LUPUS PATIENT (SLE)

[BabaGod]

Dear Guys,

i am a lupis patient. i will be using the drug mycophenolate mofetil 500g twice daily for the rest of my life. I have been looking at the drug formulary in canada.....but i seems not to have seen the drug there. i intend to reside in manitoba. Please can someone help me to see if the cost of this drug wont result into me been medically inadmissible. Thank God the annual cost has been reviewed to be approx 20,000CAD per year..

In the same vein, if you also have a case similar to mine, Please share with me personally or you can share here.

Thank you

 

[mr.preetsingh]

Dear Guys,

i am a lupis patient. i will be using the drug mycophenolate mofetil 500g twice daily for the rest of my life. I have been looking at the drug formulary in canada.....but i seems not to have seen the drug there. i intend to reside in manitoba. Please can someone help me to see if the cost of this drug wont result into me been medically inadmissible. Thank God the annual cost has been reviewed to be approx 20,000CAD per year..

In the same vein, if you also have a case similar to mine, Please share with me personally or you can share here.

Thank you

Read about Medically which diseases are allowed and which are not in Canada.

https://www.canada.ca/en/immigration-refugees-citizenship/corporate/publications-manuals/operational-bulletins-manuals/standard-requirements/medical-requirements/refusals-inadmissibility/danger-public-health-public-safety.html

 

[zardoz]

Dear Guys,

i am a lupis patient. i will be using the drug mycophenolate mofetil 500g twice daily for the rest of my life. I have been looking at the drug formulary in canada.....but i seems not to have seen the drug there. i intend to reside in manitoba. Please can someone help me to see if the cost of this drug wont result into me been medically inadmissible. Thank God the annual cost has been reviewed to be approx 20,000CAD per year..

In the same vein, if you also have a case similar to mine, Please share with me personally or you can share here.

Thank you

https://www.rexall.ca/articles/view/1250/CellCept
https://www.drugbank.ca/drugs/DB00688

 

[BabaGod]

https://www.rexall.ca/articles/view/1250/CellCept
https://www.drugbank.ca/drugs/DB00688

thank you

 

[Dannyboy-abd]

Dear Guys,

i am a lupis patient. i will be using the drug mycophenolate mofetil 500g twice daily for the rest of my life. I have been looking at the drug formulary in canada.....but i seems not to have seen the drug there. i intend to reside in manitoba. Please can someone help me to see if the cost of this drug wont result into me been medically inadmissible. Thank God the annual cost has been reviewed to be approx 20,000CAD per year..

In the same vein, if you also have a case similar to mine, Please share with me personally or you can share here.

Thank you

hello. Did you eventually get your PPR approved? My spouse also has SLE and I want to know how it went for you. i look forward to your reply

 

[BabaGod]

Yes, we are now in Canada. We were only told to do a serum creatinine test to determine the kidney function and also to submit a report from her Consultant ( a Rheumatologist ) and since my Wife is a medical Doctor ( and also she is a rheumatologist in training), it was very easy for her to get the report. Lupus is in no way a limitation to your Canadian dream. so do not be worried.

 

[skmmadison]

Hello,
I have got an invitation to apply for PR. I was diagnosed with lupus nephritis in 2013. even though I have no active disease right now, I am very much worried that my application may get rejected due to excessive cost burden. I take Plaquenil everyday, and see rheumatologist twice an year. What should I do in this condition. How can I find what could be the healthcare cost of a lupus patient per year in Canada?

 

[Banana woman]

Hello,
I have got an invitation to apply for PR. I was diagnosed with lupus nephritis in 2013. even though I have no active disease right now, I am very much worried that my application may get rejected due to excessive cost burden. I take Plaquenil everyday, and see rheumatologist twice an year. What should I do in this condition. How can I find what could be the healthcare cost of a lupus patient per year in Canada?

I am in the same situation right now, did you get your PR, please share your experience.

 

[Meghab]

I am in the same situation right now, did you get your PR, please share your experience.

Hello
Please can you share whether you got PR or not

 

[Meghab]

Hello,
I have got an invitation to apply for PR. I was diagnosed with lupus nephritis in 2013. even though I have no active disease right now, I am very much worried that my application may get rejected due to excessive cost burden. I take Plaquenil everyday, and see rheumatologist twice an year. What should I do in this condition. How can I find what could be the healthcare cost of a lupus patient per year in Canada?

Can you please email me your number as I want to share SLE and lupus condition with you in terms of PR.
meghabanga82@gmail.com

 

[Meghab]

Hello,
I have got an invitation to apply for PR. I was diagnosed with lupus nephritis in 2013. even though I have no active disease right now, I am very much worried that my application may get rejected due to excessive cost burden. I take Plaquenil everyday, and see rheumatologist twice an year. What should I do in this condition. How can I find what could be the healthcare cost of a lupus patient per year in Canada?

 

[Meghab]

Please Reply,Did you get PR.I am also suffering from lupus.I am very worried.Please reply.

 

[Porina]

Please Reply,Did you get PR.I am also suffering from lupus.I am very worried.Please reply.

Hi, i would also want if u persue with your application and how did it go

 

[BabaGod]

having Lupus does not disqualify you from applying for PR. My wife had it and we have been in Canada now for 3yrs plus. They only wanted her to do additional medical to check her EGFR and not blood creatinine ratio. Her result was OK and they passed our medical

 

[BabaGod]

you can be sure of the cost but I can assure you, My wife is in the same situation as you. she has not had any flare since we came to Canada. and she sees her Rheumatologist 2wice every year if need be. Health is free in Canada but you may have to pay for your prescription drugs after exhausting your deductible. if you get a good job, all these could be covered for you