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Seeking any info: Our son was recently diagnosed with kidney disease
Hi, I'm a parent who is looking for possible answers or similar situations out there. Our 16-year-old son was diagnosed with kidney disease in March 2024. We've been trying to find medication and treatment to help with it. This all started in January 2024, when our son was complaining about back pain
Hi, I'm a parent who is looking for possible answers or similar situations out there. Our 16-year-old son was diagnosed with kidney disease in March 2024. We've been trying to find medication and treatment to help with it. This all started in January 2024, when our son was complaining about back pain
BlueGuitar123
in
Parents of Children with Kidney Disease
1 month ago
Accord levothyroxine 100 mcgm
I take 100mcgm Levo and 15 mcgm T3 (Sigma Pharma) each day I looked back through previous years: July 2022 T4 35% through range T3 86% July21 T4 62% and T3 67% again T4 difference is noticeable Vitamins are all good , ferritin over range, waiting for
genetic
test
result for haemachromatosis as daughter
I take 100mcgm Levo and 15 mcgm T3 (Sigma Pharma) each day I looked back through previous years: July 2022 T4 35% through range T3 86% July21 T4 62% and T3 67% again T4 difference is noticeable Vitamins are all good , ferritin over range, waiting for
genetic
test
result for haemachromatosis as daughter
crimple
in
Thyroid UK
11 months ago
Genetic testing
(for information purposes) Had an appointment at the hospital today to see the lead nurse to discuss family history (looks like I am the first with my problem) and as my cardiologist still can't work out why I had heart failure I have been referred for genetic testing. She explained there are three
(for information purposes) Had an appointment at the hospital today to see the lead nurse to discuss family history (looks like I am the first with my problem) and as my cardiologist still can't work out why I had heart failure I have been referred for genetic testing. She explained there are three
uzininemm
in
British Heart Foundation
10 months ago
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Multiple menigioma
Hi had a spinal menigioma removed a few years ago and with some nerve damage to lower stomach area. Now diagnosed with frontal lobe menigioma. Anyone have more than one appear? Dr. Is watching this recent tumor, he is interested in genetic testing.
Hi had a spinal menigioma removed a few years ago and with some nerve damage to lower stomach area. Now diagnosed with frontal lobe menigioma. Anyone have more than one appear? Dr. Is watching this recent tumor, he is interested in genetic testing.
Saraschild2
in
Meningioma Support
10 months ago
Color Genetic Test
Hi all: I am on AS and was advised to get the color
genetic
test
, which tests genes corresponding to three dimensions: cancer, heart, and medication response. [1] No mutations identified for genes corresponding to cancer and heart disease. [2] Genes corresponding to medication response.
Hi all: I am on AS and was advised to get the color
genetic
test
, which tests genes corresponding to three dimensions: cancer, heart, and medication response. [1] No mutations identified for genes corresponding to cancer and heart disease. [2] Genes corresponding to medication response.
witantric
in
Prostate Cancer Network
1 year ago
PSA rockets up to 344
Hello - I received quite shocking news during my visit to the Mayo Clinic last week. My PSA has jumped to 344 from a low of 3.6 last November, when I completed chemo with cabazitaxel. PSA did start to rise quite soon, into double digits, but this is by far my highest PSA ever. Dr. Kwon recommended
Hello - I received quite shocking news during my visit to the Mayo Clinic last week. My PSA has jumped to 344 from a low of 3.6 last November, when I completed chemo with cabazitaxel. PSA did start to rise quite soon, into double digits, but this is by far my highest PSA ever. Dr. Kwon recommended
Arcticfox44
in
Advanced Prostate Cancer
2 months ago
lost my brother to SADS
Hello, I recently lost my brother at Christmas, he was only 30 years old and was fit, active and health. Was studying at university to become a physiotherapist and had his whole life ahead of him. We recently got his cause of death which was due to SADS. I’m due to go for genetic testing and have
Hello, I recently lost my brother at Christmas, he was only 30 years old and was fit, active and health. Was studying at university to become a physiotherapist and had his whole life ahead of him. We recently got his cause of death which was due to SADS. I’m due to go for genetic testing and have
MeganR13
in
British Heart Foundation
2 months ago
Transcobalamin
Likely as that is the only time that
genetic
test
is performed and then only rarely tested. What little I can find about treatment of transcobalamin is administration of large amounts of B12 and 'various' forms of B12. Which I find rational.
Likely as that is the only time that
genetic
test
is performed and then only rarely tested. What little I can find about treatment of transcobalamin is administration of large amounts of B12 and 'various' forms of B12. Which I find rational.
WIZARD6787
in
Pernicious Anaemia Society
1 year ago
Arcticfox44
Hello - I'm about to return to the Mayo for the first review since my previous visit last November. As I've reported here, my last major treatment was chemo with cabazitaxel at the Oncology Center in Nicosia, Cyprus, where I live. This was successful: PSA fell from 83 at the start of chemo to about 3
Hello - I'm about to return to the Mayo for the first review since my previous visit last November. As I've reported here, my last major treatment was chemo with cabazitaxel at the Oncology Center in Nicosia, Cyprus, where I live. This was successful: PSA fell from 83 at the start of chemo to about 3
Arcticfox44
in
Advanced Prostate Cancer
2 months ago
Bloodwork is stable, watchful waiting,stage 1(ish).What's the chance that the bone marrow biopsy will show anything different or additional?
Thoughts? Should I bother? I don't really feel like we have a decent staging. Memorial Sloan Kettering Dr says we can do a bone marrow biopsy and some mutation/genetic testing? Am I wasting my time? Or should I do it to get more peace of mind?
Thoughts? Should I bother? I don't really feel like we have a decent staging. Memorial Sloan Kettering Dr says we can do a bone marrow biopsy and some mutation/genetic testing? Am I wasting my time? Or should I do it to get more peace of mind?
HeatherW71
in
CLL Support
11 months ago
can rapid growth be malignant
I was diagnosed with AN in left ear 3 years ago. It is not growing but a routine scan a year ago showed another AN on the right side 4mm. I had genetic testing but it is not NF2. A year later it is 9.5mm and I was sent to an oncologist regarding Gamma knife. The oncologist says the growth has been
I was diagnosed with AN in left ear 3 years ago. It is not growing but a routine scan a year ago showed another AN on the right side 4mm. I had genetic testing but it is not NF2. A year later it is 9.5mm and I was sent to an oncologist regarding Gamma knife. The oncologist says the growth has been
Operalovers
in
Acoustic Neuroma Support
11 months ago
Moving on...to olaparib
Orme phoned me to report that after another
genetic
test
result came in, we now have the option of olaparib. I live in Nicosia, Cyprus, but travel to the Mayo in Rochester when necessary.
Orme phoned me to report that after another
genetic
test
result came in, we now have the option of olaparib. I live in Nicosia, Cyprus, but travel to the Mayo in Rochester when necessary.
Arcticfox44
in
Advanced Prostate Cancer
1 year ago
Please may I get your thoughts on 2nd round of thyroid tests?
Get a
genetic
test
from Regenerus Labs for possible conversion issues – not sure if this is useful in my case as not on thyroid replacement hormones? 4. Get a multi-point saliva test to assess if adrenal issues could be playing a part? Thank you for managing to get this far!
Get a
genetic
test
from Regenerus Labs for possible conversion issues – not sure if this is useful in my case as not on thyroid replacement hormones? 4. Get a multi-point saliva test to assess if adrenal issues could be playing a part? Thank you for managing to get this far!
Bertiepuss
in
Thyroid UK
6 months ago
Ductal Component
RARP with wide excision was 07/18/23. Pathology showed Gleason 4+3 - grade group 3 - adenocarcinoma with Ductal components- No LN involvement and PET scan before tx was clear of other spots in body. Genetic Testing will be done -no results for several weeks Is the “Ductal components” in the pathology
RARP with wide excision was 07/18/23. Pathology showed Gleason 4+3 - grade group 3 - adenocarcinoma with Ductal components- No LN involvement and PET scan before tx was clear of other spots in body. Genetic Testing will be done -no results for several weeks Is the “Ductal components” in the pathology
Jroeder
in
Advanced Prostate Cancer
11 months ago
Statins
I’ve just had a telephone consultation with hospital lipid dr and the
genetic
test
they did which looks for one definite familial link, but instead the results show various genetic anomalies which I have been told still puts me at a high risk of heart disease and strokes.
I’ve just had a telephone consultation with hospital lipid dr and the
genetic
test
they did which looks for one definite familial link, but instead the results show various genetic anomalies which I have been told still puts me at a high risk of heart disease and strokes.
Flecmac
in
Thyroid UK
1 year ago
Genetic testing of embryo
Is it worth to get your embryos tested when over 40 with low egg reserve? The problem is that money could be put into more cycles, also it requires to wait till blastocyst stage but with only let's say 2 or 3 embryos you might lose them before getting to blastocyst. Waiting till blastocyst is higher
Is it worth to get your embryos tested when over 40 with low egg reserve? The problem is that money could be put into more cycles, also it requires to wait till blastocyst stage but with only let's say 2 or 3 embryos you might lose them before getting to blastocyst. Waiting till blastocyst is higher
Kalinka1979
in
Fertility Network UK
11 months ago
Xeloda
I was on ibrance 100 mg and anastrozel for 3.5 years. Starting Xeloda 1500 morning and 1500 night. Took me off ibrance and anastrozel because not working. I have a biopsy Monday of an area in my lung which has grown a little I had a PET scan. I have a great oncologist and I was stable. Genetic testing
I was on ibrance 100 mg and anastrozel for 3.5 years. Starting Xeloda 1500 morning and 1500 night. Took me off ibrance and anastrozel because not working. I have a biopsy Monday of an area in my lung which has grown a little I had a PET scan. I have a great oncologist and I was stable. Genetic testing
1glajon
in
SHARE Metastatic Breast Cancer
1 year ago
We came out of the cycle with one normal fertilised egg, should we get it tested for genetic abnormalities?
It looks like I have a polyp... we only have one egg after a round of IVF stims. Should I do as much as possible to make sure the uterine environment is perfect and risk the embryo dying in the genetic testing/freezing/thawing process? Or should we just throw caution to the wind and try a fresh transfer
It looks like I have a polyp... we only have one egg after a round of IVF stims. Should I do as much as possible to make sure the uterine environment is perfect and risk the embryo dying in the genetic testing/freezing/thawing process? Or should we just throw caution to the wind and try a fresh transfer
Venster
in
Fertility Network UK
1 year ago
Genetic testing for ADHD and Anxiety?
Does anyone have experience with getting genetic testing for their child to help with diagnosis and medication management? I'm just learning this is available and I'm trying to do some research on what tests might actually provide useful information. Thanks!
Does anyone have experience with getting genetic testing for their child to help with diagnosis and medication management? I'm just learning this is available and I'm trying to do some research on what tests might actually provide useful information. Thanks!
MA_CHADD_Dad
in
CHADD's ADHD Parents Together
1 year ago
Webinar: Research into inherited retinal disease and the benefits of genetic counselling
Research optometrist Shelley Black and genetic counsellor Claire Kirk join us from the Northern Ireland Clinical Research Network (NICRN) this month for our second My Macular and Me webinar. Shelley will be sharing information on the latest macular and inherited retinal disease research, while Claire
Research optometrist Shelley Black and genetic counsellor Claire Kirk join us from the Northern Ireland Clinical Research Network (NICRN) this month for our second My Macular and Me webinar. Shelley will be sharing information on the latest macular and inherited retinal disease research, while Claire
Carol_MacularSociety
Partner
in
Macular Society
9 months ago
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