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Links to other HU forums
Just a very short signposting post to other relevant forums on Health Unlocked
Our sister forums, with shared admin support teams:
(We have a shared passion about all things running, walking and cross training)
✦ Couch to 5K (C25K) https://healthunlocked.com/couchto5k ✦ Bridge to 10K
Just a very short signposting post to other relevant forums on Health Unlocked
Our sister forums, with shared admin support teams:
(We have a shared passion about all things running, walking and cross training)
✦ Couch to 5K (C25K) https://healthunlocked.com/couchto5k ✦ Bridge to 10K
CBDB
Administrator
in
Strength & Flex
3 years ago
Some helpful advice
My husband has been diagnosed with lung cancer at a very advanced stage which is also in his chest and lymph nodes diagnosed late February and been told there is no cure he is currently receiving 12 days of radiotherapy in to his gullet which is definitely taking its toll on him. With a bone scan also
My husband has been diagnosed with lung cancer at a very advanced stage which is also in his chest and lymph nodes diagnosed late February and been told there is no cure he is currently receiving 12 days of radiotherapy in to his gullet which is definitely taking its toll on him. With a bone scan also
Bai72
in
The Roy Castle Lung Cancer Foundation
3 years ago
vitamin b12 deficency in sojgrens
hi anyone had sore tongue like you've had something too hot and burnt your tongue also is the shortage of vit b12 related to sjogrens ?
hi anyone had sore tongue like you've had something too hot and burnt your tongue also is the shortage of vit b12 related to sjogrens ?
Gran54
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
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Rapid aging of facial skin with Pegasys?
I am almost embarrassed to ask this but here goes. Since starting on Pegasys (have had 9th injection today given every 2 weeks 45mg until today upped to 67.5ish) I have noted my eyelid skin drooping over my eye to the point that it almost obscures full vision, my cheeks have sunken without weight loss
I am almost embarrassed to ask this but here goes. Since starting on Pegasys (have had 9th injection today given every 2 weeks 45mg until today upped to 67.5ish) I have noted my eyelid skin drooping over my eye to the point that it almost obscures full vision, my cheeks have sunken without weight loss
Planti
in
MPN Voice
3 years ago
Blurry vision
Hi everyone! I am at work right now and my vision keeps going blurry. I was very upset this morning due to teenager drama so I am not sure if it’s related. I have never had optic neuritis so not sure what it feels/looks like. I’m on the computer all day and the words keep going blurry and then are
Hi everyone! I am at work right now and my vision keeps going blurry. I was very upset this morning due to teenager drama so I am not sure if it’s related. I have never had optic neuritis so not sure what it feels/looks like. I’m on the computer all day and the words keep going blurry and then are
Tulip77
in
My MSAA Community
3 years ago
Ramble
I live in the West of England and there is a website for people with sight loss, from any condition, called Sight Support West of England, Looking at the website recently I noted they've partnered up with the Ramblers Association which will pair up a blind or partially sighted person with a sighted
I live in the West of England and there is a website for people with sight loss, from any condition, called Sight Support West of England, Looking at the website recently I noted they've partnered up with the Ramblers Association which will pair up a blind or partially sighted person with a sighted
Jennymary
in
Glaucoma UK
3 years ago
Loss of appetite suddenly with PSP
My mom was diagnosed with CBD (one of the PSP variants). Since then her health was deteriorated and now suddenly she is eating very slow and doesn't look like she has appetite. We had seen issues with her eyes, ptosis, gait problems, walking slow and not interested in talking and incontinence. Now this
My mom was diagnosed with CBD (one of the PSP variants). Since then her health was deteriorated and now suddenly she is eating very slow and doesn't look like she has appetite. We had seen issues with her eyes, ptosis, gait problems, walking slow and not interested in talking and incontinence. Now this
skom1
in
PSP Association
3 years ago
I graduated
I'm so pleased to say that on Saturday, I completed my final run of the Couch to 5K app. As so many of us have said before, I too never believed that I would be able to run. I've always been overweight (and still am), and I would use this as an excuse for running. Give me a group game like rounders
I'm so pleased to say that on Saturday, I completed my final run of the Couch to 5K app. As so many of us have said before, I too never believed that I would be able to run. I've always been overweight (and still am), and I would use this as an excuse for running. Give me a group game like rounders
iamhallie
in
Couch to 5K
3 years ago
Treatment end
So yesterday was advised that scan shows progression in the lung and a liver met. Treatment is not helping so discontinued. Carry on now with palliative care. In some ways I’m relieved but also feeling a bit lost.
So yesterday was advised that scan shows progression in the lung and a liver met. Treatment is not helping so discontinued. Carry on now with palliative care. In some ways I’m relieved but also feeling a bit lost.
mundy
in
The Roy Castle Lung Cancer Foundation
3 years ago
Little money spent on DMO research it all goes on AMD
I have DMO diabetic macular oedema a condition caused because my diabetes team mistakenly thought I should lower my sugar levels quickly and it caused terrible sight loss. I lost my career and my driving licence in my early 40’s. Time and time again I hear of the amount of money and research for those
I have DMO diabetic macular oedema a condition caused because my diabetes team mistakenly thought I should lower my sugar levels quickly and it caused terrible sight loss. I lost my career and my driving licence in my early 40’s. Time and time again I hear of the amount of money and research for those
tallyho
in
Macular Society
3 years ago
Eye Drops
When I saw my nervy eye doctor (neuro opthamologist), a couple of months ago,, he gave me 2 medicated eye drop bottles, and told me to use the drops first thing in the morning for my Dry Eye condition. My nervy eye doctor is an excellent neuro opthamologist who specializes in MS-related
When I saw my nervy eye doctor (neuro opthamologist), a couple of months ago,, he gave me 2 medicated eye drop bottles, and told me to use the drops first thing in the morning for my Dry Eye condition. My nervy eye doctor is an excellent neuro opthamologist who specializes in MS-related
CrazyCatWom
in
My MSAA Community
3 years ago
PIO Knots!!
Hello ladies, its me again lol. So I recently finished my first FET on 04/20/21, and have been taking progesterone injections. I am sure most of you are aware that these injections can cause knots. I have knots on each side and I am not sure what to do to get rid of them or if there is anything I can
Hello ladies, its me again lol. So I recently finished my first FET on 04/20/21, and have been taking progesterone injections. I am sure most of you are aware that these injections can cause knots. I have knots on each side and I am not sure what to do to get rid of them or if there is anything I can
Sunflower24
in
Fertility Network UK
3 years ago
Retinal thinning anyone? A sign of NPSLE?
Something funny to start the day! ☺️ A sign from an actual Texas restaurant that always has hilarious postings. Don’t you love when you have something wrong and no one tells you? Saw neuro-optho for follow up yesterday and apparently I have retinal thinning in upper, outer portion of my retina. I saw
Something funny to start the day! ☺️ A sign from an actual Texas restaurant that always has hilarious postings. Don’t you love when you have something wrong and no one tells you? Saw neuro-optho for follow up yesterday and apparently I have retinal thinning in upper, outer portion of my retina. I saw
Jmiller623
in
LUPUS UK
3 years ago
"I have always known that I am not alone in this treatment, but therapy has helped me accept that I am not the problem."
For years my name has been drug through the mud, and for years I obsessed over how to clear it. How to "set the record straight"- I thought I was losing my mind because I could not figure out why. I could not understand what I did. At one point, I convinced myself this was my karma, that maybe I deserved
For years my name has been drug through the mud, and for years I obsessed over how to clear it. How to "set the record straight"- I thought I was losing my mind because I could not figure out why. I could not understand what I did. At one point, I convinced myself this was my karma, that maybe I deserved
silentdreamer20
in
Anxiety and Depression Support
3 years ago
Advice please
I have recently been diagnosed with Glaucoma and finding it all very stressful. I am a contact lens wearer due to my very high prescription and during the last week I think I have dry eyes. I have purchased over the counter drops, which are helping slightly. Could it be my glaucoma drops causing this
I have recently been diagnosed with Glaucoma and finding it all very stressful. I am a contact lens wearer due to my very high prescription and during the last week I think I have dry eyes. I have purchased over the counter drops, which are helping slightly. Could it be my glaucoma drops causing this
Nala2509
in
Glaucoma UK
3 years ago
Post cataract surgery update etc etc
Hi all, I hope you’re doing well. Just before my eye surgery my doctors clinic called to say that my Astra Zeneca vaccination was ready for me. I had it on the 6th April. On the 7th April I stopped my ibrutinib 10 days before my surgery. On Friday I saw my doctor because I had an msg like allergy/rash
Hi all, I hope you’re doing well. Just before my eye surgery my doctors clinic called to say that my Astra Zeneca vaccination was ready for me. I had it on the 6th April. On the 7th April I stopped my ibrutinib 10 days before my surgery. On Friday I saw my doctor because I had an msg like allergy/rash
josephinef
in
CLL Support
3 years ago
Covid injection side effects
Since having my Oxford jab,some 6 weeks ago now my various arthritis's are much worse and just won't settle back to normal, I just wondered if anyone else has experienced the same? My costoscondritis is much worse, dry eyes and rheumatoid arthritis too.
Since having my Oxford jab,some 6 weeks ago now my various arthritis's are much worse and just won't settle back to normal, I just wondered if anyone else has experienced the same? My costoscondritis is much worse, dry eyes and rheumatoid arthritis too.
Jacqui2017
in
NRAS
3 years ago
Double vision/blurred vision with thyroid issues?
Hello, I woke up after a night with a sore and irritated eye with double vision. Have any of you had eye problems that accompany thyroid issues?
Hello, I woke up after a night with a sore and irritated eye with double vision. Have any of you had eye problems that accompany thyroid issues?
BC1980
in
Thyroid UK
3 years ago
Do you have vision changes from MS?
Good afternoon my friends, I was wondering how others are addressing vision difficulties. Initially i had shared my double vision was happening late in the day. The steroids were hard on my body but worked on my double vision symptoms. However today it started first thing in the morning (I was driving
Good afternoon my friends, I was wondering how others are addressing vision difficulties. Initially i had shared my double vision was happening late in the day. The steroids were hard on my body but worked on my double vision symptoms. However today it started first thing in the morning (I was driving
Sandydemop
in
My MSAA Community
3 years ago
Pegasys and high levels of liver enzyme or
Hi everyone! I was diagnosed with PV Jak2 back in 2012 and was advised to continue aspirin regimen with Phlebotomys every 3 months as I was not high risk. So, I turned 60 last fall (considered high risk now) and was placed on low dose Pegasys interferon. I've only been on this drug for 2 months and
Hi everyone! I was diagnosed with PV Jak2 back in 2012 and was advised to continue aspirin regimen with Phlebotomys every 3 months as I was not high risk. So, I turned 60 last fall (considered high risk now) and was placed on low dose Pegasys interferon. I've only been on this drug for 2 months and
ritaandscooter1
in
MPN Voice
3 years ago
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