Symptoms and Diagnosis; PSP, CBD and MSA

This video is for healthcare professionals to use as a reference when diagnosing PSP, CBD and MSA. It shows what to look for in a patient when making a correct diagnosis.

[@aleidabianchi1434]

This time I will use Weedborn CBD products to heal myself.

[@elenidudi1940]

Do you find that in every dispensery

[@romeliapolly1212]

@@elenidudi1940 Just google for it. All the best for U !

[@hammondmiers3789]

I think I will be continuing my CBD treatment. I was just given CBD products from Weedborn and I feel so much better these days : D

[@johnlewis1640]

Thanks to the Patients for allowing to be filmed. We appreciate it.

[@allencrider]

I especially enjoyed the very end.

[@herpderp7264]

My sister has CBD. Within a year she was in a wheel chair unable to move her legs, had lost the ability to speak but still could write messages on her phone with one of her hands. Now her arms don't work either and she needs a eye tracking computer to talk for her. We all believe huge amounts of stress brought the illness on.

[@drew9312]

Excellent video- thank you. Would welcome any more you could provide.

[@MRradicalmj]

Thank you for the demonstrations

[@amritanandi2410]

My mom in law has just been diagnosed with CBD. THANKS for your video it generates awareness in me. Please make some videos on how to make QOL better for CBD patients.

[@CurePSP]

Thanks for the feedback, Amrita, we are sorry about your mom-in-law. We will try to make some videos about techniques for CBD patients to improve quality of life.

[@ingernag3649]

thanks, brilliant video

[@halslanina2001]

Thank you for the information. As this video is dated 2016, have there been any promising breakthroughs in treatment for CBD since then?

[@materialobject2412]

excellent resource.remarkable clinical diversity. i have identified numerous patients with mild/early symptomology in osteopathic practice overlooked by experienced neurologists and GP.

[@CurePSP]

That is great, Craig, we haven't heard of an Osteo being able to make this diagnosis before. Can you tell us where your practice is?

[@prithvinayak3133]

Thank u sir. Very useful video...

[@lowamc86]

I know there might not be a classic progression in these diseases. Knowing that my mother only presents lack of strength in the lower and upper limbs, which leads to difficulty walking, she has had multiple tendinitis in both extremities, multiple surgeries to her feet (Morton's neuroma, hallux valgus), could these explain her difficulties? Or could it be MSA, as diagnosed by a doctor?

[@SweetTeaTvTeaSippers]

Does it cause a person to be violent

[@mini-nh7ux]

very nice video .My father in law too is having PSP.From past few days his arms have become lifeless and swelling has appeared.He opens his mouth with great difficulty,folds his legs and is unable to walk.Now a days he mostly sleeps for 20 hours a day.I want to know if this a final stage of a PSP.Please help me as I can't see him in such horrid condition.

[@CurePSP]

Hi there, if you like, call us at 347-294-2873 and we can put you in touch with the right person to talk to.

[@mini-nh7ux]

CurePSP , Thanks for your concern,but my father in law passed away in July last year

[@KickDoez]

So sorry to hear about ure father in-law. My father in-law has Psp & CBD. It's been a tough seeing his progression over the past few months. I've been doing research trying to gather info and advice from others. God bless.

[@maryamali9826]

My mother she have psp .. its star in 2015.. hows your father now.. my mom she is so tired

[@jamestucker1068]

Guys we need cure for this terrible diseases.

[@Grecco202]

It's literally worth a Nobel prize!

[@rinkle786]

Hey ! My father is Suffering from PSP. Please tell if there is any cure. I can't see him like this. I am from India.

[@YOGESHH1]

unfortunately there is no cure because it is related to brain disease.

[@lokeswarikoppu62]

My mother is also suffering from psp,how can we cute it..please help.

[@curcumin417]

There seems to be some overlap with PSP, Corticobasilar degeneration, and Parkinsons disease -Would recommend some general measures, including healthy diet: Increase Omega3 Fatty acid consumption/supplement, containing good amount of DHA and EPA. Studies suggest that omega-3 fats may help reduce nerve inflammation, improve neurotransmission, and slow neurodegeneration. Eat healthy foods containing Anti-oxidants and Probiotics, Fresh fruits and vegetables -due to relation of gut-brain axis. Avoid fast food, refined processed foods. Also for PSP patients with Parkinsons type symptoms, a trial of carbidopa-levodopa is worth a try, under the guidance of a neurologist. Fava beans have natural levodopa, so if your father is not allergic to Fava beans and does not have G6PD deficiency (in which case you would want to avoid Fava beans), this food may help. Supplement with vitamins -containing vitamin C, D, iron, zinc. Please keep us posted. Take care.

[@maryamali9826]

My mother same .. anyone now how we can help them

[@johncorroon6562]

my daddy has passed away 5 months ago now we got the news today that he had CBD God help him me and my wife looked after him I did not no that we can get this in Ireland it's so hard I miss him so much xx

[@CurePSP]

Really sorry to hear that John. I hope knowing the official diagnosis helped to deal with his loss.

[@Matdogg2k]

My dad has CBD and was diagnosed with it a year and a half ago. It's a terrible thing

[@kidaz]

The echo at the end is freaky

[@diastoleny]

Lost my patient of 4 years just 2 months ago to PSP. So unfair.

[@christinemorgan1829]

Hello

[@saviorofmyfamily6796]

Or gait