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Experiences with
Amyotrophic lateral sclerosis (ALS)
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Titan-Implantate gegen RLS ?
Mehr
als
1 oder 2 Stunden Schlaf pro Nacht gibt es nicht. Ich habe Anfang Februar einen Termin bei einem RLS-Spezialisten in Deutschland, welcher Titan-Implantate in die Ohren einsetzt. In 80 % der Fälle soll die Therapie erfolgreich sein. Hat jemand von euch bereits Erfahrung mit dieser Methode?
Mehr
als
1 oder 2 Stunden Schlaf pro Nacht gibt es nicht. Ich habe Anfang Februar einen Termin bei einem RLS-Spezialisten in Deutschland, welcher Titan-Implantate in die Ohren einsetzt. In 80 % der Fälle soll die Therapie erfolgreich sein. Hat jemand von euch bereits Erfahrung mit dieser Methode?
Feenkind
in
Restless Legs Syndrome
4 years ago
Therapist suffering with health anxiety.
A close friend of mines family friend was diagnosed with
ALS
about two months ago. Shes my age 29. I began to obsess over her symptoms (muscle weakness on her right side and abnormalities with her voice.) I then began to manifest these symptoms myself.
A close friend of mines family friend was diagnosed with
ALS
about two months ago. Shes my age 29. I began to obsess over her symptoms (muscle weakness on her right side and abnormalities with her voice.) I then began to manifest these symptoms myself.
AnxiousAng
in
Anxiety and Depression Support
4 years ago
Mental Health Counselor Struggling with Health Anxiety
A close friend of mines family friend was diagnosed with
ALS
about two months ago. Shes my age 29. I began to obsess over her symptoms (muscle weakness on her right side and abnormalities with her voice.) I then began to manifest these symptoms myself.
A close friend of mines family friend was diagnosed with
ALS
about two months ago. Shes my age 29. I began to obsess over her symptoms (muscle weakness on her right side and abnormalities with her voice.) I then began to manifest these symptoms myself.
AnxiousAng
in
Living with Anxiety
4 years ago
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Latest test results
Hi everyone, I have gone through lab tests three months after first diagnosis of T2DM in late Nov'19. Results are mentioned below with earlier results in brackets and reference ideal values. - HbA1c: 5.7 % [ 16.1 %] # Ref. non-diabetic < 5.7% - FBS: 100 mg/dL [266 mg/dL] # Ref. non-diabetic < 100
Hi everyone, I have gone through lab tests three months after first diagnosis of T2DM in late Nov'19. Results are mentioned below with earlier results in brackets and reference ideal values. - HbA1c: 5.7 % [ 16.1 %] # Ref. non-diabetic < 5.7% - FBS: 100 mg/dL [266 mg/dL] # Ref. non-diabetic < 100
prashantr
in
Diabetes India
4 years ago
Advice on latest TSH results & High vitB12-take PPIs for acid reflux....
Hi Would welcome your thoughts on my latest TSH and whether my sluggish, low energy, weight gain, constant bloated stomach, brain fog, bad short term memory and fungal rash on breasts-Is it all hypo symptoms or B12 deficiency masked by the taking of PPI Omaprazole for hiatus hernia and acid reflux.
Hi Would welcome your thoughts on my latest TSH and whether my sluggish, low energy, weight gain, constant bloated stomach, brain fog, bad short term memory and fungal rash on breasts-Is it all hypo symptoms or B12 deficiency masked by the taking of PPI Omaprazole for hiatus hernia and acid reflux.
DizzLizzie
in
Thyroid UK
4 years ago
High GGT & Raised Lymphocytes
Hello all, Attended GP a couple of months ago re. nasal polyps and was prescribed fluticasone fuorate, which I used for a month until I started with nosebleeds on the affected side. Went back and he asked on other symptoms, which I mentioned a change in bowel habits from once daily to maybe 3 times a
Hello all, Attended GP a couple of months ago re. nasal polyps and was prescribed fluticasone fuorate, which I used for a month until I started with nosebleeds on the affected side. Went back and he asked on other symptoms, which I mentioned a change in bowel habits from once daily to maybe 3 times a
MiCoHi
in
British Liver Trust
4 years ago
Blood Results Antibodies Positive..Any Help or Guidance?
Below are my lab results. Diagnosed Graves Disease February 2019. Off thyroid medication. Feel awful. Pain left side of my head, shoulder, arm, hip and thigh. Itchy eyebrows. Also flush cheeks. Have deviated septum and possible TMJ. Recently put on estrogen patch. Been a year of feeling sick. Why if
Below are my lab results. Diagnosed Graves Disease February 2019. Off thyroid medication. Feel awful. Pain left side of my head, shoulder, arm, hip and thigh. Itchy eyebrows. Also flush cheeks. Have deviated septum and possible TMJ. Recently put on estrogen patch. Been a year of feeling sick. Why if
Kim327
in
Thyroid UK
4 years ago
My latest Endo letter and need research to dispute TSH only
Hi, I've been around reading but not posting much. Have been continuing with T4/T3 combination but still symptomatic. Read ISTH book and have been slowly upping T3. I had a last minute appointment come through to see Endocrinologist, they must have forgotten and left it 14 months not 12, which I was
Hi, I've been around reading but not posting much. Have been continuing with T4/T3 combination but still symptomatic. Read ISTH book and have been slowly upping T3. I had a last minute appointment come through to see Endocrinologist, they must have forgotten and left it 14 months not 12, which I was
tzracer
in
Thyroid UK
4 years ago
Just having a bad time of it.
My sister who is only 15 months older then me (66) has been diagnosed with
ALS
on Friday....2019 can kiss my butt and I don't see 2020 being any better. I better have cheese with my wine Thanks for reading. Dee
My sister who is only 15 months older then me (66) has been diagnosed with
ALS
on Friday....2019 can kiss my butt and I don't see 2020 being any better. I better have cheese with my wine Thanks for reading. Dee
Hidden
in
PSP Association
4 years ago
Wanting to add t3 to NDT
Hello, once again I went to another dr that didnt know what to do with me! Short story of 2019- had an adrenal crash in June, looked around for another doctor, previous one just wanted to run test and not listen to symptoms. Was told about functional medicine doctor so thought she could help. Saw her
Hello, once again I went to another dr that didnt know what to do with me! Short story of 2019- had an adrenal crash in June, looked around for another doctor, previous one just wanted to run test and not listen to symptoms. Was told about functional medicine doctor so thought she could help. Saw her
GentleSoul
in
Thyroid UK
4 years ago
Help Needed...
Been tested for
ALS
, MS, Parkinson's etc. I do have diagnosis of Multi-Sensory Axonal Polyneuropathy and a slew of other issues such as spacticity, seizures, dysphagia, and on goes the list.
Been tested for
ALS
, MS, Parkinson's etc. I do have diagnosis of Multi-Sensory Axonal Polyneuropathy and a slew of other issues such as spacticity, seizures, dysphagia, and on goes the list.
Hooha215
in
Neuropathy Support
4 years ago
Those with (mostly Ashkenazi) GBA1 gene mutation will be interested to know of gene therapy targeting this.
try to report on the results) From https://www.prevailtherapeutics.com/our-science/ Parkinson's Disease with GBA1 Mutation We are developing a broad pipeline of gene therapies for a range of neurodegenerative diseases including Parkinson’s disease, frontotemporal dementia, Alzheimer’s disease, and
ALS
try to report on the results) From https://www.prevailtherapeutics.com/our-science/ Parkinson's Disease with GBA1 Mutation We are developing a broad pipeline of gene therapies for a range of neurodegenerative diseases including Parkinson’s disease, frontotemporal dementia, Alzheimer’s disease, and
ALS
pmmargo
in
Cure Parkinson's
4 years ago
Stinging skin, no rash. Ideas?
I have been on Lupron for 10 1/2 months and have tolerated it reasonably well. Obvious testicular atrophy and new belly fat past 2 months. For a few days I have had what feels like a symmetric severe sunburn with quite painful constant skin-superficial sq stinging but no redness or rash. It hurts to
I have been on Lupron for 10 1/2 months and have tolerated it reasonably well. Obvious testicular atrophy and new belly fat past 2 months. For a few days I have had what feels like a symmetric severe sunburn with quite painful constant skin-superficial sq stinging but no redness or rash. It hurts to
Milkweed
in
Advanced Prostate Cancer
4 years ago
Annual update, DNA testing, Gastric Bypass, Fungal Skin Infection, Brittle Nails, Looking for GI doc
So almost a year has gone by, now I am headed into being 47, still struggling with Dupuytrens in my right hand, but had the cataract surgery and things are looking "brighter" LOL. I recently did my DNA through 23 and Me, did not tell me much healthwise, but I did find out that I am 83% Irish and English
So almost a year has gone by, now I am headed into being 47, still struggling with Dupuytrens in my right hand, but had the cataract surgery and things are looking "brighter" LOL. I recently did my DNA through 23 and Me, did not tell me much healthwise, but I did find out that I am 83% Irish and English
Cooper6
in
PBC Foundation
4 years ago
Thyroid results, do I need to do anything?
Hi, First time posting so a little information I am a 28 year old male with hypothyroidism symptoms, not diagnosed with anything. Got my results but I am unsure what they mean or if I need to do anything, I'll post them with the values included and ranges and hopefully someone can help. Serum TSH Level
Hi, First time posting so a little information I am a 28 year old male with hypothyroidism symptoms, not diagnosed with anything. Got my results but I am unsure what they mean or if I need to do anything, I'll post them with the values included and ranges and hopefully someone can help. Serum TSH Level
Freece_
in
Thyroid UK
4 years ago
L-serine
I have read that there were positive research results using the amino acid L-serine in the treatment of
ALS
or Lou Gehrig's disease and that this may also help in Parkinsons amongst others. I have no info regarding dosage and wondered if anyone here knows anything about it.
I have read that there were positive research results using the amino acid L-serine in the treatment of
ALS
or Lou Gehrig's disease and that this may also help in Parkinsons amongst others. I have no info regarding dosage and wondered if anyone here knows anything about it.
Dizlizz
in
Cure Parkinson's
5 years ago
References for the Dietrich SPINA summary of 2019
Adaptive Veränderungen des Schilddrüsenstoffwechsels
als
Risikoindikatoren bei Traumata. Trauma Berufskrankh 21, 260–267 (2019) doi:10.1007/s10039-019-00438-z https://doi.org/10.1007/s10039-019-00438-z
16.
Adaptive Veränderungen des Schilddrüsenstoffwechsels
als
Risikoindikatoren bei Traumata. Trauma Berufskrankh 21, 260–267 (2019) doi:10.1007/s10039-019-00438-z https://doi.org/10.1007/s10039-019-00438-z
16.
diogenes
in
Thyroid UK
4 years ago
Finally good news/PSA heading down.(first time in 13 months..Fenben? Delayed miracle from The Mayo Clinic? Ribeye steaks/chocolate sundaes?
well...after 13 months of PSA going steadily upward...rather quickly, actually, My PSA FINALLY dropped from 5.34 last month to 3.94 this month. My ALK Phos also dropped from 80 to 61) ** For the past 18 months I have been on just Lupron and Xtandi...I stopped doing BIRM about a year ago...and added
well...after 13 months of PSA going steadily upward...rather quickly, actually, My PSA FINALLY dropped from 5.34 last month to 3.94 this month. My ALK Phos also dropped from 80 to 61) ** For the past 18 months I have been on just Lupron and Xtandi...I stopped doing BIRM about a year ago...and added
greatjohn
in
Advanced Prostate Cancer
4 years ago
Muscle twitching
Does anyone experience constant twitching in different part of my body not sure if it’s my anxiety I keep reading
ALS
cause twitching freaking out
Does anyone experience constant twitching in different part of my body not sure if it’s my anxiety I keep reading
ALS
cause twitching freaking out
Dperez1223
in
Anxiety Support
5 years ago
Can I have PMR with normal CRP
However due to normal CRP I have been put through all kinds of test from
ALS
,MR and cancer to polymyositis and Lyme disease (borrelia). They all said that if they did not find anything it must be PMR ON TILL they changed their mind.
However due to normal CRP I have been put through all kinds of test from
ALS
,MR and cancer to polymyositis and Lyme disease (borrelia). They all said that if they did not find anything it must be PMR ON TILL they changed their mind.
krillemy
in
PMRGCAuk
5 years ago
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