@@conniehoyle2669they all make a lot of money NOT helping people what seems to be the problem! I am sorry but arthritis and these problems have been around for years and years!
The part that drives me nuts is having to explain myself over and over again. "I'M NOT FEELING WELL. I AM SICK!" I tell people. They just don't get it. "Well you don't look sick." My family has been gaslighting me for over 30 years.
I understand if I say I’m Not feeling well maybe next time I know they talk about me and the roll Of eyes behind my back . I wish there was a cure , but I’m Not finding it .
It because there not much the doctors can do.... alot of doctors see that you have this & it really doesn't benefit them to treat you they don't make much off you you$$$$$$$$$$$$$$$$$$$ when they test or do byopsis & give pills & expensive medicine that don't do anything...but give you more problems like more pain Diarria... then ur left worse.... sorry to disappoint or b negative but it's the truth... raw truth doctors want to make money off you if you keep letting them that's were they will have you, like there PET!🤣 $$$$$$$$$$$$$$$$$$$$$$$$$we pay there house payments & cars!🤣 & the more medicine they prescribe the doctors are happy! & your left with more issues that they cause ...to keep u coming back😂
I am in the beginning of this search, but I feel awful, dry mouth, eyes, v, headaches stomach issues,joint pain that comes and goes......brain fog ...the list goes on...........I am seeing a Rheumatologist on the 20th cant wait. I started looking up dry mouth and found my way to sjogrens which sums up a lot for me. Also I have had RMSF 2x and Babesiosis, covid. Thanks for sharing this
The host is wonderful. She kept trying to reel in the guest. The guest rambled on and on about menstrual problems, teaching art, etc. I came here to learn more about Sjogrens. And BTW, they did have the ANA ( Anti Nuclear Antibody) test in 1980.
I could have accomplished so much more in my youth if I had been diagnosed correctly. My Ana was always high but never was diagnosed til later when my sister was diagnosed with sjogrens. I feel so much better with the right treatment now.
I was told for two years to see a mental doctor that I was fine after two years I went back to see the do tor finally he se t me to see a RA doctor which said I had fibromialga sjogens lupus..
I am barely in the process of diagnoses. I first started 4 yrs ago with a high fever that lasted 3 days. I felt sick and crummy. And everyone at work got sick, even my husband. Didn't think much of it. But this was two weeks before Covid was declared officially in the U.S and quarintine. To make the story short, it triggered an chronic eye disease called keratitis dendritic. I was fine after treatment. Yet, two years I got sick from a respetory infection working with kids ( I was a teacher). I had to be in medical leave because I had 5 ulcers in my eye (keratitis dendritic aka herpedic eye).Took strong doces of acyclovir. From there on, I had dry eye syndrome, the trigeminal nerve pain, the 8 months after,ezcema on my neck and chin, then I became sensitive to most sunblocks, acept the one with zinc oxide. Then after fighting this for 4 years, in mid August I almost fainted. And I started have other symptoms like, sever trigeminal shock pain, dehydration. I would drink water and nothing helped, my eye were more dry than usual. My knees and ankles started to hurt. Then my stomach, lower back and last my hands and feel started to burn. So here I am trying to get things figured out in Mexico because here in the USA there is no appointments with the rheumatologist till Feb.24th 2025. I already have had 3 espisodes of pain in this month and a half. No treatment yet, till testing is done. I feel scared. I am a mother of 3 young children. I want to be able to live long for them. Is there hope for me? I need guidance.Also, no one in my family has this disease. Could have covid triggered this autoimmune disease? I also tested high on ANA Test (1:320) yet negative in all autoimmune disease. However, I have ALL the symptoms of Sjogren's Disease and rheumatologist and my cornea specialisr said the same thing. But tomorrow I have to have a biopsy of mu salavary glands. I am in so much pain and they still don't give me treatment yet. My family doesn't believe what I am going through. My oldest son laughs when I tell him my hands hurt. My husband is acting apathetic towards my pain; he tells me he will take me to the doctor another day "but not today because I have to go to work..." My mom thinks that other autoimmune disease are worse and this is not life threatening. Even general doctors in the U.S have told me " I don't think you have Sjogren's. I am so frausterated.
The hardest thing is friends and family thinking you’re just making it up. For the last 10 years it was always something with me. Not fun for me. Migraines. Dizzy, fatigue, bladder IC, weight gain and weight loss, sometimes I hurt from the air pressure as someone is just passing me in a store, now I have no slobber my esophagus is sloughing off , I’m coughing up tissue, RA now ,and I had a girlfriend say to me what are you dying from now. I have a small circle of friends it just got smaller. Finally I have a new PCP that looked at me and said you have Sjogren disease. I just cried like a baby. I see the RA doctor the end of July . PCP put me on hydroxyclorquine I hope it helps. I’m now 1 month on it.
I had Glandular fever (mononuclosis) at 21 and and a viral infection in my late 40's that behaved like meningitis I. noticed a big difference in my 2 pregnancies. Second one at 34 was like I had low thyroid, less amniotic fluid at the end, shingles on my tummy. Stomach problems throughout my adult years but i felt like a malingerer all my younger adult years. I had an infected parotid gland at about 49 and soon after lost 2 molars after unsuccessful root canal attempts. Also it should be mentioned that 90% of sufferers are women and it gets much worse after menopause. It seemed to be menopause that really stepped up the symptoms and I started to get Raynauds in my hands. Stabbing pains in my eyes. The Raynauds and a strange condition of nodules that showed on my knuckles that actually drained joint fluid was what finally made me "demand' a referral from a random GP to a Rheumatologist. The GP was reluctant to give me the referral or a steroid puffer for my struggling lungs after the swine flu outbreak in Australia. (I haven't stuck with one GP as they seem to retire or not take me seriously) The Rheumy asked if I had dry eyes and did the blood tests which had a very high ANA result. Many years now struggling with the dry mouth and dry eyes. I have tried every drop and gel available. The usual medications, pilocarpine, hydroxychloroquine etc, for dry eye had too many side-effects. As part of my flares I get shingles outbreaks and keep anti-virals on hand. I have damaged eyes, I had shingles in an eye which has made it very dry and easily infected now. I've had punctal cauterization (not a great help) and dental issues. Now I can't eat a meal or swallow without water. My lungs are getting weaker very gradually and my bowels are mostly constipated. My diagnosis took 20 years. It's time-consuming and expensive to see specialists and most GPs do not connect the dots. There was little info out there 20 years ago. I am 72 and just live with the condition and try to stay on top of what keeps it under control. Looking back, My 6 siblings haven't shown symptoms that I am aware of, but perhaps my father had some symptoms and went undiagnosed. He had hiatus hernia, heart problems and high blood sugar. I feel viruses and hormones have played a big part and hope there are more treatments in the future!
What helped me the most is a carnivore diet, fasting, taking 500 mg of magnesium citrate a day to keep the bowels going, and yes, antivirals are a must.
Omg, I’ve never seen anyone be so ill mannered in a conversation. Cindy is bad for interrupting and just mowing down the very gracious host , who is trying to honor her story. Learn how to take turns respectfully.
My medical doctor just confirmed me better and very okay after undergoing DR Madida herbal treatment plan for my Meniere disease and Parkinson Disease.
Question…. Has Anyone gotten hives, elevated itching nearly Everywhere while on hydroxy?? I’m stressed at how I seem to react to nearly All meds?! Help?
It took 35 years for me to get a diagnosis - 35 years of hell.
I am so sorry 😞 I understand for me really it’s about 15 years I think
@@conniehoyle2669they all make a lot of money NOT helping people what seems to be the problem! I am sorry but arthritis and these problems have been around for years and years!
The part that drives me nuts is having to explain myself over and over again. "I'M NOT FEELING WELL. I AM SICK!" I tell people. They just don't get it. "Well you don't look sick." My family has been gaslighting me for over 30 years.
I understand if I say I’m
Not feeling well maybe next time I know they talk about me and the roll
Of eyes behind my back . I wish there was a cure , but I’m
Not finding it .
I am living this right now, and I feel alone and unsupported.
@@marie.theartist I'm truly sorry.
I have Sjogren’s and it took years to be diagnosed! Having Jesus has really helped me cope with the disease!
I've had this disease for years but no doctor was at all interested in diagnosing me.
Same with me.
My experience was the same.
It because there not much the doctors can do.... alot of doctors see that you have this & it really doesn't benefit them to treat you they don't make much off you you$$$$$$$$$$$$$$$$$$$ when they test or do byopsis & give pills & expensive medicine that don't do anything...but give you more problems like more pain Diarria... then ur left worse.... sorry to disappoint or b negative but it's the truth... raw truth doctors want to make money off you if you keep letting them that's were they will have you, like there PET!🤣 $$$$$$$$$$$$$$$$$$$$$$$$$we pay there house payments & cars!🤣 & the more medicine they prescribe the doctors are happy! & your left with more issues that they cause ...to keep u coming back😂
Me too. Thanks you for your channel.
I am in the beginning of this search, but I feel awful, dry mouth, eyes, v, headaches stomach issues,joint pain that comes and goes......brain fog ...the list goes on...........I am seeing a Rheumatologist on the 20th cant wait. I started looking up dry mouth and found my way to sjogrens which sums up a lot for me. Also I have had RMSF 2x and Babesiosis, covid. Thanks for sharing this
The host is wonderful. She kept trying to reel in the guest. The guest rambled on and on about menstrual problems, teaching art, etc. I came here to learn more about Sjogrens. And BTW, they did have the ANA ( Anti Nuclear Antibody) test in 1980.
Me too. Wish they’d have a guest who didn’t ramble and one could learn something helpful.
It was so difficult to follow along. Gesh! I learned more about her work career😅
This was disappointing.
I could have accomplished so much more in my youth if I had been diagnosed correctly. My Ana was always high but never was diagnosed til later when my sister was diagnosed with sjogrens. I feel so much better with the right treatment now.
What is the right treatment
I was told for two years to see a mental doctor that I was fine after two years I went back to see the do tor finally he se t me to see a RA doctor which said I had fibromialga sjogens lupus..
I love you sister.If i am allowed to say that.Sitting in that boat too.Jesus calms the storm❗️☀️
I am barely in the process of diagnoses. I first started 4 yrs ago with a high fever that lasted 3 days. I felt sick and crummy. And everyone at work got sick, even my husband. Didn't think much of it. But this was two weeks before Covid was declared officially in the U.S and quarintine. To make the story short, it triggered an chronic eye disease called keratitis dendritic. I was fine after treatment. Yet, two years I got sick from a respetory infection working with kids ( I was a teacher). I had to be in medical leave because I had 5 ulcers in my eye (keratitis dendritic aka herpedic eye).Took strong doces of acyclovir. From there on, I had dry eye syndrome, the trigeminal nerve pain, the 8 months after,ezcema on my neck and chin, then I became sensitive to most sunblocks, acept the one with zinc oxide. Then after fighting this for 4 years, in mid August I almost fainted. And I started have other symptoms like, sever trigeminal shock pain, dehydration. I would drink water and nothing helped, my eye were more dry than usual. My knees and ankles started to hurt. Then my stomach, lower back and last my hands and feel started to burn. So here I am trying to get things figured out in Mexico because here in the USA there is no appointments with the rheumatologist till Feb.24th 2025. I already have had 3 espisodes of pain in this month and a half. No treatment yet, till testing is done. I feel scared. I am a mother of 3 young children. I want to be able to live long for them. Is there hope for me? I need guidance.Also, no one in my family has this disease. Could have covid triggered this autoimmune disease? I also tested high on ANA Test (1:320) yet negative in all autoimmune disease. However, I have ALL the symptoms of Sjogren's Disease and rheumatologist and my cornea specialisr said the same thing. But tomorrow I have to have a biopsy of mu salavary glands. I am in so much pain and they still don't give me treatment yet. My family doesn't believe what I am going through. My oldest son laughs when I tell him my hands hurt. My husband is acting apathetic towards my pain; he tells me he will take me to the doctor another day "but not today because I have to go to work..." My mom thinks that other autoimmune disease are worse and this is not life threatening. Even general doctors in the U.S have told me " I don't think you have Sjogren's. I am so frausterated.
I had Sjogrens for at least 20 years before diagnosis, my family doesn’t understand how it makes me feel 😢
It's the same with me
The hardest thing is friends and family thinking you’re just making it up. For the last 10 years it was always something with me. Not fun for me. Migraines. Dizzy, fatigue, bladder IC, weight gain and weight loss, sometimes I hurt from the air pressure as someone is just passing me in a store, now I have no slobber my esophagus is sloughing off , I’m coughing up tissue, RA now ,and I had a girlfriend say to me what are you dying from now. I have a small circle of friends it just got smaller. Finally I have a new PCP that looked at me and said you have Sjogren disease. I just cried like a baby. I see the RA doctor the end of July . PCP put me on hydroxyclorquine I hope it helps. I’m now 1 month on it.
Dry mouth and lips?
@@Hew.Jarsol my mouth is full of lesions it’s so dry. My eyes are worse.
I have several autoimmunes and I’m also experiencing the systems of Srhojns
I know! Same here 😢
It's trying to keep going to doctors. When it takes years, it's like a career - getting a diagnosis.
Helpful and definitely can relate on the good, bad, and ugly. Resiliency and agency indeed so valuable.
I had Glandular fever (mononuclosis) at 21 and and a viral infection in my late 40's that behaved like meningitis I. noticed a big difference in my 2 pregnancies. Second one at 34 was like I had low thyroid, less amniotic fluid at the end, shingles on my tummy. Stomach problems throughout my adult years but i felt like a malingerer all my younger adult years. I had an infected parotid gland at about 49 and soon after lost 2 molars after unsuccessful root canal attempts.
Also it should be mentioned that 90% of sufferers are women and it gets much worse after menopause. It seemed to be menopause that really stepped up the symptoms and I started to get Raynauds in my hands. Stabbing pains in my eyes. The Raynauds and a strange condition of nodules that showed on my knuckles that actually drained joint fluid was what finally made me "demand' a referral from a random GP to a Rheumatologist. The GP was reluctant to give me the referral or a steroid puffer for my struggling lungs after the swine flu outbreak in Australia. (I haven't stuck with one GP as they seem to retire or not take me seriously)
The Rheumy asked if I had dry eyes and did the blood tests which had a very high ANA result. Many years now struggling with the dry mouth and dry eyes. I have tried every drop and gel available. The usual medications, pilocarpine, hydroxychloroquine etc, for dry eye had too many side-effects. As part of my flares I get shingles outbreaks and keep anti-virals on hand. I have damaged eyes, I had shingles in an eye which has made it very dry and easily infected now. I've had punctal cauterization (not a great help) and dental issues. Now I can't eat a meal or swallow without water. My lungs are getting weaker very gradually and my bowels are mostly constipated.
My diagnosis took 20 years. It's time-consuming and expensive to see specialists and most GPs do not connect the dots. There was little info out there 20 years ago. I am 72 and just live with the condition and try to stay on top of what keeps it under control. Looking back, My 6 siblings haven't shown symptoms that I am aware of, but perhaps my father had some symptoms and went undiagnosed. He had hiatus hernia, heart problems and high blood sugar.
I feel viruses and hormones have played a big part and hope there are more treatments in the future!
What helped me the most is a carnivore diet, fasting, taking 500 mg of magnesium citrate a day to keep the bowels going, and yes, antivirals are a must.
It took me 3 years to find out that I have sjorgens disease
I went to the doctor today and took blood to test me for this i have alot wrong with me
Omg, I’ve never seen anyone be so ill mannered in a conversation. Cindy is bad for interrupting and just mowing down the very gracious host , who is trying to honor her story. Learn how to take turns respectfully.
Describing presence is actualy my life.i am diagnosed with AS. And suspected Sjorgen....
My medical doctor just confirmed me better and very okay after undergoing DR Madida herbal treatment plan for my Meniere disease and Parkinson Disease.
They treat my Symptoms not the disease I have had similar things I have more than one Sjogrens , Scleroderma , Fibromyalgia. Hypothyroid
Thank you so much , you remind me of me! And don’t hav e support it’s good you have
I've got this Dry mouth and lips non stop. It won't go. Tired.
I have lived 28 years with RA,Lupus,and shotguns
Question…. Has Anyone gotten hives, elevated itching nearly Everywhere while on hydroxy?? I’m stressed at how I seem to react to nearly All meds?! Help?
Try getting chemical allergy testing.
That’s interesting yes hives comes and goes. Also I get hot and fevers at times. 🤷♀️
❤
This is hard to follow along
I get tired in afternoon , red and inflamation everyday
This woman sounds like my body double. 😅
This could have gone really well if the guest didn't keep talking over the host. That made it awkward and frustrating.
Light flu.so true
I am the same way I keep going until i cant go anymore than i pay for it for days i started with this pain in my early thirtys
my eye doctor told me this at 63 i raised 5 kids i was told i have rehumatoid and fibro diabetics or cornary arteriey diease