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5 All-Natural Remedies To Treat Eczema Without The Doctor – The Alternative Daily (blog)


The Alternative Daily (blog)
5 All-Natural Remedies To Treat Eczema Without The Doctor
The Alternative Daily (blog)
The term basically refers to a variety of rash-like skin conditions. The symptoms of eczema include red, blotchy skin that is inflamed, irritated and itchy. Frequently, a person with the condition will scratch their skin incessantly, which can

eczema – Google News

6 Easy Techniques to Cure For Eczema at Home Without Any Side Effects

I believe that you are fully aware of the eczema symptoms and how painful and uncomfortable it could be. If you do not try to cure for eczema, or left it untreated, your eczema can spread to other part of your body. So, if you want to cure your eczema, but don’t want to risk yourself with the side effects from medications, then, using natural cure for eczema will be highly recommended.

If you are searching for the way to cure for eczema, you will find many methods for eczema treatment available. However, home remedies are considered to be the most effective method because they are easily available, and produce no side effects at all. Besides, home remedies are painless when you apply them on your eczema area.

Below are some of the home remedies that you can follow to cure for eczema symptoms.

– Soft fiber towel could be the perfect option to reduce the inflammation, since hard towel can lead to the further inflammation.

– Stream bath and sun bath are very effective way to cure for eczema. These two methods can kill the harmful bacteria in the skin, and clean the affected part as well.

– It may be a good idea for eczema sufferers to stay away from cashew nuts since it could be the cause of the skin inflammation.

– Dry skin can be the cause of eczema. So, you should stay away from humid and cold places because this situation could easily produce the dryness of skin.

– If possible, you should not use normal soap on your eczema area since it will cause more inflammation. Try to use herbal or unscented soap to clean your affected part.

– Do you know that mango can be used to cure for eczema? Just peel the mango’s skin and boil the pulp in the water. Then, allow 15 – 20 minutes for it to cool down, and apply the paste on your eczema area. Within 15 days of this treatment, you will be amazed by its improvement.

I hope that these 6 tips mentioned in this article can help you to cure for eczema. So, if you are having eczema, just try to follow these tips and see the improvement by yourself.

If you are suffering from eczema and have been desperately looking all over the internet to find a way to cure for your eczema, well, I was in this situation. You should know that searching internet is easy and don’t cost you any cents.

How to survive the holiday season without too many gut problems

The holiday season means many different things to different people, it is supposed to be a period of joy but often it really doesn’t live up to all those expectations that we often have. The media portray images of idealistic families around the Christmas tree having all their dreams come true. For some people the reality is somewhat different, Christmas can be a traumatic time and managing with all the family can be challenging, but it can also be a time when some people are alone too. Here are some tips to help you navigate your way through the period and avoid your gut spoiling the fun.

1. Tis the season to be jolly – really? You have my permission to be a Grinch too if you wish. You should not be expected to see people and be jolly, especially people who you never get along with during the rest of the year. If you don’t get on with someone then Christmas is not a time that somehow the ‘magic’ will make a difference, and likely if your inhibitions are lowered with the odd glass of Advocaat (add your choice of tipple here!) it will not end well! Suggest that you have other plans this year, make your apologies for not seeing them if you wish.

2. Scenes on TV cookery shows promote the domestic goddess, but don’t forget all those well choreographed scenes take time and lots of other people to help, likely months of planning too. Not so much of a goddess then! So don’t try to live up to this myth of being able to manage it all, you will only end up frazzled and this will likely make symptoms worse. You could have a Jacobs join – were everyone brings a different part of the dish. Or you could ask people to bring dishes from around the world, and think of others or you could go out to eat on Christmas day. Consider inviting someone who might be on their own on Christmas day. It really doesn’t have to be a traditional day – make new traditions!

Click on here to see what Nigella really thinks

Click on the image to see what Nigella really thinks.

3. Ensure you eat regularly on Christmas day – leaving hours between meals will not help, plan to have a light breakfast before your Christmas lunch – this doesn’t mean grazing all day either. Manage your portion sizes – use a smaller plate if you like your plate full and you will be just as satisfied and not over full and unable to move!

http://eczema.curemycondition.com/wp-content/uploads/2016/12/4320.jpg

4. Don’t slouch on the sofa eating snacks whilst watching those Christmas movies, let gravity help you gut and try to sit up when eating – or don’t snack, you will eat more than you realise if you are not being mindful about what you are eating. Alternatively plan how much you are going to eat and put it in a bowl so you know when you have had enough. Your body will thank you for it.

Seriously – not a good idea!!

5. Include some light activity mid afternoon if you are able – a gentle walk in the park perhaps or some games to get you moving around.

6. Family dynamics can be a rich source of conflict during the season, this can lead to arguments in the period leading up to Christmas and especially on the day itself. Arguments at mealtimes are really not advisable, this will do nothing to help your digestion. Stress causes your body to produce adrenaline, the fight or flight hormone, this is a response to conflict or dangerous situations, originally utilised so you can escape from predators. Your body is therefore NOT concentrating on digesting lunch. In the distant past a dose of indigestion was a very small price to pay to avoiding being eaten. So you might need to be assertive and lay down some ground rules for everyone to follow so that the meal can be as calm as possible.

7. Budget as much as you can. Planning is the key here and Christmas is for thinking of others, but not at the expense of experiencing anxiety at not being able to live up to their expectations. Again tell people in advance what you are planning, say that you are only going to be able to afford to do certain things – you may find that people are relieved that they don’t have to meet these expectations either.

8. Stick rigidly to your Low Fodmap foods (or other tolerated foods) before the day, so if you eat something that you react to, you possibly won’t have as severe symptoms as you would have with eating as you please for the full season.

9. Drink plenty of fluids through the day – a least six to eight cups of non carbonated drinks and if you do drink alcohol, match every alcoholic drink with a non alcoholic one – this will mean you drink less and stay hydrated at the same time. Drinking whilst eating slows the absorption of alcohol into the body. Stay within the healthy drinking guidelines (no more than 2-3 units per day) and watch mixers for fodmaps and fizz. Make a glass of water the final drink before going to bed to counteract the dehydrating effects of alcohol. Remember alcohol is a gut stimulant and hangovers won’t help your IBS symptoms although some people can tolerate small amounts. Try not to over indulge – intoxication can remove your resolve and you might be tempted to have more than you planned. Check out Drink Aware for details of how much alcohol is in your favourite tipple. https://www.drinkaware.co.uk/understand-your-drinking/unit-calculator

The true toll of Christmas tipple how excess plays havoc with mind and body

10. The best tip is – remember to enjoy yourself – it is not money that makes the difference but being in the presence of friends, family and company on the day – spending time with others.

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Happy Holiday!

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A World Without Downs

I will write more about ‘A World Without Down’s/NIPT soon – I need some time to gather my thoughts first (and I’ve got a poorly Ella to look after at the moment!).  The following post is cobbled together from my Facebook posts over the last few days… Alternatively, you could read ‘Losing Down’s Syndrome?‘ – a post I wrote earlier in the year.

Many of you may have noticed that Down’s Syndrome is big news at the moment. Something that I’m sure you know is important to me.

This is the week that Sally Philips’ important documentary is due to air. She will explore the ethical issues and questions arising from the proposed roll out of the new NIPT screening test for Down’s syndrome.

The biggest question being asked…

Can you imagine a world without people like Ella?

 

I am aware that I share a lot of articles, pictures, blog posts and other information relating to DS on my timeline. I am not apologising for this, Down’s Syndrome is a big part of our lives and I am very committed to educating others (maybe you) and busting some of those long-standing, ingrained cultural myths about the condition.

Mainly, I want to get across that having DS is not to suffer, is not debilitating and does not cause distress or trauma to those living with it, (unlike the media would have you believe).

I am not against testing or screening in pregnancy. Nor am I against the new NIPT screening that offers women the chance to find out earlier in their pregnancy, with greater accuracy and in a safer, less invasive way whether her unborn child has a chance of having a chromosomal abnormality – such as Down’s Syndrome.

I do believe women should have choice – in this case, to terminate or not to terminate as difficult a concept as that may be to me. What I am striving for, along with many others is for parents to be given balanced, factual, unbiased information relating to a positive diagnosis of Down’s Syndrome along with unbiased language (no ‘I’m sorry’ and using ‘chance’ instead of ‘risk’) and access to support following a diagnosis – whether that is given pre or post-natally. This is happening far too infrequently at the moment.

I’m encouraging everyone to try and watch the documentary and to think about the issues that Sally puts across.  For she speaks for the vast majority of us within the Down’s Syndrome community.

You can watch on BBC iPlayer (UK only) here:

http://www.bbc.co.uk/iplayer/episode/b07ycbj5/a-world-without-downs-syndrome

If you watched the documentary or not, please consider taking a few seconds to join our social media THUNDERCLAP for Down’s syndrome.  Supporting the need for women to be given unbiased, factual and better information regarding Down’s syndrome and the screening process itself. We’d also like to see better access to counselling and support groups at the point of diagnosis and that language used should be non-leading e.g. ‘I’m sorry…’

https://www.thunderclap.it/projects/47907-a-world-with-down-s-syndrome

 

Thank You

#worldWITHdowns

 

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A World Without Down’s Syndrome?

Some of you may have noticed (many of you won’t care!) but it’s almost a year since I posted on here. Not something I’m proud of nor ashamed of but it has made it harder each time I approach the keyboard to know where to start with all of Rosie’s achievements (and mischiefs) in the past 12 months.So I’ve chosen the eve of a potentially groundbreaking short film to ease back in and write a quick post to help spread the word…Tomorrow (Wednesday 5th October 2016) BBC2 will be airing the eagerly awaited documentary from Sally Phillips, ‘A World Without Down’s Syndrome?’”Driven by the experience of raising her son Olly, who has Down’s syndrome, Sally explores some of the ethical implications of our national screening policy.”This could be an important documentary for something that is so so important to me when new parents are faced with a pre-natal diagnosis of Down’s syndrome. That something is, ‘choice’ and not just choice but INFORMED choice. This was one of the primary reason’s I started The Future’s Rosie and it continues to be the driving force behind why I (albeit sporadically now) blog and share personal moments of Rosie’s life on social media. This in itself isn’t easy as I question myself daily about whether it’s the right thing to do – do people really see why I do this or do they carry the opinion I’m exposing what would otherwise be personal family moments as a selfish need for attention? I can answer those that think the latter by saying in all honesty life would be much simpler and less hassle for me if I didn’t do it at all, I’d much rather live in a world where Rosie’s condition wasn’t something I felt I needed to share to show ‘it’s okay’. Too many people are afraid of the ‘unknown’ with Down’s syndrome – yes I was that person too once which is why I know it’s a very real problem. I’m not and never intend to be a part of any ‘PC brigade’ most DS advocates don’t either. For me it’s always been about educating in a non-patronising way and if that means sharing my daughters life to help the cause, then for now at least I’m still positive it’s the right thing to do – even if it is a mere drop in the ocean of change.I, along with so many other parents am very grateful that Sally, who is already in the public eye for professional reasons has used her platform to reach people on a much grander scale than someone like myself could ever dream of. This isn’t a small gesture either I would imagine it’s taken an awful lot of hard work, careful contemplation and courage. Sally is now exposing herself to inevitable debate and criticism which can’t be easy – all for the greater good of educating society to the ‘other’ side of ‘Down’s syndrome, a side that many healthcare professionals would have you believe doesn’t exist – and as you may or may not know I say that from first-hand experience. If you get the chance please do tune in to watch or set your record buttons! The more people that see this short film the better so please share and spread the word too! A world without Down’s syndrome would be a world without my baby, my beautiful girl, ‘Daddy’s little Princess’ and to that I say a resounding no thank you.http://www.bbc.co.uk/programmes/b07ycbj5

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