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Thanks for that info LG. I have read about Alpha Lipoid Acid before and wondered about taking it. I spend a lot as it is on supps so I didn’t rush out to get any. So, you sound like you recommend it?
I know when things ‘work’ for me because when I run out of something and can’t afford to buy any for awhile I will notice the difference with my symptoms. e.g. Omega 3 and Multi B.
Although I am trying to keep things to a minimum while on Tx, antioxidants really are vital.
QLD Australia ☀️
G3a HCV 35 yrs Tx naive
Started Sof/Dac 13/01/16Dec ’15
AST 70
ALT 89
GGT 124
Fibroscore 8.5
F1-F2
13 Feb’16 VL UND
AST 24
ALT 26
GGT 50HHi LG, if your blood work shows you are deficient in B12 – then usually a B12 shot from the Dr is recommended. Otherwise, my understanding is that the B’s are better taken as a ‘complex’ – Multi B slow release. They don’t all carry out the same functions and finding a good balance can be hard, its always recommended that B12 needs Folate (better form for absorption than Folic Acid) and B6; in a multi, choline and biotin are very important but often these things are left out in some brands, also since Vitamins B (and C) are water-soluble, any excess is flushed straight out of the body. So, taking a max dose multi that isn’t slowly released into your system through the day means your body would digest it, assimilate what it needs and flush the rest out – big waste. If you just want B12 (with folate and B6) on its own the sub-lingual forms and liquids are assimilated faster.
As you say it’s all very complex
Come on you did intend the pun didn’t you 
QLD Australia ☀️
G3a HCV 35 yrs Tx naive
Started Sof/Dac 13/01/16Dec ’15
AST 70
ALT 89
GGT 124
Fibroscore 8.5
F1-F2
13 Feb’16 VL UND
AST 24
ALT 26
GGT 50HHi CJ, and others,
many years ago (199
I was told Betacarotene was helpful. I was told Interferon cured HepC as well, but…….I think the reasoning was that it released as much Vitamin B??? as the body needed and the rest journeyed out in the urine?
Not suggesting Betacarotene!!
Tried search on this site and it is not mentioned.
Maybe someone else knows?
Yours and all the best with treatment,
J.
Thanks Chejai, Very helpful
What pun?
Hi Sabrecat, betacarotene ( a carotenoid) is the precursor to Vitamin A, it’s what gives carrots, pumpkin, sweet potato, fruits etc., their yellow/orange colour, it is found in lots of greens too. It’s absorbed in the stomach lining and converted to Vitamin A (retinol) – a fat-soluble vitamin (like E), not water-soluble like B & C, hence Vitamin A and E are stored in the liver and fat cells.
Vitamin A is important for healthy mucous membranes (e.g. mouth, throat, lungs), skin, eyesight e.g. for night ‘blindness’, and the immune system. Betacarotene is not an ‘essential’ vitamin ( vitamins and nutrients not synthesised by the body, required through diet) but Vitamin A is. It is an antioxidant, betacarotene from food will be absorbed only in the quantity the body needs, but supplements can cause build-up if too high.Some vegans who get carried away with juicing carrots can end up with a nasty looking side-effect of orange skin! So, can people who take high doses of synthetic carotenoids. It shouldn’t be taken at the same time as Vitamin B Complex because it reduces the effect of Niacin – vitamin B3. It’s suggested Carotenoids are better taken with Vit C, E, Selenium and Zinc. It is safer to take betacarotene (either natural or synthetic) than Vitamin A if you have liver problems because of the risk of Vitamin A build-up in the liver is very toxic.
It interacts with cholesterol lowering drugs e.g. statins; weight loss pills.
Smokers, apparently should be very careful taking it as a supplement because some research has indicated higher risk of lung cancer, since smokers are already at ‘high risk’ it’s difficult to analyse the reasons for this result. So, it’s just advised that smokers don’t take this supplement.
Therefore, given our HepC compromised liver function, it’s best not to take Vitamin A supplements and if you really aren’t eating your colourful fruits and veggies then betacarotene is safer.
Ok, enough of my waffling
QLD Australia ☀️
G3a HCV 35 yrs Tx naive
Started Sof/Dac 13/01/16Dec ’15
AST 70
ALT 89
GGT 124
Fibroscore 8.5
F1-F2
13 Feb’16 VL UND
AST 24
ALT 26
GGT 50HPat, so sorry to hear that your GP put you through additional stress at a time when they should be supporting you.
But glad to hear that GP2U were able to assist both with prescribing and support with your chemist. Thank goodness they were available for you and it is reassuring to hear that at least some medical practices still have their patients interests at heart.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
I almost feel like ripping open the rant banana at the moment, but then I realise with sadness that in slightly less than 5 weeks Australian GPs like Pat’s (and some others) will be able to prescribe DAAs on PBS either with a bit of extra training or in consultation with a specialist…..and I wonder about some of the specialists too. The omens as to the success of this do not look entirely bright to me for a couple of reasons:
– Maybe they are being honest in knowing nothing about HCV; in this case I suppose there is the possibility that they can learn about it but from the stories I’ve read here there doesn’t appear to be any enthusiasm to do so.
– They are just anti-generics and will suddenly become knowledgable and compliant with the new requirements once they are able to supply PBS approved patented medications.
In either case, I sense a lack of care for their patients health and wellbeing mixed with what appears to be distaste and judgemental behaviour regarding patients with HCV. Not good signs!
OTOH I do know and hear of good GPs (and specialists) who are working with what we have now or watching with interest and learning as mine seems to be. I hope they turn out to be just the tip of the iceberg indicating the vast silent majority and in the future those with HCV can go to see their doctor with the expectation that they will be treated the same as someone with bronchitis or similar.
Edit: Rereading this 13 months later I realise I was far too pessimistic and that Australia’s doctors have stepped up to the challenge admirably. From the latest available Kirby Institute report on treatment:
The total number of DAA initiations in 2016 (March-December) is estimated to be between 30,390 and 33,390.
http://www.ashm.org.au/Documents/Kirby_HepC_Newsletter_Issue6.pdf
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
Hmmm… thyroid med, levothyroxine comes back yellow on the dac. Should i quit taking it? Didn’t quite understand what I was reading. The color code helps.
thanks all. 25mcg take in the morning with blood pressure med, take sof/dac in the eveningI’d just sent you this link in another thread.
I’m not a doctor so you should discuss this situation with one before stopping your medication. Reading the warning it seems that there is a possibility that Daclatasvir may (potentially) effect Levothyroxine rather than the other way round. It may be that you need closer monitoring of your thyroid condition during treatment and possibly a different dose of levothyroxine or maybe there is an alternative drug you could use that wouldn’t interact? But you need advice from a doctor.
G3a since ’78 – Dx ’12 – F4 (2xHCC)
24wk Tx – PEG/Riba/Dac 2013 relapsed
24wk Tx – Generic Sof/Dac/Riba 2015/16 relapsed
16wk Tx – 12/01/17 -> 03/05/17 NS3/NS5a + Generic Sof
SVR7 – 22/06/17 UND
SRV12 – 27/07/17 UND
SVR24 – 26/10/17 UND
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