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Change of access of treatment to Covid treatments.
I have attached an email which I received today. It might be relevant to some of you: 'You may have previously received a letter or email explaining that you might be suitable for treatments if you get COVID and how to get treatment, if required. We are writing again because the way that you access
I have attached an email which I received today. It might be relevant to some of you: 'You may have previously received a letter or email explaining that you might be suitable for treatments if you get COVID and how to get treatment, if required. We are writing again because the way that you access
Moomin8
in
NRAS
1 year ago
update on Covid treatments
I received a email today with updated information. This is just in case people don’t receive emails from the nhs. As of 27th June you will no longer be contacted, if you submit a positive test. The onus is on the patient to contact either their gp or specialist to consider if they should receive antivirals
I received a email today with updated information. This is just in case people don’t receive emails from the nhs. As of 27th June you will no longer be contacted, if you submit a positive test. The onus is on the patient to contact either their gp or specialist to consider if they should receive antivirals
Runrig01
in
NRAS
1 year ago
1st Long protocol ivf cycle fail
Hi I'm 39 years old and we have been through a long protocol donor sperm ivf cycle which failed, we got 6eggs and only 1 fertilised which was a top grade embryo which was transferred on day 3.We had our review consultation today and consultation said all my tests through that cycle was great for my age
Hi I'm 39 years old and we have been through a long protocol donor sperm ivf cycle which failed, we got 6eggs and only 1 fertilised which was a top grade embryo which was transferred on day 3.We had our review consultation today and consultation said all my tests through that cycle was great for my age
Curri
in
Fertility Network UK
7 months ago
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NHS COVID changing
Email from NHS England saying from 27th June they will no longer contact you if you are classed as suitable for antivirals. Instead you contact your GP,hospital dept or NHS covid telephone number. Also from 1st October the way we get the tests may be changing? Yesterday someone told me that covid jabs
Email from NHS England saying from 27th June they will no longer contact you if you are classed as suitable for antivirals. Instead you contact your GP,hospital dept or NHS covid telephone number. Also from 1st October the way we get the tests may be changing? Yesterday someone told me that covid jabs
Jackie1947
in
NRAS
1 year ago
Flu jab
As flu vaccine season will soon be on us I was wondering if my husband will get a flu jab this year (I have asthma, therefore I qualify). In previous years he has been eligible but I believe the criteria has changed. Any thoughts?
As flu vaccine season will soon be on us I was wondering if my husband will get a flu jab this year (I have asthma, therefore I qualify). In previous years he has been eligible but I believe the criteria has changed. Any thoughts?
Mayneffy
in
Asthma Community Forum
10 months ago
Just started NHS referral process for IVF / ICSI and looking for some advice
My partner (32M) and I (32F) have been trying for a year with no luck. He has been diagnosed with low morphology (1.5-3% over 3 tests). He has a very high count and normal progressive motility and my tests all came back fine, except for a small fibroid which the clinic said wasn’t an issue because of
My partner (32M) and I (32F) have been trying for a year with no luck. He has been diagnosed with low morphology (1.5-3% over 3 tests). He has a very high count and normal progressive motility and my tests all came back fine, except for a small fibroid which the clinic said wasn’t an issue because of
zbexbj
in
Fertility Network UK
7 months ago
Covid Treatments NHS Changes
Just had an email from the NHS saying that the Covid treatment contact is changing from the 27th June We are writing again because the way that you access treatment will change from Tuesday 27 June 2023. If you get COVID from Tuesday 27 June 2023: You will no longer be automatically contacted by
Just had an email from the NHS saying that the Covid treatment contact is changing from the 27th June We are writing again because the way that you access treatment will change from Tuesday 27 June 2023. If you get COVID from Tuesday 27 June 2023: You will no longer be automatically contacted by
Alan7690
in
PMRGCAuk
1 year ago
Email from NHS - suddenly COVID vulnerable
*****UPDATE******* Well I asked the Dr, about change in status. They have no idea. Then when I got home, I found that I have now been sent free COVID tests in the post. ****** anyone else had an email from the NHS, stating they are vulnerable to COVID and qualify for treatment if it's contracted? (It
*****UPDATE******* Well I asked the Dr, about change in status. They have no idea. Then when I got home, I found that I have now been sent free COVID tests in the post. ****** anyone else had an email from the NHS, stating they are vulnerable to COVID and qualify for treatment if it's contracted? (It
Wetsuiter
in
Thyroid UK
1 year ago
Small cell vasculitis and epidermis demostosis
Back in November last year,I got covered in a rash which was awful . Treatment initially was antibiotics and suspect strep infection. And then as it kept reappearing and visits to dermatology put down as vasculitis caused by covid vaccine of which I still don't really buy into. Here we are 8 months
Back in November last year,I got covered in a rash which was awful . Treatment initially was antibiotics and suspect strep infection. And then as it kept reappearing and visits to dermatology put down as vasculitis caused by covid vaccine of which I still don't really buy into. Here we are 8 months
cartwheels
in
CLL Support
1 year ago
Options for Recurrent PCa w/ RT Initial Therapy
Looking for options with intent to [u]cure[/u] if recurrence is limited to prostate only, pending PET-PSMA. Have read about these options: Prostatectomy/Brachytherapy/Cystoprostatectomy/Cryotherapy Anybody have any knowledge or studies that might suggest a direction? Still hoping for the possibility
Looking for options with intent to [u]cure[/u] if recurrence is limited to prostate only, pending PET-PSMA. Have read about these options: Prostatectomy/Brachytherapy/Cystoprostatectomy/Cryotherapy Anybody have any knowledge or studies that might suggest a direction? Still hoping for the possibility
Researcher50
in
Advanced Prostate Cancer
11 months ago
Prolapse surgery
I have suffered with uterine prolapse for approximately 4 years and have had a Gellhorn pessary for almost 3 years. Prolapse is now at stage 3 with more and more problems with the pessary, discomfort, burning bladder and infections. It came out so now have a larger pessary. This is even more uncomfortable
I have suffered with uterine prolapse for approximately 4 years and have had a Gellhorn pessary for almost 3 years. Prolapse is now at stage 3 with more and more problems with the pessary, discomfort, burning bladder and infections. It came out so now have a larger pessary. This is even more uncomfortable
Catsaloud
in
Women's Health
11 months ago
poor quality day 3 embryos
hi all, going through ICSI process currently - had egg collection on 1/11/23 where 4 mature eggs were collected they said they were happy with this (I’m 38 and my AMH was 3.9) the next day I got the call to say two eggs successfully fertilised, but today on day 3 the clinic called me to say both are
hi all, going through ICSI process currently - had egg collection on 1/11/23 where 4 mature eggs were collected they said they were happy with this (I’m 38 and my AMH was 3.9) the next day I got the call to say two eggs successfully fertilised, but today on day 3 the clinic called me to say both are
Whatemwears
in
Fertility Network UK
7 months ago
HU and prefibrotic myelofibrosis
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Recently diagnosed first with ET. put on 500mg hydroxyurea daily with platelets at 617. After bone marrow aspiration and biopsy, diagnosis changed to prefibrotic myelofibrosis. HU had brought platelets down to 270 but I suffered from bad side effects. Dr didn’t want to change med or dosage. I resisted
Apple238
in
CLL Support
1 year ago
W&W, Sepsis, Pneumonia,Cellulitis, FEVERS ! - ???
Had my first visit to the Hematologist . He was patient, he was kind , he was very informative and most important to me , he asked me what my questions and concerns were. Unlike a lot of doctors I worked with as a nurse , ( who MANY have seemed to have lost their Sensitivity chip ) , he was full
Had my first visit to the Hematologist . He was patient, he was kind , he was very informative and most important to me , he asked me what my questions and concerns were. Unlike a lot of doctors I worked with as a nurse , ( who MANY have seemed to have lost their Sensitivity chip ) , he was full
Sillysand
in
CLL Support
1 year ago
Looks like even the covid vaccination has 2 sides to the story. (Rats. And just yesterday I had my 3rd booster.)
IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein May 17 https://pubmed.ncbi.nlm.nih.gov/37243095/ Abstract "Less than a year after the global emergence of the coronavirus SARS-CoV-2, a novel vaccine platform based on mRNA technology was
IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein May 17 https://pubmed.ncbi.nlm.nih.gov/37243095/ Abstract "Less than a year after the global emergence of the coronavirus SARS-CoV-2, a novel vaccine platform based on mRNA technology was
MBAnderson
in
Cure Parkinson's
1 year ago
How can I reduce the swelling in my foot and ankle?
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
spartacus101
in
NRAS
1 year ago
Off meds because of Shingles, but maybe answers to other concerns…..
So about 18 months ago I started feeling nauseous occasionally. Moved taking my mtx tablets to the evening, and upped folic acid from 1 a week to 3, then 5. Not making much difference so moved to mtx injections. Still feeling nauseous but RA team reluctant to pin on Mtx as nauseous is generally after
So about 18 months ago I started feeling nauseous occasionally. Moved taking my mtx tablets to the evening, and upped folic acid from 1 a week to 3, then 5. Not making much difference so moved to mtx injections. Still feeling nauseous but RA team reluctant to pin on Mtx as nauseous is generally after
Hollyhock123
in
NRAS
1 year ago
significant drop in platelets after Covid Shot
I am wondering if anyone else experienced this, I received my first Covid shot in April. Within the next 3 weeks I had my labs drawn for my monthly phlebotomy. Since 2016 my platelets have consistently been in the mid 700’s. After receiving the covid shot( that was the only difference in the norm)
I am wondering if anyone else experienced this, I received my first Covid shot in April. Within the next 3 weeks I had my labs drawn for my monthly phlebotomy. Since 2016 my platelets have consistently been in the mid 700’s. After receiving the covid shot( that was the only difference in the norm)
Kids0901
in
MPN Voice
1 year ago
I am so upset and don’t know where to go from here…
I went to the doctors with 3 months of pain while going for a pee, I have been on two antibiotics and none have worked. So, I made an appointment with the doctor to speak about what to do to help with the pain and find out why it was happening, or so I thought. I went in and her answer was go on the
I went to the doctors with 3 months of pain while going for a pee, I have been on two antibiotics and none have worked. So, I made an appointment with the doctor to speak about what to do to help with the pain and find out why it was happening, or so I thought. I went in and her answer was go on the
Sky342
in
Endometriosis UK
1 year ago
*Sensitive* A bit of hope for those in need
After 7 years trying to conceive, 3 ICSI cycles, 7 embryo transfers ( including 2 doubles) , 1 MMC and 5 BFN, our baby girl finally arrived in the world on Sunday the 29th October. I just wanted to thank everyone in this forum for making me feel like I wasn't alone in this difficult journey. I don't
After 7 years trying to conceive, 3 ICSI cycles, 7 embryo transfers ( including 2 doubles) , 1 MMC and 5 BFN, our baby girl finally arrived in the world on Sunday the 29th October. I just wanted to thank everyone in this forum for making me feel like I wasn't alone in this difficult journey. I don't
TrendyDove
in
Fertility Network UK
7 months ago
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