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Chorionic villus sampling (CVS)
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missed miscarriage - I need some advice
hello, On Wednesday I had my first pregnancy scan at 7w2d. An empty pregnancy sac is all they found. My hcg on Wednesday was 914, today it is 893. I have been told to stop all medication. anyone with a similar experience, when did you start miscarrying after stopping meds? im so scared to miscarry
hello, On Wednesday I had my first pregnancy scan at 7w2d. An empty pregnancy sac is all they found. My hcg on Wednesday was 914, today it is 893. I have been told to stop all medication. anyone with a similar experience, when did you start miscarrying after stopping meds? im so scared to miscarry
Bee_86
in
Fertility Network UK
6 months ago
Measles
With info about measles cases increases I wondered if anyone had experience of being vaccinated against measles since RA diagnosis. I thought I was vaccinated as a child (pre MMR vaccine) but GP doesn't have a record of it.Thanks in advance for any info
With info about measles cases increases I wondered if anyone had experience of being vaccinated against measles since RA diagnosis. I thought I was vaccinated as a child (pre MMR vaccine) but GP doesn't have a record of it.Thanks in advance for any info
Sky42
in
NRAS
5 months ago
Shingles pain
I've had shingles with continuing pain. Wounds like a burn and a scratch are taking ages to heal. I am older, 66, and I know this can happen. Any suggestions for tests I could ask for and is there any point asking for them. Best wishes Fiona
I've had shingles with continuing pain. Wounds like a burn and a scratch are taking ages to heal. I am older, 66, and I know this can happen. Any suggestions for tests I could ask for and is there any point asking for them. Best wishes Fiona
FinneUK
in
Thyroid UK
5 months ago
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Should I be worried?
Hi All, my Haemo Lady, just called me with my Bone Marrow Biopsy results, She, said they were heavily infiltrated with CLL. A recent body scan also showed a large lump in my stomach, she is not sure if it is related to my CLL, or perhaps an aggressive lymphoma. She has ordered a needle biopsy of this
Hi All, my Haemo Lady, just called me with my Bone Marrow Biopsy results, She, said they were heavily infiltrated with CLL. A recent body scan also showed a large lump in my stomach, she is not sure if it is related to my CLL, or perhaps an aggressive lymphoma. She has ordered a needle biopsy of this
Vindicatrix
in
CLL Support
6 months ago
Tacrolimus vs cyclosporin
Hi, I am currently working with my rheumatologist to plan for second pregnancy. My daughter is 3.5 years old and I was on tacrolimus during my pregnancy (I usually take MMF). I remained relatively well and stable throughout but there were alot of issues with maintaining the tacrolimus concentration
Hi, I am currently working with my rheumatologist to plan for second pregnancy. My daughter is 3.5 years old and I was on tacrolimus during my pregnancy (I usually take MMF). I remained relatively well and stable throughout but there were alot of issues with maintaining the tacrolimus concentration
SonyaNME
in
LUPUS UK
23 days ago
Good News!!!
My dr. approved the buprenorphine for me. I am thinking positive that it will work. She is giving me the patch. I am excited. I have to discontinue the horizant though which surprised me and of course discontinue the oxycodone. Hopefully now you won't have to listen to me complaining and I will
My dr. approved the buprenorphine for me. I am thinking positive that it will work. She is giving me the patch. I am excited. I have to discontinue the horizant though which surprised me and of course discontinue the oxycodone. Hopefully now you won't have to listen to me complaining and I will
lorri214
in
Restless Legs Syndrome
27 days ago
itching
I had a transplant 18 months ago and 6 days ago the hospital reduced my Tacrolimus and increased my Prednisolone to improve my kidney function (although it was no worse than it has been since the transplant). I’m gradually increasing the Tac and decreasing the Prednisolone but today lve started itching
I had a transplant 18 months ago and 6 days ago the hospital reduced my Tacrolimus and increased my Prednisolone to improve my kidney function (although it was no worse than it has been since the transplant). I’m gradually increasing the Tac and decreasing the Prednisolone but today lve started itching
Pie-eater
in
British Liver Trust
28 days ago
venetoclax and obinutuzumab treatment for cll
Hi, I have finished the above 12 months treatment for cll tp53 mutated, I now have 2 monthly checks and my lymphocytes are low, is this a cause for concern?
Hi, I have finished the above 12 months treatment for cll tp53 mutated, I now have 2 monthly checks and my lymphocytes are low, is this a cause for concern?
dellkota
in
CLL Support
6 months ago
First six-month blood test, and my lymphocytes have gone down!
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
Jazzandblues
in
CLL Support
6 months ago
Nose sprays for colds etc
I feel as if a have a cold brewing. Some time ago there were posts of a spray used in nose. Flu Guard ? I am not sure. I think a Vick one too. Could anyone advise please. Wish to nip in the bud. Thank you.
I feel as if a have a cold brewing. Some time ago there were posts of a spray used in nose. Flu Guard ? I am not sure. I think a Vick one too. Could anyone advise please. Wish to nip in the bud. Thank you.
Dottie11
in
Lung Conditions Community Forum
5 months ago
Vasculitis in the pancreas?
Has anyone with GPA or MPA been diagnosed with pancreatic issues due to vasculitis? Hubby had has GPA for 15 years, kidney transplant and sinus involvement and most often in remission until now. He has lost 40 pounds( not trying) and must take enzymes to digest food with a very bland diet. All this happened
Has anyone with GPA or MPA been diagnosed with pancreatic issues due to vasculitis? Hubby had has GPA for 15 years, kidney transplant and sinus involvement and most often in remission until now. He has lost 40 pounds( not trying) and must take enzymes to digest food with a very bland diet. All this happened
Sandalsforever
in
Vasculitis UK
1 month ago
Slow rising HCG… 6 weeks
Hello, To update since my last post, I’m currently 6+3 with painfully slow rising HCG… Need some positive stories that are similar to mine as I can’t bear this limbo! I transferred x2 day 7 embryos on the 4th Dec via FET. My betas have been as follows: 15.12 - 11dp7dt - 33 18.22 - 14dp7dt - 56
Hello, To update since my last post, I’m currently 6+3 with painfully slow rising HCG… Need some positive stories that are similar to mine as I can’t bear this limbo! I transferred x2 day 7 embryos on the 4th Dec via FET. My betas have been as follows: 15.12 - 11dp7dt - 33 18.22 - 14dp7dt - 56
Kg44
in
Fertility Network UK
6 months ago
Heading for transfer no.6 - protocol modifications
So today I had my follow up appt after 5th failed transfer. Was hoping mr Dr would suggest something new and boy has he done that! 😊😊 5th transfer I had HCG wash before transfer but no other additional tests/treatments. This time I’m having clexane injections, prednisolone, oestrogen patches instead
So today I had my follow up appt after 5th failed transfer. Was hoping mr Dr would suggest something new and boy has he done that! 😊😊 5th transfer I had HCG wash before transfer but no other additional tests/treatments. This time I’m having clexane injections, prednisolone, oestrogen patches instead
Doodlebug23
in
Fertility Network UK
6 months ago
CLL Patients -- Venclexta
I am looking for CLL patients in the U.S. who have been diagnosed within 3-4 years and who are taking Venclexta as their treatment. I work with an organization (Patient Power) that shares patient stories to help advocate and educate others on various cancers. By sharing your journey, you can help support
I am looking for CLL patients in the U.S. who have been diagnosed within 3-4 years and who are taking Venclexta as their treatment. I work with an organization (Patient Power) that shares patient stories to help advocate and educate others on various cancers. By sharing your journey, you can help support
AlexCam
in
CLL Support
6 months ago
it’s been a rough six months.
I’m tired of winning the sickness lottery. I swear it’s been one thing after another for five months. Bad cold, chronic inflammation of my eyes (non-ms) which caused sores on my right eye, Covid, extreme vertigo that returned me to the ER, another cold and now shingles. Fortunately the shingles aren
I’m tired of winning the sickness lottery. I swear it’s been one thing after another for five months. Bad cold, chronic inflammation of my eyes (non-ms) which caused sores on my right eye, Covid, extreme vertigo that returned me to the ER, another cold and now shingles. Fortunately the shingles aren
StacyHayward
in
My MSAA Community
5 months ago
Nasal / Sinus problems and Bad Smell?
I just wanted to ask about this, as had pain in the nose/cold only on the right side, (which has since gone) all round the eyes, and top of the nose, which I am guessing is Sinusitis? The odd thing is, is that all I can smell is what can only be described as 'cow sh*t' whenever I blow my nose, or sometimes
I just wanted to ask about this, as had pain in the nose/cold only on the right side, (which has since gone) all round the eyes, and top of the nose, which I am guessing is Sinusitis? The odd thing is, is that all I can smell is what can only be described as 'cow sh*t' whenever I blow my nose, or sometimes
Jack76
in
Men's Health Forum
5 months ago
Measles risk
Hi all, Just watched the news and they said they were worried about a measles outbreak. Thanks to low vaccination rates. As a commuter, what should I think/do? best, Nix
Hi all, Just watched the news and they said they were worried about a measles outbreak. Thanks to low vaccination rates. As a commuter, what should I think/do? best, Nix
BellaBee10
in
CLL Support
5 months ago
Measles outbreak
Hi, not sure if I'm being silly so looking for abit of reassurance. I'm on rituximab, azathioprine and prednisolone. I'm up-to-date with vaccinations bit concerned about the measles outbreak in my area. Am I at risk due to being immunocompromised?
Hi, not sure if I'm being silly so looking for abit of reassurance. I'm on rituximab, azathioprine and prednisolone. I'm up-to-date with vaccinations bit concerned about the measles outbreak in my area. Am I at risk due to being immunocompromised?
Vqueen
in
Vasculitis UK
5 months ago
Shingles jab
Hi everyone, just had second shingles vaccine and suddenly thought should I stop taking methotrexate this week also on sulfasalazine as is recommended after covid jab, I didn't stop taking meds after the first shingles jab,it just didn't even enter my head, think I'm losing it 😅 wishing you all as much
Hi everyone, just had second shingles vaccine and suddenly thought should I stop taking methotrexate this week also on sulfasalazine as is recommended after covid jab, I didn't stop taking meds after the first shingles jab,it just didn't even enter my head, think I'm losing it 😅 wishing you all as much
Jeremycfc
in
NRAS
5 months ago
New to the group. Should I worry concerning my latest blood results?
New to the group. First post even if I regularly read what is posted. Dx in March 2023. But CLL for at least 2 years. Unmutated, triso 12 and q (14,19). On W&W. 53 years old. I had an appointment with my Cll doctor one month ago and a bit worried. Wbc 48 000 Monocytes 12000 ALC 29 000 LDH 550 I understood
New to the group. First post even if I regularly read what is posted. Dx in March 2023. But CLL for at least 2 years. Unmutated, triso 12 and q (14,19). On W&W. 53 years old. I had an appointment with my Cll doctor one month ago and a bit worried. Wbc 48 000 Monocytes 12000 ALC 29 000 LDH 550 I understood
povhgc
in
CLL Support
7 months ago
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