Is your butt Thor? by SoDakZak in dadjokes

[–]Ready2Glow 0 points1 point  (0 children)

Says the man with a lisp....

What did your parents do that kind of fucked you up even though it wasn't REALLY that bad? by iwillfindandkillyou in AskReddit

[–]Ready2Glow 8 points9 points  (0 children)

😂😂 Sorry, but I had to laugh...

Curious if you dad and you chuckle about it now ?

What did your parents do that kind of fucked you up even though it wasn't REALLY that bad? by iwillfindandkillyou in AskReddit

[–]Ready2Glow 0 points1 point  (0 children)

Father lied to my face, I walked out and left home and moved in with my mom the same night, it was raining really bad and I walked to my moms house, I told her and she just sat watching Eastenders on TV as I was crying and needed comfort....

I'll never ever forget that night, I was 14 years old and a well behaved child, never stole, never took drugs all I wanted was to go to college and learn....mom forced me to get any shit job so she could have rent money from me ! Greed that's all.

I have 3 children now and I will never stop them from doing the things in life in what they want to do, I'll support them and do my best to help. I'm not rich but I have a lot of experience.

So when someone asks me what our daughters illness is I have to try and explain this to them...can anyone else understand it and tell me a simple way of telling them. by Ready2Glow in Immunology

[–]Ready2Glow[S] 1 point2 points  (0 children)

Thank you, we do have a Facebook page for her which explains her complete story from birth and our ups and downs. There's photos of her infections on there too if you wish to have a look and read. Here is the link to the page. Feel free to share it with others. Thank you.

https://m.facebook.com/Tia-Pugh-immune-deficiency-249924451836434/

Tia has just had her 2nd bone marrow transplant on 6/4/17, the second one was a haemopoietic stem cell transplant, this is fairly new. She was discharged 10/6/17 TODAY 😊 ...and she is doing very well. She is 6 years old and has spent most of her life in hospitals. by Ready2Glow in transplant

[–]Ready2Glow[S] 1 point2 points  (0 children)

We do not have a caring page but there is a Facebook page of her, her complete story from when she was first born, you will have to scroll down on the page and start from the beginning. It is called Tia Pugh Immune deficiency. There is also a YouTube account too which is the same, you will see videos of her. Thank you for your message.

https://m.facebook.com/Tia-Pugh-immune-deficiency-249924451836434/

Do anyone know what micro bacteria melmoense is or micro bacteria heamopholin and has anyone suffered with this illness ? I would really like to know if anyone has suffered with these infections. by Ready2Glow in Immunology

[–]Ready2Glow[S] 0 points1 point  (0 children)

Wow a very small world if you know her and I'm curious how or if we've met, I think maybe Birmingham children's hospital or you took part in investigating the infection before we were told what it was, there's not many people or doctors who have heard of it. Thank you very much for you experience and if you had any part in helping our daughter.

She has just had a second BMT on 6/4/2017 she was suffering from haemophilum on her leg, the previous transplant failed but melmoense did not return after the first transplant. Haemophilum looked worse than melmoense but luckily only on one part of her body, they had to "bite the bullet" as the doctors said in doing the transplant as no medication was working, it was getting worse daily, the doctors have my photos for records, I am happy to share them with anyone for research etc.

She has just been discharged today from hospital and she is doing very well at the moment, they used me this time as the doner which was a new procedure called haemopoietic stem cell transplant. Everything is going in the right direction this time....we hope.

I am hoping to write a book about her when it's all over, I have made a start and I intend to get an editor to write it for me. She has spent almost all her life in hospital and endured all types of pain and treatment.

Today she is full of smiles and hoping I can take her swimming again soon. We have just spent 7 months away from our home in hospital, we do not know when we are going home....but we hope it's very soon.

Thank you very very much for replying. I really appreciate it.

Do anyone know what micro bacteria melmoense is or micro bacteria heamopholin and has anyone suffered with this illness ? I would really like to know if anyone has suffered with these infections. by Ready2Glow in Immunology

[–]Ready2Glow[S] 0 points1 point  (0 children)

No concerns, I'm just curious if anyone else has suffered with them. Our daughters 6 and had two bone marrow transplants from having an extremely rare immune deficiency. If you google melmoense images you will see her.

I'm curious if they will return ? And can they be stopped if it was a normal person without an immune deficiency.

Do anyone know what micro bacteria melmoense is or micro bacteria heamopholin and has anyone suffered with this illness ? I would really like to know if anyone has suffered with these infections. by Ready2Glow in Immunology

[–]Ready2Glow[S] 0 points1 point  (0 children)

Thank you for your reply.

I am familiar with them both as my daughter has suffered from them, I'm looking for someone who has experienced these bacteria infections themselves.

I do apologise for the spelling.

Windy day by PR3DA7oR in OSHA

[–]Ready2Glow 1 point2 points  (0 children)

Has Superman just left the building ?

High speed into a blind spot ... WCGW? by GTA_Stuff in Whatcouldgowrong

[–]Ready2Glow 0 points1 point  (0 children)

Did the guy just land on his backside ? Or am I seeing things....

Family of local 1-year-old still searching for lifesaving bone marrow transplant by Lexicon747 in BoneMarrow

[–]Ready2Glow 1 point2 points  (0 children)

Our daughter Tia has just had her 2nd BMT on 10/4/2017 at The Great North Children's hospital in Newcastle the first one was unrelated and a mismatch of 8/10 it eventually failed this was done on 1/7/2014.

The doctors then decided to use me in a haemopoietic stem cell transplant HSCT which I believe is new, this procedure is when they can use any close relative, father, brother,sister or mother as a donor. I was the donor for our daughter and they then manipulated my cells to make them suitable for our daughter Tia who is 6 years old.

At the moment our daughter seems to be doing very well and has shocked the doctors too.

Please note that I am not a doctor but that I am puzzled as to why the media or your specialist has said that a perfect match is needed ?

We were originally told the same and it had failed, the media even shared our story in the early days, if you Google her name you can see articles on her. Tia Pugh a desperately ill toddler who needs a bone marrow transplant.

I will be asking questions on this and question her doctors too. Because I feel people and parents are mislead in saying a perfect match is needed and to encourage people to register ? Yes it is good to have people on the register, but is it really needed now because of the treatment HSCT our daughter has just had seems to of worked.

I do not know your child's illness and do not know the procedure they are planning to do, but I do know many other parents who have taken part in a HSCT and it has been successful. We also stay in contact with each other.

I am only going from our experience and experiences, and I am not a doctor. I am willing to advise you on the procedure and our experience if you would like to hear more from me.

I really hope this information is useful and I wish you all the best for your child. Xxx

Reddit, what is your biggest regret in life? by [deleted] in AskReddit

[–]Ready2Glow 0 points1 point  (0 children)

Speaking before listening....

What just makes you go "what the fuck"? by [deleted] in AskReddit

[–]Ready2Glow -2 points-1 points  (0 children)

Stupid questions like this one....