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TENS machine for period cramps in stage 4 endometriosis
Hi all !!! I'm stage 4 endometriosis patient and had a laparoscopy surgery 15months ago and I get lower back pain and stomach pain during my periods .I've heard of TENS machine is it suitable for everyone and can anyone suggest which brand TENS machine i should buy . Are deep heat period pain heat
Hi all !!! I'm stage 4 endometriosis patient and had a laparoscopy surgery 15months ago and I get lower back pain and stomach pain during my periods .I've heard of TENS machine is it suitable for everyone and can anyone suggest which brand TENS machine i should buy . Are deep heat period pain heat
Chotu5
in
Endometriosis UK
1 year ago
Internal Burning
Hi,I am new here. I am desperate for answers. I had a hysterectomy 21 years ago and it was only through recurrent UTI’s that I was eventually diagnosed with vaginal atrophy. I was put on Vagifem and a vaginal moisturiser but whereas my UTI’s stopped the intense burning ( as if someone had put a tube
Hi,I am new here. I am desperate for answers. I had a hysterectomy 21 years ago and it was only through recurrent UTI’s that I was eventually diagnosed with vaginal atrophy. I was put on Vagifem and a vaginal moisturiser but whereas my UTI’s stopped the intense burning ( as if someone had put a tube
CecilyParsley
in
Pelvic Pain Support Network
1 year ago
Working full-time with a DBS
DBS Deep Brain Stimulation. 1) Are there any warriors who have received DBS and are still employed full-time? 2) Are there any IT/computers warriors who have received DBS and are still working? Just wondering if that's humanly possible. Thank you for your time.
DBS Deep Brain Stimulation. 1) Are there any warriors who have received DBS and are still employed full-time? 2) Are there any IT/computers warriors who have received DBS and are still working? Just wondering if that's humanly possible. Thank you for your time.
surdug1
in
Cure Parkinson's
1 year ago
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Very bad back pain at 25. help?
i take NSAID's,
deep
heat cream,
deep
freeze
etc, it only helps for a bit and not completely. Also can anyone recommend any supplements that have helped them?
i take NSAID's,
deep
heat cream,
deep
freeze
etc, it only helps for a bit and not completely. Also can anyone recommend any supplements that have helped them?
Amywoodx
in
Fibromyalgia Action UK
2 years ago
OFF time but so much more!
I learned so much about our disease through this video. It was about OFF time but through that lens I learned out about the medications prescribed to us. There is a clear description of the different DBS devices available. This guy made my neurologist look like an amateur. https://youtu.be/TunPzh2Lw3U
I learned so much about our disease through this video. It was about OFF time but through that lens I learned out about the medications prescribed to us. There is a clear description of the different DBS devices available. This guy made my neurologist look like an amateur. https://youtu.be/TunPzh2Lw3U
PalmSprings
in
Cure Parkinson's
1 year ago
Ibs pain
I have recently been diagnosed with ibs, well my doctor has said it’s ibs but I am awaiting further tests. I have been following a gluten free diet for about 2 months now, I have noticed that I am less bloated but that has been the only change. I am wanting to ask, does anyone else get woke up through
I have recently been diagnosed with ibs, well my doctor has said it’s ibs but I am awaiting further tests. I have been following a gluten free diet for about 2 months now, I have noticed that I am less bloated but that has been the only change. I am wanting to ask, does anyone else get woke up through
Pink_Lover
in
IBS Network
8 months ago
Gluten free diet
I have been on a Gluten Free diet for more then 10 years. Recently I have had abdominal pain, flatulence, and reflux after food. I found out you can buy a Coeliac kit from the chemist, but not sure about it. I feel I should go to the GP but have been in hospital in the past and the DR there said I had
I have been on a Gluten Free diet for more then 10 years. Recently I have had abdominal pain, flatulence, and reflux after food. I found out you can buy a Coeliac kit from the chemist, but not sure about it. I feel I should go to the GP but have been in hospital in the past and the DR there said I had
Simpson43
in
Gluten Free Guerrillas
8 months ago
Need faster research on Neuro-modulation
I attended 2 various zoom meets of Vibratory Neuro-modulation . In UK they have a CUE1 available at less than 500 dollars that is showing some amazing strides for some people. Then I watched a zoom with Dr Peter Tass who is a researcher involved with the amazing Vibratory Gloves. My wife was a participant
I attended 2 various zoom meets of Vibratory Neuro-modulation . In UK they have a CUE1 available at less than 500 dollars that is showing some amazing strides for some people. Then I watched a zoom with Dr Peter Tass who is a researcher involved with the amazing Vibratory Gloves. My wife was a participant
Furch
in
Cure Parkinson's
1 year ago
Departing the Soul
Dear friends, I have been grappling with PD now for over ten years and it is getting harder and harder to go on and I have been contemplating MAID program for a while now, but my wife, who is my only support is not letting me go through with it. She loves me dearly. Moreover, she has no one except
Dear friends, I have been grappling with PD now for over ten years and it is getting harder and harder to go on and I have been contemplating MAID program for a while now, but my wife, who is my only support is not letting me go through with it. She loves me dearly. Moreover, she has no one except
gurdeep11
in
Cure Parkinson's
1 year ago
Advice please 😌
Hi everybody, It’s nice to meet you all! So I’m sure you have loads of people posting on here about their frustrations with the NHS/GPs etc. therefore I won’t bore you with all of the details. My journey began in Dec 22 with what I thought was a bout of viral infection-induced joint pain in my hands
Hi everybody, It’s nice to meet you all! So I’m sure you have loads of people posting on here about their frustrations with the NHS/GPs etc. therefore I won’t bore you with all of the details. My journey began in Dec 22 with what I thought was a bout of viral infection-induced joint pain in my hands
Rocinante_89
in
LUPUS UK
9 months ago
VTE post thrombotic
hi, in may april 2021, i was diagnosed with bilateral multiple Pulmonary embolisms in both of my lungs, prodominantly bottom lobe and DVT of the left leg (very big DVT half my leg vein was completely covered) however i have been sufferening with swelling, discolouration and seizing legs. I wear conpression
hi, in may april 2021, i was diagnosed with bilateral multiple Pulmonary embolisms in both of my lungs, prodominantly bottom lobe and DVT of the left leg (very big DVT half my leg vein was completely covered) however i have been sufferening with swelling, discolouration and seizing legs. I wear conpression
Holliemorris
in
Anticoagulation Support
1 year ago
COQ10
👋 to allHas anyone tried COQ10 supplement? Have been recommended to try it by 'holistic' nutritionist. Was very impressed with her research into AI inflammatory diseases - one suggestion was to try Gluten free diet for 4 weeks to see if any improvements noticed and the above supplement. Going down to
👋 to allHas anyone tried COQ10 supplement? Have been recommended to try it by 'holistic' nutritionist. Was very impressed with her research into AI inflammatory diseases - one suggestion was to try Gluten free diet for 4 weeks to see if any improvements noticed and the above supplement. Going down to
Poshdog
in
PMRGCAuk
9 months ago
Satisfactory Serum free T4?
Hi everyone, First time posting anything but my latest results say satisfactory T4 result, as a comment from the health professional. The result is out of the range so I am wondering if I am being fobbed off. Results as follows: TSH - 1.64 mIU/L (0.38-5.33) Serum free T3 - 4.8 pmol/L (3.8-6.0) Serum
Hi everyone, First time posting anything but my latest results say satisfactory T4 result, as a comment from the health professional. The result is out of the range so I am wondering if I am being fobbed off. Results as follows: TSH - 1.64 mIU/L (0.38-5.33) Serum free T3 - 4.8 pmol/L (3.8-6.0) Serum
BeePurple
in
Thyroid UK
9 months ago
Am I going insane?
Hmm so I’m just wondering, do those of you with PA that self inject regularly still suffer extreme fatigue and body aches and pains or other symptoms? I have celiac disease and that’s in remission thanks to a gluten free diet and I self inject fortnightly. I follow a good gut health diet but was told
Hmm so I’m just wondering, do those of you with PA that self inject regularly still suffer extreme fatigue and body aches and pains or other symptoms? I have celiac disease and that’s in remission thanks to a gluten free diet and I self inject fortnightly. I follow a good gut health diet but was told
Mandymoos8
in
Pernicious Anaemia Society
9 months ago
DBS stimulator pros and cons
Can you turn DBS stimulator Off and control it with medication as before surgery?
Can you turn DBS stimulator Off and control it with medication as before surgery?
surdug1
in
Cure Parkinson's
1 year ago
endo diet
Hey ladies dise anyone follow a gluten free diet to help with endometriosis and if so dose it help xx 😘
Hey ladies dise anyone follow a gluten free diet to help with endometriosis and if so dose it help xx 😘
Shay30
in
Endometriosis UK
10 months ago
MDD Suffers: Avolition
I wish I knew this when I was suffering from MDD so I wanted to share. There is a clinical reason why you “can’t” do things. I knew I was supposed to excercise or walk my dog I just couldn’t do it. Which made me feel worse about myself when I chose to islolate instead. Before my DBS surgery I was talking
I wish I knew this when I was suffering from MDD so I wanted to share. There is a clinical reason why you “can’t” do things. I knew I was supposed to excercise or walk my dog I just couldn’t do it. Which made me feel worse about myself when I chose to islolate instead. Before my DBS surgery I was talking
jnelson66
in
Major Depressive Disorder (MDD) Support
1 year ago
DBS info
Where is he going? My husband had it 3 yrs ago and is thrilled even tho he had a slight brain bleed affecting his speech a tad— he says he would do it again! Rigidity/cramping are what drove him to do it— he was on 17 carba/leva a day and down to about 6! Diagnosed at 64 yrs old, 7 yrs ago.. you should
Where is he going? My husband had it 3 yrs ago and is thrilled even tho he had a slight brain bleed affecting his speech a tad— he says he would do it again! Rigidity/cramping are what drove him to do it— he was on 17 carba/leva a day and down to about 6! Diagnosed at 64 yrs old, 7 yrs ago.. you should
Studio60
in
Cure Parkinson's
1 year ago
Rytary and Deep Brain Stimulation
my husband has been taking Rytary for a year. We noticed his veins get large and tingle which he says at time hurts. It gives him a terrible headache more then the the plain C/L. The Dr wants him to consider DBS now . He said it has benefits but won’t last forever then back to square one. He doesn’
my husband has been taking Rytary for a year. We noticed his veins get large and tingle which he says at time hurts. It gives him a terrible headache more then the the plain C/L. The Dr wants him to consider DBS now . He said it has benefits but won’t last forever then back to square one. He doesn’
Blueyedgirlky
in
Cure Parkinson's
1 year ago
where to go from here
I started t3 a month ago first 2 weeks 2.5 mornings only which I definitely believe gave me more stamina and energy and then after 2 weeks added in a second afternoon 2.5, - im not sure if this made much difference, perhaps as first was going from nothing to something and this was just a small increase
I started t3 a month ago first 2 weeks 2.5 mornings only which I definitely believe gave me more stamina and energy and then after 2 weeks added in a second afternoon 2.5, - im not sure if this made much difference, perhaps as first was going from nothing to something and this was just a small increase
samking5
in
Thyroid UK
10 months ago
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