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Giant axonal neuropathy
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Gonal F.... not really feeling it!
Hi alla, so Iv started my IVF ICSI medication and I’m on Gonal F (day 4) honestly I thought I’d be feeling it more, like something around me ovaries or soreness. Up until now I’m only feeling quite tired and a little dizzy. But I don’t know for some reason I felt like once I start the medication I’d
Hi alla, so Iv started my IVF ICSI medication and I’m on Gonal F (day 4) honestly I thought I’d be feeling it more, like something around me ovaries or soreness. Up until now I’m only feeling quite tired and a little dizzy. But I don’t know for some reason I felt like once I start the medication I’d
Manooo
in
Fertility Network UK
3 years ago
In focus: approaches to symptom management - complementary therapies
Hello This month in our Health in Focus posts, we’re looking at some of the different approaches to management of cancer symptoms and side effects of treatment. Today we’ll look more closely at complementary therapies. We’ll also cover food and sleep in our future posts in the series. Complementary
Hello This month in our Health in Focus posts, we’re looking at some of the different approaches to management of cancer symptoms and side effects of treatment. Today we’ll look more closely at complementary therapies. We’ll also cover food and sleep in our future posts in the series. Complementary
OvacomeSupport
Administrator
in
My Ovacome
4 years ago
Stims time
Hi all, I’ve finished down reg now which I’m thrilled about, that 3 weeks of just sniffing a spray really seems to drag for me. I always have my worst side effects during down regulation too so glad it’s over. I started 375 of the ovaleap injection this evening, that’s new for me last year I had Gonal
Hi all, I’ve finished down reg now which I’m thrilled about, that 3 weeks of just sniffing a spray really seems to drag for me. I always have my worst side effects during down regulation too so glad it’s over. I started 375 of the ovaleap injection this evening, that’s new for me last year I had Gonal
LisaBeatrix1980
in
Fertility Network UK
3 years ago
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The importance of vitamin B6 against Parkinson's. The end of a meaningless prejudice since 1975.
A restriction or prohibition that has survived almost 50 years (1975-2020) without any scientific reason since levodopa was linked to carbidopa or benserazide. by Jesus Marquez Rivera Project "Parkinsons Here and Now" (2012-2021) "What is Science? Learn from Science that you must doubt of the experts
A restriction or prohibition that has survived almost 50 years (1975-2020) without any scientific reason since levodopa was linked to carbidopa or benserazide. by Jesus Marquez Rivera Project "Parkinsons Here and Now" (2012-2021) "What is Science? Learn from Science that you must doubt of the experts
parkinsonshereandnow
in
Cure Parkinson's
4 years ago
RA pain
Hi guys I’m writing this as the last few months I’ve been in excruciating pain . I have sero negative inflammatory arthritis. I’m on weekly benpali injection and arcoxia for day time pain along with tramadol and amitriptaylin on a night . The pain is getting worse my meds don’t seem to be working apart
Hi guys I’m writing this as the last few months I’ve been in excruciating pain . I have sero negative inflammatory arthritis. I’m on weekly benpali injection and arcoxia for day time pain along with tramadol and amitriptaylin on a night . The pain is getting worse my meds don’t seem to be working apart
LJS13
in
Fibromyalgia Action UK
4 years ago
EMG and Nerve Conduction Study
Hi everyone. Recently I underwent a n EMG (electromyograph) and Nerve Conduction Study to verify the nerve damage since I’m having symptoms of peripheral neuropathy. Both studies were normal. Have any of you underwent such study to confirm peripheral neuropathy (nerve pain, muscle weakness) due to Pernicious
Hi everyone. Recently I underwent a n EMG (electromyograph) and Nerve Conduction Study to verify the nerve damage since I’m having symptoms of peripheral neuropathy. Both studies were normal. Have any of you underwent such study to confirm peripheral neuropathy (nerve pain, muscle weakness) due to Pernicious
Dolansan
in
Pernicious Anaemia Society
4 years ago
Tocilizumab extension
Hi I wrote a couple of weeks ago asking if anyone had been told that their tocilizumab was being extended. I’ve heard nothing from rheumatology or G.P but today I’ve had a txt from the company that deliver the injections to say they are delivering early March. Not sure if it’s the normal 8 weeks supply
Hi I wrote a couple of weeks ago asking if anyone had been told that their tocilizumab was being extended. I’ve heard nothing from rheumatology or G.P but today I’ve had a txt from the company that deliver the injections to say they are delivering early March. Not sure if it’s the normal 8 weeks supply
Devoid
in
PMRGCAuk
4 years ago
Therapy light
Has anyone tried therapy lights or mood or depression that constantly accompanies Parkinson’s?
Has anyone tried therapy lights or mood or depression that constantly accompanies Parkinson’s?
Kt088
in
Cure Parkinson's
4 years ago
Started Xtandi Today after Taxotere Finished.
Three weeks ago I had my last of 6 sessions (every 3 weeks) of Taxotere and monthly Lupron shots. Post RP PSA was 63 and now after chemo undetectable. Got back Ct scans and no Mets to chest, abdomen or pelvic area. One enlarged node shrank. Staying on Lupron and starting Xtandi. I’m taking it before
Three weeks ago I had my last of 6 sessions (every 3 weeks) of Taxotere and monthly Lupron shots. Post RP PSA was 63 and now after chemo undetectable. Got back Ct scans and no Mets to chest, abdomen or pelvic area. One enlarged node shrank. Staying on Lupron and starting Xtandi. I’m taking it before
MrCatMan
in
Fight Prostate Cancer
3 years ago
Third round with pergoveris
Hello everyone . So i started my third round , i am Taking pergoveris and gonal f , i am hoping this round will lead to something good , trying my best to keep positive and hopeful. Though i am feeling physically drained , i don’t know if its the pergoveris , im new to it but since i started my stims
Hello everyone . So i started my third round , i am Taking pergoveris and gonal f , i am hoping this round will lead to something good , trying my best to keep positive and hopeful. Though i am feeling physically drained , i don’t know if its the pergoveris , im new to it but since i started my stims
Wishingforabump
in
Fertility Network UK
3 years ago
Vaccine and PN
Having jab 2Feb concerned how this will affect my Peripheral Neuropathy as it is very severe. I also have R.A. so very nervous about any reaction. Just wondered if anybody had this condition( PN) and did the vaccine cause any problems.
Having jab 2Feb concerned how this will affect my Peripheral Neuropathy as it is very severe. I also have R.A. so very nervous about any reaction. Just wondered if anybody had this condition( PN) and did the vaccine cause any problems.
orange33
in
Neuropathy Support
4 years ago
A look at the next generation of Androgen Receptor therapies--AR Degraders/PROTACS
Greetings FPC members, Recently, Cujoe the K9 Wonder asked me if ARV-110 might deserve a post and I confirmed that the next generation of AR drugs--the PROTACs / AR Degraders indeed deserve a serious look. What does one do when those second line AR drugs like abiraterone, TAK-700, enzalutamide, apalutamide
Greetings FPC members, Recently, Cujoe the K9 Wonder asked me if ARV-110 might deserve a post and I confirmed that the next generation of AR drugs--the PROTACs / AR Degraders indeed deserve a serious look. What does one do when those second line AR drugs like abiraterone, TAK-700, enzalutamide, apalutamide
NPfisherman
in
Fight Prostate Cancer
3 years ago
Magnesium
Hello friends, Is it better to take magnesium taurate than magnesium glycinate for afib? Or is it trial and error to see what works best?
Hello friends, Is it better to take magnesium taurate than magnesium glycinate for afib? Or is it trial and error to see what works best?
Nanny01
in
AF Association
4 years ago
Chemo Neuropathy on fingers
Hi all, I was due to receive my last chemo on Monday 25th Jan, but I have developed some neuropathy on both hands, on my finger tips. It seems very painful sometimes. My nails look funny as in colour and I can't open lids, jars, or sometimes find difficult to press on things. I have been told that if
Hi all, I was due to receive my last chemo on Monday 25th Jan, but I have developed some neuropathy on both hands, on my finger tips. It seems very painful sometimes. My nails look funny as in colour and I can't open lids, jars, or sometimes find difficult to press on things. I have been told that if
Shinebright2020
in
My Ovacome
4 years ago
Trigger shot
Doing trigger with 10,000 hcg + 160 units Lupron + gonal f. Is that normal? I am issues with low reserve and low egg maturation.
Doing trigger with 10,000 hcg + 160 units Lupron + gonal f. Is that normal? I am issues with low reserve and low egg maturation.
Scout82
in
Fertility Network UK
3 years ago
The more homocysteine, the worse the Parkinson's?
"You don't discover new continents if you don't have the courage to lose sight of the old shores." Andre Gide An elevated level of the amino acid homocysteine in the blood is neurotoxic and has been reported as a truly important risk factor for developing Parkinson's, as well as cardiovascular disease
"You don't discover new continents if you don't have the courage to lose sight of the old shores." Andre Gide An elevated level of the amino acid homocysteine in the blood is neurotoxic and has been reported as a truly important risk factor for developing Parkinson's, as well as cardiovascular disease
parkinsonshereandnow
in
Cure Parkinson's
4 years ago
Nervous
Sorry I'm going a bit off piste but I feel very scared. My husband has had trouble with his mobility and memory for a couple of years and yesterday got a diagnosis of Normal postural Hydrocephalus. He has been advised to have a lumber puncture to drain some fluid to see if it temporarily improves with
Sorry I'm going a bit off piste but I feel very scared. My husband has had trouble with his mobility and memory for a couple of years and yesterday got a diagnosis of Normal postural Hydrocephalus. He has been advised to have a lumber puncture to drain some fluid to see if it temporarily improves with
Suet3942
in
PMRGCAuk
4 years ago
Anaphylatic Shock Episode
Hi all, I had a severe allergic reaction to a voltaren tablet this week resulting in Anaphylatic Shock ( trip to emergency dept). I have been a work in progress patient with suspected Lupus since Oct 2019 in Uk . I am in Dubai where my son lives so have been to see a Rheumatologist here.... having
Hi all, I had a severe allergic reaction to a voltaren tablet this week resulting in Anaphylatic Shock ( trip to emergency dept). I have been a work in progress patient with suspected Lupus since Oct 2019 in Uk . I am in Dubai where my son lives so have been to see a Rheumatologist here.... having
Maloo19
in
LUPUS UK
4 years ago
Prednisone
New to this site. I have UC for last 3years and at first 6 800mg octasa tablets kept it under control but since Christmas I’ve been struggling lhave constant so called flares. My consultant has tried me on salafalk 2mg enamas and budalfalk foam enamas.at the moment I’m on prednisone 5mg suppository which
New to this site. I have UC for last 3years and at first 6 800mg octasa tablets kept it under control but since Christmas I’ve been struggling lhave constant so called flares. My consultant has tried me on salafalk 2mg enamas and budalfalk foam enamas.at the moment I’m on prednisone 5mg suppository which
Bluegirl1948
in
IBS Network
3 years ago
Severe folate deficiency
Hi I’m new to this forum. I have been diagnosed recently with severe folate deficiency, it was below 2. I had the pins and needles like tingling down my arms and legs. So went to doctor and got bloods done which resulted in folate deficiency. I have been on 5mg of folic acid now for a week. The tingling
Hi I’m new to this forum. I have been diagnosed recently with severe folate deficiency, it was below 2. I had the pins and needles like tingling down my arms and legs. So went to doctor and got bloods done which resulted in folate deficiency. I have been on 5mg of folic acid now for a week. The tingling
Hidden
in
Pernicious Anaemia Society
4 years ago
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