how ever suffer terrible constipation, bloating and am 20 kg heavier than 5 years ago, but I am in LaLa land so its not that bad!!!
I am not religious at all and have to confess I said my first prayer or what ever I can call it to who ever is up there or down there last night going to bed....." please god if you are up there, feed the starving, house the homeless and give rapist, murders, child abusers etc vulvadynia" I guess I have just wished it apon others.
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Thanks for updating despite no definites on nerves. I gained 2 stone from the Lyrica but have managed to lose one while still taking it with Slimming World (done from home using facebook groups for recipes) and I'm still working on that second stone so it is possible to lose weight but it does come off slowly. For constipation I take Magnesium Oxide tablets, I buy them from Holland and Barrett and take 2 in the morning and one in the evening and as long as I drink enough water I very rarely get constipated now. Worth a try And remember all physios are not created equal so some won't know enough to help and any clenching done in between sessions (I do this ALOT) undoes the trigger point work so could be you haven't yet met the right physio. Loving your positive attitude, keep it up!
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
thanks sarah
Thanks Sarah I appreciate your great advice. I did try magnesium about 4 years ago for the nerve pain but haven't since so I will get them again, do you remember the lady that was selling that book called ' I cured my vulvadynia naturally and so can you' ? Well she said magnesium in high doses worked for the nerve pain but no such luck for me. I would love to know more about your history with vulvadynia is your story on this forum? How has it affected your life etc...? Sorry but sometimes I feel the need to just communicate more with fellow sufferers....guess it makes me feel less alone in this journey or life sentence as it some times feels like..
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Hi again zarli, I take magnesium for constipation because in high doses it gets excreted out through the bowel and relieves constipation, I actually found out about it by stumbling onto an IBS forum where lots of members were using it. It has to be the oxide variety through to work.
My life is badly affected by Ehlers-Danlos Syndrome Type 3 along with Fibromyalgia so the V on top hasn't helped much and in fact ended my 13 year relationship but that was a couple of years ago now so I'm pretty much over that! Mine is definitely a pelvic floor issue as my pelvis is badly affected by my EDS and very loose and unstable so at the moment I'm trying prolotherapy on my pelvic joints to try and stabilise it enough to start releasing my PF. Aka going round in circles!! My V is unprovoked and constant but it started as provoked only and I wish I'd taken it more seriously then and not let it get worse. I had a resting tone of 20 last time it was checked so if you consider 2 or under is normal it's pretty obvious what's going on with me! I have a great physio though who is helping keep my pelvis aligned while I have prolo and on stand by should I ever get stable enough for her to go for it and meanwhie I'm trying to correct my lousy breathing patterns and posture and learn not to clench all day long so I'm still busy with it all. My story is buried way back because I joined when the forum first started and I can't recall what title I gave it!! It's been 3 and a half years so I think I can be forgiven for that!!
My life is badly affected by Ehlers-Danlos Syndrome Type 3 along with Fibromyalgia so the V on top hasn't helped much and in fact ended my 13 year relationship but that was a couple of years ago now so I'm pretty much over that! Mine is definitely a pelvic floor issue as my pelvis is badly affected by my EDS and very loose and unstable so at the moment I'm trying prolotherapy on my pelvic joints to try and stabilise it enough to start releasing my PF. Aka going round in circles!! My V is unprovoked and constant but it started as provoked only and I wish I'd taken it more seriously then and not let it get worse. I had a resting tone of 20 last time it was checked so if you consider 2 or under is normal it's pretty obvious what's going on with me! I have a great physio though who is helping keep my pelvis aligned while I have prolo and on stand by should I ever get stable enough for her to go for it and meanwhie I'm trying to correct my lousy breathing patterns and posture and learn not to clench all day long so I'm still busy with it all. My story is buried way back because I joined when the forum first started and I can't recall what title I gave it!! It's been 3 and a half years so I think I can be forgiven for that!!
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
thank you
Thank you Sarah for responding, you certainly have had a lot to deal with and its a credit to you how positive and proactive you remain. I also suffer from fibromyalgia that came after 'V' and it has certainly made 'V' worse. I have never herd of EDS but I'm going to have a research of it out of interest. I wish 4 years ago instead of thinking amil medication had control of my 'V' and I thought if I slowly went off them it would all be ok...bad mistake but you live and learn!! I am a very positive person and will fight to make my life the best it can be. The best thing is at least I do respond to medication for that I am grateful. All the best to you Sarah and I'm so glad your on this forum your wealth of knowledge and attitude is very much appreciated.
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Thanks zarli it's quite a rarity to feel useful when you're literally falling apart!!
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Ive had a terrible day vulva pain disgusting, burning heals, aching all over and hard day at work. I was telling myself I'm falling apart all day until that was making me feel very depressed so I told myself ...im here im alive and I have to keep moving forward for my children I want to have quality of life. Its bludyy hard some days that's all there is to it.
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
I really mean literally falling apart, if you look up EDS and all the joint dislocations we're prone to you'll see what I mean!! Do you work standing up? I do and when I struggle with it I grip with my glutes and clench my pelvic floor which in turn seems to make my burning feet much worse.
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Sorry Sarah my last post was not ment to offend you at all or make you feel bad in any way. I was venting on my own bad day which I thought might make you feel less alone. It was in no means referring to your falling apart with EDS and it makes me feel quite sad that it may have hurt your feelings, so once again I do apologise. I do work standing up all day my shifts are 12 hours so yes by the end of the bad days I am totally exhausted and frustrated, I guess we all have our own problems to bare with, I only wish you all the very best in finding any relief you can.
zarli- Posts : 182
Join date : 2013-08-11
Location : Australia
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
You didn't offend me at all zarli, I just wanted to clarify what I actually meant.
Sarah001- Posts : 1164
Join date : 2010-06-11
Age : 50
Location : UK
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
Hi Zarli,zarli wrote:Hi All
Just wondering if any one else suffers from painful burning heels/feet when unprovoked vulvodynia is present?
I strongly recommend you to go and see a neurologist since burning feet or leg is the most popular symptom of bulged discs in lumbar spine. You may need to have a lumbar MRI.
Take good care.
burningturning- Posts : 24
Join date : 2013-09-24
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
This is odd, I sometimes get burning soles and lower back pain. Interesting!
tinkerbelle2- Posts : 303
Join date : 2013-09-28
Age : 31
Location : Brighton, England, UK.
Re: HAS ANY ONE HAD PAINFUL FEET/HEELS WITH VULVODYNIA?
I too get burning feet when i get a flare up...like right now unfortunately. Most doctors i have been to say it is unrelated but I obviously do not believe that. I truly believe it is nerve related, hopefully doctors will figure it out one day so we can all be pain free and enjoy being women.
ringostarr26- Posts : 59
Join date : 2012-07-31
Similar topics
» Back pain, burning feet and vulvodynia....all related?
» Can people with generalized unprovoked vulvodynia have painful sex?
» Burning Feet?
» Can people with generalized unprovoked vulvodynia have painful sex?
» Burning Feet?
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Fri Oct 23, 2020 12:04 am by ringostarr26
» Please tell me this can get better
Sat Jul 18, 2020 7:38 pm by sammykramer
» By no means cured, but doing much better!
Mon Mar 16, 2020 1:26 pm by tinkerbelle2
» How I cured my Vulvodynia!
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» 7 months since the diagnosis
Wed Aug 14, 2019 2:38 am by agtoronto
» Gabapentin Gel. or other topical creams
Sat Jun 15, 2019 5:22 pm by mary jane
» IMPORTANT FOR UK SUFFERERS
Sat Jun 15, 2019 5:21 pm by mary jane
» Help New Diagnosis
Sat Jun 15, 2019 5:07 pm by mary jane
» 6 days post Vestibulectomy - Is this normal?? please tell me about your postop healing process!
Tue Jun 11, 2019 12:56 am by VVSSufferer