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| General chitchat Got something non-GYO related to get off your chest? Feel free to talk about anything you like! (Keep it clean) |
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| Deffo makes a huge difference to have the sun shining! Hope it stays a while!
__________________ smiling is infectious....http://www.thehudsonallotment.blogspot.com/ updated 28th May 2008 |
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| There's now an increasing realization among health professionals that growing your own is actually beneficial. There are projects springing up all over the place to provide 'Eco-therapy' (in English, gardening) experience for people with depressive illnesses. Makes you quite smug to realize that we'd figured this out all for ourselves. But if it helps people - which I'm sure it does - then I'm all in favour. |
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| Wonderful to have a couple of dry days in a row and get outdoors and do something. I have CFS (or ME) and took up veg growing to encourage me to take gentle exercise - there are days where I would not do anything if I didn't have plants to check! It keeps me moving when I would rather not bother due to pain and that is great. And of course there is the wonder of planting those tiny seeds like the calabrese I sowed today and knowing that you will get a meal from it in the future! |
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| yaay for shirl - my pal has CFS (ME) and I believe your approach is the best, not that I know of what I speak, but I am constantly trying to get him involved in 'gentle' gardening things - I hope he comes through it
__________________ aka Suzie |
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That kind of explains why my garden expands by a few feet a year compared to others who take on an overgrown lottie and get it all producing in the first 6 months! Boy is it frustrating!! |
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__________________ Hazel www.hazelandjanesallotment.blogspot.com update Sat 04/10/2008......sorry, Keats...... |
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| That's so true but it is hard to do as well. I don't have CFS/ME but I do have a chronic illness that means I'm not always as I might be. The temptation (pressure?) to 'get a grip' or 'be normal' is intense... but definitely not always (or ever) the right thing in the long term. |
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I hope my words above didn't read as 'get a grip' cos that was nowhere in my mind when I wrote them.
__________________ aka Suzie |
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| Shirl, I see several clients with ME, and Reflexology seems to work really well for them. Particularly one friend who just over a year ago found every movement of her body painful and couldn't stand up straight, she had reflex from me, weekly for about 5 months, massage from a mate of mine several times and developed the attitude that she was going to be well. Amazingly she is well now, she has full range of movement and is pain free and has lots of energy. What I'm trying to say is the Drs paint such a bleak picture with ME and because of the chemical imbalances it causes it must be really hard to get in a positive mind set about things, my freind has amazed her Drs with her recovery and it just proves that it is possible. Doing something as positive as GYO can only be a good thing, fresh air exercise and good food and like Suzie says it really is better than prozac. I know I get a high every time I go down the lottie!
__________________ Imagination is everything, it is a preview of what is to become. |
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| Told you to stay away from "those" plants, I know they're reported to have "medicinal" properties, but still... Anyway on a serious note, I'm sorry I know nothing about ME but I do know pain unfortunately, and just how much it can get you down, so you have my sympathies shirl and Seahorse. Being outside does make you feel great though doesn't it!? Mange tout, after yesterday my knees hurt and the heels of my hands are sore from all that metal bending and bashing I did yesterday. Come on spring!!! ![]()
__________________ A simple dude trying to grow veg. http://haywayne.blogspot.com/ - Tuscany update - 27th September http://tickers.baby-gaga.com/p/dev036pr___.png |
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| Deffo with you there lainey lou. I wish I could afford to have regular massage - Madmax does what he can but with him working away 'tis tricky. I am not crippled by pain or anything, I think I am fortunate that it was diagnosed early before I made it worse by trying to cope. The frustration of it is the worst thing for me. I used to be able to carry a bale of hay across the field to my horses, now I have to get mk1 son to push it in a wheelbarrow! There are other folks with ME who are much worse than me. It is such a tricky thing to describe to people coz everyone gets tired don't they? |
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| indeed they do shirl, but from what I've understood, the tired related with CFS/ME is all-consuming, there is no option to push through it. The pal I mentioned above was an ex RAF Copper, 6' 3", rugby player, always strong and doing things, when this hit it hit hard. We found it really hard to understand why he was always sleeping, getting up in the monring, eating breakfast, then having to sleep again. He isn't better at all, although there appears to be some slight improvement.
__________________ aka Suzie |
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![]() Shirl it might be worth checking with your local college, sometimes they do cheap reflex/ massage etc cause the students need to practise, you might even be able to pursued a student to take you on as a case study and thereby get some free treatments, benefit to you both! BTW did you know, they now think ME may be caused by a stomach virus?
__________________ Imagination is everything, it is a preview of what is to become. |
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smiling is infectious....
yep sun on the back and actually working is the bestest
