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What really PLEASED you?


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2 hours ago, b_emmons said:

Thank you, I hope so

Good luck mate, my gaffer on the farm suffered like you for a few years, it wasn’t MS though, turned out to be Celiacs disease. Mind you, all the chemicals we have been handling for years probably has affected us all....sheep dip through to all the sprays. Often wondered if I would have death via Metasistox:D

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1 hour ago, dm434 said:

Ms is quite painful , I have two siblings with it , it is manageable but only with plenty of meds , good luck Brian 

 

1 hour ago, chris.watson said:

Good luck mate, my gaffer on the farm suffered like you for a few years, it wasn’t MS though, turned out to be Celiacs disease. Mind you, all the chemicals we have been handling for years probably has affected us all....sheep dip through to all the sprays. Often wondered if I would have death via Metasistox:D

thank you guys :)

my worst one is if they cant find a reason

 

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On 10/14/2019 at 4:08 PM, b_emmons said:

Finally had a Doctor my Local GP practice actually listen to how I feel and how long it has been going on for, so finally after 8+ years of worsening fatigue, headaches, numbness and muscle cramps I am being referred for testing to see if I have MS :)

and yes I am pleased to be sent even if it dose mean I might have MS, as at least I will know why I feel so bad some days :)

Hope you get some answers Brian . Best off luck. ;)

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1 hour ago, jmd said:

best of luck brian sorry to hear that

 

18 hours ago, Valley Axe Man said:

Hope you get the answers your looking for Brian, it might be a long road to getting to the answer but at least your headed the right way, good luck :)

Thank you :)

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On 10/15/2019 at 11:15 PM, Kirely said:

Not knowing cannot have been easy, hopefully you can turn the corner now.

Thank you, The not knowing is a killer, so any positive diagnoses will be a step forward and allow me to get some help :)

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On ‎10‎/‎14‎/‎2019 at 4:08 PM, b_emmons said:

Finally had a Doctor my Local GP practice actually listen to how I feel and how long it has been going on for, so finally after 8+ years of worsening fatigue, headaches, numbness and muscle cramps I am being referred for testing to see if I have MS :)

and yes I am pleased to be sent even if it dose mean I might have MS, as at least I will know why I feel so bad some days :)

Hi Brian ,I was going to come and see you layout down at toytrak on sunday and say hello but I got busy helping Mr Reeve on his stand and the day just whizzed by ,anyway I was feeling like you say well over a year ago and drs just said you working to hard ,not drinking enough water etc ,cramps and tiredness got worse also had the numbness in arms and legs at times anyway about a week after I finished combining in August 2018 I went to get out of bed and I could not move my muscles was trembling and locking out like a cramp feeling it was agony could not see a Dr straight away as you have to make a appointment 2 weeks in advance(stupid system ) anyway I did see someone later that day my own dr was on leave so see a stand in one just said it would go away after a week but he is some steroids take 13mg a day with food and you will be ok after about 2hrs of taking first lot I was up and about with nothing wrong ,took tablets for the week and stopped a few days later it come back worse then before I was in my JCB loadall at the time and could not move to get out of it anyway the wife came up farm and found me helped me get out and straight down Drs ,my own Dr was back and see me straight away and said she thought I had P.M.R. which is POLYMYALGLA RHEAMATICE  and the steroids was the correct treatment but was not supposed to just stop taking them like I had been told so she put me straight back on them for the next 6 weeks I was struggling to work my mate that had helped me on odd days before was up farm everyday doing my work as I was buggered anyway I slowly felt better and over the next few months I was up hospital at least twice a month for tests ,nothing else was showing up so they presumed it was PMR so carried on with steroids but slowly reducing the dose rate I have had other tests done since as the steroids have a few nasty side effects ,only on 5mg now and I now it is still there as arms ache at times and I feel rough some days ,MS was mentioned to me at the start but they are certain it is PMR with me had another test only on wedesday of this week and got another coming up in next couple of weeks as they do wont to get me off the steroids completely and on to something else I don't know what but probably be on something for the rest of my time ,anyway keep your head up they have all sorts of treatment these days and now they are listening to you I am sure they will sort you out , I am ok on my muscles at moment but don't have the strength like I used to and I do get tired ,but I am ok and I am sure you will be as well ,Smithy        

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On 10/18/2019 at 12:58 AM, smithy said:

Hi Brian ,I was going to come and see you layout down at toytrak on sunday and say hello but I got busy helping Mr Reeve on his stand and the day just whizzed by ,anyway I was feeling like you say well over a year ago and drs just said you working to hard ,not drinking enough water etc ,cramps and tiredness got worse also had the numbness in arms and legs at times anyway about a week after I finished combining in August 2018 I went to get out of bed and I could not move my muscles was trembling and locking out like a cramp feeling it was agony could not see a Dr straight away as you have to make a appointment 2 weeks in advance(stupid system ) anyway I did see someone later that day my own dr was on leave so see a stand in one just said it would go away after a week but he is some steroids take 13mg a day with food and you will be ok after about 2hrs of taking first lot I was up and about with nothing wrong ,took tablets for the week and stopped a few days later it come back worse then before I was in my JCB loadall at the time and could not move to get out of it anyway the wife came up farm and found me helped me get out and straight down Drs ,my own Dr was back and see me straight away and said she thought I had P.M.R. which is POLYMYALGLA RHEAMATICE  and the steroids was the correct treatment but was not supposed to just stop taking them like I had been told so she put me straight back on them for the next 6 weeks I was struggling to work my mate that had helped me on odd days before was up farm everyday doing my work as I was buggered anyway I slowly felt better and over the next few months I was up hospital at least twice a month for tests ,nothing else was showing up so they presumed it was PMR so carried on with steroids but slowly reducing the dose rate I have had other tests done since as the steroids have a few nasty side effects ,only on 5mg now and I now it is still there as arms ache at times and I feel rough some days ,MS was mentioned to me at the start but they are certain it is PMR with me had another test only on wedesday of this week and got another coming up in next couple of weeks as they do wont to get me off the steroids completely and on to something else I don't know what but probably be on something for the rest of my time ,anyway keep your head up they have all sorts of treatment these days and now they are listening to you I am sure they will sort you out , I am ok on my muscles at moment but don't have the strength like I used to and I do get tired ,but I am ok and I am sure you will be as well ,Smithy        

I am sorry to hear you are also having problems Smithy, so hope they can sort them out :)

For me it is a great relief that they are finally taking notice and now trying to find out why I have gone from super fit, to barely able to fight a paper bag in less then 10 years, and I hope it is not MS I have but I have multiple problems on nearly all the symptom fields for testing, so just have to wait and see, and if I have then there are plenty of groups I can talk to and get help from, instead of the not knowing and getting worse that I have now :)

As a side note steroids are a treatment for getting over the attacks of MS if you have the progressive form of it :)

Edited by b_emmons
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10 minutes ago, Tractorman810 said:

After 5 years of worry the wife has finally been discharged from the cancer clinic with the all clear 

Brilliant news Sean, a weight off your mind I would think

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3 hours ago, b_emmons said:

and more good news my Hospital referral for MS testing has come through and I go on the 25th of November :)

Good luck Brian. I hope you get some answers that will help you manage your condition.

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