Dealing with Fibromyalgia and weather I'm eligible for PIP
Posted , 8 users are following.
Hi Guys..
I'm 20 years old and have been diagnosed with Fibromyalgia 4 months ago. I also have problems with my nerves with the doctors have not yet been able to tell me what the problem is..
I had an accident in Auguest 2014. I crashed a Go-kart in to a wall at 60mph. It was not fun! I now have numb legs ad get shooting pain through my nerves from my spine in my lower back and legs like I'm being stabbed but as quick as an electric shock. It painful to walk or to even move. Does anyone know what this could be?
I am currently on Gabapentin, Amitriptyline and dihydrocodeine. They do help with the pain but my body gets used to the mediation and I'm highly addicted to them. I can't have anymore medication. I urge anyone who is on medication to take breaks and try not to go to high with them.
I don't really have any knowledge of how to deal with fibromyalgia as well as my nerve pain. Does anyone have any advice or ways of dealing with it?
With my tablets they make me constipated and i recently went to see a dietitian who suggested i start a new diet. I currently work 16 hours a week and earn 100. I have just left college so I don't have income support anymore to help me out. The 100 pound I get a week, 3/4 of that goes on my living expensis as I support myself.
My new diet is quite expensive and I don't have the money to pay for it all.. I was told I could claim PIP whilst working to help with stuff like this. The only problem is I don't know how to start the process, can anyone help please?
I also don't know weather i'll be entitled to it as i work. I also have to pay for my medication which is 8.60 per item and I have 6 items a week. I have no idea how I'm going to pay for it all and still survive living on my own with no parents.
I can't go out and get a full time job as moving helps my pain but too much and I physically can't walk.
Can anyone help me with this or have some advice?
I also have really bad migrains and my synopsis flaire up. I had one the other day from about 5 in the afternoon on the friday until I woke up on the Sunday morning for work. I had to take the day of work on the Saturday as it was that bad. Sometimes i end up ebing sick, and i feel better afterwards. But I take medication for it, I sleep and drink lots of water. and neitehr of them help. Does anyone else with fibromyalgia suffer with this? And if so how do you deal with it?
I don't have anyone to talk to about this as im a young person with these ilnesses, So im turning to you guys to help me if you would..
Anything would be appreciated.
Many Thanks.
Kayleigh
0 likes, 19 replies
tina46759 kayleigh60814
Posted
kayleigh60814 tina46759
Posted
This has been a massive help. What do I put in my search bar to find the number?
And how do I contact equal lives as i've never heard of them. I only live in a little town called Winsford in Cheshire. I'm not sure if we have equal lives about.
Would you suggest that I get a writen letter from the doctor and all my medical proffesionals and send it with the form I fill out?
Thank you so much Tina, You've helped loads.
Kayleigh
kayleigh60814
Posted
tina46759 kayleigh60814
Posted
kayleigh60814 tina46759
Posted
You've been a masive help..I hope you get your claim and the help you need.
Thanks again
Gizmo1963 kayleigh60814
Posted
kayleigh60814 Gizmo1963
Posted
Unfortunatly I wasn't told about this as I was on income support as I was at college so I didn't need to pay at the time.
I'm already addicted to the stuff I'm on and I suffer really bad with the withdrawals, So I dearnt ask for even stronger ones.. Sometimes I don't know whats worse, the pain or the withdrawals.
This has helped me alot, so thank you so much.
Many thanks. Wish you well too.. x
Gizmo1963 kayleigh60814
Posted
I have just checked the nhs website for you and the charges are £29.10 for 3 months or £104.00 for 1 year which can be paid over 10 monthly instalments. I hope this helps x
mel77 Gizmo1963
Posted
Thought that I write you. You being in the UK and me being in the States, we have different types of medical care. I was wondering what PIP means and what that would be considered compared to our insurance? I'm just curious. Looking through these posts, I notice that prescription drugs are not as expensive as in the States. The Pharma here charge big bucks and newer medications are almost out of the range of being affordable. Big Pharmas make lots of new drugs, advertised on TV and patients who watch this, has the info asking your doctor to prescribe them. I am unable to afford the new drugs. I go to any clinical trials that I can see if these drugs do indeed work. Qualifications are pretty strict and that is just to get the first appointment. As you know a very large questionaire is filled out so these trials can check you out. Especially if you are taking too much meds, wrong kind, conflicts and using street drugs of course. That slows the process down to a few that will qualify. You don't get paid as much as it only takes care of transportation and having a burger or two. Hope yoou feel better and stay well.
mel
pollmadoll64 kayleigh60814
Posted
kayleigh60814 pollmadoll64
Posted
I'm glad I can still claime. Where could I find those questions.. Do I just look up 'questions PIP will ask me'? Something like that. I'm quite useless at this, I don't have any parents to help me either. It's quite scary.
It is tough when your young but it's tough on everyone going through this.
Wish you well
Thank you
pam_87693 kayleigh60814
Posted
kayleigh60814 pam_87693
Posted
I've already been to see a neurologist but I haven't heard anything back from them. Evbery time I call up, they just tell me someone will be in contact with me. My GP has even wrote to them a few times and tried calling.
Do you mind me asking what is POTS? I hope one day someone will get to the bottom of this, I think whats even worse than this ilness is not knowing what's causing it and how we can get better. I will ask my GP about it though, thank you..
Thank you, and I hope so too.
Wish you well x
grandmaDylan kayleigh60814
Posted
kayleigh60814 grandmaDylan
Posted
I'm glad you don't get the shooting pains anymore, I woldn't wish them on anyone. I'm having them quite bad today in my lower back.
If you don't mind me aksing, what is polymyalgia? I feel ever so sorry for you.. It sounds painful. It's horrible when you don't understand your pain, what's causing it and which diagnosis it actually is.
Arthritis too, I really don't know how you cope. I hope you get your new knees and if I was rich I'd pay for you knees
I've never really searched anything about working tax credits to be completly honest. I didn't think I was entitled to them but I shall look in to it.. Thank you.
Wish you well