Here's the latest from Motability regarding transitional support if you fail to be awarded enhanced mobility in the upcoming PIP reassessments:-
http://www.motability.co.uk/about-us/news-and-information/motability-announces-transitional-support-package
Hello!
Newbie alert :)
Hoping you can help meon this one - apologies in advance, it may be a long one!
Think I will do this in bullet form, as I do tend to go round the houses to explain things, and will probably confuse you as well as myself lol
9th Nov 09 white floater in my left eye, terrible headache, never had one like it or since. Over the course of 4 days lost sight completley in left eye.
13th Nov 09 went to walk in eye clinic - sent for an MRI scan. Optic Neurotis mentioned - of course looked up on the web and made the MS connnection!
Sight came back over about 3/4 weeks. I then had a numbness from chest down to my legs - as tho I was coming round from an op, sometimes feel like theres a very tight belt round my stomach - My feet also felt very strange - as tho I wouldn't know if I was wearing socks or not.
Early Jan 10 went to GP to see if he could speed up the neurologist appt, as I now had this numbness. He did write to the Neuro, who replied that he could not bring the appt forward, but suggested GP refered me directly to MS Clinic to speed things up. It seems very likely MS
18.2.10 Appt to see MS neuro (MS Clinic) Different Hospital, so didnt have access to the MRI scan. Sent for chest xray to eliminate anything else, also blood tests. Neuro to get copy of scan. In the meantime MS nurse will contact me this week.
With hindsight I am very sure that 2/3 separate episodes of not being able to walk properly - thinking I had a virus during 09 must have been some sort of 'attack'.
Today, I went to the orginal appt, and thankfuly the neuro, who is not MS specific, had a copy of the MRI scan - he is going to send a copy to the MS Neuro. Each of my symptons on their own would not point to MS but all of them together do.
Since yesterday afternoon, my tounge has gone numb and this morning woke up and my lips/chin numb and tingling.
Onto my question re DVLA
My 13 yr old daughter receives the higher rate mobility and care. I am looking into getting a motability car. I have more or less made up my mind that we will go for a Renault Grand Scenic, and have test driven an automatic, (never driven one before in my life lol)
I know I have to inform DVLA, but is that when I have the official diagnosis? Am worried the DVLA would take my licence, then I'd be in a right mess, as I need a car to be able to take my daugher out and about, and for me too!
Also I don't want to sign up to get the mobility car, only for DVLA to say I can't drive! Think I may be overreacting, as from reading on here, I think I am right in saying they would prob write to the neuro and let me carry on driving... and possibly give me a 3 year licence?
I am sposed to be getting back to the motability bloke to let him know what I'm doing.... should I go for it!
See, told you I went round the houses lol
Any advice welcome ;-)
Thankyou
x
My Toyota Yaris had a little oil leak and I took it in to Toyota under warranty. It also has a little water leak from the rear screen washer so its going to go back in at the end of the month too.
While I was waiting around in the showroom, I started looking at cars and their motability rep started talking to me. I said I was thinking about Motabiliy but would probably run my Yaris for a couple of years. He pointed out that I would get more for my Yaris if I sold it and got a Motability car now.
OK he's a salesman and really only wants to sell another car but at the same time he has a point. In a couple of years I will have about 72,000 miles on the clock. Not only that but he thinks I would do better with a Diesel Yaris rather than the Petrol I have now. They do about 50-60mpg. I am currently getting 42mpg.
The only downside to this idea is that I do 27000 miles more than the Motability people allow. They will charge me about
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