Search
Search
About
Log in
Join
Experiences with
DTIC-Dome
Posts
Communities
1,900 public posts
Filter results
Dr Adam Sandford & Low Dose Naltrexone
https://vimeo.com/165497733
https://vimeo.com/165497733
liveurlife
Volunteer
in
LDN Research Trust
8 years ago
Fatigue etc etc etc
Hi the last few days I feel so sick until about lunch time. Then all day I'm shivering , constant goose bumps, reals heavy head, sore neck and headache with fatigue . Surely this isn't anxiety ??? Feeling really yuck
Hi the last few days I feel so sick until about lunch time. Then all day I'm shivering , constant goose bumps, reals heavy head, sore neck and headache with fatigue . Surely this isn't anxiety ??? Feeling really yuck
Jodz
in
Anxiety Support
8 years ago
Back to work
Hi folks. I am off back to work wednesday on a phased return. So my first week Ill be doing 8-1, 2nd week 8-2, 3rd week 8-3 and the final week ill be doing normal 8-4:30 hours. I will no longer be in my old team when I return as per request of myself due to bullying. Im just alittle nervous. Going back
Hi folks. I am off back to work wednesday on a phased return. So my first week Ill be doing 8-1, 2nd week 8-2, 3rd week 8-3 and the final week ill be doing normal 8-4:30 hours. I will no longer be in my old team when I return as per request of myself due to bullying. Im just alittle nervous. Going back
AmeliaIvy
in
Mental Health Support
8 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Low Dose Naltrexone
Just an update on my LDN journey. As far as Low Dose Naltrexone (LDN) is concerned, it is an unlicensed drug which, as far as I can ascertain, means that it is not on the list of approved drugs for doctors to prescribe on the NHS, but that if they wish to prescribe it it is perfectly legal for them
Just an update on my LDN journey. As far as Low Dose Naltrexone (LDN) is concerned, it is an unlicensed drug which, as far as I can ascertain, means that it is not on the list of approved drugs for doctors to prescribe on the NHS, but that if they wish to prescribe it it is perfectly legal for them
Schenks
in
Thyroid UK
8 years ago
My holiday with pain
As you all know we are up north staying in Whitley bay for the week. We came up last year as well and we had a lovely time then and we have had a lovely time this year as well with the exeption of my health which has let me down big time. It was at Alnwick gardens that it hit me hard. I had had a lovely
As you all know we are up north staying in Whitley bay for the week. We came up last year as well and we had a lovely time then and we have had a lovely time this year as well with the exeption of my health which has let me down big time. It was at Alnwick gardens that it hit me hard. I had had a lovely
sylvi
in
NRAS
8 years ago
Low dose naltrexone, collagen, & other alternatives
Please see my posts in the NRAS community. I can't repeat everything here, but I have LONG posts there! I'm posting here because I live in N California & hope I can tie in with other RD folks in my area, particularly those trying alternatives (or complements) to steroids, mainstream DMARD's, & biologics
Please see my posts in the NRAS community. I can't repeat everything here, but I have LONG posts there! I'm posting here because I live in N California & hope I can tie in with other RD folks in my area, particularly those trying alternatives (or complements) to steroids, mainstream DMARD's, & biologics
Julie_R
in
Cure Arthritis Community
8 years ago
Just one bad day...
Day 46 of no smoking and I was feeling pretty smug. I'm still on the 7mg patch, but most of the urges had subsided until yesterday. My spouse was having a rough day and being very confrontational, and I found out my stubborn and perpetually mad brother refused shipment of a birthday gift I sent him,
Day 46 of no smoking and I was feeling pretty smug. I'm still on the 7mg patch, but most of the urges had subsided until yesterday. My spouse was having a rough day and being very confrontational, and I found out my stubborn and perpetually mad brother refused shipment of a birthday gift I sent him,
Seahoch
in
No Smoking Day
8 years ago
Low Dose Naltrexone (LDN)
Has anyone out there with Hashimotos or other auto immune conditions tried Naltrexone? It can be got here in New Zealand from a compounding pharmacy, but only with a doctor,s prescription. Has anyone tried it and found it beneficial?
Has anyone out there with Hashimotos or other auto immune conditions tried Naltrexone? It can be got here in New Zealand from a compounding pharmacy, but only with a doctor,s prescription. Has anyone tried it and found it beneficial?
Hidden
in
Thyroid UK
8 years ago
Who Says Being A Quitter Is A Bad Thing?
For me it was the best thing that ever happened in my life. It has been 10 months ago driving the 400 km back from the doctor with a box of Champix in my pocket and a X-Ray in a brown envelope showing my poor lungs in a very bad shape after my 38 years of abusing them with toxins.....that is where
For me it was the best thing that ever happened in my life. It has been 10 months ago driving the 400 km back from the doctor with a box of Champix in my pocket and a X-Ray in a brown envelope showing my poor lungs in a very bad shape after my 38 years of abusing them with toxins.....that is where
Hercu
Valued Contributor
in
No Smoking Day
8 years ago
Clumsiness & alzheimers.
Every now & again, I reach out for a door handle & miss. this is a fairly recent thing, & Iv`e read that this can be an early sign of alzheimers. I`m terrified now, & imagining my self having to check into a home & ending up incontinent & not knowing who I am anymore. What are the odds that this is down
Every now & again, I reach out for a door handle & miss. this is a fairly recent thing, & Iv`e read that this can be an early sign of alzheimers. I`m terrified now, & imagining my self having to check into a home & ending up incontinent & not knowing who I am anymore. What are the odds that this is down
hairyfairy
in
Anxiety Support
8 years ago
new diagnosis
this past week my mom was diagnosed with psp I have not ever even heard of the disease. She has had many diagnoses but none have really matched her symptoms until now. Reading the symptoms alone are scary. She has fallen backwards for about 3 years now. Very clumsy, dropping most dishes in the
this past week my mom was diagnosed with psp I have not ever even heard of the disease. She has had many diagnoses but none have really matched her symptoms until now. Reading the symptoms alone are scary. She has fallen backwards for about 3 years now. Very clumsy, dropping most dishes in the
caroleen
in
PSP Association
8 years ago
I won so glad
Okay so I have been fighting for low dose naltrexone for over a year now.. Been paying for it private for over 3 year.. I so glad I had my mum if it was not for her i don't no were I would be oh yea dead cuz I refuse to take steroids because there utterly pointless they don't work and just make u more
Okay so I have been fighting for low dose naltrexone for over a year now.. Been paying for it private for over 3 year.. I so glad I had my mum if it was not for her i don't no were I would be oh yea dead cuz I refuse to take steroids because there utterly pointless they don't work and just make u more
Karlimc93
in
PBC Foundation
8 years ago
Ablation date
I have received a date for my second ablation. 20th April. I am so so scared and worried...to the point that I am now considering not having it done. Although I hate arrythmias I have got used to living like this and wonder if I should just continue like this rather than risk stroke or cardiac tamponade
I have received a date for my second ablation. 20th April. I am so so scared and worried...to the point that I am now considering not having it done. Although I hate arrythmias I have got used to living like this and wonder if I should just continue like this rather than risk stroke or cardiac tamponade
Vony
in
AF Association
8 years ago
Low dose naltrexone
Hello everyone, Can anyone who takes LDN for hashimoto's tell me if they can return to eating gluten and still have lowered antibodies from the LDN? It's not that I'm in any big hurry to get back to eating gluten by choice, I actually think maybe we are better off without it even if we don't have a
Hello everyone, Can anyone who takes LDN for hashimoto's tell me if they can return to eating gluten and still have lowered antibodies from the LDN? It's not that I'm in any big hurry to get back to eating gluten by choice, I actually think maybe we are better off without it even if we don't have a
DonnyJam
in
Thyroid UK
8 years ago
Help!!
im an anxiety sufferer. I'm 16 and a female I'm not sure if this has anything to do with it but over the last few weeks I've been getting hot flushes and then the next minute I'll be freezing cold. When I stand up I get really dizzy and have to sit back down. I also feel like my head gets that tingly
im an anxiety sufferer. I'm 16 and a female I'm not sure if this has anything to do with it but over the last few weeks I've been getting hot flushes and then the next minute I'll be freezing cold. When I stand up I get really dizzy and have to sit back down. I also feel like my head gets that tingly
Mollieh
in
Anxiety Support
8 years ago
Urso
I was diagnosed with PBC last month. I did not have any symptoms. Then came Urso.😣. Now I itch at night, feel nauseous and have problems with anger. Too much of a coincidence for my liking. Has anyone heard of Low dose naltrexone?
I was diagnosed with PBC last month. I did not have any symptoms. Then came Urso.😣. Now I itch at night, feel nauseous and have problems with anger. Too much of a coincidence for my liking. Has anyone heard of Low dose naltrexone?
LindyRich
in
PBC Foundation
8 years ago
Fighting & treating PPP - Primary Peritoneal Carcinoma. Help?
Dear sweet community at Health Unlocked, My name is Delia, I'm 24, and almost a month ago my mom, 66, was diagnosed with stage 3 PPC. She's currently at MD Anderson in Houston, being treated by an incredible gyn-oncology team. They've told her the survival rate is 70% and things we've read that told
Dear sweet community at Health Unlocked, My name is Delia, I'm 24, and almost a month ago my mom, 66, was diagnosed with stage 3 PPC. She's currently at MD Anderson in Houston, being treated by an incredible gyn-oncology team. They've told her the survival rate is 70% and things we've read that told
Deliacarolind
in
OvaCare
8 years ago
Understanding & Beating PPC - Primary Peritoneal Carcinoma - Help?
Dear sweet community at Health Unlocked, My name is Delia, I'm 24, and almost a month ago my mom, 66, was diagnosed with stage 3 PPC. She's currently at MD Anderson in Houston, being treated by an incredible gyn-oncology team. They've told her the survival rate is 70% and things we've read that told
Dear sweet community at Health Unlocked, My name is Delia, I'm 24, and almost a month ago my mom, 66, was diagnosed with stage 3 PPC. She's currently at MD Anderson in Houston, being treated by an incredible gyn-oncology team. They've told her the survival rate is 70% and things we've read that told
Deliacarolind
in
My Ovacome
8 years ago
Son with BI
Hi, I first looked at the Headway site 2 1/2 years ago, 5 months after my son (aged 17 at the time) sustained a BI from a cycling accident. I didn't feel able to contribute then (to upsetting) but do now. To say the last 3 years have been hard work is an understatement. I am a single parent with no family
Hi, I first looked at the Headway site 2 1/2 years ago, 5 months after my son (aged 17 at the time) sustained a BI from a cycling accident. I didn't feel able to contribute then (to upsetting) but do now. To say the last 3 years have been hard work is an understatement. I am a single parent with no family
sunflower2
in
Headway
8 years ago
ibs c
Iam a female in early sixties, have had this 6 yrs now.My gi tells me to take miralax 3 times daily with stool softners,prune juice prunes and grapes,Sometimes it works but mostly just a little bowel comes out.I am at my wits end, someone suggested magnesium citrate gels, if anyone has tried this can
Iam a female in early sixties, have had this 6 yrs now.My gi tells me to take miralax 3 times daily with stool softners,prune juice prunes and grapes,Sometimes it works but mostly just a little bowel comes out.I am at my wits end, someone suggested magnesium citrate gels, if anyone has tried this can
bearfriend52
in
IBS Network
8 years ago
1
...
69
70
71
...
95
Next page
30
40
50
60
70
80
90
Filter results
Clear filters
Posted in
All communities
Headway
276 results
LDN Research Trust
194 results
ERIC
128 results
View top 10 communities
Sort by
Most Relevant
Newest