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Hi there, I have just discovered the site and wanted to ask if anyone has had similar migraine experiences to me?
I have tried a mouth guard,
hypnotherapy
and osteopathy which have not worked. I use sumitriptan for migraine which usually works but I often get the symptoms back. I wondered if anyone had any advice on anything else I haven't tried. I have gone through all medication options.
I have tried a mouth guard,
hypnotherapy
and osteopathy which have not worked. I use sumitriptan for migraine which usually works but I often get the symptoms back. I wondered if anyone had any advice on anything else I haven't tried. I have gone through all medication options.
jellybabies
in
National Migraine Centre
12 years ago
Am i Coping ?
im now on medication for anxiety, depression, heart racing and also sleeping tablets. iv had
hypnotherapy
and to help me cope, some days i feel ok but most days i feel like i dont want to live like this. i have constant hot flushes, racing heart, bad thoughts and tiredness, id like to think im coping
im now on medication for anxiety, depression, heart racing and also sleeping tablets. iv had
hypnotherapy
and to help me cope, some days i feel ok but most days i feel like i dont want to live like this. i have constant hot flushes, racing heart, bad thoughts and tiredness, id like to think im coping
sammyjoo
in
Anxiety Support
12 years ago
Endo and Anxiety/Panic disorder?
I had
hypnotherapy
for a few months a couple of years ago and it was brilliant - but as soon as I stopped the sessions, the panic came back I wonder if endo and anxiety are somehow linked?
I had
hypnotherapy
for a few months a couple of years ago and it was brilliant - but as soon as I stopped the sessions, the panic came back I wonder if endo and anxiety are somehow linked?
Chrissie66
in
Endometriosis UK
12 years ago
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Hello all, I'm a new member on this particular site and have found it interesting so far, I've not read all the blogs so please forgive me if I am repeating things :-) I think, most anxiety problems are usually from past negative experiences or from Significant Emotional Experience. I know about these
Hello all, I'm a new member on this particular site and have found it interesting so far, I've not read all the blogs so please forgive me if I am repeating things :-) I think, most anxiety problems are usually from past negative experiences or from Significant Emotional Experience. I know about these
Hidden
in
Anxiety Support
12 years ago
Does Hypnosis treatment work for Anxiety ?
My Anxiety was caused when I felt dizzy in a bar on a Sunday afternoon, I had only 1 drink but from that day onwards I feel anxious when going near a bar and cannot drink socially. I have been on on computer based CBT courses and have taken Mirtazapine. The feeling is still there when I enter places
My Anxiety was caused when I felt dizzy in a bar on a Sunday afternoon, I had only 1 drink but from that day onwards I feel anxious when going near a bar and cannot drink socially. I have been on on computer based CBT courses and have taken Mirtazapine. The feeling is still there when I enter places
KevinManchester
in
Anxiety Support
12 years ago
Should Dyslexia be labeled a learning disability?
I've since got a degree in medical and clinical
hypnotherapy
and I am a NLP (neuro linguistic programing) and trainer of it.
I've since got a degree in medical and clinical
hypnotherapy
and I am a NLP (neuro linguistic programing) and trainer of it.
Hidden
in
The Dyslexia Community
12 years ago
is anyone on here trying out the hypnotherapy at NMC?
rosianna
in
National Migraine Centre
12 years ago
I am thinking of trying clinical hypnotherapy to help my anxiety. What are other people's experiences of it?
Chloe
in
Anxiety Support
12 years ago
hydrotherapy
I commented on a question about hydrotherapy. My comment is below. Not sure if i'm allowed to make this offer, if I'm not someone please tell me. It's just that I've been going for about 2 years and it really helps. as stated below, I just want to help out if I can. xx "It's soooo wonderful. I actually
I commented on a question about hydrotherapy. My comment is below. Not sure if i'm allowed to make this offer, if I'm not someone please tell me. It's just that I've been going for about 2 years and it really helps. as stated below, I just want to help out if I can. xx "It's soooo wonderful. I actually
charlie_2
in
Fibromyalgia Action UK
12 years ago
hydrotherapy
I am being referred to have hydrotherapy, has anyone else had it and wat is it like.
I am being referred to have hydrotherapy, has anyone else had it and wat is it like.
lash
in
Fibromyalgia Action UK
12 years ago
hi eveyone i live in Haydock does anyone know where i can find either warm swimming pool or hydrotherapy pool gentle hugs to everyone xx
please help i really need some help,
please help i really need some help,
tramar
in
Fibromyalgia Action UK
12 years ago
Hydrotherapy or a warm swimming pool?
Does anybody know of a warm pool in central London, that is maybe not too expensive...not a private 5 star hotel pool which are great but cost the earth for a day membership. I would love to have hydrotherapy but not through my docs as the physios in my local hospital are masachists. (seriously) I
Does anybody know of a warm pool in central London, that is maybe not too expensive...not a private 5 star hotel pool which are great but cost the earth for a day membership. I would love to have hydrotherapy but not through my docs as the physios in my local hospital are masachists. (seriously) I
fibrodude
in
Fibromyalgia Action UK
12 years ago
First do no harm????
Sorry need to sound off, have had a so called professional being very nasty on the phone to me. I was diagnosed with RA at the beginning of April and have started treatment with the BRI, which is a hospital a bus or car journey away. At first I was a bit disapointed as I live a short walk from Southmead
Sorry need to sound off, have had a so called professional being very nasty on the phone to me. I was diagnosed with RA at the beginning of April and have started treatment with the BRI, which is a hospital a bus or car journey away. At first I was a bit disapointed as I live a short walk from Southmead
Traceyanne
in
NRAS
12 years ago
Gym for back pain and fibro
I am going to Ashford Hospital (near Heathrow Airport) for physiotherapy. I have had hydrotherapy and now I have been put into a physio gym for back pain. My first session was yesterday (Friday 20th April) I didnt know what to expect. I thoroughly enjoyed it. Met another lady who has fibro there. Trouble
I am going to Ashford Hospital (near Heathrow Airport) for physiotherapy. I have had hydrotherapy and now I have been put into a physio gym for back pain. My first session was yesterday (Friday 20th April) I didnt know what to expect. I thoroughly enjoyed it. Met another lady who has fibro there. Trouble
VonnyM
in
Fibromyalgia Action UK
12 years ago
Hydrotherapy
Back from hydro today after several weeks break due to hospital and Easter. Didnt manage any exercises at all today, just spent half hour having a float. Heaven
Back from hydro today after several weeks break due to hospital and Easter. Didnt manage any exercises at all today, just spent half hour having a float. Heaven
julieru
in
Fibromyalgia Action UK
12 years ago
Could my assault have caused my FM??
saying that FM can be triggered by a traumatic experience.....when I was 13 I was attacked and brutally raped by a gang of 3 boys...i have found it very hard over the past 13 years trying to cope with what happened to me, I have nightmares all the time, ive seen psycologists, psychiatrists, councellers,
hypnotherapy
saying that FM can be triggered by a traumatic experience.....when I was 13 I was attacked and brutally raped by a gang of 3 boys...i have found it very hard over the past 13 years trying to cope with what happened to me, I have nightmares all the time, ive seen psycologists, psychiatrists, councellers,
hypnotherapy
Tess1
in
Fibromyalgia Action UK
12 years ago
My first blog-its on my profile.Hope you'll all understand?
Diagosed in 2008, along with hearing impairment,wear a hearing aid now. Then a year ago diagnosed with Type 2 diabetes. Looking back I probably had it for years but kept relatively active,good diet and luckily didnt smoke or drink so probably masked and kept at bay alot of the symtoms. I really have
Diagosed in 2008, along with hearing impairment,wear a hearing aid now. Then a year ago diagnosed with Type 2 diabetes. Looking back I probably had it for years but kept relatively active,good diet and luckily didnt smoke or drink so probably masked and kept at bay alot of the symtoms. I really have
asasmum
in
NRAS
12 years ago
No not more!!
Well i went to the podiatrist yesterday who was lovely and said he would make me two pairs of special shoes and insoles and let me choose a lovely pair i like!! So i was pleased and thought great i can tell work that i will be able to walk better as i have new shoes. Today i went to see a physio who
Well i went to the podiatrist yesterday who was lovely and said he would make me two pairs of special shoes and insoles and let me choose a lovely pair i like!! So i was pleased and thought great i can tell work that i will be able to walk better as i have new shoes. Today i went to see a physio who
allanah
in
NRAS
12 years ago
Becoming an Expert Patient - article 3: Dealing with Doctors
[u]Dealing with Doctors[/u]
Something many people with Fibromyalgia Syndrome (Fibro) find difficult is working out how to best deal with doctors. Establishing a good working relationship with your healthcare team is often a crucial part of getting control of your condition and keeping control
[u]Dealing with Doctors[/u]
Something many people with Fibromyalgia Syndrome (Fibro) find difficult is working out how to best deal with doctors. Establishing a good working relationship with your healthcare team is often a crucial part of getting control of your condition and keeping control
LindseyMid
in
Fibromyalgia Action UK
12 years ago
Physiotherapy and Fibro
It has come to my attention that a few of our members here have struggled to access useful physiotherapy. This is such a shame as appropriate physiotherapy can make such a difference to someone with Fibro and may actually be an essential part of getting control of your symptoms. I have therefore copied
It has come to my attention that a few of our members here have struggled to access useful physiotherapy. This is such a shame as appropriate physiotherapy can make such a difference to someone with Fibro and may actually be an essential part of getting control of your symptoms. I have therefore copied
LindseyMid
in
Fibromyalgia Action UK
12 years ago
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