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Few years ago i had a accessment i went there and it was full with people waiting, i was overcome with stress panic anxiety i had to get out of there, i phoned pip told them what happend they reccomenfed a home assessment which iv had helpd me big time fortunate to have understanding pip workers.🎉

So amazing! Came across your RUclips totally by fluke… I was a client of yours a few years ago. You inspired me to take a new career! Thank you and take care. Nye ❤

I'm so sorry to bother you, I applied for pip in march had my phone call 2nd may, had a txt on 3rd may saying my assessment is with the assessor and then a txt on the 20th saying the still haven't made a decision, so I requested my assessment letter and at the back page it says based on the claimant's likely future circumstances it would be appropriate to review the claim in 2 years what does that mean please? Thank you x

You are beautiful

Hi Laura, my name is Kerrick. I live in Pennsylvania. Have MS and similar story, had a very active lifestyle and rode motorcycles, a Black Beauty. 1981 Yamaha 650 Midnight Maxim. Noticed I was loosing my balance when riding, thought it may have something to do with blood pressure, fatigue, whatever. Quickly afterwards went numb from waist down. Went to family doctor about symptoms, he immediately sent me to hospital for testing. All of them including spinal tap, MRI, etc. I thought that it would be temporary at first. Was wrong. Immediately lost all balance in my mobility, walking, speaking, eating, bowels and bladder. Diagnosed 4 years ago, same as when you posted this video. Bummer it took that long for me to discover it especially since I've been doing not much of anything besides watching RUclips since I'm now disabled. Coping has been difficult, I miss the great lifestyle that I had and I'm sure that you do too.

You are better off being an illegal migrant you get everything on a plate no questions asked. England today

Are yoj ok?

It's the twisted brain and emotional issues I have. It's hard to explain.

Since birth? You're not born with it.

When I went for a PIP Appeal, as soon as I reached the minimum necessary points, the assessment was stopped and I was awarded it. As a person might have a stroke or heart attack proceeding I can in one way understand it, but it also stops the person carrying on and being awarded the complete number of points relevant to their case. That is important as PIP could be stopped or questioned as valid if just one issue is reassessed in later interviews, when the person might have had many points more on their claim, rendering that as irrelevant to questioning PIP.

THANK YOU FOR GIVING US ALL THIS INFORMATION, THAT YOU RESEARCHED ABOUT L-LYSINE. I HOPE TO CONTINUE TO LISTEN TO YOUR VEDIO'S ..YOU HAVE A NICE AND CALM VOICE ....THANK YOU. BE BLESSED 🙂

I have optic neuritis in my left eye, i had intermittent vision issues and pain which grew in intensity and frequency over many months. Then it grew to a point where vision in the left eye was badly affected and it no longer hurt. I had lost my mum and dad in the space of four months, so i wasnt in the best of places mentally so didnt take action like i should have done. When i finally did go to the opticians all the layers of my eye had thinned out, the optic nerve was badly damaged and my left eye is not reactive to light. The optician told me there is little chance i will recover sight in that eye. Im now awaiting an urgent referral to eye department in hospital and referral for neurology as MS is suspected.

I am always left confused when told to avoid stress. How does one do that? If life is sending so many dreadful and frightening things to navigate, how does one avoid the resulting stress?

What other medications have you tried

Totally cleared up shingles in me in 3 days.... outrageous ... I watched Dave Letterman wait 3 months to get rid of his shingles using some other treatment. Epstein Barr Virus is a Herpavirus ... so... L-Lysine is effective.... My wife has MS and is gaining ground against the symptoms of MS using LYsine

Hi Laura..hope you are ok?x

They are limited as to how many they let through AND get cash for turning you down. The Tory government are a criminal & terrorist organisation. They want to steal from the needy to feed greedy pensionscroungers. The generation that steals off everyone.

I’m looking at using these soon , cutting down my supplements and taking one multivitamin. The b1 and b2 seems quite high. I will only be taking one a day

The benefits of lysine supplementation are more related to its antiviral properties and less about directly influencing MS. There is no significant evidence to suggest that lysine can affect MS directly. On the other hand, BPC-157, a peptide with potential regenerative effects, is known for its healing properties in various tissues, including muscle, tendon, and nervous system tissues. Its regenerative capabilities suggest it could help in repairing the myelin sheath or nerve cells damaged by MS, although direct research on BPC-157 specifically for MS is limited.

Hi, have you heard of low dose naltraxone (LDN)? It's not a normal ms drug but immune system modifier. I'm starting it tonight. There is lots of good results for different autoimmune conditions including ms

A great deal of the process is how questions are answered, both written and verbal. Never say words like 'sometimes', this is a 50/50, we don't have our conditions 'sometimes'. If asked how many minutes you can walk for, your answer, if you have limited mobility, has to be i don't measure my walking in minutes, but steps. You have to bring your conditions into the environment and let them know what it is like 'most of the time'. The 'enemy' is not the assessor, but the person with no medical background who issues the points for each of the descriptors, from the information provided. Under all circumstances, get a brief summary from your GP's practice manager, this is free and legally should be made available to you and takes no more than a day or 2 to collect. The DWP will not contact your GP, or any other medical team, regardless of what the GP receptionist tells you. If you have no medical papertrail, you will receive 0 points

What a rude dog lol. That would get you 0 points lol

I had a liver transplant and did not get pips

The pips don’t want me to got again ..

Hi since my last assessment I have moved to a bungalow with a wet room , will this go against me ?

I got my decision less than 24 hours after my assessment, this week. Dodgy af

For my first PIP claim I had to have two assessments after mandatory appeal In my first assessment they scored me zero second assessment I scored 4 went to tribunal where there is a judge because it’s a court a doctor and a disability specialist and scored 28 awarded full PIP never give up it’s what they want

Assessors have a target of rejecting 65% of cases. The case manager has no medical experience at all

I had my first episode of optical neuritis this morning. I woke up and all of sudden I felt like my eye was being stabbed. Vision was blurry, but the pain-OMG I couldn’t bear it. I start crying and screaming. My husband ran in our bedroom and no did not know what to do. I went to the ER and they gave me a steroid shot. It definitely helped. But my eye feels like something is in it nonstop. Tomorrow morning I see the specialist eye doctor. I’m scared. I don’t want to lose my sight. Thanks for sharing.

Hello How much time does take to get carars allowance approval letter

Been watching your videos and thanks for your information and advice, by the way gorgeous saluki dog you've got just like you ❤

luck seems to play a big part of the assessment, I got my pip based on my mental health but not on mobility which I am in the process of appealing , I hope My reassessment is a tribunal as I think it will give me a reasonable chance to show I need it ,,

What do I do about these old people, NHS, the Left, Employers and Government people in the benefits department who all conspire with each other deny me jobs and also deny me benefits and try to award me lower amount of benefits? How is a person suppose to survive financially?

Diagnosis should be enough for them. I can't stand having to do this each year. It's like they want you to fake it or lay it on thick in front of them so they can deliberately catch you out if you do. It's a ridiculous and draconian method. My condition worsens year after year. I still only get the basic even though I haven't been able to work since 1999 and have recognised mobility issues by my council and GP , I have never been awarded anything for my mobility from PIP. When I was on mobility with DLA previously for years. I'm suprised that they haven't asked for the money back if PIP claim I have no mobility issues. It's unbearable the stress of being unfortunate enough to have a progressive disabled that you are pressured to prove it when your diagnosis already proves it for you. I have more than 10 major disabilities. I get lowest standard rate on PIP. On DLA Before half my disabilities I received Higher rate care and I think it was mid rate mobility. Before I was diagnosed with 5 physical disabilities on pip . Bog standard for getting progressively worse.

I live next to a pip assessor,who has told me me that after stopping being an assessor. They are not fully trained in anything,apart from reading a computer screen. They get £80 per refusal,and that is better for their pockets. Never say sometimes,maybe,or anything they can twist. These people are profiteering,never trust any of them,they try and be friendly,but really after you to make a mistake they can use against you.

Hi Laura -- Thanks for all your valuable tips which you've been so kind to post. My friend Gretchen has MS, so I watched diligently to learn new tips from you, which I then shared with her. She says "thanks!", and so do I for providing this valuable service. Please come back for updates and just to say Hi, as you're a great communicator. 😊

Yes itis very difficult to get the PIP and to get the PIP assessment face to face I was apply 2 time and they was declined and the third time application I was right in the filed that I need one person to see my condition and after to take the decision. Then I was there and now i waiting to see what gone happen they was telling me that is for 2 years and after 2 years I have to go again with them . Please if you know how they are working and how much time will take I will like to know . Thanks

Hi, my friend was given pip in 2016, after going to court, and his health has not improved, but if they stop his pip, he said he will fight it in the courts because the decision that they made back in 2016 was wrong and he will pay back all of that money from 2016 even if becomes homeless in doing so

I had a review back in october filled the forms in sent them back and had 1 message off them 2 say they have received my review application but its now apirl still havent heard nothing ..every time i phone them i dont get through so ive got my local mp on to it ..still waiting tho

there’s a symptom that had been affecting my life,it’s numbness,happen to be numb from head to toe,

What a great video. I checked out description and you put everything in the video spelled out. I am taking this as my example and template for fasting

Such a pretty female to have such an awful illness and helping all with good advice. Thank you !

I am going through same I've got leukemia look fine but inside I'm struggling with aches pains and cramps in muscles find it hard to explain

Why do you have to go through this every 3 years? Even if you tick "no change"

Just got mine renewed for 4 years! So relieved because the job centre did me over on my esa!

you were lucky my assessor was a bare faced liar

Do you need a doctors prescription to get this?

Such an informative video, thank you so much for sharing.

Thank you for this comprehensive information on lysine. I’ve taken lysine for years to control cold sores. There have been times when I’ve forgotten to renew my lysine supply and have gotten a cold sore, but of lesser severity (size). During the C19 lockdowns I got shingles during a period where I was not taking lysine. My doctor prescribed the antiviral medication but it still took nearly two weeks to fully recover. I now buy a 250 gram packet of lysine powder and take 1/4 teaspoon every second day. I’ve have been considering whether to get the shingles vaccination but I’m wary about vaccines now, so I’ll just keep taking lysine.

i was very luck as well to have a lovely lady that helped me feel human and not as anxious i was exspecting something completely differnt i have another one coming up soon and hoping i have a good and fare exsperience good luck to anybody having to claim