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recurrence of viral meningitis
Hi, I am new to posting! I first had VM in 2014 and spent a week in hospital where I had a lumber puncture to confirm diagnosis. For several months I had headaches and tingling in my legs. Apart from tiredness my recovery was not too bad. About a month ago I started having back pain and headaches.
Hi, I am new to posting! I first had VM in 2014 and spent a week in hospital where I had a lumber puncture to confirm diagnosis. For several months I had headaches and tingling in my legs. Apart from tiredness my recovery was not too bad. About a month ago I started having back pain and headaches.
fran39
in
Meningitis Now
8 years ago
Is Acyclovir ok to take with HU?
Can we take antivirals for herpes outbreaks? I can call my dr tomorrow but thought someone might know. Thanks
Can we take antivirals for herpes outbreaks? I can call my dr tomorrow but thought someone might know. Thanks
DH65
in
MPN Voice
8 years ago
Itchy skin
Hi first post to this site though I've read others and it doesn't appear that any post is seen as trivial. I was diagnose with nhl about 13 years ago which was later classified as cll. After initial chlorambucil treatment I was on w and w until last year when my white cell and neutrophils count were
Hi first post to this site though I've read others and it doesn't appear that any post is seen as trivial. I was diagnose with nhl about 13 years ago which was later classified as cll. After initial chlorambucil treatment I was on w and w until last year when my white cell and neutrophils count were
Lolleper
in
CLL Support
8 years ago
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Starting Ibrutinib
Hello all, I've been w&w for 6 years and now have several bothersome nodes, severe fatigue and labs are indicating CLL progression. Due to my non-mutated status the doctors at MDA gave me the choice of ibrutinib, or a trial of ibrutinib w/ venetoclax. I opted for the ibrutinib alone and will start
Hello all, I've been w&w for 6 years and now have several bothersome nodes, severe fatigue and labs are indicating CLL progression. Due to my non-mutated status the doctors at MDA gave me the choice of ibrutinib, or a trial of ibrutinib w/ venetoclax. I opted for the ibrutinib alone and will start
kimiD
in
CLL Support
8 years ago
First outbreak of herpes
I'm In my first outbreak and in soo much pain. My jobs physically demanding so I'm off work. I can't even drive my car. I know everyone says the breakouts will not be as server as the first one but im worried about keep needing time off work and what to say to them. Also how long does breakout last for
I'm In my first outbreak and in soo much pain. My jobs physically demanding so I'm off work. I can't even drive my car. I know everyone says the breakouts will not be as server as the first one but im worried about keep needing time off work and what to say to them. Also how long does breakout last for
alice87
in
BASHH
8 years ago
Aciclovir mood swings
i presume that most of us are on immunosuppressive medications so when something like shingles comes along they deal with it quite agressively. i have a suspected shingles rash and my doctors put me on Aciclovir 800mg 5 times a day and since then I have been feeling quite bad- hysterical crying, mood
i presume that most of us are on immunosuppressive medications so when something like shingles comes along they deal with it quite agressively. i have a suspected shingles rash and my doctors put me on Aciclovir 800mg 5 times a day and since then I have been feeling quite bad- hysterical crying, mood
maeows
in
LUPUS UK
8 years ago
Exposure to Chickenpox
I know this subject has been discussed a number of times in the past, although there appears to be no official guidance on the Vasculitis UK website. Clearly the big risk in immunosuppressed people is if you have never had it and you are exposed to it. However if you have already had chickenpox a child
I know this subject has been discussed a number of times in the past, although there appears to be no official guidance on the Vasculitis UK website. Clearly the big risk in immunosuppressed people is if you have never had it and you are exposed to it. However if you have already had chickenpox a child
Chris-Bromsgrove
in
Vasculitis UK
8 years ago
Newbie
Hi I have been a 'browser' here for a while but never posted for personal reasons. I am 64 (65 next week) and was 32 when I was diagnosed with ET. I think I must have had every treatment available in the last 32 years; radio active phosphorus injections, interferon, Hydrea, Busulphan, Anagrelide, aspirin
Hi I have been a 'browser' here for a while but never posted for personal reasons. I am 64 (65 next week) and was 32 when I was diagnosed with ET. I think I must have had every treatment available in the last 32 years; radio active phosphorus injections, interferon, Hydrea, Busulphan, Anagrelide, aspirin
Wychwoodbabe
in
MPN Voice
8 years ago
Advice on T3 dose
I posted my results recently but I thought as I have just received my T3 in the post I would re post them and ask for advise on dosage. I am not on any medication except for vitamins. TSH 2.79 0.35 – 5 mu/L T4 12.7 9.00 – 22.00pmol/L T3 3.9
I posted my results recently but I thought as I have just received my T3 in the post I would re post them and ask for advise on dosage. I am not on any medication except for vitamins. TSH 2.79 0.35 – 5 mu/L T4 12.7 9.00 – 22.00pmol/L T3 3.9
gisa12
in
Thyroid UK
8 years ago
Support for a newbie
Hello, I was diagnosed with viral meningitis in February and after 8 days in hospital treating VZV with acyclovir and receiving morphine and T3 for pain I was released. I have been off my medicine for a month now and have been struggling. I will be totally fine one week and the next I will have the horrible
Hello, I was diagnosed with viral meningitis in February and after 8 days in hospital treating VZV with acyclovir and receiving morphine and T3 for pain I was released. I have been off my medicine for a month now and have been struggling. I will be totally fine one week and the next I will have the horrible
Hidden
in
Meningitis Now
8 years ago
should i take Aciclovir Tablets 800mg
hi was put on this tablets and they are making me sick have stopped taking them
hi was put on this tablets and they are making me sick have stopped taking them
iowssgroup
in
Diabetes Research & Wellness Foundation
9 years ago
Advise please... Sorry, long post!
Hi, I have lurked for a while trying to pluck up courage to post... My name is Laura and I am 53. I was very ill 10 months ago, taken into hospital suffering from Confusion. I couldn't swallow so didn't eat anything or drink anything for a good week. I didn't recognise who my hubby and Sister were, was
Hi, I have lurked for a while trying to pluck up courage to post... My name is Laura and I am 53. I was very ill 10 months ago, taken into hospital suffering from Confusion. I couldn't swallow so didn't eat anything or drink anything for a good week. I didn't recognise who my hubby and Sister were, was
Hidden
in
Hughes Syndrome APS Forum
9 years ago
Another episode
Ok it has happened again. I moved to a new community, and wanted to get established with a Physician. My headaches and neck / back ache and the burning feeling has returned. Upon meeting the doctor I explained I have Mollaretts meningitis and he said ( what is that). I explained it is reoccurring meningitis
Ok it has happened again. I moved to a new community, and wanted to get established with a Physician. My headaches and neck / back ache and the burning feeling has returned. Upon meeting the doctor I explained I have Mollaretts meningitis and he said ( what is that). I explained it is reoccurring meningitis
sopie
in
Meningitis Now
9 years ago
Hi, I am new to this site and thyroid issues so I'd be grateful for some advice as I have my first endo appointment this week.
I was diagonised with stage 4 Hodgkin's lymphoma in oct 2012, 7 different types of chemo and 2 stem cell transplants later I'm still here and hodgkins free for 11 months. Due to treatments I have a non functioning spleen so I was on 961mg septrin, 500mg of amoxicillin & Aciclovir every day. Many meds
I was diagonised with stage 4 Hodgkin's lymphoma in oct 2012, 7 different types of chemo and 2 stem cell transplants later I'm still here and hodgkins free for 11 months. Due to treatments I have a non functioning spleen so I was on 961mg septrin, 500mg of amoxicillin & Aciclovir every day. Many meds
Hidden
in
Thyroid UK
9 years ago
Acyclovir and PMR?
Hello fellow travellers, this is my first post. I have had PMR for almost 2years now and recently got a whacking dose of Shingles and was given Acyclovir tablets for a week, I soon experienced a complete absence of pain, and although very sore, an absence of fatigue. I reduced my prednisolone tablets
Hello fellow travellers, this is my first post. I have had PMR for almost 2years now and recently got a whacking dose of Shingles and was given Acyclovir tablets for a week, I soon experienced a complete absence of pain, and although very sore, an absence of fatigue. I reduced my prednisolone tablets
Zoshie
in
PMRGCAuk
9 years ago
Acyclovir - Anti-virals? B12 interaction?
Hi all, I am investigating new routes along with B12. I have been suggested Acyclovir 400mg 3x per day for 3 months in case it is a viral illness. Does anyone know anything about this as I am concerened about taking prescription meds and worried it will interact badly with my B12? This article I
Hi all, I am investigating new routes along with B12. I have been suggested Acyclovir 400mg 3x per day for 3 months in case it is a viral illness. Does anyone know anything about this as I am concerened about taking prescription meds and worried it will interact badly with my B12? This article I
Qunk
in
Pernicious Anaemia Society
9 years ago
Can't get off the couch!
I'm new this is my first post, I was diagnosed around 2000 after a very traumatic divorce and many years of stress my immune system was shot and my herpes problem was out of control I went to a Chinese Doctor and she said the Herpes was a problem in my gut the health of your dictates the health of your
I'm new this is my first post, I was diagnosed around 2000 after a very traumatic divorce and many years of stress my immune system was shot and my herpes problem was out of control I went to a Chinese Doctor and she said the Herpes was a problem in my gut the health of your dictates the health of your
Angiebaby9
in
Thyroid UK
10 years ago
FLAIR Trial - FCR for me
Apologies first for the slowness of getting my post out here but thankfully the roller-coaster has just slowed down enough for a few words on my progress with the FLAIR trial. As explained before FLAIR compares IR (Ibrutinib plus Rituximab) against FCR (Fludarabine, Cyclophosphamide and Rituximab):
Apologies first for the slowness of getting my post out here but thankfully the roller-coaster has just slowed down enough for a few words on my progress with the FLAIR trial. As explained before FLAIR compares IR (Ibrutinib plus Rituximab) against FCR (Fludarabine, Cyclophosphamide and Rituximab):
Ernest2
in
CLL Support
10 years ago
wobbily moments??
As some of you will know, because you have kindly supported and responded to me and my queries........ more............. my husband has now overcome shingles,(except for one 6mm lesion which has remained intact for over two weeks and a biopsy will be carried out next week). he will re-start ibrutinib
As some of you will know, because you have kindly supported and responded to me and my queries........ more............. my husband has now overcome shingles,(except for one 6mm lesion which has remained intact for over two weeks and a biopsy will be carried out next week). he will re-start ibrutinib
lartington
in
CLL Support
10 years ago
Anagrelide and herpes
I was on hydroxyurea and had a bad case of herpes on my face. Now into about 5th week of anagrelide and now bad herpes on face. Taking aciclovir tabs but seems to be taking a while to clear. Has anyone else experienced herpes as a result of taking anagrelide and if so, any advice? Tinkerbell13
I was on hydroxyurea and had a bad case of herpes on my face. Now into about 5th week of anagrelide and now bad herpes on face. Taking aciclovir tabs but seems to be taking a while to clear. Has anyone else experienced herpes as a result of taking anagrelide and if so, any advice? Tinkerbell13
Tinkerbell13
in
MPN Voice
10 years ago
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