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Interferon beta-1a
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has anyone in the UK been started on the sovaldi for Hep C
Hi everyone just curious to find out if there has been anyone started on the new non interferon drug sovaldi yet..just read the NHS has delayed the decision to treat for 6mths because of the cost. I have geno type 4 and have cirhossis and was hoping to be treated ASAP as time is not in my favour to sit
Hi everyone just curious to find out if there has been anyone started on the new non interferon drug sovaldi yet..just read the NHS has delayed the decision to treat for 6mths because of the cost. I have geno type 4 and have cirhossis and was hoping to be treated ASAP as time is not in my favour to sit
ballie52
in
British Liver Trust
9 years ago
1st Endo visit
Hi, would appreciate your comments/advice.... I'm seeing an Endo on Thursday because I was diagnosed with auto immune rheumatoid arthritis and thyroiditus a few months ago. Theses are my latest bloods TSH. 0.01. (0- 5) Free T4. 31.5. (9-28) Free T3 5.5. (0-7.7) B12. 1328ng (200-900) Folate 17.2
Hi, would appreciate your comments/advice.... I'm seeing an Endo on Thursday because I was diagnosed with auto immune rheumatoid arthritis and thyroiditus a few months ago. Theses are my latest bloods TSH. 0.01. (0- 5) Free T4. 31.5. (9-28) Free T3 5.5. (0-7.7) B12. 1328ng (200-900) Folate 17.2
Trewoof
in
Thyroid UK
9 years ago
Help please to interpret test results
Comments please on the supplements I need from the test results below. I already take a good Univite brand multi vitamin and minerals daily and also: Calcium and Vitamin D3 3000mg/800IU tablets per day; 1 Solgar Ginko 60 ; 1 Beta Glucans and Beta Sitosterol to boost immune system (is this good idea
Comments please on the supplements I need from the test results below. I already take a good Univite brand multi vitamin and minerals daily and also: Calcium and Vitamin D3 3000mg/800IU tablets per day; 1 Solgar Ginko 60 ; 1 Beta Glucans and Beta Sitosterol to boost immune system (is this good idea
arty123
in
Thyroid UK
9 years ago
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Switching Hydroxiurea with Interferon alpha
I'm 54 years old and I have PV,discovered 7 years ago. Initially I was on interferon alpha one year , which I agreed very well but due high price, doc. switched on Hydrea until now. Now for 3-4 month I have possibility to use again interferon alpha. Has somebody made this changes? How have you affected
I'm 54 years old and I have PV,discovered 7 years ago. Initially I was on interferon alpha one year , which I agreed very well but due high price, doc. switched on Hydrea until now. Now for 3-4 month I have possibility to use again interferon alpha. Has somebody made this changes? How have you affected
cata
in
MPN Voice
10 years ago
should I wait to see an endocrinologist?
I have been taking medication for an MPN ( high platelets) and about 2 years ago, it was observed that I had problems with fluctuating TSH levels. I reduced the medication by over 50% ( Interferon Alpha). I currently have some symptoms of hypothyroidism ( severe eyebrow loss, hair loss, weight gain
I have been taking medication for an MPN ( high platelets) and about 2 years ago, it was observed that I had problems with fluctuating TSH levels. I reduced the medication by over 50% ( Interferon Alpha). I currently have some symptoms of hypothyroidism ( severe eyebrow loss, hair loss, weight gain
Florence1961
in
Thyroid UK
10 years ago
What is the treatment for Sweet's syndrome?
The main form of treatment for Sweet's syndrome is the steroid (corticosteroid), prednisone. After steroids, first-line treatments include colchicine and potassium iodide. They can be given instead of or alongside steroid medication. Second-line treatments include indomethacin, clofazimine, ciclosporin
The main form of treatment for Sweet's syndrome is the steroid (corticosteroid), prednisone. After steroids, first-line treatments include colchicine and potassium iodide. They can be given instead of or alongside steroid medication. Second-line treatments include indomethacin, clofazimine, ciclosporin
Shell567
Sweet's Syndrome UK
in
Sweet's Syndrome UK
10 years ago
I need your help!
Hi all.Please advise me with your experience. After 9 years of just venesections and aspirin to treat my PV, I am told it's time to start treatment to lower my platelets. As I am 47 and have always said that i don't want hydroxie because of the leukemia risk, my heam has told me it's my choice whether
Hi all.Please advise me with your experience. After 9 years of just venesections and aspirin to treat my PV, I am told it's time to start treatment to lower my platelets. As I am 47 and have always said that i don't want hydroxie because of the leukemia risk, my heam has told me it's my choice whether
harleydavidson
in
MPN Voice
10 years ago
Unfair treatm ty tent for geno type1 4 5 6
I have just read that Nice have recomended the new non interferon. treatment for hep c that we all have been waiting for...the shock is that they are not treating geno type 4 with the new drugs while most other geno types get treated...i have cirhossis and failed on interferon after 48wks of treatment
I have just read that Nice have recomended the new non interferon. treatment for hep c that we all have been waiting for...the shock is that they are not treating geno type 4 with the new drugs while most other geno types get treated...i have cirhossis and failed on interferon after 48wks of treatment
226mt
in
British Liver Trust
10 years ago
POST MENOPAUSE WOMEN - PLSE GIVE ADVICE for ANXIETY / SLEEPLESSNESS from Menopause
Others please join me.... ADVICE FROM POST MENOPAUSAL WOMAN WHO WENT THROUGH ANXIETY, MIGRAINES,ETC. Here is the good news. YOU WILL ALL GET YOUR LIFE BACK!!!!! The most severe symptoms last MAXIM 1 1/2 yrs. RE: WELLBUTRIN -wellbutrin does work! it will however cause weight gain...less than other
Others please join me.... ADVICE FROM POST MENOPAUSAL WOMAN WHO WENT THROUGH ANXIETY, MIGRAINES,ETC. Here is the good news. YOU WILL ALL GET YOUR LIFE BACK!!!!! The most severe symptoms last MAXIM 1 1/2 yrs. RE: WELLBUTRIN -wellbutrin does work! it will however cause weight gain...less than other
thegemprincess
in
Thyroid UK
10 years ago
hep c treatment
hi hope everyone is as well as could be does anyone know or been on the triple treatment for hep c genoe type 3 interferon ,ribovirin,sofosbuvir this treatment is for 13wks would like to know more about it if anyone can help thanks
hi hope everyone is as well as could be does anyone know or been on the triple treatment for hep c genoe type 3 interferon ,ribovirin,sofosbuvir this treatment is for 13wks would like to know more about it if anyone can help thanks
lippy_lou
in
British Liver Trust
10 years ago
PV side effects and denied Pegasus Interferon
Hello! Now this one is just for the ladies! I am not too sure if it is a side effect but i keep getting irregular periods and they are really getting me down now! Did anyone else get these?? I've been checked out for all sorts and have nothing but PV so I think it must be down to that as my periods have
Hello! Now this one is just for the ladies! I am not too sure if it is a side effect but i keep getting irregular periods and they are really getting me down now! Did anyone else get these?? I've been checked out for all sorts and have nothing but PV so I think it must be down to that as my periods have
noodles26
in
MPN Voice
10 years ago
Are all my symptoms Hep C related or is it something else?
Last November I had a liver review with my Consultant re. my Hep C. For various personal reasons I cannot commit to treatment and am hoping for a new drug for Genotype 3 that doesn't contain interferon to come along before I pop my clogs. I took a list of all my worsening symptoms and was sent for an
Last November I had a liver review with my Consultant re. my Hep C. For various personal reasons I cannot commit to treatment and am hoping for a new drug for Genotype 3 that doesn't contain interferon to come along before I pop my clogs. I took a list of all my worsening symptoms and was sent for an
patti62
in
British Liver Trust
10 years ago
Interferon 2a or Pegasys----how different are they regarding effect on the body and possible molecular remission?
Hi everyone, I am 74 years old, have ET, Jak2 and exon12 negative. I have been on interferon 2a for 2 1/2 years and am sick of having painful legs and lower back. My bloods are normal, platelets 250-300. I would like to stop the meds but haem is reluctant. Would there be any point in switching to Pegasys
Hi everyone, I am 74 years old, have ET, Jak2 and exon12 negative. I have been on interferon 2a for 2 1/2 years and am sick of having painful legs and lower back. My bloods are normal, platelets 250-300. I would like to stop the meds but haem is reluctant. Would there be any point in switching to Pegasys
graymare
in
MPN Voice
10 years ago
hydroxycarbamide side effects
Hello! I have been switched from interferon to hydroxycarbamide...after 1 week on 500mg a day i felt much brighter within myself...until i went to my haemotologist!my platelets had shot up!now i'm on 1g a day and having some strange side effects....migraines, upset stomach - feel like i am losing weight
Hello! I have been switched from interferon to hydroxycarbamide...after 1 week on 500mg a day i felt much brighter within myself...until i went to my haemotologist!my platelets had shot up!now i'm on 1g a day and having some strange side effects....migraines, upset stomach - feel like i am losing weight
noodles26
in
MPN Voice
10 years ago
PV Hangover!
Morning! Does anyone else wake up and feel hungover?I haven't touched a drop of alcohol and yet feel like i've had one too many cosmo's! I've been on interferon for a month now and I am just fed up of the side effects!I'm 26 and feel like i've aged 10 years within the last month!! I'm realy struggling
Morning! Does anyone else wake up and feel hungover?I haven't touched a drop of alcohol and yet feel like i've had one too many cosmo's! I've been on interferon for a month now and I am just fed up of the side effects!I'm 26 and feel like i've aged 10 years within the last month!! I'm realy struggling
noodles26
in
MPN Voice
10 years ago
Difficulty injecting Fragmin
Hello everybody, I have to inject fragmin daily and interferon 3x a week but since sunday i am struggling with the fragmin injecton. It feel like the tip of the needle just won't go into the skin as my skin is feeling very bruised from all the injections. it's strange as the interferon goes in fine
Hello everybody, I have to inject fragmin daily and interferon 3x a week but since sunday i am struggling with the fragmin injecton. It feel like the tip of the needle just won't go into the skin as my skin is feeling very bruised from all the injections. it's strange as the interferon goes in fine
noodles26
in
MPN Voice
10 years ago
Peg Interferon - Anyone found bone structure changing?
Hi The meds we are taking affect the bone. Has anyone noticed any changes in their joints / bone structure? I am on Pegylated Inteferon and I think I am noticing some changes but cannot be 100% sure. Sherry.
Hi The meds we are taking affect the bone. Has anyone noticed any changes in their joints / bone structure? I am on Pegylated Inteferon and I think I am noticing some changes but cannot be 100% sure. Sherry.
Sherry2
in
MPN Voice
10 years ago
New to PV
Hello! I have been recently diagnosed with PV and have been on Interferon for a week now but I am experiencing really achey legs, it literally feels like my bone could snap! Did anyone else experience this? I am hoping it goes soon! I am having to go to hospital for regular venesections and my blood
Hello! I have been recently diagnosed with PV and have been on Interferon for a week now but I am experiencing really achey legs, it literally feels like my bone could snap! Did anyone else experience this? I am hoping it goes soon! I am having to go to hospital for regular venesections and my blood
noodles26
in
MPN Voice
10 years ago
Considering changing from Hu to Interferon and need support to make right decision.
Diagnosed with ET Oct. 2011 and been on Hu ever since different dosages. I am doing well and now my dosage is reduced to 1gr. one day and rest week days 500mg. I am also on 75mg aspirin and Bisoprolol 1.25mg a day. My platelets are under control. Hu side effects are anxiety, fatigue, restlessness, chemo
Diagnosed with ET Oct. 2011 and been on Hu ever since different dosages. I am doing well and now my dosage is reduced to 1gr. one day and rest week days 500mg. I am also on 75mg aspirin and Bisoprolol 1.25mg a day. My platelets are under control. Hu side effects are anxiety, fatigue, restlessness, chemo
light
in
MPN Voice
10 years ago
THE IMPORTANCE OF GREEN SALADS !! = HEALTH
THE IMPORTANCE OF GREEN SALADS !! = HEALTH = Green salads are an excellent source of vitamins, minerals and fiber, but people do not generally include salads in their diet. This is because they do not realize the benefits which they can derive from them. Arugula, lettuce, romaine and other greens,
THE IMPORTANCE OF GREEN SALADS !! = HEALTH = Green salads are an excellent source of vitamins, minerals and fiber, but people do not generally include salads in their diet. This is because they do not realize the benefits which they can derive from them. Arugula, lettuce, romaine and other greens,
harsta
in
Diabetes India
10 years ago
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