Hi I found this out by accident. Fibro can cause premature aging of the brain, the grey matter which I find very alarming. My Doctor also said the medication I take does have have a bigger impact as I get older. 😣
Aging of the brain : Hi I found this... - Fibromyalgia Acti...
Aging of the brain
Is there anything else that Fibro wants to do to f*** up my life??!!!!
I know it's difficult but I also think it's important to keep pushing back and that's really hard to do especially when I'm knackered and sore. When I was diagnosed early 2000 I was told to look it up on the Internet, I know we have come a long way since then and now there is more awareness. One day at a time.
I agree, I have stopped eating for two days now as my brain even reacts to chewing food.
When I went outside this morning for a fresh air I had a fall due to dizziness. I can see and feel the premature ageing of my brain which in turn make me look over 100 despite being half of that age.
Oh man o man.....it’s tough 🤞🌻
Not eating can cause collapse
Painny please have something to eat - even if it is soft food like soup or scrambled egg. Take care hun x
Do you have a link to the evidence relating to this?
jneurosci.org/content/27/15...
I am the evidence and can vouch for what was said about the brain. I am a scientist but not medical science and can see how fibro ruins lives 🦋
that is the study I am aware of for this but it is a single study that is pilot, limited and using a small cohort.
The results are a discussion point until they are replicated, explained and understood. The age matching with such a small group of people could be an inadequate comparison.
I can't remember where I saw it as it was months ago but when I check it on line it did say that. I was upset about it and if this is the case we should be told about it. I asked my doc about it and he did not say anything but gave me a yes nod however that's when he said as you get older the medication has a bigger impact.
Oh no , getting hurt by our own act is the worst things, and I am sorry that you still not right, if I am hungry I know the kind of reaction I get but the nausea this morning was more than that
Thank you for sharing the love 💕 I will be careful 🥰
I am 40 and have noticed slurred speech and my brain is slow to react. Im so scared I have kept it too myself.
Hi purple I'm 54 and I have noticed.my speech gets really delayed sometimes especially more so.when.im.tired and I lòose my concentration aswell which isnt good when I'm.dealing with money everyday but he ho I just joke about it as if I think about it to much it will really get me down try not to let it get you down try not to think about it as it will really affect your life and lifes to short to let it beat us take care big gentle hugs xx
On question of money ! I went to a famous market in London for food. I gave the guy £20 and the food cost only £9.99. He gave a P back without realising it should have come with another £10 but I was such a dumb on the day because of the brain fog. The Turkish guy saw the vulnerability in my face and took advantage of it
My brain is is a mystery 🙈🦥I cry and laugh at the same time 😓😂
Bless you hunny can gp change the meds, there is so much attributed to fibro these days that all of em cant be right they find a few of us share a symptom and put it as a new symptom im sure head falling off will be on there one day lol all you can do to keep your brain healthy is eat the right foods n exercise it i do scrabble on line (word feud) writ3 doodle anything to stretch the mind its fun you make new friends at same time anything to stave off old age brain or otherwise good luck warm gentle hugs xxxxxxx
If it helps, I recently had a brain MRI. The neurologist got very excited when he showed me the results. He said I had a total absence of any plaque and the brain of someone in their 20s. I’m much older than that and have fibromyalgia. Interestingly I meditate daily and have done for years and we discussed findings from latest research that demonstrates that Meditation can increase the grey matter and shrink the amygdala. I get forgetful/foggy brain when I have a flare up but I’ve grown used to it and accept it is my body’s way of telling me to rest and nurture myself😊😊
Scary! I have Fibro, and am experiencing forgetfulness lately. Up to now I have put it down to Fibrofog; but I am 72, It could be Alzheimers'.
Cheers, Midori
If it is, it is. No point worrying about it
I have had a good innings, done many things. As long as I leave my son well provided for after him spending his youth taking care of me.
Cheers, Midori
Hi Elay,
It’s so scary finding another thing to add to the fibromyalgia list bless you I have days dizziness I do eat regularly I cut back on my medication because I couldn’t function the Gabapentine made me unable to speak properly someone called me a drunk 🥴 I don’t drink.
Have a chat with your doctor see if there is any other medication without the side affects.
Bug hug Hel52
Hi Hel52, I too am cutting down on the gabapentin, with a view of stopping taking it altogether. I have also stopped taking Co-codamol, except if I get a really bad flare up. I don't like what these drugs are doing to me. It is scary.
Hi Welshcatlady,
Well done it’s not easy I think we need to be on them to fully understand what they do but trying to function on these evil medications is absolutely impossible We are all individuals with differing levels of fibromyalgia my daughter has it at age 32 she’s just got diagnosed she’s taking everything thing her doctor is prescribing worry I can’t talk to her she’s as stubborn as hell
I have a few more gabapentine to ween off at night I to do one tablet over 4 weeks so I can lessen the side affects.
I only take paracetamol and ibuprofen BP medication plus others for other health issues I take supplements to help with the fibromyalgia.
Good luck big hugs Hel52 🤗
I'm sorry to hear that your daughter has this evil disease, I can understand her need to take anything and everything that her GP gives her. I was exactly the same. I should be weaned off the Gabapentin in just over 3 weeks time, I am noticing improvements already. I still take 50mg of Amitriptyline at night, so will be tackling that next, but not immediately. I can't take Ibuprofen because I took diclofenac for year, blissfully unaware of the damage it was doing to my stomach. So it's Paracetamol for me and Co-codomol if the pain becomes unbearable. I would never have started on these meds if I had realised what effect they would have, but hindsight is a fine thing! Hope all goes well with you coming off the Gabapentin. Take care.
Yes I totally agree mr_zoonie that is me 😂
I agree with Hel52 - meds can slow and dampen all functions down which makes everything harder including processing information. I came off all meds 6 months ago and now I feel much more capable of coping with the fibro AND life’s issues. I’ve started Win Hof breathing and walking meditation helping me to sleep better and clear the overwhelming distractions in my mind that fibro symptoms cause.
When I had my MRI they said I had white round spots which they see in older people. So yes I would agree with you.
Yes that's me too, I get frustrated by it, and my husband gets frustrated too, waiting for me to answer him. I say to him it's just the Fibro Fog.
Sorry that's her response it's a shame she doesn't understand, at least my husband realises that it's here for the very long term, well forever. He is really quite understanding.
Well done Mr Zoonie, I have just over 3 weeks before I am hopefully free from Gabapentin, then next I will be tackling the Amitriptyline, although not immediately. I am feeling more like me again already.
Hi, please can you tell me what CBD you take as I really want to try this. Thanks
Mr Zoonie, it definitely is! I have definitely felt much since coming of the Co-codamol, it was a struggle, but I'm so glad I persevered, and I've found that my pain is much the same as when I was taking the maximum dose. As for being educated there is so much literature on line these days. When I spoke to one of my GP's about coming off the Gabapentin, I told him that one of my symptoms was difficulty in peeing, and I explained that it is a noted side effect, he said he didn't know that. They can't be expected to know every side effect can they. He was very please to hear that I have all but knocked the co-codamol on the head.
Thankfully I have never taken it. 😊
There is a substantial amount of research that does link fibro to a CNS cause or at the very least a very substantial component in how it operates.
I am wondering what you are trying to convey with "Fibro is a collection of symptoms not a diagnosis."?
differentials like thyroid, MS, arthritis et al should be ruled out just like any medical investigation for any condition. But there is a distinct, discrete criteria that has evolved over time to identify the condition.
Theories exist that fibro, vulvodynia, IBS and other conditions may actually be conditions that have a common origin and present as pain/ nerve dysfunctions that will over time be better identified.
However, until we have theories that gather evidence and traction and become facts we are where we are and the existing evidence base is what we should work from. I know that there have been hypothesis's presented that have sought to establish other conditions as being the origin of fibro symptoms but unfortunately these have not yet made their way to being evidence based with adequate replication and peer review and still fall within the differential criteria.
I wish some one would beam you up. You obviously haven't felt the pain of fibromyalgia. It was around in biblical times . Yes fibromyalgia has lots of different problems . It's easy to say see a neurologist but you can't always choose who you see. I find your item very rude nasty insulting. Maybe one day you may feel it.
Hello
My son swears by cbd oil . His dog had cancer he used cbd on her . The vet was surprised when he went back and it had shrunk . His other dog has cushions he's now trying the cbd on her . They are sister and twelve years old Labrador's . He idolises them. He also had cancer in the roof of his mouth which they had to cut away . He had a metal plate to go over the hole . They said it would grow part the way back but not fully then they would operate and fill the hole in. He has taken cbd for a long time as he also has fibromyalgia . Now the hole in the roof of his mouth has gone. I have tried it but it does nothing for me . He was dreading another operation as it was sore for a long time.
Thanks for posting, I keep playing word games and scrabble online when Im resting with family to try keep the grey matter active, another symptom then to add to the Fibro list🤣