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very hard time today…need support
today I woke up not feeling well. Where I live we’re going through a heat wave. The day before I was outside quite a bit, and I went to a concert so I didn’t get a ton of sleep. I went to breakfast with a friend and then napped for two hours. I felt better and drove home from my boyfriend’s house to
today I woke up not feeling well. Where I live we’re going through a heat wave. The day before I was outside quite a bit, and I went to a concert so I didn’t get a ton of sleep. I went to breakfast with a friend and then napped for two hours. I felt better and drove home from my boyfriend’s house to
Daisy425
in
Anxiety and Depression Support
1 month ago
News we've all been waiting for!
Ralph's had the most amazing few days. On Tuesday he had the swallow x-ray and the speech therapist was amazed at the results. Firstly he gave him some sour tasting stuff, which Ralph insisted he tried to see how horrible it was, lol. Then he had barium mixed with water, then barium with yoghurt then
Ralph's had the most amazing few days. On Tuesday he had the swallow x-ray and the speech therapist was amazed at the results. Firstly he gave him some sour tasting stuff, which Ralph insisted he tried to see how horrible it was, lol. Then he had barium mixed with water, then barium with yoghurt then
Gardenview10
in
British Heart Foundation
1 month ago
Seeking Advice: Non-Medication Methods for Managing Hand Joint Pain Flare-Ups
Hello everyone, I'm reaching out to this community for some advice and personal experiences. I have been living with lupus for six years now, and I've been dealing with joint pain in my hands for quite a while. I'm particularly interested in non-medication methods to manage flare-ups. I've heard
Hello everyone, I'm reaching out to this community for some advice and personal experiences. I have been living with lupus for six years now, and I've been dealing with joint pain in my hands for quite a while. I'm particularly interested in non-medication methods to manage flare-ups. I've heard
Sophieeeee
in
LUPUS UK
1 month ago
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cruise next week
next week I am going on a cruise with my boyfriend and his family. I have been on a cruise before but with my family. I am scared of getting sea sick from rough seas. We are going from NYC to Bermuda. Last summer I went on a. Girls trip to Nashville and I struggled a lot. Since then I have done outpatient
next week I am going on a cruise with my boyfriend and his family. I have been on a cruise before but with my family. I am scared of getting sea sick from rough seas. We are going from NYC to Bermuda. Last summer I went on a. Girls trip to Nashville and I struggled a lot. Since then I have done outpatient
Daisy425
in
Anxiety and Depression Support
1 month ago
The T3-4-Hypo trial (Netherlands)
[i]
The T3-4-Hypo trial
[/i] [i]A Dutch national randomized placebo-controlled double-blind multicenter trial of LT4/LT3
combination
therapy
in patients with autoimmune hypothyroidism.
[i]
The T3-4-Hypo trial
[/i] [i]A Dutch national randomized placebo-controlled double-blind multicenter trial of LT4/LT3
combination
therapy
in patients with autoimmune hypothyroidism.
helvella
Thyroid UK
in
Thyroid UK
2 years ago
Feeling awful again
therapy
my T3 has dropped a little and my TSH has risen an infinitesimal amount, which are probably related.
therapy
my T3 has dropped a little and my TSH has risen an infinitesimal amount, which are probably related.
Pearlteapot
in
Thyroid UK
1 year ago
Upcoming Webinar - Enjoy the Beat: Music, Brain Health, and MS
Music plays an important role in our lives. Research also suggests that music can benefit our physical and mental health in numerous ways. Join MSAA’s upcoming webinar “Enjoy the Beat: Music, Brain Health, and MS” Monday, June 17th, at 8:00PM Eastern with MS specialist Dr. Augusto Miravalle and MS
Music plays an important role in our lives. Research also suggests that music can benefit our physical and mental health in numerous ways. Join MSAA’s upcoming webinar “Enjoy the Beat: Music, Brain Health, and MS” Monday, June 17th, at 8:00PM Eastern with MS specialist Dr. Augusto Miravalle and MS
DanaMSAA
Partner
in
My MSAA Community
1 month ago
My DIY red light therapy / photobiomodulation helmet build. If you have built one and would like to share pictures please do.
I originally posted here asking some questions about building a red light therapy hat. https://healthunlocked.com/cure-parkinsons/posts/150630223/a-question-for-anyone-who-built-a-red-light-therapy-helmet-hat.?responses=150932897 I would like to say thank you to the people in that thread for helping
I originally posted here asking some questions about building a red light therapy hat. https://healthunlocked.com/cure-parkinsons/posts/150630223/a-question-for-anyone-who-built-a-red-light-therapy-helmet-hat.?responses=150932897 I would like to say thank you to the people in that thread for helping
Glenfarclas
in
Cure Parkinson's
1 month ago
Has anyone done the proton therapy?
Just curious if anyone had their MO suggest doing the proton therapy? When I have my discussion with my new MO, I want to ask if proton therapy would be a fit for myself. I have to deal with the prostate cancer and the met pelvic lymph nodes as well as the met bone issue.
Just curious if anyone had their MO suggest doing the proton therapy? When I have my discussion with my new MO, I want to ask if proton therapy would be a fit for myself. I have to deal with the prostate cancer and the met pelvic lymph nodes as well as the met bone issue.
PARKER3237
in
Advanced Prostate Cancer
1 month ago
update on oxygen therapy
a friend with MS got me into this, we are lucky to have an MS centre with a hyperbaric chamber in Hereford. It’s not NHS They kindly accepted me as a trial as it’s usually MS patients, burns patients and cancer recovery but also fibromyalgia and inflammation. I’ve just completed my 20th session which
a friend with MS got me into this, we are lucky to have an MS centre with a hyperbaric chamber in Hereford. It’s not NHS They kindly accepted me as a trial as it’s usually MS patients, burns patients and cancer recovery but also fibromyalgia and inflammation. I’ve just completed my 20th session which
Regenallotment
in
Thyroid UK
2 months ago
surely no more - - -
wonderful supportive group, I contacted you with my chronic constipation, really seems I have inability to poop, currently having biofeedback , was so hopeful at first but session today shows little if any improvement- messing with diet, ( fibre that doesn’t block me up) active cultures that made things
wonderful supportive group, I contacted you with my chronic constipation, really seems I have inability to poop, currently having biofeedback , was so hopeful at first but session today shows little if any improvement- messing with diet, ( fibre that doesn’t block me up) active cultures that made things
Dudders123
in
IBS Network
2 months ago
Pneumocystis pneumonia - PCP
I am just making people aware of the above. This is fungi that in a healthy person would resolve in days. However, in immunosuppressed it can be fatal. I have never heard of this before. Because of taking immune surpression, this fungi has knocked me off my feet. I have been admitted to hospital, now
I am just making people aware of the above. This is fungi that in a healthy person would resolve in days. However, in immunosuppressed it can be fatal. I have never heard of this before. Because of taking immune surpression, this fungi has knocked me off my feet. I have been admitted to hospital, now
TEDDYM
in
LUPUS UK
2 months ago
Working on overcoming FND
Hello friends, in Dec 2008 I started having vocal issues during a cold. It has continue to come and go for the last 15 1/2 years. In addition to my voice after about 2 years, I began having myoclonic jerks, swallowing issues, dystonia, tremors, gait issues, spasms in my face. Tics, non epileptic & EPILEPTIC
Hello friends, in Dec 2008 I started having vocal issues during a cold. It has continue to come and go for the last 15 1/2 years. In addition to my voice after about 2 years, I began having myoclonic jerks, swallowing issues, dystonia, tremors, gait issues, spasms in my face. Tics, non epileptic & EPILEPTIC
cgarff
in
Functional Neurological Disorder - FND Hope
2 months ago
Aspen Neuroscience to Present at International Society for Cell & Gene Therapy (ISCT) Annual Meeting
As part of the ISCT 2024 Translational Pathway Sessions, as well as the ISCT main program, Aspen's Chief Scientific Officer Xiaokui Zhang, Ph.D., and Chief Technology Officer Kim Raineri will discuss developments in autologous research and development, including for ANPD001, Aspen's autologous iPSC-derived
As part of the ISCT 2024 Translational Pathway Sessions, as well as the ISCT main program, Aspen's Chief Scientific Officer Xiaokui Zhang, Ph.D., and Chief Technology Officer Kim Raineri will discuss developments in autologous research and development, including for ANPD001, Aspen's autologous iPSC-derived
Farooqji
in
Cure Parkinson's
2 months ago
Just Tired
Hi Everyone - this is such a valuable community. I just wanted to vent a little. Are any parents on this journey just feeling tired? We have weathered the nasty teachers, the disinterested teachers, the play therapy, the behavior therapy, the unconventional treatments, the medications, the school
Hi Everyone - this is such a valuable community. I just wanted to vent a little. Are any parents on this journey just feeling tired? We have weathered the nasty teachers, the disinterested teachers, the play therapy, the behavior therapy, the unconventional treatments, the medications, the school
Uptowngirl12121
in
CHADD's ADHD Parents Together
2 months ago
The 40 Hz flickering light restores synaptic plasticity and mitochondrial phenotype in experimental model of Alzheimer's disease May 2024
The 40 Hz flickering light restores synaptic plasticity and mitochondrial phenotype in experimental model of Alzheimer's disease May 2024
- https://www.researchgate.net/publication/380600451_The_40_Hz_flickering_light_restores_synaptic_plasticity_and_mitochondrial_phenotype_in_experimental_model_of_Alzheimer
The 40 Hz flickering light restores synaptic plasticity and mitochondrial phenotype in experimental model of Alzheimer's disease May 2024
- https://www.researchgate.net/publication/380600451_The_40_Hz_flickering_light_restores_synaptic_plasticity_and_mitochondrial_phenotype_in_experimental_model_of_Alzheimer
Bolt_Upright
in
Cure Parkinson's
2 months ago
Moving forward
Before my diagnosis, I had various symptoms that I could not control, and afterward would lose parts of my memories, it was people's names and events later I had a seizure but sometimes in my sleep. It was either when I was fully awake and alert and I could see my surroundings but then if I did have
Before my diagnosis, I had various symptoms that I could not control, and afterward would lose parts of my memories, it was people's names and events later I had a seizure but sometimes in my sleep. It was either when I was fully awake and alert and I could see my surroundings but then if I did have
mavem100
in
Functional Neurological Disorder - FND Hope
2 months ago
school anxiety
I’m in speech therapy grad school, something I’ve worked towards for a VERY long time. I made so many sacrifices to be here and I got a C in a clinical experience. In my program you have to get a B to pass and move forward. I have to redo this clinical experience and any time I have a meeting for it
I’m in speech therapy grad school, something I’ve worked towards for a VERY long time. I made so many sacrifices to be here and I got a C in a clinical experience. In my program you have to get a B to pass and move forward. I have to redo this clinical experience and any time I have a meeting for it
Pupsandpeonies
in
Anxiety and Depression Support
2 months ago
Supporting evidence for PIP
I’m ploughing through the online form and it keeps saying about supporting evidence. I was diagnosed in 2021 by my then GP in the midlands over the Covid period - so not many doctor visits. Not much prescribed, using paracetamol and/or ibuprofen as and when necessary. Basically have been self-managing
I’m ploughing through the online form and it keeps saying about supporting evidence. I was diagnosed in 2021 by my then GP in the midlands over the Covid period - so not many doctor visits. Not much prescribed, using paracetamol and/or ibuprofen as and when necessary. Basically have been self-managing
Gulfstream_Maggie
in
Fibromyalgia Action UK
2 months ago
List of good Genetic Tests in Homologous Recombination Deficiency in PCa and the Mechanisms of Resistance to PARP Inhibitors
I was searching RAD50 and PARPinhibitors and since i am going for a high risk genetic consult i came across this good explanation of different genetic testing. Title of article:
Homologous Recombination Deficiency in Ovarian, Breast, Colorectal, Pancreatic, Non-Small Cell Lung and Prostate Cancers
I was searching RAD50 and PARPinhibitors and since i am going for a high risk genetic consult i came across this good explanation of different genetic testing. Title of article:
Homologous Recombination Deficiency in Ovarian, Breast, Colorectal, Pancreatic, Non-Small Cell Lung and Prostate Cancers
KocoPr
in
Advanced Prostate Cancer
2 months ago
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