dude. I can’t believe I’m not the only one . I’ve had parvo since last December. And nothing has changed. Your story of it getting slightly better is giving me hope. I hope you are better and thank you for making me feel a little less alone in the world.
April Lindsay typing this literally from my bed bc I cant move. I’ve had it since December 2018, so in a couple months it’ll be four years. This is crazy
Thanks for posting this,i was just finally diagnosed with Parvo yesterday and it was at my own request for this specific blood test about a week ago at patient first,i am 44 male carpenter,and this infection kicked my ass,made it impossible to work for a couple months because the pain was so severe and would come on so fast, tried working for a while but hips were so bad i had to hobble everywhere,hands/wrists were basically useless,could barely turn the ignition let alone hold things up and hammer/nailgun them,getting in and out of work vehicle was hell would have to physically lift my leg up and put it on the brake pedal,and lots of other things were just PURE HELL with so many painful swollen joints not to mention no sleep due to the pain.The bright side is after about 4 months of this, the pain jumping all around my body it is only slight now and easily tolerable,i feel this is due to my very strict low carb diet and fasting,the benefits of fasting are amazing especially with illnesses,research has shown that this virus can be found in body tissue for years later,and can also be found in your synovial fluid which is the fluid that lubricates tendons/joints so my goal was to try to get as much regeneration going as i could and produce as much human growth hormone and stem cells as i could in my own body and fasting is awesome at this, stem cells are important because they are blank and become whatever your body needs the most and go there i just cant say enough about the benefits of fasting with this condition,mix that with a low carb no sugar diet like Keto,eat a lot of leafy greens like spinach and kale,broccoli,cauliflower and add in some supplements like oil of oregano,garlic,apple cider vinegar,pure licorice and lots of other natural virus/bacteria/fungus fighters and do some research,and i will bet your condition will improve,there is just no way in hell i was about to just accept the fact that this disease was gonna win and be a lifelong problem,without me at least fighting back and learning as much as i could about it,on the days when you just feel like face planting exhausted,you just have to walk,move and burn this crap out of you,and turn your body into a hostile environment where nothing bad wants to live,good luck to anybody going through this virus,and i hope you kick its sorry ass.
@@mrfake675 started only eating every 8 hrs, then 12,then OMAD one meal a day ,have been doing that for a while and once a month 72 hour fast,i found for me switching between 16/8 style of fasting and OMAD works best for me.
I had parvo 5 years ago. Before that I was perfectly healthy. It took me about a year to recover, but then I developed hashimoto (pretty common to develop an autoimmune disease after a virus completely messes up your immune system), which lead to its own set of symptoms. I never had the rash but I had the severe joint pain, brain fog, hair loss, weight loss, issues to my eyes, inflammation, insomnia, gut issues, etc. I saw so many doctors who had no understanding of what parvo is and how it can affect adults, especially women. They think it is a ´kid disease’ that goes away within 2 weeks. This virus has completely ruined my health ...
Hey, thank you for posting this. It's so hard to find anything on this on the web. I am 36 and Ive been living with it for more than six years. I have found that diet has a lot to do with the amount of pain i will have the next morning. Eating clean helps a lot but anything can make it flare up. Ibuprofen is my last grab but it works. Glad i am not the only one with this thing. Stay positive.
@@AMGGT63DRIVER Sorry to have to give you bad news... but Iv had Parvo since 2014 and it still sucks just as much. Symptoms dont really improve. The only thing that improves is that you can tell when you are going to have a flare up. It really is a terrible disease because no one really understands it. No one really understands the immense joint pain. Best of luck
Amazing that this is about the only vid I could find about this. I have an infection, in week 6 now and it doesn't seem to get any better. Some days were somewhat better but then it slips back. I became from a 3x per week gym guy suddenly an old man shuffling through life. Hope it clears up. I will report here when it does (or doesn't).
Update: Still have terrible join pain and flare ups. Symptoms have NOT gotten better and it is still very much a problem Ill see you all again in 4 years lol
@@Kojo2338 Thanks for this update. Good to know at least that I'm not the only one experiencing this although 5 years sounds like 5 wasted years. Good luck.
I think it gave me Mcas. I contracted it 6 mounts ago and I feel miserabel. Fatigue, joint pain, muscle pain, itchy skin, eyes, flashing on the Face, tremmor, insomnia.. i stil have sollen lymph nodes on my neck, i have nausia, weight loss and a lot more. I still cant believe it, what one kids virus did to me...
Deterrence/Prevention Phase I clinical trials are currently evaluating vaccine candidates against parvovirus B19. [2, 8] I’m glad to see they are working on a vaccine. My pain finally started for real today achy and sore all my joints but especially hips shoulders knees ankles and the sole of my feet is so sore this is a rotten thing I hope my body can pass it soon
I was so lucky that my parvo left nearly as quickly as it came. But it was horribly painful, and yes exhausting, and the pain and fear when I woke up & it had shifted to my knees is something I wouldn’t wish on anyone. I hope you feel better soon
I wish I’d seen this sooner. I got it around Christmas 2018. I was 34 and in the hospital for about 11 days. No one could give me any answers. They thought it was lupus. I finally saw a infectious disease doc in the hospital who said “let run the test for Parvo, I don’t think it’s that but maybe” and sure enough. It was hell! I feel much better now but still have residual issues.
How are you feeling now? I have a family member who just been recently tested positive for it. How long did it take to fully go away? Or is there possibilities that it becomes a chronic situation?
I was diagnosed in 2015 at age 39. The doctor said that it was Still's disease (rheumatoid arthritis) but all blood tests showed parvo. I suffer to this day with random symptoms like joint pain and fevers, extreme fatigue.
Are you seeing a rheumatologist? I was referred to one initially because nobody could figure out what was wrong with me. The rhuemy ran the parvo labs, came back positive, and had me stay in their care. I was prescribed flexeril for pain as needed. I have been in joint pain from this since 2019. Slowly it's been getting better. Since 2021 I now only get random flares of it around my period, and when the weather is stormy. I am do for a follow up with my rhuemy but haven't made the appointment yet. But perhaps seeing one could be more helpful if you are not already.
Why would a rheumatologist be maintaining for parvovirus patients? Several mention it here. I've been to a rheum several times since parvo, and I'm sure I mentioned I had parvo prior, but they never seemed to care a whit about it. (Not saying I know this is my problem - lingering parvo - but it could be.)
What is parvovirus? What is a parvovirus infection (parvovirus B19)? The parvovirus in humans is different than the one by the same name found in dogs and cats. Humans get a different type: B19. Parvovirus B19 is a common infectious disease that spreads from person to person and most often results in no or very mild symptoms. The virus sometimes targets the cells that mature into red blood cells. Infection causes a temporary stoppage of the production of these cells. The effect of this stoppage is only apparent in individuals who don’t produce normal red blood cells. The parvovirus causes fifth disease, also known as “slapped cheek” disease, which is very common in school-aged children. How common is parvovirus b19? Up to 50% of adults in the United States have had a parvovirus B19 infection. Most experience no symptoms or mild symptoms. How is a parvovirus infection spread? Human parvovirus is present in the nasal mucus, spit or saliva. The virus can be spread through airborne droplets when an infected person coughs or sneezes. It may also spread through blood or contaminated blood products. Pregnant people with parvovirus can spread the virus to the fetus through the placenta. What are the symptoms of a parvovirus infection? Symptoms of a parvovirus B19 infection in children can be different than in adults. Symptoms include: Swollen and/or painful joints (more common in adults). Fatigue. Low-grade fever. Headache. Upset stomach. Arthritis (some cases have caused chronic arthritis or even rheumatoid arthritis). Gloves and socks syndrome (less common and usually in adults). The parvovirus can also, rarely, cause you or your child’s body to stop making new blood cells. This is a serious symptom because it can cause severe anemia. You may experience this symptom if you have: Sickle cell anaemia Other blood disorders How long does a parvovirus B19 infection last? The parvovirus B19 incubation period (the time between when you’re exposed to the virus to when you have symptoms) is between three days and three weeks. If you have symptoms, you’ll only have them for a short time, about five to seven days. You are no longer infectious after the rash from fifth disease appears. Symptoms of fifth disease caused by the parvovirus include: The “slapped cheek” rash. Four to 14 days after your child is infected, you may see a pink or red rash on their chin and cheeks. This rarely happens in adults. A raised “lacy” rash on their torso, arms and legs. The rashes can stick around for several weeks - getting better or worse, coming and going. Heat, sunlight and stress can make the rashes worse. Sometimes a second rash occurs several days after the slapped cheek rash appears. It may be present on your arms, legs, chest, back or butt. The rash might cause itching and discomfort. It usually disappears after seven to 10 days, but sometimes it lasts for several weeks. Sources my.clevelandclinic.org/health/diseases/16633-parvovirus-infection
I've been suffering with extremely bad joint pain swelling stomach problems headaches I've been in and out of the er different doctors no one knew what was wrong finally one thought to test me for it sadly that's what I had I'm still dealing with it if I'm being honest it's only gotten worse it's been about 2 years now all they say it it'll get better on its own or maybe it won't but one thing if anyone can answer for me ik the virus itself can cause extreme joint pain/swelling but will it actually affect your joints like arthritis does? or is it just you get the pain but perfectly "healthy" in the sense it's not attacking your joints? I've been so worried because idk if it will tear at my joints like arthritis does or if I just have to deal with the pain but still be healthy
Hi @ahna lopez . I had heart/ kidney transplant in May, and finally tested positive for Parvo 3 weeks ago. Due to immunosuppresant drugs I was left open for this. My issue was/is severe anemia. The joint pain is secondary for me, sorry if yours is that bad. My team explained that it is reliably treated with Intravenous Immunoglobin. ( Iv Ig) . It is essentially a boost for your immune system to kick Parvo's ass in your bones. I went to an infusion center five days in a row and was given this treatment each day. This concluded one week ago. I can't say I feel any different, but def not worse. My white blood cells are coming back slowly, red blood cells and hemoglobin take longer to rebound and mature, so there will be a delayed recovery there. I've had the same idea/question as you: Are these effects reversible once healed, or have we done lasting damage to our joints and bone marrow? I've not found a concise answer yet . Tl:Dr: Ask you doctors about Iv Ig treatments. www.medicinenet.com/what_is_intravenous_immunoglobulin_used_for/article.htm
What about immunoglobulin therapy? I believe that is available. On a side note, I believe, based on my research on the internet, that HIV does not cause AIDS but may in fact be caused by the parvovirus. Have you ever been tested for HIV? I would be interested to know the results. An HIV test may turn up positive but you will not die of AIDS. That is, HIV particles in your blood is just a side effect of the parvo infection. Anybody with adult parvo out there testing positive for HIV? It's just a pet theory.
Hey guys! I was diagnosed with the parvob19 virus last year. I had 5.8 igg and 0.2 igm immunoglobbins. Last year, October 2018, I was admitted into the er for almost a week with hives, anaphylaxis, severe joint pain, joint swelling. Just a few weeks ago, I downloaded my medical app and collected all my medical records. I found that I had tested positive for parvob19 virus. Nobody told me. I found it on my app in the middle of the night. The past month I have been diagnosed with a right ovarian cyst, gastroenteritis(stomach virus)(parvovirus), hives, joint pain/neuropathy, extreme exhaustion, nausea, vomiting, low tsh, low lipase, high platelet count and increased inflammatory response. Abs basinophills, c-reactive protein etc. I've had over a year and half of acute systematic problems correlating with my ovulation. Long story short each month around ovulation, I get hives, joint pain, nerve pain and I am itchy. It's as if this virus activates when my body tries to get pregnant/ovulates. Which makes sense as this virus gets in your bone marrow and can replicate via your DNA. This virus is no joke and we need to come together and manifest funding for more research and get a vaccine for this "immunogobblin," virus. I am 26 and I've had two miscarriages. There are so many women out there who are having complications from this virus and we need to unite and eradicate it. The symptoms we all have are way too similar and it is too uncanny. I am a nurses aide and I am slowly going through school for pharmacy. Please add the support page on Facebook. Together we will get through this! If you have any questions please reach out to me. Happy healing and eradicating! m.facebook.com/Parvob19-Virus-support-group-101931927985867/
dude. I can’t believe I’m not the only one . I’ve had parvo since last December. And nothing has changed. Your story of it getting slightly better is giving me hope. I hope you are better and thank you for making me feel a little less alone in the world.
I’ve had it since Jan 2019. Still dealing with severe joint pain
April Lindsay typing this literally from my bed bc I cant move. I’ve had it since December 2018, so in a couple months it’ll be four years. This is crazy
Thanks for posting this,i was just finally diagnosed with Parvo yesterday and it was at my own request for this specific blood test about a week ago at patient first,i am 44 male carpenter,and this infection kicked my ass,made it impossible to work for a couple months because the pain was so severe and would come on so fast, tried working for a while but hips were so bad i had to hobble everywhere,hands/wrists were basically useless,could barely turn the ignition let alone hold things up and hammer/nailgun them,getting in and out of work vehicle was hell would have to physically lift my leg up and put it on the brake pedal,and lots of other things were just PURE HELL with so many painful swollen joints not to mention no sleep due to the pain.The bright side is after about 4 months of this, the pain jumping all around my body it is only slight now and easily tolerable,i feel this is due to my very strict low carb diet and fasting,the benefits of fasting are amazing especially with illnesses,research has shown that this virus can be found in body tissue for years later,and can also be found in your synovial fluid which is the fluid that lubricates tendons/joints so my goal was to try to get as much regeneration going as i could and produce as much human growth hormone and stem cells as i could in my own body and fasting is awesome at this, stem cells are important because they are blank and become whatever your body needs the most and go there i just cant say enough about the benefits of fasting with this condition,mix that with a low carb no sugar diet like Keto,eat a lot of leafy greens like spinach and kale,broccoli,cauliflower and add in some supplements like oil of oregano,garlic,apple cider vinegar,pure licorice and lots of other natural virus/bacteria/fungus fighters and do some research,and i will bet your condition will improve,there is just no way in hell i was about to just accept the fact that this disease was gonna win and be a lifelong problem,without me at least fighting back and learning as much as i could about it,on the days when you just feel like face planting exhausted,you just have to walk,move and burn this crap out of you,and turn your body into a hostile environment where nothing bad wants to live,good luck to anybody going through this virus,and i hope you kick its sorry ass.
How long do you fast?
@@mrfake675 started only eating every 8 hrs, then 12,then OMAD one meal a day ,have been doing that for a while and once a month 72 hour fast,i found for me switching between 16/8 style of fasting and OMAD works best for me.
@@Lambo-op2oj no personally I didn't have any crunching
Thank you for sharing your story. I hope you are doing better today.
I had parvo 5 years ago. Before that I was perfectly healthy. It took me about a year to recover, but then I developed hashimoto (pretty common to develop an autoimmune disease after a virus completely messes up your immune system), which lead to its own set of symptoms. I never had the rash but I had the severe joint pain, brain fog, hair loss, weight loss, issues to my eyes, inflammation, insomnia, gut issues, etc. I saw so many doctors who had no understanding of what parvo is and how it can affect adults, especially women. They think it is a ´kid disease’ that goes away within 2 weeks. This virus has completely ruined my health ...
Hey, thank you for posting this. It's so hard to find anything on this on the web. I am 36 and Ive been living with it for more than six years. I have found that diet has a lot to do with the amount of pain i will have the next morning. Eating clean helps a lot but anything can make it flare up. Ibuprofen is my last grab but it works. Glad i am not the only one with this thing. Stay positive.
Hi there, thanks for sharing your experience. Has your symptoms improved?
@@AMGGT63DRIVER Sorry to have to give you bad news... but Iv had Parvo since 2014 and it still sucks just as much. Symptoms dont really improve. The only thing that improves is that you can tell when you are going to have a flare up.
It really is a terrible disease because no one really understands it. No one really understands the immense joint pain.
Best of luck
Amazing that this is about the only vid I could find about this. I have an infection, in week 6 now and it doesn't seem to get any better. Some days were somewhat better but then it slips back. I became from a 3x per week gym guy suddenly an old man shuffling through life. Hope it clears up. I will report here when it does (or doesn't).
Update. In week 13. Last week I had two days where I thought it was gone. Fully recovered. But it came back with a bite. Bizarre.
@@georgeoreilly1546 Hi, Do you have only joint pain as a symptome? I am on my 6th mount , but i have a lot more to deal with....
Thank you for your videos. I just got a positive result on my parvovirus B19 at the age of 35. And it’s kicking my butt. Everything hurts so bad.
Has anyone else had this for more than 5 years? I keep reading online that it should "go away on its own" but it is still very much a problem.
Update: Still have terrible join pain and flare ups. Symptoms have NOT gotten better and it is still very much a problem
Ill see you all again in 4 years lol
@@Kojo2338 Thanks for this update. Good to know at least that I'm not the only one experiencing this although 5 years sounds like 5 wasted years. Good luck.
I was never the same, but have a very rare immune reaction to the disease. I was later diagnosed with Fibromyalgia.
I think it gave me Mcas. I contracted it 6 mounts ago and I feel miserabel. Fatigue, joint pain, muscle pain, itchy skin, eyes, flashing on the Face, tremmor, insomnia.. i stil have sollen lymph nodes on my neck, i have nausia, weight loss and a lot more. I still cant believe it, what one kids virus did to me...
Deterrence/Prevention
Phase I clinical trials are currently evaluating vaccine candidates against parvovirus B19. [2, 8]
I’m glad to see they are working on a vaccine. My pain finally started for real today achy and sore all my joints but especially hips shoulders knees ankles and the sole of my feet is so sore this is a rotten thing I hope my body can pass it soon
Where do I find this info at!? I’ve suffered with this for over 5years. It’s exhausting
I was so lucky that my parvo left nearly as quickly as it came. But it was horribly painful, and yes exhausting, and the pain and fear when I woke up & it had shifted to my knees is something I wouldn’t wish on anyone. I hope you feel better soon
I wish I’d seen this sooner. I got it around Christmas 2018. I was 34 and in the hospital for about 11 days. No one could give me any answers. They thought it was lupus. I finally saw a infectious disease doc in the hospital who said “let run the test for Parvo, I don’t think it’s that but maybe” and sure enough. It was hell! I feel much better now but still have residual issues.
How are you feeling now? I have a family member who just been recently tested positive for it. How long did it take to fully go away? Or is there possibilities that it becomes a chronic situation?
I was diagnosed in 2015 at age 39. The doctor said that it was Still's disease (rheumatoid arthritis) but all blood tests showed parvo. I suffer to this day with random symptoms like joint pain and fevers, extreme fatigue.
Hello Rachel and thanks for sharing your story. How are you doing today? Better I hope.
Is there a different video, that is more detailed in your journey?
Thank you for the hope❤️
Omg, this is so frustrating! I just want to get better
Did you b19 goes low when you did you blood test or no?
I've been sick over a month just diagnosed with parvo and I'm dying I'm so miserable I can't walk I haven't been offered anything
Are you seeing a rheumatologist? I was referred to one initially because nobody could figure out what was wrong with me. The rhuemy ran the parvo labs, came back positive, and had me stay in their care. I was prescribed flexeril for pain as needed. I have been in joint pain from this since 2019. Slowly it's been getting better. Since 2021 I now only get random flares of it around my period, and when the weather is stormy. I am do for a follow up with my rhuemy but haven't made the appointment yet. But perhaps seeing one could be more helpful if you are not already.
Why would a rheumatologist be maintaining for parvovirus patients? Several mention it here. I've been to a rheum several times since parvo, and I'm sure I mentioned I had parvo prior, but they never seemed to care a whit about it. (Not saying I know this is my problem - lingering parvo - but it could be.)
What is parvovirus? What is a parvovirus infection (parvovirus B19)?
The parvovirus in humans is different than the one by the same name found in dogs and cats. Humans get a different type: B19. Parvovirus B19 is a common infectious disease that spreads from person to person and most often results in no or very mild symptoms. The virus sometimes targets the cells that mature into red blood cells. Infection causes a temporary stoppage of the production of these cells. The effect of this stoppage is only apparent in individuals who don’t produce normal red blood cells.
The parvovirus causes fifth disease, also known as “slapped cheek” disease, which is very common in school-aged children.
How common is parvovirus b19?
Up to 50% of adults in the United States have had a parvovirus B19 infection. Most experience no symptoms or mild symptoms.
How is a parvovirus infection spread?
Human parvovirus is present in the nasal mucus, spit or saliva. The virus can be spread through airborne droplets when an infected person coughs or sneezes. It may also spread through blood or contaminated blood products. Pregnant people with parvovirus can spread the virus to the fetus through the placenta.
What are the symptoms of a parvovirus infection?
Symptoms of a parvovirus B19 infection in children can be different than in adults. Symptoms include:
Swollen and/or painful joints (more common in adults).
Fatigue.
Low-grade fever.
Headache.
Upset stomach.
Arthritis (some cases have caused chronic arthritis or even rheumatoid arthritis).
Gloves and socks syndrome (less common and usually in adults).
The parvovirus can also, rarely, cause you or your child’s body to stop making new blood cells. This is a serious symptom because it can cause severe anemia. You may experience this symptom if you have:
Sickle cell anaemia
Other blood disorders
How long does a parvovirus B19 infection last?
The parvovirus B19 incubation period (the time between when you’re exposed to the virus to when you have symptoms) is between three days and three weeks. If you have symptoms, you’ll only have them for a short time, about five to seven days.
You are no longer infectious after the rash from fifth disease appears.
Symptoms of fifth disease caused by the parvovirus include:
The “slapped cheek” rash. Four to 14 days after your child is infected, you may see a pink or red rash on their chin and cheeks. This rarely happens in adults.
A raised “lacy” rash on their torso, arms and legs.
The rashes can stick around for several weeks - getting better or worse, coming and going. Heat, sunlight and stress can make the rashes worse.
Sometimes a second rash occurs several days after the slapped cheek rash appears. It may be present on your arms, legs, chest, back or butt. The rash might cause itching and discomfort. It usually disappears after seven to 10 days, but sometimes it lasts for several weeks.
Sources
my.clevelandclinic.org/health/diseases/16633-parvovirus-infection
My daughter is 24 and I think she has Parvo! I am so worried about her!
I’ve had for 20 years now
Cindy Khos omg !!!! No!! I’m going on year 2 now. Does it get any better at all ?!?
This is not encouraging at all. I’m only on month 3. Cindy- do you feel any better?
We never know of our genetic weaknesses.
I this helped a lot but I'm 48 and it has kept me bed ridden unfortunately my life has totally changed I'm so depressed and frustrated
I've been suffering with extremely bad joint pain swelling stomach problems headaches I've been in and out of the er different doctors no one knew what was wrong finally one thought to test me for it sadly that's what I had I'm still dealing with it if I'm being honest it's only gotten worse it's been about 2 years now all they say it it'll get better on its own or maybe it won't but one thing if anyone can answer for me ik the virus itself can cause extreme joint pain/swelling but will it actually affect your joints like arthritis does? or is it just you get the pain but perfectly "healthy" in the sense it's not attacking your joints? I've been so worried because idk if it will tear at my joints like arthritis does or if I just have to deal with the pain but still be healthy
Hi @ahna lopez . I had heart/ kidney transplant in May, and finally tested positive for Parvo 3 weeks ago. Due to immunosuppresant drugs I was left open for this. My issue was/is severe anemia. The joint pain is secondary for me, sorry if yours is that bad.
My team explained that it is reliably treated with Intravenous Immunoglobin. ( Iv Ig) . It is essentially a boost for your immune system to kick Parvo's ass in your bones. I went to an infusion center five days in a row and was given this treatment each day. This concluded one week ago. I can't say I feel any different, but def not worse. My white blood cells are coming back slowly, red blood cells and hemoglobin take longer to rebound and mature, so there will be a delayed recovery there.
I've had the same idea/question as you: Are these effects reversible once healed, or have we done lasting damage to our joints and bone marrow? I've not found a concise answer yet .
Tl:Dr: Ask you doctors about Iv Ig treatments.
www.medicinenet.com/what_is_intravenous_immunoglobulin_used_for/article.htm
can humans get parvo from dogs
you cannot! you also cannot die like dogs can from getting the virus
@@rachelknight705 thanks for reply
@@vannasagwal6031 Different strain.
I believe the opposite to be true
I have a parvo story... it was a year ago.
Since when do we have the parvo virus here in Australia so much for our tough bio-security laws & regulations its all a bunch of bullshit
What about immunoglobulin therapy? I believe that is available.
On a side note, I believe, based on my research on the internet, that HIV does not cause AIDS but may in fact be caused by the parvovirus. Have you ever been tested for HIV? I would be interested to know the results. An HIV test may turn up positive but you will not die of AIDS. That is, HIV particles in your blood is just a side effect of the parvo infection. Anybody with adult parvo out there testing positive for HIV? It's just a pet theory.
Hey guys! I was diagnosed with the parvob19 virus last year. I had 5.8 igg and 0.2 igm immunoglobbins. Last year, October 2018, I was admitted into the er for almost a week with hives, anaphylaxis, severe joint pain, joint swelling. Just a few weeks ago, I downloaded my medical app and collected all my medical records. I found that I had tested positive for parvob19 virus. Nobody told me. I found it on my app in the middle of the night. The past month I have been diagnosed with a right ovarian cyst, gastroenteritis(stomach virus)(parvovirus), hives, joint pain/neuropathy, extreme exhaustion, nausea, vomiting, low tsh, low lipase, high platelet count and increased inflammatory response. Abs basinophills, c-reactive protein etc. I've had over a year and half of acute systematic problems correlating with my ovulation. Long story short each month around ovulation, I get hives, joint pain, nerve pain and I am itchy. It's as if this virus activates when my body tries to get pregnant/ovulates. Which makes sense as this virus gets in your bone marrow and can replicate via your DNA. This virus is no joke and we need to come together and manifest funding for more research and get a vaccine for this "immunogobblin," virus. I am 26 and I've had two miscarriages. There are so many women out there who are having complications from this virus and we need to unite and eradicate it. The symptoms we all have are way too similar and it is too uncanny. I am a nurses aide and I am slowly going through school for pharmacy.
Please add the support page on Facebook. Together we will get through this! If you have any questions please reach out to me.
Happy healing and eradicating!
m.facebook.com/Parvob19-Virus-support-group-101931927985867/
@@cranberryfrank530Hi, how are you doing now?
I thought only dogs can get it...? 😂
Austin. Nope, I have parvo
Australian Mapping uhhh ok... Idk....🤨
can humans get parvo from dogs? plz reply
vanna sagwal no lmao
There is a canine, feline, and human strain.