I’ve kinda always had a high white blood cell count, but since I’ve been complaining about fatigue for a while now, my MD referred me to the hematologist oncology department at my local hospital, and my appointment is tomorrow. The timing of seeing this is incredible!!! Thank you!
@@Kattykat63 Apologies I didn’t see this earlier! My bloodwork didn’t raise any issues with that department, thank goodness. So even though my count was rated as high, it would have to be 10x high to be suspect of cancer. Thanks goodness!!!! I haven’t solved the fatigue issue, but what a blessing to I be cancer free. Thank you so very much for your concern!! I also had a radial scar excised from my left breast, and the pathology came back on that, which also cancer-free! I feel like I dodged a bullet here.
I was ecstatic when my wbc hit 50,000. I was at 249,000 when i was first diagnosed. At 4000 now after 1 and a half months of obinutuzimab and venetoclax. Keep fighting, and i hope you are well. I am blessed to be in the care of the Wilmot Cancer Center's CLL team, and they are up to date with the newest treatments available.
My husband was diagnosed with CLL a year ago (uk) the haematologist was brilliant and explained everything. I’m always astounded that in the USA, you have to find your own doctors. It’s such a tough time anyway you kind of need people to tell you how/why things are happening. We were told watch and wait…and my husband has bloods taken every 3 months and is doing brilliantly. Such a lovely lady with some excellent advice.
As soon as I heard you say, "Let's get aggressive", I wanted to scream at you, NO!! My blood count has been consistently high also, not by much, and I said to my doctor, we have to do something right away. He said, "Why would you want treatment that will kill your immune system, if you really may never need it. We will watch it and wait". I'm so glad he said that, because all of my research is saying the same thing. I would go back to your doctor and say something. That was just wrong of them. You can have a super high white blood count and still not need chemo if all of the other pieces of the CLL puzzle aren't there.
I have a tentative diagnosis of CLL, finding out exactly on Jan 11. I hope and pray if I have leukemia, this is the one. This video was most informative.
Wow did I need to hear this today. Just diagnosed with CLL/SLL at the age of 54. Really tanked two years ago with progressive spine pain multi level cord compression and rising lymphocyte counts. In the process of getting worked up with regard to lymphoma, on my second hematologist already because the first doctor did no history and no physical. I just knew that wasn’t right. Oncology workup and Neurosurgery workup simultaneously and Im scared. Im scared in so much pain andI m too exhausted to function. I need a good team. Good luck everyone ❤
I have mantle cell lymphoma. It can't be cured and has a short life expectancy. I took chemo for 8 months and had a pet scan and was told I need more chemo, radiation, and a bone marrow transplant. That would give me 10 to 15 months. Otherwise I had less than 6 left. I went ho.e and started eating apricot seeds and walking and praying a lot. That was 5 years ago now. I still have lots of pain, but I enjoy life. My oncologist recently did blood work and instead of giving me a short sentence, said my cancer has turned into cll, and my count is only 10000. She also said she doesn't understand how that happened that it shouldn't go backwards like that,but it has. Don't be scared, don't give up. Honestly, I am at peace with the lord and dying. I did, for how I felt give in to what they said and didn't expect to live. But all of this happened over 5 years ago and I'm still living life. May God give you peace and bless you.
Hi, how do you feel after 6 months? I just got my diagnosis....so I'm just taking it in...and I try to gather information. I live in sweden and we have excellent healtcare over here......but I have had to reconsider my future plans....I had a dream of moving to a warmer climate....But if that means that the treatment would be dried bat wings and spider web, then I may have to stay put.
@@scottcummings8074Hi Scott, glad to hear your great news! Could you tell me how many apricot seeds you would take and if it was daily, weekly, and do you still take them. Very much appreciated and may you continue to be in good health.
@@ASpectacular3777 sorry I didn't see this sooner. I started out eating 2 in the morning and 2 in the evening. I increased 1every dose for a couple weeks until I was taking 25 a day. You want to start slow so you can stop if it kills the cancer cells to fast. After a couple months I cut back down to 8 to 12 a day. If I feel worse like my counts are going up ill increase the seeds for a while. By doing this and just going by how I feel I've controlled my lymphoma for close to 6 years now. I suggest doing your own research and deciding for yourself on what treatments you want to take. I have stage 4 mantel cell lymphoma and clls. To me choosing apricot seeds over being put into a choma for more chemo, radiation, and a bone marrow transplant just to live 10 to 15 months more was not much of a choice. But I can say I made that decision over 5 years ago and have hardly seen a dr since. I just don't want to cause someone to avoid a dr when there might be a possible cure for their cancer. There was not for mine though.
I am a 75 year old male with stage 3 non Hodgkin’s Lymphoma. I am looking for an appropriate support group. Any ideas or suggestions would be appreciated
I was diagnosed with CLL three weeks ago. I have felt tired at work the last few years, but now I got the answer why I lacked the extra supply of energy. They are very understanding where I work which is great.
Your story is terrific, I actually live in Louisville and I go to Doctor Stevens so that makes me feel so much better! Thank you for posting this! Chris N.
What An Incredible Story And An Incredible Lady ❤🙌. I LOVE YOUR HAIR!!! Congratulations On The Adoptions Of Your Two Amazing Boys 🙏💙🩵!!! What A Gift For Them AND You And Your Husband 💕🎉!!! May You ALL Grow Old Together!!!
Wow What a great lady you are Hannah honestly you spoke the language and brought this cancer to the Ask the questions! Instinct matters. Have a specialist work with your Doctors. Thankyou for sharing.
I have cll and was in watch and wait for 2 years and that is not better. I had 2 years of stress. Once it progressed and my white count was very high I went into 6 months chemo. I could have stopped after 4 months but I wanted full treatment. I also never had a bone marrow test just lymph removal biopsy. I like how my oncologist handled it and still like him .
I saw Dr Stevens for the first time yesterday, due to your video, and will keep your Cincy expert, Dr Berg, in mind for the future. Thank you for Dr Stevens name. I live in your town, too, and was very happy with his whole practice. Being newly diagnosed, there may be a long road ahead. I’ve got an excellent start. Thank you!
God is trying to get your attention. He is there, with you, patiently waiting for you to reach out to Him! It's going to be OK my friend, you can do this!!! 💪 ❤ 🙏
I was told by my Dr that I had leukemia 8 years ago but I still do t feel sick until about 5 months ago stomic hurts and hard to use the bathroom all kinds of things the list goes on and I'm a single father of two wonderful kids and the mother left us over 8 years ago and started a whole new family dnt pay child support or anything or even see them I'm just scared of leaving them alone I work 6 days aweek started to get to me now idk what to do I have to figure something out to stay for them they are my world ill work every day even when I'm sick, no matter what
Sadly I don't think it's about deserving but affording for a lot of people and things like dealing with insurance and transportation can be big barriers . I like what you said about CLL being aggressive but science being aggressive to counter it and I'm glad you hung in there !
We would love to hear your questions! If you sign up here: www.thepatientstory.com/newsletter/ we can get a better idea of what your looking for and help you answer any questions!
@@davewagner5408 great and thank you,ok here it is I have positive CD marks and no one will tell me what to look for cd3, cd5 cd20 cd79a cd23 and pax5 Bcl2,I have been told not to worry about it by a doctor so can you help
I'm not sure what those numbers mean,Kim. My oncologist told me I had,CLL and SLL. The only other thing I remember was she told me I was a deletion 13,which was better than deletion 17. I can't explain what it means exactly,but it was something to do with the genetics of the cancer cells. I agreed to immunotherapy,a form of chemotherapy that helps your body kill the cancer cells itself. I had 10 infusions of Obinatuzomab,excuse any wrong spelling,and one year is oral Venetoclax. 4 pills,once a day. It worked wonders for me. My wbc was 58000 when diagnosed and with steroids it was brought down to 20000. Then the chemo reduced it to 6000 after one infusion. It's not been above 8000 since. And I felt pretty good throughout the whole thing. Other than being very tired. Never lost hair and wasn't sick one time. Don't be scared of immunotherapy. I don't know where you live,but I'm in Pennsylvania,Milton Hershey medical center treated ne,the doctor was great. Hope this helps. Please ask if I can answer anything else for you. I'm happy to help. Good luck
✔Emotional testimony is good, but we would like rational elements : how many "white blood cells? what was his blood pressure,? the number of his heartbeats? finally as many concrete numerical elements within the reach of the patient in 2023 !
The leukemic cells are not just in your blood. They're in your bone marrow too. They can do a stem cell or bone marrow transplant to cure some forms of leukemia but, unfortunately, there is no cure for CLL.
![Noob To Max With DRAGON REWORK In Blox Fruits [FULL MOVIE]](http://i.ytimg.com/vi/LnBMOinoOvA/mqdefault.jpg)
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EMZL patient stories
I’ve kinda always had a high white blood cell count, but since I’ve been complaining about fatigue for a while now, my MD referred me to the hematologist oncology department at my local hospital, and my appointment is tomorrow. The timing of seeing this is incredible!!! Thank you!
Praying for healing for you. In Jesus's name I pray. AMEN
Many blessings for healing!! Stay positive
How did you're appointment go, did you get any answers?
Any update? What happened?
@@Kattykat63 Apologies I didn’t see this earlier! My bloodwork didn’t raise any issues with that department, thank goodness. So even though my count was rated as high, it would have to be 10x high to be suspect of cancer. Thanks goodness!!!! I haven’t solved the fatigue issue, but what a blessing to I be cancer free. Thank you so very much for your concern!! I also had a radial scar excised from my left breast, and the pathology came back on that, which also cancer-free! I feel like I dodged a bullet here.
I was ecstatic when my wbc hit 50,000. I was at 249,000 when i was first diagnosed. At 4000 now after 1 and a half months of obinutuzimab and venetoclax. Keep fighting, and i hope you are well. I am blessed to be in the care of the Wilmot Cancer Center's CLL team, and they are up to date with the newest treatments available.
I was on the same meds myself,3 years ago. They worked wonders for me immediately,and with almost no side affects.
Such a beautiful human being she is . Living with any disease is hard but dealing with a chronic condition is worse
My husband was diagnosed with CLL a year ago (uk) the haematologist was brilliant and explained everything. I’m always astounded that in the USA, you have to find your own doctors. It’s such a tough time anyway you kind of need people to tell you how/why things are happening. We were told watch and wait…and my husband has bloods taken every 3 months and is doing brilliantly. Such a lovely lady with some excellent advice.
I'm in Mexico, I need to guess where to go, guessing. Here a real Public health system is practically inexistent.
As soon as I heard you say, "Let's get aggressive", I wanted to scream at you, NO!! My blood count has been consistently high also, not by much, and I said to my doctor, we have to do something right away. He said, "Why would you want treatment that will kill your immune system, if you really may never need it. We will watch it and wait". I'm so glad he said that, because all of my research is saying the same thing. I would go back to your doctor and say something. That was just wrong of them. You can have a super high white blood count and still not need chemo if all of the other pieces of the CLL puzzle aren't there.
I have a tentative diagnosis of CLL, finding out exactly on Jan 11. I hope and pray if I have leukemia, this is the one.
This video was most informative.
I was diagnosed with CLL April 2000.
Wow did I need to hear this today. Just diagnosed with CLL/SLL at the age of 54. Really tanked two years ago with progressive spine pain multi level cord compression and rising lymphocyte counts. In the process of getting worked up with regard to lymphoma, on my second hematologist already because the first doctor did no history and no physical. I just knew that wasn’t right. Oncology workup and Neurosurgery workup simultaneously and Im scared. Im scared in so much pain andI m too exhausted to function. I need a good team. Good luck everyone ❤
I have mantle cell lymphoma. It can't be cured and has a short life expectancy. I took chemo for 8 months and had a pet scan and was told I need more chemo, radiation, and a bone marrow transplant. That would give me 10 to 15 months. Otherwise I had less than 6 left. I went ho.e and started eating apricot seeds and walking and praying a lot. That was 5 years ago now. I still have lots of pain, but I enjoy life. My oncologist recently did blood work and instead of giving me a short sentence, said my cancer has turned into cll, and my count is only 10000. She also said she doesn't understand how that happened that it shouldn't go backwards like that,but it has. Don't be scared, don't give up. Honestly, I am at peace with the lord and dying. I did, for how I felt give in to what they said and didn't expect to live. But all of this happened over 5 years ago and I'm still living life. May God give you peace and bless you.
PTL!
Hi, how do you feel after 6 months? I just got my diagnosis....so I'm just taking it in...and I try to gather information. I live in sweden and we have excellent healtcare over here......but I have had to reconsider my future plans....I had a dream of moving to a warmer climate....But if that means that the treatment would be dried bat wings and spider web, then I may have to stay put.
@@scottcummings8074Hi Scott, glad to hear your great news! Could you tell me how many apricot seeds you would take and if it was daily, weekly, and do you still take them. Very much appreciated and may you continue to be in good health.
@@ASpectacular3777 sorry I didn't see this sooner. I started out eating 2 in the morning and 2 in the evening. I increased 1every dose for a couple weeks until I was taking 25 a day. You want to start slow so you can stop if it kills the cancer cells to fast. After a couple months I cut back down to 8 to 12 a day. If I feel worse like my counts are going up ill increase the seeds for a while.
By doing this and just going by how I feel I've controlled my lymphoma for close to 6 years now.
I suggest doing your own research and deciding for yourself on what treatments you want to take. I have stage 4 mantel cell lymphoma and clls. To me choosing apricot seeds over being put into a choma for more chemo, radiation, and a bone marrow transplant just to live 10 to 15 months more was not much of a choice. But I can say I made that decision over 5 years ago and have hardly seen a dr since. I just don't want to cause someone to avoid a dr when there might be a possible cure for their cancer. There was not for mine though.
I am a 75 year old male with stage 3 non Hodgkin’s Lymphoma. I am looking for an appropriate support group. Any ideas or suggestions would be appreciated
Non-hodgkins lymphoma support
So sorry we missed this! The Leukemia & Lymphoma Society has a great peer to peer resource: www.lls.org/support-resources/peer-peer-support
CLL Support group on Facebook
I was diagnosed with CLL three weeks ago. I have felt tired at work the last few years, but now I got the answer why I lacked the extra supply of energy. They are very understanding where I work which is great.
Your story is terrific, I actually live in Louisville and I go to Doctor Stevens so that makes me feel so much better! Thank you for posting this! Chris N.
Oh wow. My husband has CLL and I am so sorry you were with that doctor.
I was diagnosed in 2019. Still on w&w. I look forward to treatment. I feel so tired legs so weak.
I’m still w and w also. I need 11 to 14 hours a day….
Sleep…
I'm so glad you are in such good hands now, you seem like an amazing person. I hope you can enjoy your life and live it to the fullest!
10 yrs of W&W for me , WBC @ 182 , A symptomatic but not sure if the aching bones is age(62) or CLL , informative vid -good story
Diagnosed at 51 with CLL. No symptoms, praying I'm one that never needs treatment, its scary and stress inducing. I am grateful for these videos.
What An Incredible Story And An Incredible Lady ❤🙌. I LOVE YOUR HAIR!!! Congratulations On The Adoptions Of Your Two Amazing Boys 🙏💙🩵!!! What A Gift For Them AND You And Your Husband 💕🎉!!! May You ALL Grow Old Together!!!
Wow What a great lady you are Hannah honestly you spoke the language and brought this cancer to the Ask the questions! Instinct matters. Have a specialist work with your Doctors. Thankyou for sharing.
Such a helpful and hope full interview. Thank you!
I have cll and was in watch and wait for 2 years and that is not better. I had 2 years of stress. Once it progressed and my white count was very high I went into 6 months chemo. I could have stopped after 4 months but I wanted full treatment. I also never had a bone marrow test just lymph removal biopsy. I like how my oncologist handled it and still like him .
CLL starts in the bone marrow so the test would be pointless.☹️
I saw Dr Stevens for the first time yesterday, due to your video, and will keep your Cincy expert, Dr Berg, in mind for the future. Thank you for Dr Stevens name. I live in your town, too, and was very happy with his whole practice. Being newly diagnosed, there may be a long road ahead. I’ve got an excellent start. Thank you!
I have leukemia cll, and it destroyed me mentally. I battle with anxiety and depression every day. I also developed white coat syndrome😢
So sorry to hear that! We are thinking about you here at The Patient Story!
I have cll for 4years l had chemotherapy, and other medications. Now lam on ibrutinib capsules not bad on me, But very expensive.
try cannabis
God is trying to get your attention. He is there, with you, patiently waiting for you to reach out to Him! It's going to be OK my friend, you can do this!!! 💪 ❤ 🙏
@@cornyconnie. 🙏🏼🙏🏼🙏🏼😊
I was told by my Dr that I had leukemia
8 years ago but I still do t feel sick until about 5 months ago stomic hurts and hard to use the bathroom all kinds of things the list goes on and I'm a single father of two wonderful kids and the mother left us over 8 years ago and started a whole new family dnt pay child support or anything or even see them I'm just scared of leaving them alone I work 6 days aweek started to get to me now idk what to do I have to figure something out to stay for them they are my world ill work every day even when I'm sick, no matter what
I’m praying for you❤️
Sadly I don't think it's about deserving but affording for a lot of people and things like dealing with insurance and transportation can be big barriers . I like what you said about CLL being aggressive but science being aggressive to counter it and I'm glad you hung in there !
It amazes me how doctors can become so numb to the point that they have no human compassion.
good doctors never become numb... just find someone else!
Your right lam on ibrutinib capsules but it very expensive.
Shes right...find the best
I go to Dr. Kommor in Louisville. He is a cll specialist.
Thank you🤗
2:35 "I can't, I don't have time." 😂😅
They rush in and out. They hardly listen. Too absorbed with their computer. They don’t want to give you time.
I have questions but no one will answer them and the more I look on line
We would love to hear your questions!
If you sign up here: www.thepatientstory.com/newsletter/ we can get a better idea of what your looking for and help you answer any questions!
I will gladly answer any questions I can. I'm a survivor,3 years in remission.
@@davewagner5408 great and thank you,ok here it is I have positive CD marks and no one will tell me what to look for cd3, cd5 cd20 cd79a cd23 and pax5 Bcl2,I have been told not to worry about it by a doctor so can you help
@@davewagner5408 thank you,will here it goes I have positive CD marks cd3 cd5 cd20 cd79a cd23 and pax5 Bcl2 so what to look for
I'm not sure what those numbers mean,Kim. My oncologist told me I had,CLL and SLL. The only other thing I remember was she told me I was a deletion 13,which was better than deletion 17. I can't explain what it means exactly,but it was something to do with the genetics of the cancer cells. I agreed to immunotherapy,a form of chemotherapy that helps your body kill the cancer cells itself. I had 10 infusions of Obinatuzomab,excuse any wrong spelling,and one year is oral Venetoclax. 4 pills,once a day. It worked wonders for me. My wbc was 58000 when diagnosed and with steroids it was brought down to 20000. Then the chemo reduced it to 6000 after one infusion. It's not been above 8000 since. And I felt pretty good throughout the whole thing. Other than being very tired. Never lost hair and wasn't sick one time. Don't be scared of immunotherapy. I don't know where you live,but I'm in Pennsylvania,Milton Hershey medical center treated ne,the doctor was great. Hope this helps. Please ask if I can answer anything else for you. I'm happy to help. Good luck
✔Emotional testimony is good, but we would like rational elements :
how many "white blood cells?
what was his blood pressure,?
the number of his heartbeats?
finally as many concrete numerical elements within the reach of the patient in 2023 !
Definitely the right decision to see a different Dr. Claims to be the 'local expert' but can't answer basic questions on the treatment plan? Yeeesh...
Why don’t they just clean your blood? Take it out , remove the WBC, re inject clean blood, etc…
The leukemic cells are not just in your blood. They're in your bone marrow too. They can do a stem cell or bone marrow transplant to cure some forms of leukemia but, unfortunately, there is no cure for CLL.
🙏 ❤️ 🙏
🤍
Red flag doctor - so terrible! Lesson to listen to your instinct and advocate for yourself! So sorry you had this experience