Waking up with pain.

I wish we didnt all have to wake up like this each morning. 

Amen 

I wish it wasnt like that for us christine 1 day hopefully it wount be until then onwards upwards xx

rolleyes

Yes, I agree Kaz, it is so tiring and depressing, but we somehow have to find a way of not letting it get us down, I don't know what that might be yet, but maybe something to look forward to. We have to put our minds on something pleasant, I feel it's the only way rolleyes

Hope you enjoy something in your day

Gentle hugs

we are planning to decorate our bathroom and sons bedroom. so Im decideing on paint colour and what flooring to have. I love designing choosing different looks for each of your rooms. A friend of mne who lives 2 doors away from me asked invited me to hers tonight so Im looking forward to that. and tomorrow hopeing to go out for the day. I also treat my self now again as it helps to lift the spirits. also I help our local charity shop by donateing to them unwanted goods to help raise money. so sorting out stuff today for them. finding other things to focus on Ive found helps me. Hope you have agood weekend and not too much pain ake care gentle hug

Ive forgotten what its like to feel normal, especially  in the mornings

Sue

Thank you Kaz, sounds like you're going to be busy, have fun and enjoy your weekend 😊

It's sad, isn't it, that we feel this way, life changes so much especially when you look back to a few years ago. But you know things could be worse. I went to the Dr and he said that to me, Ireplied that I didn't see how things could be any worse, a couple of weeks later I broke a rib, so well, yes, things can always be worse. 😊

Take care and be gentle with yourself

smile Thank you x take care big hug x

I know Kaz it's horrendous! T.c.xx

Hi susan would be great to feel normal again free from pain .life has certainly changed since having fibro the impact this condition has had on our lives is unbelievable.all we can do is take each day at a time get through it as best we can take care gentle hugs

Don't think I remember a time when I didn't ache, now I have trouble working out if what I feel is fibro or something else. Apparently my hospital notes say I have a high tolerance for pain, not always a good thing, explains why it took me 12 hours to realise what I thought was a stomach upset was something more by which time I was jaundiced and very ill with trapped gallstones. And why my husband was convinced I'd a minor sprain to my ankle not actually broken it (and a bone in my foot) as he thought I should be at least crying if not screaming in pain.

Its hard when we have fibro as it throws so many different things at us you never know whether it is fibro or something else going on. Ive found that if unsure its always best to speak to a dr.I have a high pain level, but fibro pain is a different sort of pain, not what I would personal call a normal pain. If you can understand what I mean

HI Kaz and all, was researching into  colloidal silver for a friend with a very sore mouth, cant beleive what i read scrolling down..look

Fibromyalgia

My fibromyalgia is such that I ache throughout my body, all day, every day of my life. I get out of bed in the morning and my body hurts. It’s worse in the cold weather – which we have plenty of in Syracuse. Every part of me hurts: my legs, arms, back, my connective tissue. On bad days, it’s debilitating. Because I’m also allergic to everything under the sun and almost all medications —I should be in plastic bubble! — I can’t even take anything for it. A few months, ago, I took some Mesosilver for an ear abscess and noticed that my fibromyalgia symptoms lessened. It was pretty subtle at first: I just sort of noticed, “Wait, I’m a lot less achy than I was.” I didn’t understand it, and kept asking myself, “What’s going on – is this real?” But there was no question that once I started taking Mesosilver, I felt a lot better. I am in a lot less pain, and movement is so much easier, like I can get up out of a chair now without pain and major effort. It’s quite unbelievable! I've never been so impressed with anything! I feel like I have a new lease on life! How spectacular is that? I thank God for you for giving me my life back! This really works! It truly is a miracle!

Tammie Thomas

Syracuse, NY

My fibromyalgia had me in a state of total exhaustion. I couldn’t walk, couldn’t think clearly, could barely function. Colloidal Silver got me out of bed, helped my brain to function and got me off my prescription drugs, which means a lot to me because I don’t like taking drugs and really prefer more natural healing approaches.

Firbromyalgia is a cyclical condition, in which the symptoms come and go. I notice with Mesosilver, the waxing and waning of the symptoms is so much less drastic and much less severe. If I run out of the Mesosilver, my fibromyalgia symptoms flare up immediately, so I know there is a definite cause and effect relationship between my relief and the Mesosilver. And I love it that it’s a natural solution and I can get relief without the terrible side effects of the prescription drugs.

Also, I use Mesogold to help with fibromyalgia muscle pain. And my 12-year-old daughter who is just starting to manifest the beginning symptoms of the disease also takes gold to help with her pain, as well as her confusion and lack of focus. The Mesogold really helps her to think more clearly and follow through on assignments and tasks, both at home and at school.

My friend Deborah who also has Fibromyalgia uses both the silver and the gold, and finds them necessary for good daily functioning.

Could this help us?

Sue x

 

Hi Susan556  I am going to go on google and research into it, and also when I am able to speak to my gp ask her about it. I am only speaking for my self but I would never take anything before running it past my gp 1st. mainly because I have problems where medications are concerned and the affects they have on me.its up to us all where our health is concerned to do what we think is right and best for ourselves. But I do think its best to ask gp for advice before taking anything which isnt prescribed. Just to be on the safe side. x

Hi Susan556  I have just been on wikpedia go on their read up about it x

Hi Kaz I definitely agree there in absolute agony today and so tired interview at jobcentre a complete joke told me should be on sick then wouldn't have to visit them made it clear to her that this is my final chance at work and if I don't go there will no money coming in as getting nothing from them anyway with my own car in the garage and looking at a bill of near one thousand pounds approx there will be little left to shop with plus have to get boys school shoes uniform and sports shoes for return to school in September got call this week to go Torquay for Atos PIP assessment but because on job club day and car problems turned it down plus the added stress of not being where I live just puts more on my already broken body which gets weaker by the day hands are really sore and shoulders giving me grief together with back of my head where headrest impacted and back agony too booked in with Dr next week as can't take much more what with IBS diarhoea confining me to home too more than had enough.  Had call from my sons DAF lead as have asked her to be my support for assessment when get another appointment she is his school nurse and I hope this will get the assessor to see that I am not pulling any strings and of course they are unaware if this further trauma and she is also to ring my pain management team as feel they should be taking my physical needs more seriously and providing me with suitable mobility aids crutches or walking stick but all depends on what I can cope with given tennis elbow, splinted left hand/wrist and two painful hands too.  Four weeks today and feel nowhere near in the road to recovery absolutely no energy and totally shattered cleaned toilet and bathroom fully for first time in that time and my right knee was agony oh for a new body.  Gentle hugs.  Julia

Hi Julia54537 I know youve applied for pip, but if your on a low income would you be able to claim working tax credit. I know their is a thresh hold to what you can earn. But if its under the threshold you could cliam. I know claiming anything is very stressful.you have to jump through hoops to get anything now a days.You could definitly do with aids to help you.My physio got me a walking frame and stick I have 2 commodes bath board perching stool for kitchen. I had occupational health come out to see me they were from local council.They assess you and see what you need to help you. My dr refered me to them. Its good that your sons school nurse go with you. Having some one like that should be a big help in them hopefully seeing that you are not swinging the lead. not that you are.I have found that when I am ill fibro does 2 thinkgs makes the illness 10x worse and the recovery period takes alot lot longer. you have had a massive trauma with having your accident. so you could find with you having fibro the recovery period will take longer.I know its easier said than done saying to some one dont stress worry, but when we do it just makes our condition sooooo much worse.Have a word with your gp see what help support she can get you as you really do need it. cab are really good when you need advice. My heart goes out to you with all that you have going on dealing with fibro is bad enough, with out other things added to it. I certainly would not worry where house work is concerned youve enough on your plate.Im thinking of you I feel so bad for you. The ibs is down to stress and worry ive had it past 2 weeks because of stress worry. you take care gentle hugs xx . 

I am so sorry you are in pain, you poor poor thing. I wish the doctors could help you, you need some relief from this. I know you have tried all the prescription drugs, is there any point trying smaller doses of the traditional fibro drugs and then titrating up to the level with minimum side effects and yet some relief from the fibro. 

I just do do not know the answer to all this but I feel anything is worth trying at this stage. I personally get some relief from Lyrica, even though I am on a low dose.

gentle gentle hugs

Meg

🌺