@@macchiatolashes8211 I adjust the immune system not to let it destroy herself. When inflammation is reduced, Fibrosis will not occur, disease will calm and suppress. This is how I adjust my immune system to not destroy herself :- 1. I eat nutritious foods. Avoid certain foods that will trigger the disease. 2. Focus on exercising the mouth, lungs, joints, muscles. 3. Get enough rest. 4. Not stressful, encouraging yourself. 5. I decided to reduce the Immunosuppressants or Immunosuppressive Agents in order not to get too low immunity and to prevent complication of infections. 6. I have been taking a supplement to help detoxify residues in the blood and lymph system. 7. Avoid contact with toxic chemicals. Important Note : Anyhow, it depends on each individual condition how severe the disease as my condition was not severe at the time of diagnosis 6 years back. Nothing like finger deformed or no ulcer on the fingertips, only little fibrosis to the lung.
hello, this is an informative video on scleroderma. my cousin was also suffering from this condition. she visited many hospitals but didnt get any relief. then one day she visited planet ayurveda and got sclero care pack. now she is fine. thanks to planet ayurveda.
@StratosFear1992 Appreciate Video! Forgive me for butting in, I would appreciate your initial thoughts. Have you researched - Pefincoln Illustrious Precedence (Sure I saw it on Google)? It is a great one of a kind guide for erasing your hives once and for all without the hard work. Ive heard some extraordinary things about it and my m8 after a lifetime of fighting got amazing results with it.
I have had Systemic scleroderma for over 10 years and found it impossible to explain how dreadful it is, as people only see me when I'm between flares, when I appear relatively normal. This video is excellent. Thank you x
@@monikasicz9736 I have systemic sclerosis besides other autoimmune diseases and the rheumo told me to carry on with my high level of methotrexate and i know how you feel 🤗
I have Limited Scleroderma. 😢 It's really an awful disease. I hope scientists, pharmaceuticals please find a medication to stop the collagen over production. 🙏🏼 There's nothing yet. It's a complex disease and so misunderstood yet. Hopefully soon? Scientists can find medications to really stop 🫷 this disease. 🙏🏼
I have systemic scleroderma and I will confirm this video is very accurate thank you for giving correct information and making it simple enough for us to explain to your typical person
@Tony sabroso A Rheumatologist diagnosed me at 14yrs old I’m a rare case being a male and young when diagnosed nonetheless I had very heavy treatment at first and over time my treatment has now only been to target certain symptoms I still have I believe being young helped me if I was older I believe o would’ve been in a worse situation
This is a superb video. Very useful for all in understanding these problems.. I would be pleased to see this shown to all newly diagnosed patients, gives a good overview. Clear information and explanation. Great Resource.
Do Yogasan 1 hour daily especially lungs exercise. Don't come in contact with cold weather directly and drink plenty water and eat turmeric, ginger,dry food,Ashwagandha these are the best alternative to treat PSS and one more things try to avoid milk and milk products at least 4 months
Why have you turned comments off on your Ankylosing Spondylitis video? Is it because you are completely WRONG that men are 3 x more likely to have it? Might be. Says a woman with Psoriatic Spondylitis. VERY OLD HAT, sir!
Living with MS is terrible but thankGod for making me Negative of MS recently, after I meant a channel on TH-cam ( Dr mason channel )...thank you Doctor
I'm a 20yr old male with cracking joints, deteriorating eyes, and calcium buildup under the already dry skin on my knees and chin/center neck.. at this point I don't know what the cost of these 'rare case treaters' are and I'm already anxious the way it is with how far it has seemingly progressed....
My thoughts are with all the people suffering from this horrible disease. Somebody I know has recently been diagnosed with scleroderma and it’s the most traumatic thing that’s ever happened in our lives. Please have an extensive read about Helminthic therapy.
If PM-Scl is positive on ENA test but ANA test is negative. Does it mean the person has scleroderma? Symptoms are limited to Raynaud's and blood vessels only. No skin related issues are there at all. Does it mean that there is presence of another disease that mimics scleroderma?
If you find out PLEASE let me know. I have zero symptoms of scleroderma and still tested positive for Antiscl-70 antibodies. I don’t even get Reynolds’s at all.
reat video, but why not try diet change? I would try the Seignalet diet for one full month: - remove ALL cereals 100% - remove ALL milk&dairy products from my diet. for one full month, and then see!
I had Renauds gor many now i been diagnosed of systemic antibodies my fingers splits under the nails i tought i had fungal nails infection im suffering of pain they put me on steroids recently thank for some of info
Hi, I have many symptoms with positive Ana cytoplasmic staining but neg Ena panel. I have Reynauds and alot of nail issues as well. Not sure if its fungal but almost feels like the sidewalls of my nails are always infected or something and my nails are growing into my skin if that makes sense. I kept going to hand surgeon for ingrowns but they said they arent ingrown nails. its always on sides of thumb nails and painful.
I just brought kindle version of the book… I just have one query and I would appreciate if you can reply back…. Is the book suitable for post graduate in medicine? I hope you understand what I mean. Btw the video and the book both are awesome. Great work
In Ayurved, Scleroderma is correlated with “Uttana Vatarakta” that causes imbalance of dosha, dhatu, & dushya. The imbalance of three doshas (vata, pitta, & kapha) is responsible for the scleroderma
I have been living with this disease for 8 years without any further serious conditions. Living with normal and healthy life.
wau, how about your medicine or diet? just got diagnosed and falling into depression mode currently
@@nursha206 I have been using alternative health care.
@@toistory732 don't mind to tell more about it?
@@macchiatolashes8211 I adjust the immune system not to let it destroy herself.
When inflammation is reduced, Fibrosis will not occur, disease will calm and suppress.
This is how I adjust my immune system to not destroy herself :-
1. I eat nutritious foods. Avoid certain foods that will trigger the disease.
2. Focus on exercising the mouth, lungs, joints, muscles.
3. Get enough rest.
4. Not stressful, encouraging yourself.
5. I decided to reduce the Immunosuppressants or Immunosuppressive Agents in order not to get too low immunity and to prevent complication of infections.
6. I have been taking a supplement to help detoxify residues in the blood and lymph system.
7. Avoid contact with toxic chemicals.
Important Note :
Anyhow, it depends on each individual condition how severe the disease as my condition was not severe at the time of diagnosis 6 years back. Nothing like finger deformed or no ulcer on the fingertips, only little fibrosis to the lung.
@@toistory732 I see thanks!
The best resource out there for ALL basic medical knowledge!!! Videos, notes, podcasts, Instagram questions, etc. Thank you so much, Tom.
Glad to help!
hello, this is an informative video on scleroderma. my cousin was also suffering from this condition. she visited many hospitals but didnt get any relief. then one day she visited planet ayurveda and got sclero care pack. now she is fine. thanks to planet ayurveda.
Wow that's interesting pls give more information
What’s the sclero pack?
Just found your channel. Thank you this video lines up well with my school lecture notes on this disorder/disease
watch at x2 speed
👍
thanks sir💙🤍
Your videos are SO good! You’re such an underrated medical channel. Will recommend you to my medical colleagues. You deserve way more exposure.
Thanks! Thats great to hear
Is this the same as Sjogren's syndrome...
@StratosFear1992 Appreciate Video! Forgive me for butting in, I would appreciate your initial thoughts. Have you researched - Pefincoln Illustrious Precedence (Sure I saw it on Google)? It is a great one of a kind guide for erasing your hives once and for all without the hard work. Ive heard some extraordinary things about it and my m8 after a lifetime of fighting got amazing results with it.
I have had Systemic scleroderma for over 10 years and found it impossible to explain how dreadful it is, as people only see me when I'm between flares, when I appear relatively normal. This video is excellent. Thank you x
What was your treatment? I have it also,and I really interested!!😪😪
@@monikasicz9736 I have systemic sclerosis besides other autoimmune diseases and the rheumo told me to carry on with my high level of methotrexate and i know how you feel 🤗
Hi.. currently my sister’s in same condition for 2years now.. tell me more about how to get treatment and diagnosed please..
Great video! I would love to see them more regularly, but I can imagine it takes you a long, long time to make them 😅👍
Planning on making them more regular. Hopefully at least once a week!
@@ZeroToFinals that would be awesome! I will be waiting 👍
@@howtomedicate Thanks for your support!
I have Limited Scleroderma. 😢 It's really an awful disease. I hope scientists, pharmaceuticals please find a medication to stop the collagen over production. 🙏🏼 There's nothing yet. It's a complex disease and so misunderstood yet.
Hopefully soon? Scientists can find medications to really stop 🫷 this disease.
🙏🏼
I have systemic scleroderma and I will confirm this video is very accurate thank you for giving correct information and making it simple enough for us to explain to your typical person
@Tony sabroso A Rheumatologist diagnosed me at 14yrs old I’m a rare case being a male and young when diagnosed nonetheless I had very heavy treatment at first and over time my treatment has now only been to target certain symptoms I still have I believe being young helped me if I was older I believe o would’ve been in a worse situation
Oh I’m so happy reading this :)) I was also diagnosed at a really young age and hope it will also get better for me in the future!!
This is a superb video. Very useful for all in understanding these problems.. I would be pleased to see this shown to all newly diagnosed patients, gives a good overview.
Clear information and explanation. Great Resource.
Thanks
My father died of this when i was 6 years old (He got to live till 36)
It is an evil disease.
I'm 36 n recently diagnosed. 😔 terrifying
@@cindyreyes91 I got diagnosed on 29 th December 2021 and because of my diet and medication it is better please go for whole plant based diet
My sister in law died from this in her mid 40s after a lot of painful years.
Great video 👍🏻
Clear explanation & covered the most important points.
THANKS 🙏🏻
Don't mind me just looking at what to expect from my future
Do Yogasan 1 hour daily especially lungs exercise. Don't come in contact with cold weather directly and drink plenty water and eat turmeric, ginger,dry food,Ashwagandha these are the best alternative to treat PSS and one more things try to avoid milk and milk products at least 4 months
Has ANYONE tested positive for Antiscl-70 antibodies and NOT had scleroderma? I have zero symptoms and every organ is normal
Your video’s are the best, and very helpful because my mom has this illness this type of information is very helpful 🙏🏼✨🤳🏻😘 keep up the good work.
Why have you turned comments off on your Ankylosing Spondylitis video? Is it because you are completely WRONG that men are 3 x more likely to have it? Might be. Says a woman with Psoriatic Spondylitis. VERY OLD HAT, sir!
Please read the correction in the video description.
Living with MS is terrible but thankGod for making me Negative of MS recently, after I meant a channel on TH-cam ( Dr mason channel )...thank you Doctor
I have GERD and Raynaud syndrome but not Scleroderma apparently, no doctor mentioned it.
Thank you so much for making such a amazing lecture the most rated channel for medicos on tube will suggest to all of the medicos
Garcia David Jackson Shirley Jones Edward
Jones Kimberly Moore Linda Thomas William
Lopez Joseph Rodriguez Amy Perez Daniel
THANK YOU SO MUCH for all your videos. They have helped me more than overpriced nursing school.
Moore Betty Walker Joseph Jones Ruth
thank you for sharing. i appreciate it so much. May God bless your effort.
I'm a 20yr old male with cracking joints, deteriorating eyes, and calcium buildup under the already dry skin on my knees and chin/center neck.. at this point I don't know what the cost of these 'rare case treaters' are and I'm already anxious the way it is with how far it has seemingly progressed....
I'm sorry for that,but I know who can help you with a cure
Do you have diagnosis?
My thoughts are with all the people suffering from this horrible disease. Somebody I know has recently been diagnosed with scleroderma and it’s the most traumatic thing that’s ever happened in our lives. Please have an extensive read about Helminthic therapy.
Lopez Angela Garcia Carol Harris Brian
Has anyone experienced or heard of CREST being aggravated by physical trauma (following a fall or accident?)? TIA!
If PM-Scl is positive on ENA test but ANA test is negative. Does it mean the person has scleroderma?
Symptoms are limited to Raynaud's and blood vessels only. No skin related issues are there at all.
Does it mean that there is presence of another disease that mimics scleroderma?
If you find out PLEASE let me know. I have zero symptoms of scleroderma and still tested positive for Antiscl-70 antibodies. I don’t even get Reynolds’s at all.
@@PaarthurnaxdovaI have the same, one year passed and nothing wrong is happening :)
These are brilliant! I wish I had these in medical school 20 years ago. I’m using them to revise for my occupational health OSPE exams.
Young Jose Thomas James Allen Jason
so underrated channel. one of the best. thanks sir
Thanks Shivir!
I was diagnosed two months ago and am physically and mentally exhausted every day, had to retire early I just feel like a burden to my wife.
I'm sorry to hear that. I hope you feel better
Don't worry freind , hope you are get well soon
తెలుగు బాష లో దయచేసి తర్జుమా చేయగలరు (please Telugu)
Very helpful. Thank you so much!🙏
Saya sdh mengalami 3tahun penyakit ini apkh saya bisa berkosulltasi pada anda.karena saya belum mendapatkan dokter yg tepat
Thanks for this. I have CREST & since I was about 20.
How old are you now
hi , your all videos are very helpful, can you please make a video on Raynaud's disease. thanks
Check out the one of systemic sclerosis - it has a section all about Raynauds!
I'll do a short!
thank you. appreciated. @@ZeroToFinals
Can systemic sclerosis patient take HemoHim supplement(korian product)??
41343 Jones Plaza
I'm wondering if the drug sulodexide would help in this case? Anyone got any experience using it?
Very useful thank you!
Ini yg. Saya alami bagaimana saya bisa membuatnya normal kembali.can you help me
is this mercury poison 3rd stage..i thought it was mercury poison while i find circles on nail
Ihave been living in deases since 2007 nowi iam improve
Amazing exposition in a concise manner. Thank you!
Thanks Adeola!
Awesomely explained everything!
Very useful, thanks so much from Egypt 💖💖
How'd we get this
reat video, but why not try diet change?
I would try the Seignalet diet for one full month:
- remove ALL cereals 100%
- remove ALL milk&dairy products from my diet.
for one full month, and then see!
Hello dear Dr, would you please tell me how did you make this nice video? Which app did you use? Many thanks
I had Renauds gor many now i been diagnosed of systemic antibodies my fingers splits under the nails i tought i had fungal nails infection im suffering of pain they put me on steroids recently thank for some of info
Hi, I have many symptoms with positive Ana cytoplasmic staining but neg Ena panel. I have Reynauds and alot of nail issues as well. Not sure if its fungal but almost feels like the sidewalls of my nails are always infected or something and my nails are growing into my skin if that makes sense. I kept going to hand surgeon for ingrowns but they said they arent ingrown nails. its always on sides of thumb nails and painful.
waw♥️♥️♥️
I just brought kindle version of the book…
I just have one query and I would appreciate if you can reply back….
Is the book suitable for post graduate in medicine? I hope you understand what I mean. Btw the video and the book both are awesome. Great work
Yes, it should be helpful for learning general medicine at any stage
Your channel is a perfection 💙
Good video man, I had to break out the pen and paper on this one. Ha-Ha!
Awesome! You can find written information on the website!
Fantastic👌🏻👍🏻
:)
Glomerolonephritis is not associated with Scleroderma
In Ayurved, Scleroderma is correlated with “Uttana Vatarakta” that causes imbalance of dosha, dhatu, & dushya. The imbalance of three doshas (vata, pitta, & kapha) is responsible for the scleroderma
Can it be treated using ayurvedic medicine?
thank u so much , that was very helpful
Thank you sir for the information given
Great
Great video! One of the inspirations behind my videos! Keep it up buddy
Thanks for the information.
Pls make a video on SLE
Brilliant work, so good
💜too good! thanx!
Glad you like it!
Beautifully explained
Thank you for this information!
Great video
Thank you so much 😊
wow thank you
Amazing explanation!!!!
Thank you so much!!
Thank you!
Thank you
very helpful 👍🏻
great video thank u
thankyou doc :)
Thank you 😊
thx a loot 👍❤
Thanks
Vanaja =
Bitte in Deutsch
This was so goodddddd
Very greatful. Thank you a lot for such a great videos. 🙂
Glad to help!
Amazing illustration 🤩
Really fantastic & brilliant presentation within short time with huge information.Thanks a lot.
Glad to help
У меня скеледермия Рено
Thank you!!!
Thank you!!!!! Thank you!!!!!
lov u soooo much ....from india
Hi India. cant wait to visit one day!
Great 👌
Brilliant !!!