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Giant axonal neuropathy
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Laxido for fecal impaction. What to expect?
Hi, I was in hospital yesterday and told I have a fecal impaction and given laxido, told to take 8 sachets in six hours. I am on my glass now and already starting to feel the effects. I had imagined that it would just soften the blockage enough for me to pass as a type 4 stool? I currently have diarrhoea
Hi, I was in hospital yesterday and told I have a fecal impaction and given laxido, told to take 8 sachets in six hours. I am on my glass now and already starting to feel the effects. I had imagined that it would just soften the blockage enough for me to pass as a type 4 stool? I currently have diarrhoea
Chloeanzani123
in
IBS Network
4 years ago
PA and blood group A connection ?
I found a Haematologist consultant's powerpoint presentation about the "[i]diagnosis and management of vitamin B12 disorders"[/i] which, in discussing pernicious anaemia, made reference to an association with blood group A. No more detail than that, it being mainly bulletpoint prompts, but this interested
I found a Haematologist consultant's powerpoint presentation about the "[i]diagnosis and management of vitamin B12 disorders"[/i] which, in discussing pernicious anaemia, made reference to an association with blood group A. No more detail than that, it being mainly bulletpoint prompts, but this interested
Cherylclaire
Forum Support
in
Pernicious Anaemia Society
4 years ago
Swelling of anus
Hello everyone, I am male 24 . From the last whole month I have been getting blood in my stool. And these are not just patches of blood, thr quantity is a lot. And I started taking medicines consulting genral doctors but it didn't stopped. Now I have changed diet, increased my water intake, lotsbof fibre
Hello everyone, I am male 24 . From the last whole month I have been getting blood in my stool. And these are not just patches of blood, thr quantity is a lot. And I started taking medicines consulting genral doctors but it didn't stopped. Now I have changed diet, increased my water intake, lotsbof fibre
Brad1379
in
IBS Network
4 years ago
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Peripheral Neuropathy?
I was treated for a Burketts Lymphoma 20 years ago and I know that I had an infection in my left foot whilst I was undergoing chemotherapy, since then I have had a numb foot with pins and needles and it aches more when it is damp or wet weather. I have never had peripheral neuropathy diagnosed and was
I was treated for a Burketts Lymphoma 20 years ago and I know that I had an infection in my left foot whilst I was undergoing chemotherapy, since then I have had a numb foot with pins and needles and it aches more when it is damp or wet weather. I have never had peripheral neuropathy diagnosed and was
Milko
in
Neuropathy Support
4 years ago
Rucaparib side effects
Hi I have been on rucaparip for 15months was diagnosed in 2007 and now have brain metastases .Have been doing well but have recently developed tingling and itching in both arms. Wondered if anyone else had these effects from a parp Thanks Morag x
Hi I have been on rucaparip for 15months was diagnosed in 2007 and now have brain metastases .Have been doing well but have recently developed tingling and itching in both arms. Wondered if anyone else had these effects from a parp Thanks Morag x
govanhill
in
My Ovacome
4 years ago
Mucus
Hello - I had mucus around around my poo last week, four days ago there was a bit of red blood in it, the doc said if it didn't clear up ring back, no more blood but still mucus so rang back this morning. Different doc, I asked if it could be piles as I was sore and itchy and felt swollen, she said
Hello - I had mucus around around my poo last week, four days ago there was a bit of red blood in it, the doc said if it didn't clear up ring back, no more blood but still mucus so rang back this morning. Different doc, I asked if it could be piles as I was sore and itchy and felt swollen, she said
greatgran28
in
IBS Network
4 years ago
Tocilizumab patients and the COVID Vaccine
My Rheumatologist has let me know that it is fine for me to have the COVID Vaccine and to continue having my Tocilizumab injections. I am also on 10 mgs of Prednisalone. I have Giant Cell Arteritis/Large Vessel Vasculitis.
My Rheumatologist has let me know that it is fine for me to have the COVID Vaccine and to continue having my Tocilizumab injections. I am also on 10 mgs of Prednisalone. I have Giant Cell Arteritis/Large Vessel Vasculitis.
SheffieldJane
in
PMRGCAuk
4 years ago
Gonal F
Hi all, Can someone please help...once Gonal F is opened is it still stored in the fridge or can it be left at room temp? I’m really confused as in the past I’ve always stored it in the fridge but on the leaflet it says once it’s opened it can be stored at room temp.. Thank you x ***Updated: Thank
Hi all, Can someone please help...once Gonal F is opened is it still stored in the fridge or can it be left at room temp? I’m really confused as in the past I’ve always stored it in the fridge but on the leaflet it says once it’s opened it can be stored at room temp.. Thank you x ***Updated: Thank
Hope_JN
in
Fertility Network UK
4 years ago
Interesting twist of events
Hi, hope everyone is staying safe and well. We are again in lockdown and California looks to be pretty high on the exposure list. Please keep us in your thoughts and prayers as i can only imagine how tired health care employees must be. A good friend of mine recently tested positive as she was around
Hi, hope everyone is staying safe and well. We are again in lockdown and California looks to be pretty high on the exposure list. Please keep us in your thoughts and prayers as i can only imagine how tired health care employees must be. A good friend of mine recently tested positive as she was around
JennaShi
in
LUPUS UK
4 years ago
Teenage son has thyroid function slightly low
Testing showed he is just above the normal range however 2 years ago he was in the normal range for TSH so they say he has slight hypothyroid. I am trying to get the rest of his results sent to me as dr rang him with results so of course as a teenager he was very vague. Due to privacy laws he has to
Testing showed he is just above the normal range however 2 years ago he was in the normal range for TSH so they say he has slight hypothyroid. I am trying to get the rest of his results sent to me as dr rang him with results so of course as a teenager he was very vague. Due to privacy laws he has to
LAJ12345
in
Thyroid UK
4 years ago
Would love some advice
Hi. Firstly, I just want to say how grateful I am to have found this forum. It is invaluable and has answered some of my questions before I have even asked them - ie. blurry eyes etc. I would love some advice though if you can still put up with me. My consultant reduced my 40mg dose of prednisolone
Hi. Firstly, I just want to say how grateful I am to have found this forum. It is invaluable and has answered some of my questions before I have even asked them - ie. blurry eyes etc. I would love some advice though if you can still put up with me. My consultant reduced my 40mg dose of prednisolone
Sophiestree
in
PMRGCAuk
4 years ago
BPPV Vertigo and Pernicious Anaemia
I keep reading in the posts about Vertigo. My question is does Benign Proximal Positional Vertigo BPPV have a connection to pernicious anaemia and Vit B12 deficiency? I have had bouts of it for the past 20 years and always thought it was due to a virus.
I keep reading in the posts about Vertigo. My question is does Benign Proximal Positional Vertigo BPPV have a connection to pernicious anaemia and Vit B12 deficiency? I have had bouts of it for the past 20 years and always thought it was due to a virus.
DBHolland
in
Pernicious Anaemia Society
4 years ago
Neuropathy
Hi Ladies, I have had my 4th chemo of Carboplatin and paclitaxel last week. During the 3 chemos, numbness, tingling in hands and feet was not too bad and seemed to get better by day 7/8, no sleep problems, able to walk some distance....this last one has been worse and I am now 15 days later still suffering
Hi Ladies, I have had my 4th chemo of Carboplatin and paclitaxel last week. During the 3 chemos, numbness, tingling in hands and feet was not too bad and seemed to get better by day 7/8, no sleep problems, able to walk some distance....this last one has been worse and I am now 15 days later still suffering
Dubai18
in
My Ovacome
4 years ago
Restless Legs Syndrome
Restless Body Syndrome. Last night I had electric impulses going down my arms & legs, some seem to go from my brain through my heart which I find a bit worrying. I have peripheral neuropathy. Any feedback gratefully received.
Restless Body Syndrome. Last night I had electric impulses going down my arms & legs, some seem to go from my brain through my heart which I find a bit worrying. I have peripheral neuropathy. Any feedback gratefully received.
Boxer215
in
Restless Legs Syndrome
4 years ago
Neuropathy symptoms variable?
Hi, When my monthly B12 injections were cut to every 3 months I developed a range of symptoms including peripheral neuropathy. I am still trying to get this situation resolved (my GP insists I will need to be seen by a neurologist which could take months so I may need to try self-injecting) but in
Hi, When my monthly B12 injections were cut to every 3 months I developed a range of symptoms including peripheral neuropathy. I am still trying to get this situation resolved (my GP insists I will need to be seen by a neurologist which could take months so I may need to try self-injecting) but in
Brocher
in
Pernicious Anaemia Society
4 years ago
Sotalol
I saw my cardiologist last week and because of the increase in my AF episodes and continuing ectopics felt that a change of medication would be advisable and wanted me to start taking 25mgs of metoprolol 3 times a day to start with I’ve been taking 80mgs of Sotalol twice a day for 7 years following a
I saw my cardiologist last week and because of the increase in my AF episodes and continuing ectopics felt that a change of medication would be advisable and wanted me to start taking 25mgs of metoprolol 3 times a day to start with I’ve been taking 80mgs of Sotalol twice a day for 7 years following a
colingee
in
Atrial Fibrillation Support
4 years ago
Diagnosed with pelvic floor dysfunction.
Hi all, Just an update. I had a proctogram examination today and it has confirmed pelvic floor dysfunction. I'm a 44 year old man and have been suffering for years with pelvic pain which was made worse after pooping. I'd suffered constipation and developed haemorrhoids from straining to defecate. It
Hi all, Just an update. I had a proctogram examination today and it has confirmed pelvic floor dysfunction. I'm a 44 year old man and have been suffering for years with pelvic pain which was made worse after pooping. I'd suffered constipation and developed haemorrhoids from straining to defecate. It
Lovetocycle76
in
Pelvic Pain Support Network
4 years ago
Amitripyline
Has anyone ever taken Amitripyline for spasms in the esophagus? I am new—-this is my first post. I have been having severe pain in between my breast that radiates through my back —last about five to ten minutes then totally no pain at all. It happens a lot after rushing and being stresses and after
Has anyone ever taken Amitripyline for spasms in the esophagus? I am new—-this is my first post. I have been having severe pain in between my breast that radiates through my back —last about five to ten minutes then totally no pain at all. It happens a lot after rushing and being stresses and after
Fraunfelter
in
Pain Concern
4 years ago
Overwhelming Pain (I am new)
First, my screen name, say it like this `eye see you a lot`! I have had kyphoscoliosis, which causes overwhelming pain in my lower back. Recently I had Radio Frequency denervation, it did not work. I have also suffered for a long time with pain in joints, muscle weakness, and spasms, headaches, upset
First, my screen name, say it like this `eye see you a lot`! I have had kyphoscoliosis, which causes overwhelming pain in my lower back. Recently I had Radio Frequency denervation, it did not work. I have also suffered for a long time with pain in joints, muscle weakness, and spasms, headaches, upset
Hidden
in
Fibromyalgia Action UK
4 years ago
A different pain!
I have had fibromyalgia for years now and I get all kinds of pain. We fibro sufferers know the pains take turns. Today I woke up with a pain I had never had before. The skin of my left thigh is hurting sooo much. I can't touch it because then I'll scream! Even if I touch it gently the pain is terrible
I have had fibromyalgia for years now and I get all kinds of pain. We fibro sufferers know the pains take turns. Today I woke up with a pain I had never had before. The skin of my left thigh is hurting sooo much. I can't touch it because then I'll scream! Even if I touch it gently the pain is terrible
Micafe
in
Fibromyalgia Action UK
4 years ago
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