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Giant axonal neuropathy
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’Modified’ natural FET - anyone ovulated before trigger?
I have a modified natural FET. So I take low levels of gonal f to stimulate ovaries to produce 1 or 2 follicles which naturally creates oestrogen and thickens my lining. I normally take a trigger when it’s ready. However I went for my scan today and they said I’d already ovulated! My ov sticks have
I have a modified natural FET. So I take low levels of gonal f to stimulate ovaries to produce 1 or 2 follicles which naturally creates oestrogen and thickens my lining. I normally take a trigger when it’s ready. However I went for my scan today and they said I’d already ovulated! My ov sticks have
Daisy-Delilah
in
Fertility Network UK
4 months ago
Scientific opinion on the tolerable upper intake level for vitamin B6
The new scientific opinion (EFSA) revised in Europe the Tolerable Upper Intake Level
(UL) for vitamin B6 of 12.5 mg/day
for adults (including pregnant and lactating women), down from the previous UL of 30 mg/day set in 2000. For infants and children the ULs are: 2.2-2.5 mg/day (4-11 months), 3.2
The new scientific opinion (EFSA) revised in Europe the Tolerable Upper Intake Level
(UL) for vitamin B6 of 12.5 mg/day
for adults (including pregnant and lactating women), down from the previous UL of 30 mg/day set in 2000. For infants and children the ULs are: 2.2-2.5 mg/day (4-11 months), 3.2
Esperanto
in
Cure Parkinson's
9 months ago
Feeling a little disillusioned about TTFD and High Dose Thiamine (HDT):
My opinion: You can watch videos that say other B1’s are better; they are more powerful; they cross the BBB; etc. but you cannot find much (if any) info on long-term positive results [success stories]. Best to leave Benfothiamine, TTFD, Sulbutiamine, etc. alone and stay with what works for other people
My opinion: You can watch videos that say other B1’s are better; they are more powerful; they cross the BBB; etc. but you cannot find much (if any) info on long-term positive results [success stories]. Best to leave Benfothiamine, TTFD, Sulbutiamine, etc. alone and stay with what works for other people
Gcf51
in
Cure Parkinson's
9 months ago
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Hope neuro is right
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did , He has taken me off temgesic as well and informed the other drs looking after me not to put me on it again..
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did , He has taken me off temgesic as well and informed the other drs looking after me not to put me on it again..
Hidden
in
Neuropathy Support
9 months ago
Hope neuro is right
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did , He has taken me off temgesic as well and informed the other drs looking after me not to put me on it again..
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did , He has taken me off temgesic as well and informed the other drs looking after me not to put me on it again..
Hidden
in
Neuropathy Support
9 months ago
Hope neuro is right
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did and to ring your dr also, he said he is not looking at someone's sob letter. He has taken me off temgesic as well
Hope neurologist is right or I'm done.Well the neurologist said it is not restless legs but nerve damage. He flatly refused to give me subutex without scientific proof, I told him that I did and to ring your dr also, he said he is not looking at someone's sob letter. He has taken me off temgesic as well
Hidden
in
Restless Legs Syndrome
9 months ago
Losing Hope of a good life
Sitting here jerking away, feels like someone has a cattle prod stuck in my thigh and sending shocks down my leg..my foot is twisting up....I'm about done with this. My husband may as well go and find someone else that can give him a happy retirement...the last 2 days I have had to drug myself up to
Sitting here jerking away, feels like someone has a cattle prod stuck in my thigh and sending shocks down my leg..my foot is twisting up....I'm about done with this. My husband may as well go and find someone else that can give him a happy retirement...the last 2 days I have had to drug myself up to
Hidden
in
Restless Legs Syndrome
9 months ago
Benefits of knowing your illness/condition/disease to help others as well as yourself
It’s about time I posted that a couple of months ago my husband was diagnosed with Giant Cell Arteritis. I was somewhat overwhelmed by the diagnosis having had PMR, GCA/LVV myself over the past 5 and a half years and haven’t, until now, felt ready to share his story on the forum.
It’s about time I posted that a couple of months ago my husband was diagnosed with Giant Cell Arteritis. I was somewhat overwhelmed by the diagnosis having had PMR, GCA/LVV myself over the past 5 and a half years and haven’t, until now, felt ready to share his story on the forum.
123-go
in
PMRGCAuk
7 months ago
v non-invasive treatment may offer significant relief to and restore gait function in patients with neurological disorders
To this end, the clinical researchers from Japan recruited twenty-three patients with PD or Parkinson’s syndrome. All study participants were randomly assigned to receive either the active treatment or a “sham” treatment that mimics the active treatment but does not offer any therapeutic benefit.
To this end, the clinical researchers from Japan recruited twenty-three patients with PD or Parkinson’s syndrome. All study participants were randomly assigned to receive either the active treatment or a “sham” treatment that mimics the active treatment but does not offer any therapeutic benefit.
Farooqji
in
Cure Parkinson's
9 months ago
tramadol
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
I was on tramadol for at least 10 years----100 mg. then my doc took me off because a neurologist put me on Clonazepam for REM/SBD (rapid eye movement sleep behavior disorder.) But I was also getting cervical and lumbar rhizotomies...and still do every 12-14 months or so. I am now working with the VA
Shadowperson
in
Pain Concern
9 months ago
Low B6... taking a complex with pyridoxine which obviously doesn't suit
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
Back to the search for the best B complex (Thorne being elusive at the moment and didn't do particularly well at keeping my B12 up)... one which contains pyridoxal 5' phosphate Does anyone rate Igennus Super B Complex? All suggestions welcome 🤗
TiggerMe
in
Thyroid UK
9 months ago
Free auto injector : )
Hi all - I am in Germany and have a new, unused Union Medico Needle Guide Assistant with English instructions. I don't need it and don't want to just toss it. I know some of you struggle with injections and might need it. I'm happy to send free to anyone in Europe or the UK. Please just let me know
Hi all - I am in Germany and have a new, unused Union Medico Needle Guide Assistant with English instructions. I don't need it and don't want to just toss it. I know some of you struggle with injections and might need it. I'm happy to send free to anyone in Europe or the UK. Please just let me know
SigNi
in
Pernicious Anaemia Society
9 months ago
Neuropathy AFTER Chemo: Treatment?
I had 14 docetaxel treatments a little over a year ago with no neuropathy. Approximately two months after completing these 14 treatments, I began to have peripheral neuropathy in my fingertips and a small amount in my toes. The neuropathy is worse at night and has continued (at about the same severity
I had 14 docetaxel treatments a little over a year ago with no neuropathy. Approximately two months after completing these 14 treatments, I began to have peripheral neuropathy in my fingertips and a small amount in my toes. The neuropathy is worse at night and has continued (at about the same severity
VLBIV
in
Advanced Prostate Cancer
9 months ago
Hypnotherapy for Primary Raynaud's
Hello, there are some websites that state that Hypnotherapy can help Raynaud's. There are some Hypnotherapists that offer treatments for Raynaud's which are very expensive, £400 for just 2 sessions, https://www.emmaarmes.com/fees I would want hypnotherapy to stop my central nervous system from overreacting
Hello, there are some websites that state that Hypnotherapy can help Raynaud's. There are some Hypnotherapists that offer treatments for Raynaud's which are very expensive, £400 for just 2 sessions, https://www.emmaarmes.com/fees I would want hypnotherapy to stop my central nervous system from overreacting
mike444
in
Scleroderma & Raynaud's UK (SRUK)
9 months ago
TSH increased but no medication change
Hi, My recent blood tests showed my TSH has increased from 1.12 to 2.4 and I haven’t changed anything. Is there a reason this would happen or does it just fluctuate? I have been eating a lot of cruciferous everyday. Would that have an impact? My FT4 has remained pretty constant.
Hi, My recent blood tests showed my TSH has increased from 1.12 to 2.4 and I haven’t changed anything. Is there a reason this would happen or does it just fluctuate? I have been eating a lot of cruciferous everyday. Would that have an impact? My FT4 has remained pretty constant.
Emj001
in
Thyroid UK
9 months ago
Could these symptoms be CANVAS
Diagnosed with Large fibre polyneuropathy in 2021 but symptoms have progressed more towards CANVAS. Is anyone familiar with it? Stands for Cerebellar Ataxia (CA), Neuropathy (N) and Vestibular Areflexia (VA). There is a genetic RFC1 type and one without a genetic type. I have positive Rhomberg and loss
Diagnosed with Large fibre polyneuropathy in 2021 but symptoms have progressed more towards CANVAS. Is anyone familiar with it? Stands for Cerebellar Ataxia (CA), Neuropathy (N) and Vestibular Areflexia (VA). There is a genetic RFC1 type and one without a genetic type. I have positive Rhomberg and loss
rideabike
in
Ataxia UK
9 months ago
Infections during Chemo
After my LRP (2010) I had UTI's continually for ~2 years. I have no idea what finally shook them off -- a change from a tropical to a temperate climate, maybe? I am not coming to the end of the oral treatments available to me. At some time in the not too distant future I will be moving to docetaxel
After my LRP (2010) I had UTI's continually for ~2 years. I have no idea what finally shook them off -- a change from a tropical to a temperate climate, maybe? I am not coming to the end of the oral treatments available to me. At some time in the not too distant future I will be moving to docetaxel
BrentW
in
Advanced Prostate Cancer
9 months ago
Tooth extraction and tocilizumab
Hi I am going to have to have a tooth extraction....dentist says chance of jaw necrosis from tocilizumab and I wonder if anyone has had this ....I know from here that it is only a small chance but its scary ! Also will I need to come off medications (tocilizumab and methotrexate) first? Advice appreciated
Hi I am going to have to have a tooth extraction....dentist says chance of jaw necrosis from tocilizumab and I wonder if anyone has had this ....I know from here that it is only a small chance but its scary ! Also will I need to come off medications (tocilizumab and methotrexate) first? Advice appreciated
WaltzG
in
PMRGCAuk
7 months ago
what test should i ask for??!
Hi all, On my 3rd FET & although not due to test until next week i have the gut feeling it hasn't worked as i have had brown watery type spotting/discharge since Tuesday. This is the last embryo of my 2nd ivf round. My question is with 3 failed transfers & having stage 4 endo is there any tests
Hi all, On my 3rd FET & although not due to test until next week i have the gut feeling it hasn't worked as i have had brown watery type spotting/discharge since Tuesday. This is the last embryo of my 2nd ivf round. My question is with 3 failed transfers & having stage 4 endo is there any tests
NM19
in
Fertility Network UK
5 months ago
5 days of provera done - now waiting for a period to start letrozole.
Hi everyone , as you all may know I have decided to put my second IVF on hold to give my body a chance on Letrozole. After the loss of my baby at 21 weeks and a failed fet and not responding great (112 gonal f) which was probably why! I have decided to try and trust my body . I say try because i
Hi everyone , as you all may know I have decided to put my second IVF on hold to give my body a chance on Letrozole. After the loss of my baby at 21 weeks and a failed fet and not responding great (112 gonal f) which was probably why! I have decided to try and trust my body . I say try because i
Hidden
in
Fertility Network UK
5 months ago
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