@jamesmerrellofficial1: 💓🧠 Living with PoTS After Long COVID? You Might Qualify for PIP 💷📄 If standing up makes your heart race, your vision blur, or you feel like you might faint this might be PoTS, and it’s a common after-effect of Long COVID. 😞 But here’s what most people don’t know: 👉 You don’t need to be in a wheelchair to be eligible for PIP. 👉 If your daily life is affected, you might qualify for support. As a nurse and former PIP assessor, I’ve supported many of people with PoTS, fatigue, and brain fog through the PIP process even after their claims were initially denied. 📝 If PoTS or Long COVID makes it hard to: Cook safely without help 🍳 Manage medication consistently 💊 Travel alone due to symptoms 🧍♀️ Walk more than 20–50 metres without rest 🚶♂️ Concentrate or complete tasks 🔄 You could be eligible for Personal Independence Payment (PIP). 📩 Email me if you’re unsure, I’m here to help. 📢 YOU DESERVE SUPPORT. DON’T STRUGGLE SILENTLY. 💬 Share this post if you know someone who’s suffering in silence with PoTS or Long COVID. #PIP #PersonalIndependencePayment #PIPApplication #PIPHelp #PIPAdvice #PIPClaim #PIPSupport #PIPForm #PIPTribunal #PIPAssessor #PIPUK #ApplyForPIP #PIPGuide #DisabilityPIP #PIPRights #PIPReview #PIPDecision #MandatoryReconsideration #PIPAppeal #PIPQuestions #UKBenefits #UKDisabilityBenefits #PIPProcess #ChronicIllnessSupport #InvisibleDisability #PoTS #LongCovid #PoTSAwareness #BrainFog #ChronicFatigueSyndrome #DWP #DisabilitySupport #PIPNurseHelp #FatigueWarrior #HiddenDisability #DisabilityBenefitsUK #NurseTips #PoTSRecovery #SpoonieSupport #FunctionalNeurologicalDisorder #AutonomicDysfunction #PostViralSyndrome #BenefitHelp #UKDisability #EDS #PIPTips #PIPClaim #DisabledSupport #NHS #Spoonie #SpoonieSupport #HealthAdvocate #ChronicPain #EndTheStigma #PIPSuccess #BenefitsAdvice #DisabilityBenefits #LongCovidSupport #PostViralSyndrome #PoTSAwareness #LivingWithPoTS #LongCovidUK #DisabilityUK #NursesOfTikTok #PIPTribunal #ChronicIllnessCommunity #NurseAdvice #ChronicLife #DisabilityInclusion #PIPJourney #DisabledVoices #AdvocateForYourself #PoTSSymptoms #CovidRecovery #DisabilityTikTok #FibroFighter #ChronicFatigueSyndrome #Neurodivergent #fyp
jamesmerrellofficial1
Region: GB
Friday 02 May 2025 08:36:43 GMT
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Caz :
could I get pip I have emphysema and a brain aneurysm
2025-05-03 08:24:14
4
goth chick :
thank you for covering this subject i have pots and severe orthostatic hypotension plus other ilnesses people dont understand as its not a well known disability
2025-05-02 14:29:50
15
Qwertytheiggy :
So just to clarify I should answer the questions based of a flare day? This has been really helpful. Thank you x
2026-05-06 13:21:59
2
BrittanyXWhelan🤍 :
I have sent off my PIP assessment and awaiting my actual assessment. which I'm worried about because POTs is "invisible"
2026-04-01 07:12:49
3
Noni Horwell :
I have POTs, hEDS and getting assessed for adhd, I didn’t even know you could apply for PIP with POTs, well documented my fainting 😭
2026-02-16 23:25:36
1
paulsome7 :
I have my paper assessment next Tuesday the 14th really worried about it it's my first time had a heart attack in January
2025-05-02 09:25:26
3
Zoë 🎄💙⚽️ :
My daughter is 16 and has had long COVID for the last 3 years it’s so rubbish x
2025-05-03 12:18:45
2
User123456 :
Can I just say you can get POTS for many reasons, some are born with it , some get it from brain injuries ect ect it's not just from long covid !!
2025-11-24 07:55:44
3
Miriam Tb :
😁
2025-05-06 18:26:50
0
Denni :
💝💝💝
2025-05-03 20:20:15
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Miriam Tb :
🥰
2025-05-06 18:26:57
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jegoodwill :
Heart fast (pulse) and when I stand up i nearly flatline 110/115, the pulse pressure not there and gives me dizziness and chest pains. Go figure 😂 people get angry when I walk out my wheelchair…
2025-05-03 17:15:31
0
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