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don't know what to do next re pudendal nerve treatment
Hi all. I was diagnosed with pudendal neuralgia in june after having a period of 2 weeks of no pain at all following an x-ray guided pudendal nerve block into the nerve via the buttock. The anaeasthetic part didn't work at all but the steroid kicked in exactly 2 weeks after and I really thought I'd
Hi all. I was diagnosed with pudendal neuralgia in june after having a period of 2 weeks of no pain at all following an x-ray guided pudendal nerve block into the nerve via the buttock. The anaeasthetic part didn't work at all but the steroid kicked in exactly 2 weeks after and I really thought I'd
sweetpea02
in
Pelvic Pain Support Network
12 years ago
Pudendal Pain
Hi Ladies I am glad I have found this site because I have been in a great deal of pain following a hystorectomy, front and back prolapse. After giving up with my local hospital I asked my doctor for a second opinion. I was referred to another hospital where i have found the most wonderful man who has
Hi Ladies I am glad I have found this site because I have been in a great deal of pain following a hystorectomy, front and back prolapse. After giving up with my local hospital I asked my doctor for a second opinion. I was referred to another hospital where i have found the most wonderful man who has
Marion35
in
Pelvic Pain Support Network
12 years ago
occipital nerve block injections
hi has anybody had occipital nerve block injections for their migraines ? and if so did they work ?
hi has anybody had occipital nerve block injections for their migraines ? and if so did they work ?
saphire72
in
National Migraine Centre
12 years ago
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hi guys
hi all, been a while since i posted, i got feed back that via the n.h.s the ct guided injection won't be til april,so dr de mello has offered me a transvaginal nerve block into the pudendal nerve to see if that will help and am soon to have it done,yet to send me appoint but have been told end nov,beginnning
hi all, been a while since i posted, i got feed back that via the n.h.s the ct guided injection won't be til april,so dr de mello has offered me a transvaginal nerve block into the pudendal nerve to see if that will help and am soon to have it done,yet to send me appoint but have been told end nov,beginnning
electricjaws
in
Pelvic Pain Support Network
12 years ago
Back to life
Words… searching, searching… any second now… … … almost… actually, nope.., it’s not going to happen. As if there’d be ANY words for me to explain how I feel writing this post. So please gear up with me, imagine the drum rolls and the biggest mountain you can imagine with me standing on the tippy top
Words… searching, searching… any second now… … … almost… actually, nope.., it’s not going to happen. As if there’d be ANY words for me to explain how I feel writing this post. So please gear up with me, imagine the drum rolls and the biggest mountain you can imagine with me standing on the tippy top
Hidden
in
Pelvic Pain Support Network
12 years ago
Hi, has anyone tried a Tens machine for migraine.
I have tried lots treatment including Botox, Nerve Block injection and loads of different Medications but still suffering daily very painful headaches and full blown Migraine with vomiting at least once a week. Thanks Alison
I have tried lots treatment including Botox, Nerve Block injection and loads of different Medications but still suffering daily very painful headaches and full blown Migraine with vomiting at least once a week. Thanks Alison
hattie2
in
National Migraine Centre
12 years ago
Has anyone tried greater occiptal nerve block injections for migraine prevention?
My migraines have got much worse this year and I am now having on average one a week. I had an appt at the NMC yesterday and they suggested I try these injections - preventative supplements and medication haven't worked so far. I'd be interested to hear if anyone else has tried them and whether they
My migraines have got much worse this year and I am now having on average one a week. I had an appt at the NMC yesterday and they suggested I try these injections - preventative supplements and medication haven't worked so far. I'd be interested to hear if anyone else has tried them and whether they
MonicaG
in
National Migraine Centre
12 years ago
Pudendal Neuralgia and Pelvic Floor Exercises
I recently had prostate surgery (HIFU) for cancer which has left me partially incontinent.I have been recommended by my urologist to undertake pelvic floor exercises. I also suffer from pudendal neuralgia for five years which has been kept under reasonable control with pregabalin and three previous nerve
I recently had prostate surgery (HIFU) for cancer which has left me partially incontinent.I have been recommended by my urologist to undertake pelvic floor exercises. I also suffer from pudendal neuralgia for five years which has been kept under reasonable control with pregabalin and three previous nerve
Hidden
in
Pelvic Pain Support Network
12 years ago
Antidepressants and Statins.
I have been taking antidepressants for approx 12 years. (present dose is 300mg per day of venlafaxine). I had a heart bypass in 2010 and have been taking statins since then. Is it okay to take these together? Also, I've heard that statins can cause muscle problems. I have a lot of muscle pain
I have been taking antidepressants for approx 12 years. (present dose is 300mg per day of venlafaxine). I had a heart bypass in 2010 and have been taking statins since then. Is it okay to take these together? Also, I've heard that statins can cause muscle problems. I have a lot of muscle pain
Hidden
in
Cholesterol Support
12 years ago
Has anyone experienced pudendal nerve block injections? I may have to have these.
I am in the scottish borders and could travel to Edinburgh to hospital there. I have pudendal neuralgia as a result of a mistake during surgery and don't want the same surgeon to gave me the injections.
I am in the scottish borders and could travel to Edinburgh to hospital there. I have pudendal neuralgia as a result of a mistake during surgery and don't want the same surgeon to gave me the injections.
juliahall
in
Pelvic Pain Support Network
12 years ago
Hi I am new to this.Wondering if anyone can advise me on Drs. who treat GAVE. for my husband.
He has GAVE (watermelon stomach). He is having transfusions every 2-3 months now, used to be 6 months. Also has laser once a year which does not do anything for him. We live on the mid North Coast NSW but we will go anywhere if we can get a Dr who specialises in this area. I also want to know if there
He has GAVE (watermelon stomach). He is having transfusions every 2-3 months now, used to be 6 months. Also has laser once a year which does not do anything for him. We live on the mid North Coast NSW but we will go anywhere if we can get a Dr who specialises in this area. I also want to know if there
franny1
in
PBC Foundation
12 years ago
Living with ADPKD
Hi I was diagnosed with Poly cystic Kidney disease many years ago and am stable within stage 3 renal failure. I am a nurse in a children's hospice I work part time. My main problem has been pain due to the size of my kidneys and liver . I have recently been referred to a pain specialist and am at
Hi I was diagnosed with Poly cystic Kidney disease many years ago and am stable within stage 3 renal failure. I am a nurse in a children's hospice I work part time. My main problem has been pain due to the size of my kidneys and liver . I have recently been referred to a pain specialist and am at
cmcginily
in
Early CKD Support
12 years ago
INTRAVENOUS LIGNOCAINE ???? anyone any idea?
letter from pain clinic drs says consideration is to be given for occipital nerve block or intravenous Lignocaine, anyone any idea about the intravenous Lignocaine thingy, ?? (for headaches caused by fibro so they say )
letter from pain clinic drs says consideration is to be given for occipital nerve block or intravenous Lignocaine, anyone any idea about the intravenous Lignocaine thingy, ?? (for headaches caused by fibro so they say )
jue2829
in
Fibromyalgia Action UK
12 years ago
nerve block
Hi anybody had an ultra sound guided nerve block in the neck, im having one Thursday and am looking for comments
Hi anybody had an ultra sound guided nerve block in the neck, im having one Thursday and am looking for comments
jancross
in
Fibromyalgia Action UK
12 years ago
Nerve blocks
I have just had my second nerve block to help with my Fibro/Lupus. They really do make living these these conditions more tolerable. As anyone had these for a number of years and can you tell me if they are still effective or do you wear off more quickly the more you have?. Would welcome any comments
I have just had my second nerve block to help with my Fibro/Lupus. They really do make living these these conditions more tolerable. As anyone had these for a number of years and can you tell me if they are still effective or do you wear off more quickly the more you have?. Would welcome any comments
Alexandria
in
LUPUS UK
12 years ago
What's new in managing pelvic pain ?
I attended the Convergences PP congress in Nimes recently. There were several interesting presentations including the results of the nerve block trial carried out by several pain teams in France. The results show that diagnostic blocks are still important but that therapeutic nerve blocks
I attended the Convergences PP congress in Nimes recently. There were several interesting presentations including the results of the nerve block trial carried out by several pain teams in France. The results show that diagnostic blocks are still important but that therapeutic nerve blocks
PPSN_JudyB
Pelvic Pain Support Netwo
in
Pelvic Pain Support Network
12 years ago
Pain management
What suggestions do people have for pain management? I have tried chiropratic intervention, massage therapy, cortizone shots and nerve blocks, accupuncture, heat and cold pacs but still have an unbelievable amount of pain. I cannot do a quarter of what i used to do and my sleep is constantly interrupted
What suggestions do people have for pain management? I have tried chiropratic intervention, massage therapy, cortizone shots and nerve blocks, accupuncture, heat and cold pacs but still have an unbelievable amount of pain. I cannot do a quarter of what i used to do and my sleep is constantly interrupted
tinanyc
in
LUPUS UK
13 years ago
Cluneal nerve problems/neuralgia?
Hi all, i've been to see Dr B in London, i was referred to him because of possible PN, but he thought it was the cluneal nerves causing my sitting/pain problems. Anyway he did a diagnositic bilateral nerve block, which didn't really help much. He wants to repeat the procedure to see if it helps the second
Hi all, i've been to see Dr B in London, i was referred to him because of possible PN, but he thought it was the cluneal nerves causing my sitting/pain problems. Anyway he did a diagnositic bilateral nerve block, which didn't really help much. He wants to repeat the procedure to see if it helps the second
Igno
in
Pelvic Pain Support Network
12 years ago
Should I be worrying
Hi - I had a double heart bypass in 2007 and have been reasonably well since. I work in a hospital and yesterday they had a day where staff could go and have their BP taken by a professional. Well it was taken three times and was very high 1. 170/92 2. 172/91 3. 177/90. I was told to go back a
Hi - I had a double heart bypass in 2007 and have been reasonably well since. I work in a hospital and yesterday they had a day where staff could go and have their BP taken by a professional. Well it was taken three times and was very high 1. 170/92 2. 172/91 3. 177/90. I was told to go back a
Hidden
in
Cholesterol Support
12 years ago
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